CA1305271C - Photochromic articles - Google Patents
Photochromic articlesInfo
- Publication number
- CA1305271C CA1305271C CA000536229A CA536229A CA1305271C CA 1305271 C CA1305271 C CA 1305271C CA 000536229 A CA000536229 A CA 000536229A CA 536229 A CA536229 A CA 536229A CA 1305271 C CA1305271 C CA 1305271C
- Authority
- CA
- Canada
- Prior art keywords
- photochromic
- oxazine
- article according
- spiro
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/72—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/20—Spiro-condensed systems
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/685—Compositions containing spiro-condensed pyran compounds or derivatives thereof, as photosensitive substances
Abstract
ABSTRACT
PHOTOCHROMIC ARTICLES
A plastic organic photochromic article, typically a lens such as an ophthalmic lens or a window such as a vehicle roof light, comprising a plastics host material having a photochromic compound incorporated therein or applied thereto, the article exhibiting the following properties, measured at Air Mass 2 at 25°C:
(a) an integrated visible transmission in the faded state (B.IVT) ranging from 90 to 25%, (b) an integrated visible transmission in the darkened state (D.IVT) ranging from 1 to 50X, preferably 4 to 30X, (c) the rate of darkening of the article when it is exposed to actinic radiation is such that 88X of the darkening range is achieved in 30 seconds or less, i.e. T88 ? 30 secs, (d) the rate of fading of the article from its fully darkened condition is such that more than 60% of the optical density range is recovered in 60 seconds, i.e. % ODG-1 ? 60%, and (e) the induced optical density of the article, i.e. the change in the optical density of the article, in moving from the faded state (B.IVT) to the darkened state (D.IVT), is greater than 0.45 Typically, the photochromic compound is a spiro-oxazine compound of general formula (II),
PHOTOCHROMIC ARTICLES
A plastic organic photochromic article, typically a lens such as an ophthalmic lens or a window such as a vehicle roof light, comprising a plastics host material having a photochromic compound incorporated therein or applied thereto, the article exhibiting the following properties, measured at Air Mass 2 at 25°C:
(a) an integrated visible transmission in the faded state (B.IVT) ranging from 90 to 25%, (b) an integrated visible transmission in the darkened state (D.IVT) ranging from 1 to 50X, preferably 4 to 30X, (c) the rate of darkening of the article when it is exposed to actinic radiation is such that 88X of the darkening range is achieved in 30 seconds or less, i.e. T88 ? 30 secs, (d) the rate of fading of the article from its fully darkened condition is such that more than 60% of the optical density range is recovered in 60 seconds, i.e. % ODG-1 ? 60%, and (e) the induced optical density of the article, i.e. the change in the optical density of the article, in moving from the faded state (B.IVT) to the darkened state (D.IVT), is greater than 0.45 Typically, the photochromic compound is a spiro-oxazine compound of general formula (II),
Description
13052~1 PHOTOCHROMIC ARTICLES
FIELD OF THE INVENTION
The present invention relates to photochromic articles, particularly to articles having organic photochromic material in a plastic matrix, 5 for example photochromic ophthalmic lenses and windows such as vehicle roof lights.
DESCRIPTION OF THE PRIOR ART
10 Photochromism is a reversib1e physical phenomenon which is observed with certain classes of chemical compounds which are found to change colour when they are exposed to actinic light and which return to their original colour when they are removed from the influence of the actinic radiation.
Plastic organic photochromic lenses are known and have been described, for examp1e, in U.S. Patent 4215010, European Patent Application No.
0141407, U.K. Patent Application No. 2117390 and Wbrld PCT Patent Application No. 85/02619, These patent specifications describe a 20 var~ety of sp~ro-oxazine compounds which have been found to be suitable for incorporation into a polymerised host material thereby ~mparting photochromic propert~es to the host material.
Plastic organic photochromlc windows are known and have been 25 described, for example in U.S. Patent 3508810 which describes a photochromic window having a photochromic spiro-pyran incorporated into a polyvinyl butyral interlayer between sheets of glass.
SUMMARY OF THE INVENTION
We have now produced plastic organic photochromic articles having a denser colouring in their darkened conditlon than previously known plastic organic photochromic articles.
'" ' ' - 130~Z~l ' Accordingly, the present invention provides a plastic organic photochromic article comprising a plastics host materia1 having a photochromic compound incorporated therein or applied thereto, the article being characterised in that it exhibits the following 5 properties, measured at Air Mass 2 at 25C:
(a) an integrated visible transmission in the faded state (B.IVT) ranging from 90 to 25~, lO (b) an integrated visible transmission in the darkened state (D.IVT) ranging from l to 50%, preferably 4 to 30~, (c) the rate of darkening of the article when it is exposed to actinic radiation is such that 88X of the darkening range is achieved in 30 seconds or less, i.e. T88 ~ 30 secs, (d) the rate of fading of the article from its fully darkened condition is such that more than 60~ of the optical density range is recovered in 60 seconds, i.e. ~ ODG-l >~ 60~, and (e) the lnduced optical density of the article, i.e. the change in the optical density of the article, in moving from the faded state (B.IVT) to the darkened state (D.IYT), ls greater than 0.45.
Throughout this specification the term "integrated visible transmission" or IVT is used to mean the weighted average transmission taking into account the emission from the source SA (in this case Illum~nant C ~dayl1ght) as defined by the International Commission of 30 Lighting CIE 1964) and the sensitivity of the detector DA (in this case as defined by the CIE 1964 standard colourimetric observer).
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DETAILED DESCRIPTION OF THE INVENTION
We ha~e found in particular that photochromic articles having such dense colouring can be obtained by applying to or incorporating within 5 a solid transparent plastic host material a photochromic compound represented by the general formula (I):
~Rl~n ~R7 , (1) R4 ~R23m wherein n is an integer of 1 to 4, and m is 1, 2 or 3, each of Rl and R2 independently represents (i) a hydrogen atom or an amine functionality of genera1 formula -NR'R " , whereln each of R' and R "
independently represents a hydrogen atom or an alkyl, cycloalkyl or 25 phenyl group or a subst~tuted derivative thereof, or an amine functionality which is a cycloheteroalkyl ring or a substituted cycloheteroalkyl ring which ring includes one or more heteroatoms, (~l) a group of formula -R, -OR, -SR, -COR, or -COOR wherein R
represents H, alkyl, aryl or heteroaryl, (iii) -X, -CH2X, -CHX2, -CX3 wherein X represents halogen, or (iv) -NO2, -CN, -SCN, with the proviso that r~ng A ls always subst.ituted at the 6' position by a group R2 which is an amine-func~lonality as def~ned above;
R4 represents -H, alkyl, alkenyl, phenyl, phenyla1kyl, mono-, di- or tri-substituted phenyl or alkoxy, , . . .
, :
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each of Rs and R6 independently represents -H, alkyl, alkenyl, phenyl, phenylalkyl such as benzyl, mono-, di- or tri-substituted phenyl, or Rs and R6 together represent an alicyclic ring including spiro carbons, norbornane, and adamantane, R3 represents a hydrogen atom, or an alkyl, aryl or heteroaryl group, R7 is as defined for Rl and R2 above, or is a ring system fused to ring A, which ring system may incorporate aromatic and/or alicyclic 10 rings, the said ring system optionally carrying one or more substituents R8, the substituent R8 being as defined above for Rl and R2, and Ring B may optionally contain one or more ring nitrogen atoms.
The terms "aromatic" and "alicyclic" used herein should be interpreted to include hetero-aromatic and hetero-alicyclic systems.
:i ' Preferably, the photochromic spiro-oxazine compounds of generalformula (I) are spiro-oxazines of the formula (II) below:
~, ~
R5 R6 R3 (R1o)q (Rl~n~ (Il) 30 ~Rg)p ,, , ' ~, , , :
, "j :
~:
,~
,' ~".:,, . ~, .
,~ , .
- s -wherein each of Rl, Rg and Rlo independently represents (i) a hydrogen atom or an amine functionality of general formula -NR'R " , where each o~ R' and R " independently represents a hydrogen atom or an alkyl, cycloalkyl or phenyl group or a substituted derivative thereof, or an 5 amine functionality which is a cycloheteroalkyl ring or a substituted cycloheteroalkyl ring, which ring includes one or more heteroatoms, (ii) a group of formula -R, -OR, -SR, -COR, or -COOR wherein R
represents H, alkyl, aryl or heteroaryl, (iii) -X, -CH2X, -CHX2, -CX3 wherein X represents halogen, or (iv) -N02, -CN, -SCN: with the 10 proviso that the group (Rg)p always includes an amine-functionality as defined immediately above at the 6'-position, n is an integer of l to 4, p is l or 2, q is l, 2 or 3, and ~X- and zY- each independently represents ~ N or \/ C-Rlo wherein Rlo is as def~ned above, and R3, R4, Rs and R6 are as defined above for formula (I).
For convenience, the structural formula (II) depicted above shows the -X~ group in the 7'-posit~on of the molecule and the ~Y- group in the 7-pos~t~on, but ~t should be noted that the -X~ group can equally well be located at the 8', 9' or lO' - position of the molecule and the =Y-group can equally well be located at the 4 , 5 , or 6 -position in addition to, or in place of, the depicted position.
In this specificat~on the term "lower a1kyl" is intended to mean an alkyl group of from 1 to 8 carbon atoms.
The group R3 is preferably a hydrogen atom, ' ,~' ".
SZ~
For the avoidance of doubt, when the substituents Rl, R2, Rg or Rlo represent an amine functionality which is a substituted cycloheteroalkyl ring as defined above, the substituent on the said cycloheteroalkyl ring can take the form of a system of one or more further rings fused to the cycloheteroalkyl ring, which ring system may incorporate saturated and/or unsaturated rings. Typical examples of such a substituted amine functionality include a tetrahydroisoquinoline substituent of formula --N~
: or an indoline substituent of formula ~
or a hexahydrocarbazole substituent of formula ' ~O ' C~
:
~.-!i, :
.' ~ .. ,,..~, ,;,-," :, ~, `` 1305Z71 Preferred photochromic materials for incorporation into or application to the plastic host material are compounds of general formula (II) in which n is 1 and Rl is a hydrogen atom, or a 5-alkoxy substituent, preferably 5 methoxy, or a 5-halogen substituent, preferably a 5 5-chloro substituent; R3 is a hydrogen atom; each of R4, R~ and R6 is an alkyl group, preferably methyl; p is 1 and Rg for example is a 6'-piperidino, 6'-morpholino, 6'-N-methylpiperazino, 6'-N-phenylpiperazino, 6'-tetrahydroisoquinolino, 6'-indolino, 6'-thiomorpholino, 6'-homopiperidino, 6'-(1,2,3,4,4a,9a-10 hexahydrocarbazolino, or 6' aziridino substituent; q is 1 and Rlo is ahydrogen atom or an 9'-alkoxy substituent, preferably 9'-methoxy; X is -CH= or -N= located in the 7' position; and Y is -CH= or -N=.
Particularly preferred compounds of general formula (II) are 15 6'-indolino-1,3,3-trimethylspiro ~indoline-2,3'-3H-naphtho[2,1-b][1,4]
oxazine] of formula CH3 C~3 CH3 ~
and 5-methoxy-6'-morpholino-1,3,3-trimethylspiro [indoline-2,3'-3H-naphtho~2,1-b]~1,4] oxazine] of formula 1`3~
The novel photochromic compounds of formula (II) may be prepared by a general preparative method based on the following reaction scheme:
NO
HO ~ ( IVa) R R6 ~ ~ (RlO)q ~Rl~n ~= (Rg) p R4 10 q (R9)p ( I \l ) (R~ R10)q : ~ R4 ( I I ) Th1s methot 1s based on the react~on of an a-n~tro B-naphthol derlvat~ve w~th a 2-methylene~ndole compound such as descr~bed in U.S.
Patent No. 3578602.
, : , ~' The compounds of general ~ormula (I) may be prepared by a s~m~lar process, us1ng the correspondlng start~ng mater~als.
,. ~,,,~, ,, - ~
"., "
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.
,, . - , . .
~ : . , . : -.~, ~ . .
.
130~ ~'3.
In order to prepare the compounds of formula (II), the appropriate nitroso-hydroxy derivative of formula (IY) is reacted with the appropriate indoline of formula (III). Alternatively, an indolenium salt, such as a methiodide, can be used instead of the indoline of 5 formula (III).
The t~o starting materials are generally reacted together by refluxing in a solvent such as trichloroethylene or toluene. If an indolenium salt is used, a base such as the triethylamine should be present. The lO desired spiro-oxazine product is separated and purified by conventional techniques such as chromatographic separation and crystallisation.
Examples of suitable plastics host materials are optically clear plastics selected from polymers of polyol(allyl carbonate)-monomers, polyacrylates, poly(alkylacrylates) such as polymethylmethacrylates, cellulose acetate, cellulose triacetate, cellulose acetate propionate, cellulose acetate butyrate, poly(vinyl acetate), poly(vinyl alcohol), polyurethanes, polycarbonates, polyethylene terephthalate, polystyrene, poly(styrene methylmethacrylate) copolymers, poly(styrene acrylonitrile) copolymers, and polyvinylbutyral. Transparent copolymers and blends of the transparent polymers are also suitable as host mater1als.
Preferably, the host mater1al is an optically clear polymerized organic mater1al such as tr1ethylene glycol dimethacrylate (TEGDM) or di~thylene ~lycol bi~(allyl carb6~ate). , ~
, The photochromic spiro-oxaz1ne compounds of formula (ll may be applied to or incorporated in the plast1c host mater1al by any of the convent10nal methods known ~n the art, for example by the methods exempl1f1ed in European Patent Spec1f1cat10n No. 141407, TypicallY, ~a~
130SZ:71 such methods include dissolving or dispersing the photochromic compound in the host material. The photochromic compound may be dispersed into the host material by "imbibition", i.e. diffusion of the photochromic compound into the host material by a suitable 5 transfer mechanism such as immersion, thermal transfer or vapour phase transfer.
In addition, when the plastic host material is one which is formed from a highly reactive polyfunctional monomer the photochromic lO compounds can be incorporated in the plastic 'nost material by a direct casting process as described in our published European Patent Application Nb. 0227~37. This direct casting process uses a highly reactive polyfunctional monomer and a low catalyst concentration in order to prevent degradation of the spiro-oxazine compound; the process 15 comprises incorporating into a mixture comprising a highly reactive polyfunctional monomer and 0.01 to 1~J by weight, based on the volume of the monomer, of a polymerisation catalyst, O.OS to 5~ by weight, based on the volume of the monomer, of a photochromic spiro-oxazine compound; introducing the resultant polymerisable composition into a ~ould, and curing the composition to form the shaped synthetic plastic artic1e.
Typica11y a p1astic lens is formed by using a conventional direct casting process in which the polymer~sab1e composit10n ~ncorporating the photochromic spiro-oxazine compound is introduced into a mould and is then cured by heating. Suitable curing conditions are, for example, heating at a temperature ranging from room temperature to 100C, generally over a period of about 5 'nours. A typical cur1ng schedule is to subject the material to be cured to a temperature be~inning at 40C r1sing up to a temperature within the range 80 -90C over a per~od of about 5 hours.
~, , ~ ,:
~ ~, i , -,~ , ' -130S2'71 The highly reactive polyfunctional monomers used in the said direct casting process are preferably methacrylates or acrylates of linear or branched aliphatic or aromatic liquid polyols such as glycols or bisphenols. Examples of specific monomers include ethylene glycol 5 dimethacrylate or diacrylate and the corresponding dimethacrylates or diacrylates of di-, tri- and tetra-ethylene glycol; the dimethacrylates of 1,2-propyleneglycol, of 1,2-dipropylene glycol, of 1,2-tripropylene glycol and of 1,3-butylene glycol; dimethacrylates of propanediol, butanediol, hexanediol and decanediol; trimethylol ethane 10 trimethacrylate, ~rimethylol propane trimethacrylate, pentaerythritol trimethacrylate, ~,2,4-trimethyl-1,3-pentanediol dimethacrylate and 1,4-cyclohexanediol dimethacrylate.
Mixtures of the reactive polyfunctional monomers may also be used.
The highly reactive polyfunctional monomer or monomers may be used alone or in the presence of other copolymerisable monofunctional monomers which may be added to modify the physical properties - such as impact strength, castability and tintability - of the resultant 20 polymer. The amount of co-monomer which may be added is up to 30% by we~ght, preferably 5 to 15% by weight, based on the volume of the reactive polyfunctional monomer.
Typical co-monomers are alkyl methacrylates such as cyclohexyl 25 methacrylate, n-butyl methacrylate and lauryl methacrylate, which may be added to ~mprove the impact reslstance of the finished lens;
ethoxylated bisphenol-A dimethacrylate, which is added to reduce the shrinkage which is found to occur during formation of the moulded article; and hydroxyalkyl methacrylates such as hydroxyethyl ~o methacrylate and hydroxybutyl methacrylate which improve adhesion of the po1ymer to the mould surface dùring polymer~sation.
:
Other co-monomer additives include methacryl~c acid, aryl methacrylates such as benzyl methacrylate, allyl methacrylate, ,I , ''''''''1 ~ , ", ~
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tetrahydrofurfurylmethacrylate; and polyether monoacrylates or mono-methacrylates such as ethoxyethyl methacrylate.
The catalysts used in the said direct casting process are the 5 conventional free-radical polymerisation catalysts used in the art, in particular, organic peroxides such as benzoyl peroxide and peroxydicarbonates such as isopropylperoxydicarbonate. The amount of catalyst used is kept as low as possible, and is from 0.01 to 1% by weight, based on the volume of the monomer.
1~
The amount of the photochromic compound incorporated into the plastic host material is usually of the order of from 0.05% to 5% by weight, based on the volume of the host material. However, the amount of photochromic compound is not critical and can be varied depending upon 15 the method which is used to apply or incorporate the photochromic compound. In particular, when the spiro-oxazine compound is applied to or imbibed into the surface of the article, the amount used will usually be significantly less than 0.05g by weight.
20 Art~cles ~n accordance with the present invention typically exhibit a pale colouration in the faded condition, dependant on the nature of the compound used and a purple to blue colour in the darkened cond~t~on.
25 If desired, the colour of the article can be modified with conventional water-based dyes or tints. For example, it is possible to make an art1cle which is grey or brown in its faded condition and darkens to a blue/grey colouration when exposed to sunlight.
30 The present invention is illustrated further by the following Examples.
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~ ' ' .
3(~ 7 Example 1 Preparation of 6'-indolino-1,3,3-trimethylspiro~indoline-2,3'-3H-naphtho[2,1-b] [1,4]oxazine]
l-Nitroso-2-naphthol (17.3 g; 0.1 mol) and indoline (23.8 9; 0.2 mol) were dissolved in trichloroethylene (150 cm3) by heating under reflux. A solution of 1,3,3-trimethyl-2-methyleneindoline (17.3 g;
10 0.1 mol) in trichloroethylene (100 cm3) was added dropwise over 30 min to the boiling solution. Boiling under reflux was continued for three hours.
The solvent was removed and the oil was adsorbed onto silica and 15 chromatographed in silica using ethyl acetate - light petroleum as eluant. Evaporation of the solvent gave 6'-indolino-1 ,3,3-trimethyl spiro[indoline-2,3'-3H-naphtho[2,1-b] [1,4]oxazine], mp 25~-257C, lH nmr (CDC13): ~1.36, s, (6H), 3,3-Me2; 2.77, s, (3H), NMe; 3.17, m, (2H), CH2; 3.93, m, (2H), NCH2; 6.93, s, (lH), 5'-H;
20 7.69, s, ~lH)J 2'-H.
~, Preparation of 1 ,3,3-trimethyl-6'-piperidinospiro[indoline-2,3'-3H-25 naphtho~2,1-b]~1,4]oxazine]
4-Piperidino-1,2-naphthoquinone (2.419, 0.01 mol) was prepared by the same method as is known for the preparation of 4-morpholino-1,2-30 naphthoquinone. The product was then heated under reflux withhydroxylam~ne hydrochloride (0.83g, 0.012 mol) for two hours. The pyr1dine was removed and the residue dissolved in methylene chloride, washed with water and brine, dried and finally the solvent evaporated to y~eld an oil. The oil was adsorbed onto silica and chromatographed 35 in silica using methanol/methylene chloride as e1uent. Evaporation of ., , ~31~2; ~
the solvent gave 4-piperidino-1,2-naphthoquinone monoxime, m.p.
135-7C, ~a compound of general formula IY in the tautomeric form having general formula IVb]. This compound was reacted with 1,3,3 trimethyl-2-methyleneindoline in boiling trichloroethylene. The solvent was removed and the resulting oil chromatographed in silica to give:
1,3,3-trimethyl-6'-piperindinospiro~indoline-2,3'-3H-naphtho[2,1-b]~1,4 oxazine] m.p. 230-2C, lH nmr (CDC13); ~ 1.35,s,(6H)3,3-Me2;
1.71,br,(6H)(CH2)3; 2.75,s,(3H) NMe; 3.01,br,(4H) N(CH2)2;
6.57,s,(1H)S'-H; 7.61,(lH)2'-H.
Examples 3 - 20 15 Table I below lists a number of photochromic spiro-oxazine compounds which were made by a process analogous to that described in Example 1 or Example 2; the melting point and partial nmr data obtained for each compound are given in the Table.
Table I
_ Example Spiro-oxaz~ne compound and physical data 3. 9'-Methoxy-1,3,3-trimethyl-6'-piperidinospiro~indoline-2,3-3H-naphtho ~2,1-b]~1,4]oxazine] mp 180-181C, lH nmr (CDC13); ~1.36, s, (6H), 3,3-Me2; 1.70 brm, (6H), (CH2)3;
FIELD OF THE INVENTION
The present invention relates to photochromic articles, particularly to articles having organic photochromic material in a plastic matrix, 5 for example photochromic ophthalmic lenses and windows such as vehicle roof lights.
DESCRIPTION OF THE PRIOR ART
10 Photochromism is a reversib1e physical phenomenon which is observed with certain classes of chemical compounds which are found to change colour when they are exposed to actinic light and which return to their original colour when they are removed from the influence of the actinic radiation.
Plastic organic photochromic lenses are known and have been described, for examp1e, in U.S. Patent 4215010, European Patent Application No.
0141407, U.K. Patent Application No. 2117390 and Wbrld PCT Patent Application No. 85/02619, These patent specifications describe a 20 var~ety of sp~ro-oxazine compounds which have been found to be suitable for incorporation into a polymerised host material thereby ~mparting photochromic propert~es to the host material.
Plastic organic photochromlc windows are known and have been 25 described, for example in U.S. Patent 3508810 which describes a photochromic window having a photochromic spiro-pyran incorporated into a polyvinyl butyral interlayer between sheets of glass.
SUMMARY OF THE INVENTION
We have now produced plastic organic photochromic articles having a denser colouring in their darkened conditlon than previously known plastic organic photochromic articles.
'" ' ' - 130~Z~l ' Accordingly, the present invention provides a plastic organic photochromic article comprising a plastics host materia1 having a photochromic compound incorporated therein or applied thereto, the article being characterised in that it exhibits the following 5 properties, measured at Air Mass 2 at 25C:
(a) an integrated visible transmission in the faded state (B.IVT) ranging from 90 to 25~, lO (b) an integrated visible transmission in the darkened state (D.IVT) ranging from l to 50%, preferably 4 to 30~, (c) the rate of darkening of the article when it is exposed to actinic radiation is such that 88X of the darkening range is achieved in 30 seconds or less, i.e. T88 ~ 30 secs, (d) the rate of fading of the article from its fully darkened condition is such that more than 60~ of the optical density range is recovered in 60 seconds, i.e. ~ ODG-l >~ 60~, and (e) the lnduced optical density of the article, i.e. the change in the optical density of the article, in moving from the faded state (B.IVT) to the darkened state (D.IYT), ls greater than 0.45.
Throughout this specification the term "integrated visible transmission" or IVT is used to mean the weighted average transmission taking into account the emission from the source SA (in this case Illum~nant C ~dayl1ght) as defined by the International Commission of 30 Lighting CIE 1964) and the sensitivity of the detector DA (in this case as defined by the CIE 1964 standard colourimetric observer).
, ' 770 T~,.S~,D~ dA
i . e 770 D1~ S~ dA
3~0 , 1 ' .
....
~ , . . , .; - -~ ' .
, , ~;~05Z~f~
DETAILED DESCRIPTION OF THE INVENTION
We ha~e found in particular that photochromic articles having such dense colouring can be obtained by applying to or incorporating within 5 a solid transparent plastic host material a photochromic compound represented by the general formula (I):
~Rl~n ~R7 , (1) R4 ~R23m wherein n is an integer of 1 to 4, and m is 1, 2 or 3, each of Rl and R2 independently represents (i) a hydrogen atom or an amine functionality of genera1 formula -NR'R " , whereln each of R' and R "
independently represents a hydrogen atom or an alkyl, cycloalkyl or 25 phenyl group or a subst~tuted derivative thereof, or an amine functionality which is a cycloheteroalkyl ring or a substituted cycloheteroalkyl ring which ring includes one or more heteroatoms, (~l) a group of formula -R, -OR, -SR, -COR, or -COOR wherein R
represents H, alkyl, aryl or heteroaryl, (iii) -X, -CH2X, -CHX2, -CX3 wherein X represents halogen, or (iv) -NO2, -CN, -SCN, with the proviso that r~ng A ls always subst.ituted at the 6' position by a group R2 which is an amine-func~lonality as def~ned above;
R4 represents -H, alkyl, alkenyl, phenyl, phenyla1kyl, mono-, di- or tri-substituted phenyl or alkoxy, , . . .
, :
, os~
each of Rs and R6 independently represents -H, alkyl, alkenyl, phenyl, phenylalkyl such as benzyl, mono-, di- or tri-substituted phenyl, or Rs and R6 together represent an alicyclic ring including spiro carbons, norbornane, and adamantane, R3 represents a hydrogen atom, or an alkyl, aryl or heteroaryl group, R7 is as defined for Rl and R2 above, or is a ring system fused to ring A, which ring system may incorporate aromatic and/or alicyclic 10 rings, the said ring system optionally carrying one or more substituents R8, the substituent R8 being as defined above for Rl and R2, and Ring B may optionally contain one or more ring nitrogen atoms.
The terms "aromatic" and "alicyclic" used herein should be interpreted to include hetero-aromatic and hetero-alicyclic systems.
:i ' Preferably, the photochromic spiro-oxazine compounds of generalformula (I) are spiro-oxazines of the formula (II) below:
~, ~
R5 R6 R3 (R1o)q (Rl~n~ (Il) 30 ~Rg)p ,, , ' ~, , , :
, "j :
~:
,~
,' ~".:,, . ~, .
,~ , .
- s -wherein each of Rl, Rg and Rlo independently represents (i) a hydrogen atom or an amine functionality of general formula -NR'R " , where each o~ R' and R " independently represents a hydrogen atom or an alkyl, cycloalkyl or phenyl group or a substituted derivative thereof, or an 5 amine functionality which is a cycloheteroalkyl ring or a substituted cycloheteroalkyl ring, which ring includes one or more heteroatoms, (ii) a group of formula -R, -OR, -SR, -COR, or -COOR wherein R
represents H, alkyl, aryl or heteroaryl, (iii) -X, -CH2X, -CHX2, -CX3 wherein X represents halogen, or (iv) -N02, -CN, -SCN: with the 10 proviso that the group (Rg)p always includes an amine-functionality as defined immediately above at the 6'-position, n is an integer of l to 4, p is l or 2, q is l, 2 or 3, and ~X- and zY- each independently represents ~ N or \/ C-Rlo wherein Rlo is as def~ned above, and R3, R4, Rs and R6 are as defined above for formula (I).
For convenience, the structural formula (II) depicted above shows the -X~ group in the 7'-posit~on of the molecule and the ~Y- group in the 7-pos~t~on, but ~t should be noted that the -X~ group can equally well be located at the 8', 9' or lO' - position of the molecule and the =Y-group can equally well be located at the 4 , 5 , or 6 -position in addition to, or in place of, the depicted position.
In this specificat~on the term "lower a1kyl" is intended to mean an alkyl group of from 1 to 8 carbon atoms.
The group R3 is preferably a hydrogen atom, ' ,~' ".
SZ~
For the avoidance of doubt, when the substituents Rl, R2, Rg or Rlo represent an amine functionality which is a substituted cycloheteroalkyl ring as defined above, the substituent on the said cycloheteroalkyl ring can take the form of a system of one or more further rings fused to the cycloheteroalkyl ring, which ring system may incorporate saturated and/or unsaturated rings. Typical examples of such a substituted amine functionality include a tetrahydroisoquinoline substituent of formula --N~
: or an indoline substituent of formula ~
or a hexahydrocarbazole substituent of formula ' ~O ' C~
:
~.-!i, :
.' ~ .. ,,..~, ,;,-," :, ~, `` 1305Z71 Preferred photochromic materials for incorporation into or application to the plastic host material are compounds of general formula (II) in which n is 1 and Rl is a hydrogen atom, or a 5-alkoxy substituent, preferably 5 methoxy, or a 5-halogen substituent, preferably a 5 5-chloro substituent; R3 is a hydrogen atom; each of R4, R~ and R6 is an alkyl group, preferably methyl; p is 1 and Rg for example is a 6'-piperidino, 6'-morpholino, 6'-N-methylpiperazino, 6'-N-phenylpiperazino, 6'-tetrahydroisoquinolino, 6'-indolino, 6'-thiomorpholino, 6'-homopiperidino, 6'-(1,2,3,4,4a,9a-10 hexahydrocarbazolino, or 6' aziridino substituent; q is 1 and Rlo is ahydrogen atom or an 9'-alkoxy substituent, preferably 9'-methoxy; X is -CH= or -N= located in the 7' position; and Y is -CH= or -N=.
Particularly preferred compounds of general formula (II) are 15 6'-indolino-1,3,3-trimethylspiro ~indoline-2,3'-3H-naphtho[2,1-b][1,4]
oxazine] of formula CH3 C~3 CH3 ~
and 5-methoxy-6'-morpholino-1,3,3-trimethylspiro [indoline-2,3'-3H-naphtho~2,1-b]~1,4] oxazine] of formula 1`3~
The novel photochromic compounds of formula (II) may be prepared by a general preparative method based on the following reaction scheme:
NO
HO ~ ( IVa) R R6 ~ ~ (RlO)q ~Rl~n ~= (Rg) p R4 10 q (R9)p ( I \l ) (R~ R10)q : ~ R4 ( I I ) Th1s methot 1s based on the react~on of an a-n~tro B-naphthol derlvat~ve w~th a 2-methylene~ndole compound such as descr~bed in U.S.
Patent No. 3578602.
, : , ~' The compounds of general ~ormula (I) may be prepared by a s~m~lar process, us1ng the correspondlng start~ng mater~als.
,. ~,,,~, ,, - ~
"., "
- .
.
,, . - , . .
~ : . , . : -.~, ~ . .
.
130~ ~'3.
In order to prepare the compounds of formula (II), the appropriate nitroso-hydroxy derivative of formula (IY) is reacted with the appropriate indoline of formula (III). Alternatively, an indolenium salt, such as a methiodide, can be used instead of the indoline of 5 formula (III).
The t~o starting materials are generally reacted together by refluxing in a solvent such as trichloroethylene or toluene. If an indolenium salt is used, a base such as the triethylamine should be present. The lO desired spiro-oxazine product is separated and purified by conventional techniques such as chromatographic separation and crystallisation.
Examples of suitable plastics host materials are optically clear plastics selected from polymers of polyol(allyl carbonate)-monomers, polyacrylates, poly(alkylacrylates) such as polymethylmethacrylates, cellulose acetate, cellulose triacetate, cellulose acetate propionate, cellulose acetate butyrate, poly(vinyl acetate), poly(vinyl alcohol), polyurethanes, polycarbonates, polyethylene terephthalate, polystyrene, poly(styrene methylmethacrylate) copolymers, poly(styrene acrylonitrile) copolymers, and polyvinylbutyral. Transparent copolymers and blends of the transparent polymers are also suitable as host mater1als.
Preferably, the host mater1al is an optically clear polymerized organic mater1al such as tr1ethylene glycol dimethacrylate (TEGDM) or di~thylene ~lycol bi~(allyl carb6~ate). , ~
, The photochromic spiro-oxaz1ne compounds of formula (ll may be applied to or incorporated in the plast1c host mater1al by any of the convent10nal methods known ~n the art, for example by the methods exempl1f1ed in European Patent Spec1f1cat10n No. 141407, TypicallY, ~a~
130SZ:71 such methods include dissolving or dispersing the photochromic compound in the host material. The photochromic compound may be dispersed into the host material by "imbibition", i.e. diffusion of the photochromic compound into the host material by a suitable 5 transfer mechanism such as immersion, thermal transfer or vapour phase transfer.
In addition, when the plastic host material is one which is formed from a highly reactive polyfunctional monomer the photochromic lO compounds can be incorporated in the plastic 'nost material by a direct casting process as described in our published European Patent Application Nb. 0227~37. This direct casting process uses a highly reactive polyfunctional monomer and a low catalyst concentration in order to prevent degradation of the spiro-oxazine compound; the process 15 comprises incorporating into a mixture comprising a highly reactive polyfunctional monomer and 0.01 to 1~J by weight, based on the volume of the monomer, of a polymerisation catalyst, O.OS to 5~ by weight, based on the volume of the monomer, of a photochromic spiro-oxazine compound; introducing the resultant polymerisable composition into a ~ould, and curing the composition to form the shaped synthetic plastic artic1e.
Typica11y a p1astic lens is formed by using a conventional direct casting process in which the polymer~sab1e composit10n ~ncorporating the photochromic spiro-oxazine compound is introduced into a mould and is then cured by heating. Suitable curing conditions are, for example, heating at a temperature ranging from room temperature to 100C, generally over a period of about 5 'nours. A typical cur1ng schedule is to subject the material to be cured to a temperature be~inning at 40C r1sing up to a temperature within the range 80 -90C over a per~od of about 5 hours.
~, , ~ ,:
~ ~, i , -,~ , ' -130S2'71 The highly reactive polyfunctional monomers used in the said direct casting process are preferably methacrylates or acrylates of linear or branched aliphatic or aromatic liquid polyols such as glycols or bisphenols. Examples of specific monomers include ethylene glycol 5 dimethacrylate or diacrylate and the corresponding dimethacrylates or diacrylates of di-, tri- and tetra-ethylene glycol; the dimethacrylates of 1,2-propyleneglycol, of 1,2-dipropylene glycol, of 1,2-tripropylene glycol and of 1,3-butylene glycol; dimethacrylates of propanediol, butanediol, hexanediol and decanediol; trimethylol ethane 10 trimethacrylate, ~rimethylol propane trimethacrylate, pentaerythritol trimethacrylate, ~,2,4-trimethyl-1,3-pentanediol dimethacrylate and 1,4-cyclohexanediol dimethacrylate.
Mixtures of the reactive polyfunctional monomers may also be used.
The highly reactive polyfunctional monomer or monomers may be used alone or in the presence of other copolymerisable monofunctional monomers which may be added to modify the physical properties - such as impact strength, castability and tintability - of the resultant 20 polymer. The amount of co-monomer which may be added is up to 30% by we~ght, preferably 5 to 15% by weight, based on the volume of the reactive polyfunctional monomer.
Typical co-monomers are alkyl methacrylates such as cyclohexyl 25 methacrylate, n-butyl methacrylate and lauryl methacrylate, which may be added to ~mprove the impact reslstance of the finished lens;
ethoxylated bisphenol-A dimethacrylate, which is added to reduce the shrinkage which is found to occur during formation of the moulded article; and hydroxyalkyl methacrylates such as hydroxyethyl ~o methacrylate and hydroxybutyl methacrylate which improve adhesion of the po1ymer to the mould surface dùring polymer~sation.
:
Other co-monomer additives include methacryl~c acid, aryl methacrylates such as benzyl methacrylate, allyl methacrylate, ,I , ''''''''1 ~ , ", ~
. ~ ~ .. ..... .....
- .
.
: - - . .
,. . .
' .
.
13(~SZ
tetrahydrofurfurylmethacrylate; and polyether monoacrylates or mono-methacrylates such as ethoxyethyl methacrylate.
The catalysts used in the said direct casting process are the 5 conventional free-radical polymerisation catalysts used in the art, in particular, organic peroxides such as benzoyl peroxide and peroxydicarbonates such as isopropylperoxydicarbonate. The amount of catalyst used is kept as low as possible, and is from 0.01 to 1% by weight, based on the volume of the monomer.
1~
The amount of the photochromic compound incorporated into the plastic host material is usually of the order of from 0.05% to 5% by weight, based on the volume of the host material. However, the amount of photochromic compound is not critical and can be varied depending upon 15 the method which is used to apply or incorporate the photochromic compound. In particular, when the spiro-oxazine compound is applied to or imbibed into the surface of the article, the amount used will usually be significantly less than 0.05g by weight.
20 Art~cles ~n accordance with the present invention typically exhibit a pale colouration in the faded condition, dependant on the nature of the compound used and a purple to blue colour in the darkened cond~t~on.
25 If desired, the colour of the article can be modified with conventional water-based dyes or tints. For example, it is possible to make an art1cle which is grey or brown in its faded condition and darkens to a blue/grey colouration when exposed to sunlight.
30 The present invention is illustrated further by the following Examples.
.'~ ~,....
~ ' ' .
3(~ 7 Example 1 Preparation of 6'-indolino-1,3,3-trimethylspiro~indoline-2,3'-3H-naphtho[2,1-b] [1,4]oxazine]
l-Nitroso-2-naphthol (17.3 g; 0.1 mol) and indoline (23.8 9; 0.2 mol) were dissolved in trichloroethylene (150 cm3) by heating under reflux. A solution of 1,3,3-trimethyl-2-methyleneindoline (17.3 g;
10 0.1 mol) in trichloroethylene (100 cm3) was added dropwise over 30 min to the boiling solution. Boiling under reflux was continued for three hours.
The solvent was removed and the oil was adsorbed onto silica and 15 chromatographed in silica using ethyl acetate - light petroleum as eluant. Evaporation of the solvent gave 6'-indolino-1 ,3,3-trimethyl spiro[indoline-2,3'-3H-naphtho[2,1-b] [1,4]oxazine], mp 25~-257C, lH nmr (CDC13): ~1.36, s, (6H), 3,3-Me2; 2.77, s, (3H), NMe; 3.17, m, (2H), CH2; 3.93, m, (2H), NCH2; 6.93, s, (lH), 5'-H;
20 7.69, s, ~lH)J 2'-H.
~, Preparation of 1 ,3,3-trimethyl-6'-piperidinospiro[indoline-2,3'-3H-25 naphtho~2,1-b]~1,4]oxazine]
4-Piperidino-1,2-naphthoquinone (2.419, 0.01 mol) was prepared by the same method as is known for the preparation of 4-morpholino-1,2-30 naphthoquinone. The product was then heated under reflux withhydroxylam~ne hydrochloride (0.83g, 0.012 mol) for two hours. The pyr1dine was removed and the residue dissolved in methylene chloride, washed with water and brine, dried and finally the solvent evaporated to y~eld an oil. The oil was adsorbed onto silica and chromatographed 35 in silica using methanol/methylene chloride as e1uent. Evaporation of ., , ~31~2; ~
the solvent gave 4-piperidino-1,2-naphthoquinone monoxime, m.p.
135-7C, ~a compound of general formula IY in the tautomeric form having general formula IVb]. This compound was reacted with 1,3,3 trimethyl-2-methyleneindoline in boiling trichloroethylene. The solvent was removed and the resulting oil chromatographed in silica to give:
1,3,3-trimethyl-6'-piperindinospiro~indoline-2,3'-3H-naphtho[2,1-b]~1,4 oxazine] m.p. 230-2C, lH nmr (CDC13); ~ 1.35,s,(6H)3,3-Me2;
1.71,br,(6H)(CH2)3; 2.75,s,(3H) NMe; 3.01,br,(4H) N(CH2)2;
6.57,s,(1H)S'-H; 7.61,(lH)2'-H.
Examples 3 - 20 15 Table I below lists a number of photochromic spiro-oxazine compounds which were made by a process analogous to that described in Example 1 or Example 2; the melting point and partial nmr data obtained for each compound are given in the Table.
Table I
_ Example Spiro-oxaz~ne compound and physical data 3. 9'-Methoxy-1,3,3-trimethyl-6'-piperidinospiro~indoline-2,3-3H-naphtho ~2,1-b]~1,4]oxazine] mp 180-181C, lH nmr (CDC13); ~1.36, s, (6H), 3,3-Me2; 1.70 brm, (6H), (CH2)3;
2.75, s, (3H), NMe; 2.85, brm, (4H), N(CH2)2; 3.99, s, (3H), OCH3; 6.44, s, (lH), 5'-H; 7.59, s, (lH) 2'-H
30 4. 5-Methoxy-1,3,3-tr1methyl-6'-piperidinospiro~indoline-2,3'-3H-naphtho~2,1-b~1,4]oxazine] mp 150-2C, lH nmr (CDC13);
~ 1.35, s, (6H), 3,3-Me2; 1.70, br, (6H), (CH2)3; 2.70, s, (3H), NMe; 3.01, br, (4H), N(CH2)2; 3.80, s, (3H), OMe; 6.58, s, (lH), S'-H; 7.60, s, (lH), 2'-H.
13(~S2 -- l5 --5. 1,3,3-Trimethyl-6'-morpholinospiroCindoline-2,3'-3H-naphtho C2,1-b]Cl,4]oxazine] mp 196C, 1H nmr (CDC13); ~1.36, s, (6H), 3,3-Me2; 2.75, s, (3H), NMe; 3.06, m, (4H), N(CHz)2;
30 4. 5-Methoxy-1,3,3-tr1methyl-6'-piperidinospiro~indoline-2,3'-3H-naphtho~2,1-b~1,4]oxazine] mp 150-2C, lH nmr (CDC13);
~ 1.35, s, (6H), 3,3-Me2; 1.70, br, (6H), (CH2)3; 2.70, s, (3H), NMe; 3.01, br, (4H), N(CH2)2; 3.80, s, (3H), OMe; 6.58, s, (lH), S'-H; 7.60, s, (lH), 2'-H.
13(~S2 -- l5 --5. 1,3,3-Trimethyl-6'-morpholinospiroCindoline-2,3'-3H-naphtho C2,1-b]Cl,4]oxazine] mp 196C, 1H nmr (CDC13); ~1.36, s, (6H), 3,3-Me2; 2.75, s, (3H), NMe; 3.06, m, (4H), N(CHz)2;
3.96, m, (4H), O(CH2)2; 6.62, s, (lH), 5'-H; 7.47, s, (lH), 2'-H.
6. 5-Methoxy-1,3,3-trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphtho~2,1-b]~1,4]oxazine] mp 172-3C, lH nmr (CDC13);
~1.35, s, (6H), 3,3 Me2; 2.74, s, (3H), N-Me; 3.07, m, (4H), N(CH2)2; 3-81, s, (3H), O-Me; 3.95, m, (4H), O(CH2)2; 6.64, s, (lH), 5'-H; 7.52, s, lH 2'-H.
7. 9'-Methoxy-1,3,3-trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphtho~2,1-b]~1,4]oxazine] mp 197-200C, lH nmr (CDC13);
~1.36, s, (6H), 3,3-Me2; 2.76, s, (3H), NMe; 3.04, brm, (4H), N(CH2)2; 3.94, brm, (4H), O(CH2)2; 4.00, s, (3H), OMe;
6.48-8.03, m, (8H) aromatic H.
8. 5-Chloro-1,3,3-trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphthoC2,1-b]Cl,4]oxazine], mp 196C, lH nmr (CDC13);
~1.34, s, (6H), 3,3-Me2; 2.73, s, (3H), NMe; 3.07, m, (4H), N(CH2)2; 3.96, m, (4H), O(CH2)2; 6.60, s, (lH), 5'-H; 7.62, s, (lH), 2'-H.
z5 9. 1,3,3-Trimethyl-6'-thiomorpholinospiroCindoline-2,3'-3H-naphtho C2,1-b~Cl,4]oxazine], mp 184-5C, lH nmr (CDC13); ~ 1.34, s, (6H), 3,3-Me2; 2.75, s, (3H), NMe; 2.90, m, (4H), N(CH2)2;
3.30, m, (4H), S(CH2)2; 6.61, s, (lH), 5'-H; 7.64, s, (lH), 2'-H.
10. 1,3,3-Trimethyl-6'-(N-methylpiperazino)spiroCindoline-2,3'-3H-naphthoC2,1-b]Cl,4]oxazine] mp 203-4C, lH nmr (CDC13);
~1.35, s, (6H), 3,3-Me2; 2.41, s, (3H), NMe; 2.75 m, (3H), NMe and (4H) N(CH2)2; 3.10, m, (4H), N(CH2)2; 6 61, s, (lH) 5'-H; 7.64, s, (lH), 2'-H.
,, .~ ,, . ., 11. 1,3,3-Trimethyl-6'-(N-phenylpiperazino)spiro[indoline-2,3'-3H-naphtho[2,1-b][1,4~oxazine] mp 207-208C, lH nmr (CDC13);
~1.37, s, (6H), 3,3-Me2; 2.77, s, (3H), NMe; 3.35, br m, (8H), (N(CH2)2)2; 6.66, s, (lH), 5'-H; 7.65, s, (lH), 2'-H.
12. 6'-(1,2,3,4-Tetrahydroisoquinolino)-1,3,3-trimethylspiro [indoline-2,3'-3H-naphtho[2,1-b][1,4]oxazine], mp 188-190C, lH nmr (CDC13); ~1.37J s, (6H), 3,3-Me2; 2.77, s, (3H) NMe;
3.26, m, (4H), (CH2)2; 4.25, br. s, (2H), CH2; 6.70, s, (lH), 5'-H; 7.65, s, (lH), 2'-H.
13. 6'-Homopiperidino-1,3,3-trimethylspiro[indoline-2,3'-3H-naphtho C1,2-b]~1,4]oxazine], mp 225C, lH nmr (CDC13); ~ 1.35, s, (6H), 3,3-Me2; 1.80, br. s, (8H), (CH2)4; 2.75, s, (3H), NMe;
3.25, br, (4H), N(CH2)2; 6.63, s, (lH), 5'-H; 7.60, s, (lH), 2'-H.
14, 6'-Aziridino-1,3,3-trimethylspiroCindoline-2,3'-3H-naphtho ~2,1-b]~1,4~oxazine] mp 168-170C, lH nmr (CDC13); ~1.35, s, (6H), 3,3-Me2; 2.25, br. s, (4H), N(CH2)2; 2.75, s, (3H), NMe; 6.50, s, (lH), 5'-H; 7.62, s, (lH), 2'-H.
6'-Dimethylamlno-1,3,3-tr~methylspiro~ndoline-2,3'-3H-naphtho ~2,1-b~Cl,4~oxazine] mp 172 - 173C, lH nmr (CDC13); ~1.36, s, (6H), 3,3-Me2; 2.75, (3H), NMe; 2.88, s, (6H), NMe2; 6.59, s, (lH), 5'-H; 7 62, s, (lH), 2'-H.
16. 6'-Dimethylamino-1,3,3-trimethylspiro[1ndoline-2,3'-3H-benzo ~1,4]oxazine], mp 138-9C, lH nmr (CDC13); ~1.30, s, (3H), 3-Me; 1.35, s, (3H), 3-Me; 2.76, s, (3H), NMe; 2.92, s, (6H), NMe2 . ~r 13~ 5;~
17. 6'-Diethylamino-1,3j3-trimetbylspir~-indoline-2,3'-3~-~enzoCl,
6. 5-Methoxy-1,3,3-trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphtho~2,1-b]~1,4]oxazine] mp 172-3C, lH nmr (CDC13);
~1.35, s, (6H), 3,3 Me2; 2.74, s, (3H), N-Me; 3.07, m, (4H), N(CH2)2; 3-81, s, (3H), O-Me; 3.95, m, (4H), O(CH2)2; 6.64, s, (lH), 5'-H; 7.52, s, lH 2'-H.
7. 9'-Methoxy-1,3,3-trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphtho~2,1-b]~1,4]oxazine] mp 197-200C, lH nmr (CDC13);
~1.36, s, (6H), 3,3-Me2; 2.76, s, (3H), NMe; 3.04, brm, (4H), N(CH2)2; 3.94, brm, (4H), O(CH2)2; 4.00, s, (3H), OMe;
6.48-8.03, m, (8H) aromatic H.
8. 5-Chloro-1,3,3-trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphthoC2,1-b]Cl,4]oxazine], mp 196C, lH nmr (CDC13);
~1.34, s, (6H), 3,3-Me2; 2.73, s, (3H), NMe; 3.07, m, (4H), N(CH2)2; 3.96, m, (4H), O(CH2)2; 6.60, s, (lH), 5'-H; 7.62, s, (lH), 2'-H.
z5 9. 1,3,3-Trimethyl-6'-thiomorpholinospiroCindoline-2,3'-3H-naphtho C2,1-b~Cl,4]oxazine], mp 184-5C, lH nmr (CDC13); ~ 1.34, s, (6H), 3,3-Me2; 2.75, s, (3H), NMe; 2.90, m, (4H), N(CH2)2;
3.30, m, (4H), S(CH2)2; 6.61, s, (lH), 5'-H; 7.64, s, (lH), 2'-H.
10. 1,3,3-Trimethyl-6'-(N-methylpiperazino)spiroCindoline-2,3'-3H-naphthoC2,1-b]Cl,4]oxazine] mp 203-4C, lH nmr (CDC13);
~1.35, s, (6H), 3,3-Me2; 2.41, s, (3H), NMe; 2.75 m, (3H), NMe and (4H) N(CH2)2; 3.10, m, (4H), N(CH2)2; 6 61, s, (lH) 5'-H; 7.64, s, (lH), 2'-H.
,, .~ ,, . ., 11. 1,3,3-Trimethyl-6'-(N-phenylpiperazino)spiro[indoline-2,3'-3H-naphtho[2,1-b][1,4~oxazine] mp 207-208C, lH nmr (CDC13);
~1.37, s, (6H), 3,3-Me2; 2.77, s, (3H), NMe; 3.35, br m, (8H), (N(CH2)2)2; 6.66, s, (lH), 5'-H; 7.65, s, (lH), 2'-H.
12. 6'-(1,2,3,4-Tetrahydroisoquinolino)-1,3,3-trimethylspiro [indoline-2,3'-3H-naphtho[2,1-b][1,4]oxazine], mp 188-190C, lH nmr (CDC13); ~1.37J s, (6H), 3,3-Me2; 2.77, s, (3H) NMe;
3.26, m, (4H), (CH2)2; 4.25, br. s, (2H), CH2; 6.70, s, (lH), 5'-H; 7.65, s, (lH), 2'-H.
13. 6'-Homopiperidino-1,3,3-trimethylspiro[indoline-2,3'-3H-naphtho C1,2-b]~1,4]oxazine], mp 225C, lH nmr (CDC13); ~ 1.35, s, (6H), 3,3-Me2; 1.80, br. s, (8H), (CH2)4; 2.75, s, (3H), NMe;
3.25, br, (4H), N(CH2)2; 6.63, s, (lH), 5'-H; 7.60, s, (lH), 2'-H.
14, 6'-Aziridino-1,3,3-trimethylspiroCindoline-2,3'-3H-naphtho ~2,1-b]~1,4~oxazine] mp 168-170C, lH nmr (CDC13); ~1.35, s, (6H), 3,3-Me2; 2.25, br. s, (4H), N(CH2)2; 2.75, s, (3H), NMe; 6.50, s, (lH), 5'-H; 7.62, s, (lH), 2'-H.
6'-Dimethylamlno-1,3,3-tr~methylspiro~ndoline-2,3'-3H-naphtho ~2,1-b~Cl,4~oxazine] mp 172 - 173C, lH nmr (CDC13); ~1.36, s, (6H), 3,3-Me2; 2.75, (3H), NMe; 2.88, s, (6H), NMe2; 6.59, s, (lH), 5'-H; 7 62, s, (lH), 2'-H.
16. 6'-Dimethylamino-1,3,3-trimethylspiro[1ndoline-2,3'-3H-benzo ~1,4]oxazine], mp 138-9C, lH nmr (CDC13); ~1.30, s, (3H), 3-Me; 1.35, s, (3H), 3-Me; 2.76, s, (3H), NMe; 2.92, s, (6H), NMe2 . ~r 13~ 5;~
17. 6'-Diethylamino-1,3j3-trimetbylspir~-indoline-2,3'-3~-~enzoCl,
4]oxazine], mp 143-5C, lH nmr (CDC13); ~1.12, t, (6H), ~CH3)2; 1.28, s, (3H), 3-Me; 1.35, s, (3H), 3-Me; 2.76, s, (3H), NMe; 3.29, q, (4H), N(CH2)2.
18. 6'-Indolino-1,3,3-trimethylspiro[indoline-2,3'-3H-pyrido~3,2-f]
[1,4]benzooxazine], mp 231-3C, lH nmr (CDC13); ~1.36, s, (6H), 3,3-Me2; 2.78, s, (3H), NMe; 3.20, m, (2H), CH2; 4.23, m, (2H), NCH2; 7.64, s, (lH), 2'-H.
19. 1,3,3-Trimethyl-6'-piperidinospiro[7-azaindoline-2,3'-3H-naphtho ~2,1-b][1,4]oxazinei, mp 211C, lH nmr (CDC13);
~1.36,s,(6H),3,3-Me2; 1.71,br,(6H),(CH2)3; 2.94,s(3H),NMe;
6.56,s,(1H),5'-H; 7.60,s,(1H),2'-H.
20. 6'-Indolino-1,3,3-trimethylspiro~7-azaindoline-2,3'-3H-naphtho~
2,1-b]~1,4]oxazine], mp 192C, lH nmr(CDC13);
~1.37,s,(6H)3,3-Me2; 2.98,s,(3H) NMe; 3.25,m,(2H)CH2;
4.00,m,(2H)NCH2; 6.73-8.70,m,(12H)aromatic H;
7,67,s,(1H)2'-H.
A correlat1On between the spiro-oxazine compounds of each of Examples 1 to 20 and the general form~lae I and II ~s g1ven in Tables II and ; III below, :i' ~.?.
~ .. .
;~3~5~
r T ~ T S
C~ I T ~ I T
C~. _ _ _ _ _ r _ _ _ --Oc c Oc O Oc O O ~O ~ c _ r- r~
O _ ~ S S S O ~
~ , ~ L ~ E E E E ~ E Z c~.
_~O S I = T I T , T T T
~C Cl~
_~ O ll'~ I S I T S = 2 I T I
~ J C~ ~S: ~
Z ~ = S 2 S 2 = ~ ~ I S
,~? 2 2 = 2 2 T . 2 2 S
C _ _ _ _ _ _ _ _ _ _ ~ T 2 2 ~ S ~ ~ T 2 11 111~ ~I 11 11 11 11 11 y I~ ~ I~ I~
ll llll ll ll ll ll ll 11 ll ll C.) ~ t~
X
r~
~ = u~
, ~13~
.
V' _ _ _ _ _ _ _ _ ~ _ . = = = = = _ C~
C
.~ o C- ._Co o ~ I ~ ' o E o _ ~ ~ C _ o _ o C~ ,c~ ~ ~0 C~ " ~ C ~
c C~l ~ o~ ' ~ o ~ o -- -C o ,~ .E ~ o~
_ ~ C ~ ~
_ _ ,~, _ _ _ _ _ _ V _.
C ~
~c =~ ~D ~ = S S =
O O ~
~ t~7 ~ = I = = s s S =
~ = ~ S ~ = = S
,, ,' ~ - S - S S S = S
.. ~ S = = S S S
' 11 I~ 11 11 11 11 I~11 ll ~ ~ ~ ~ Z
~_ I~
: 1~ 11 11 11 11 ~1 11 11 X~ _1 _1 _~ I _1 _1 .
,~ ~
_ _ N '7 ~r ~ 0 0~ O
, ' .
, '' ' i' ' ' ' :
- 130~Z~7~
,o~,cC
~I
~3(~S; ~
Some of the spiro-oxazine compounds of Examples 1 to 20 and two other spiro-oxazines (for comparative purposes) were incorporated into a plastic host material to prepare a plastic photochromic lens.
The ophthalmic lenses were made by a conventional direct casting method using a plano lens mould comprising a pair of glass moulds sealed by a flexible gasket at their interface. The mould cavity was filled with a thermosettable composition consisting of, as monomer, triethyleneglycol dimethacrylate (TEGDM), with O.lX by weight (based lo on the volume of monomer) of benzoyl peroxide, as initiator, and 0.2~
by weight (based on the volume of monomer) of a spiro-oxazine compound of formula I or II. The mixture in the mould was cured by heating at a temperature of 75 - 95C over a period of about four hours.
15 The results obtained with lenses incorporating each of the spiro-oxazine compounds of Examples 1 to 20 and the two comparative materials are given in Table IV.
The chromophores used in Comparative Examples 1 and 2 were 20 sp~ro-oxazines from which substituents of amine functionality were absent. The spiro-oxazine of Comparative Example 1 was 'l ~
9'-methoxy-1,3,3-trimethylspiro~ndol~ne-2,3'-3H-naphthot2,1-b]~1,4 ,~ oxazine], while that of Comparative Examp1e 2 was 1,3,3-trimethylspiro~indoline-2,3'-3H-naphtho~2,1-b]~1,4]oxazine].
The results in Table IV include the integrated visible transmission of the lens in the faded or bleached state (ibbreviated as B.IVT) and the ;~ 1ntegrated vis1ble transmission of the lens in the darkened state (abbreviated as D.IVT). These values show for each material the typical v~sual photochromic range which can be achieved, and show the j' 35 suitability of the materials for use in sunlenses. The fully darkened ; ',~, , , , ~
~ , :, ~ ~3V~Z'7~1 state of a lens made in accordance with the present invention is defined as the state reached by a lens at 25C after exposure to standard solar simulation conditions at Air Mass 2 for 10 minutes [see Parry Moon J. Franklin Inst 230 (1940) P583-617]. It can be seen from
18. 6'-Indolino-1,3,3-trimethylspiro[indoline-2,3'-3H-pyrido~3,2-f]
[1,4]benzooxazine], mp 231-3C, lH nmr (CDC13); ~1.36, s, (6H), 3,3-Me2; 2.78, s, (3H), NMe; 3.20, m, (2H), CH2; 4.23, m, (2H), NCH2; 7.64, s, (lH), 2'-H.
19. 1,3,3-Trimethyl-6'-piperidinospiro[7-azaindoline-2,3'-3H-naphtho ~2,1-b][1,4]oxazinei, mp 211C, lH nmr (CDC13);
~1.36,s,(6H),3,3-Me2; 1.71,br,(6H),(CH2)3; 2.94,s(3H),NMe;
6.56,s,(1H),5'-H; 7.60,s,(1H),2'-H.
20. 6'-Indolino-1,3,3-trimethylspiro~7-azaindoline-2,3'-3H-naphtho~
2,1-b]~1,4]oxazine], mp 192C, lH nmr(CDC13);
~1.37,s,(6H)3,3-Me2; 2.98,s,(3H) NMe; 3.25,m,(2H)CH2;
4.00,m,(2H)NCH2; 6.73-8.70,m,(12H)aromatic H;
7,67,s,(1H)2'-H.
A correlat1On between the spiro-oxazine compounds of each of Examples 1 to 20 and the general form~lae I and II ~s g1ven in Tables II and ; III below, :i' ~.?.
~ .. .
;~3~5~
r T ~ T S
C~ I T ~ I T
C~. _ _ _ _ _ r _ _ _ --Oc c Oc O Oc O O ~O ~ c _ r- r~
O _ ~ S S S O ~
~ , ~ L ~ E E E E ~ E Z c~.
_~O S I = T I T , T T T
~C Cl~
_~ O ll'~ I S I T S = 2 I T I
~ J C~ ~S: ~
Z ~ = S 2 S 2 = ~ ~ I S
,~? 2 2 = 2 2 T . 2 2 S
C _ _ _ _ _ _ _ _ _ _ ~ T 2 2 ~ S ~ ~ T 2 11 111~ ~I 11 11 11 11 11 y I~ ~ I~ I~
ll llll ll ll ll ll ll 11 ll ll C.) ~ t~
X
r~
~ = u~
, ~13~
.
V' _ _ _ _ _ _ _ _ ~ _ . = = = = = _ C~
C
.~ o C- ._Co o ~ I ~ ' o E o _ ~ ~ C _ o _ o C~ ,c~ ~ ~0 C~ " ~ C ~
c C~l ~ o~ ' ~ o ~ o -- -C o ,~ .E ~ o~
_ ~ C ~ ~
_ _ ,~, _ _ _ _ _ _ V _.
C ~
~c =~ ~D ~ = S S =
O O ~
~ t~7 ~ = I = = s s S =
~ = ~ S ~ = = S
,, ,' ~ - S - S S S = S
.. ~ S = = S S S
' 11 I~ 11 11 11 11 I~11 ll ~ ~ ~ ~ Z
~_ I~
: 1~ 11 11 11 11 ~1 11 11 X~ _1 _1 _~ I _1 _1 .
,~ ~
_ _ N '7 ~r ~ 0 0~ O
, ' .
, '' ' i' ' ' ' :
- 130~Z~7~
,o~,cC
~I
~3(~S; ~
Some of the spiro-oxazine compounds of Examples 1 to 20 and two other spiro-oxazines (for comparative purposes) were incorporated into a plastic host material to prepare a plastic photochromic lens.
The ophthalmic lenses were made by a conventional direct casting method using a plano lens mould comprising a pair of glass moulds sealed by a flexible gasket at their interface. The mould cavity was filled with a thermosettable composition consisting of, as monomer, triethyleneglycol dimethacrylate (TEGDM), with O.lX by weight (based lo on the volume of monomer) of benzoyl peroxide, as initiator, and 0.2~
by weight (based on the volume of monomer) of a spiro-oxazine compound of formula I or II. The mixture in the mould was cured by heating at a temperature of 75 - 95C over a period of about four hours.
15 The results obtained with lenses incorporating each of the spiro-oxazine compounds of Examples 1 to 20 and the two comparative materials are given in Table IV.
The chromophores used in Comparative Examples 1 and 2 were 20 sp~ro-oxazines from which substituents of amine functionality were absent. The spiro-oxazine of Comparative Example 1 was 'l ~
9'-methoxy-1,3,3-trimethylspiro~ndol~ne-2,3'-3H-naphthot2,1-b]~1,4 ,~ oxazine], while that of Comparative Examp1e 2 was 1,3,3-trimethylspiro~indoline-2,3'-3H-naphtho~2,1-b]~1,4]oxazine].
The results in Table IV include the integrated visible transmission of the lens in the faded or bleached state (ibbreviated as B.IVT) and the ;~ 1ntegrated vis1ble transmission of the lens in the darkened state (abbreviated as D.IVT). These values show for each material the typical v~sual photochromic range which can be achieved, and show the j' 35 suitability of the materials for use in sunlenses. The fully darkened ; ',~, , , , ~
~ , :, ~ ~3V~Z'7~1 state of a lens made in accordance with the present invention is defined as the state reached by a lens at 25C after exposure to standard solar simulation conditions at Air Mass 2 for 10 minutes [see Parry Moon J. Franklin Inst 230 (1940) P583-617]. It can be seen from
5 the results in ~he Table that in general purple colouring compounds show a wider range than blue colouring materials.
The range at ~max gives the bleached and darkened trans~issions at the point of maximum absorption of the chromophore, and allows the calculation of induced optical density (IOD):
IOD = loglo BT
DT
The high IOD's of the spiro-oxazines of the invention ranging from 0.76 to 2.6 demonstrate the very dense colouring of the samples.
These results contrast markedly with the values of induced optical density of 0.29 and 0.23 obtained with the chromophores of Comparative Examples l and 2.
An ~ndication of the speed of the photochromic response can be obtained by comparing the time required for the lens, in its darkening phase, to cover 88% of its total available transmission range (Tgg) The Table shows all the compounds of the invention exh~bit fast rates of darkening as indicated by T88 less than 60 secs, generally less than 30 secs.
Comparison of the speed at which lenses fade from the darkened state is obtained by comparing % ODG - 1 values, This gives the percentage of the induced optical density range recovered after one minute's fading. The higher the value of % ODG-l, the faster is the fading rate of the lens. A fast fading rate would be shown by % ODG-l greater than 50~; the results in the Table ind1cate that all compounds of the invention exhibit a % ODG-l value greater than 50, in general greater than 70~.
..
~" 130~Z71 We have also found that lenses in accordance with the present invention exhibit good fatigue resistance.
, ! .
... .
~ . ., ~ `' ? ' ~ ~ .,"1 -. . , i , ~ ~ ' :~ , , ~` 131~S;~ il . ,~
. _ . .
co ~ ~ In C~ _ cn a 0 O ~ D
~o C~
~ ~ ~ 0 0 -- ~
,.
N ~ 1~
1-- a:~ ~ ~ cn 0 ~ ~ ~
C~
O ~ 0 ~ ~D
0 ~ ~
~ I
_ 1 ~3~S~i - ~-`. . ~ ' _. _ ~ ~, ~. _ C~l , C ~
_ J ~ a~ ~ ~ . _ a~
~ C~
~o ~ ~ ~ o ~ ~
~ _ U ~ C~ o _ C~ ' ~ U~ CO ~ N ~ CO
~ ~ In ~ O
c ~ ~ ~ n _ , ~
U~
.~ _ C~
e _ ~ C~
~ C2 o ~ J ~
~I LL~I
U~ ~ O C~
~ CL ~ C~
~ O ~ ~ ~ ~ ~ O
. ' ., :, ~ - ` ' .
, 3~5271 .
L~
~, ~ ~ ~, ,~
O x~ _ ~ u:~ O~ ~ ~ r~
c~ o cn o ~C ~ Ln ~ d o X _ o -, oo o C~.
CO o ,' CO
O O ~ O cr~
~ N
c~ I ~ I~
J LLJ N
~ ~ ~ ~ ~ ? ~
~ ~ O d' o ~ U~
,~
. ~`
~ ~ ,` -- o ~ C~l U'~
CL ~
oo Z
z ~
~o~ o ~
130SZ7~
EXAMPLES ZI and 22 Lenses made as described in Example l were modified by pretinting with "SOLA" fast tint brown and "SOLA" fast tint grey, respectively, supplied by Yorkshire Chemicals to produce lenses having a brown pretint (Example 21) or a grey pretint (Example 22).
The optical properties of the lenses were as follows:
Example 21 22 PRETINT BROWN GREY
lS B.IVT(~) 31 38 D.IVT(~) 9 9 Range at A max 37/2.5 44/1.6 lOD 1.17 1.44 T88 (secs) 6 6 ,~, ~OOG-l 65 69 from the results above 1t w111 be seen that 1n Example 21 a brown pre-t1nted 1ens shows an IVT range of 31/9 and darkens to a grey brown - w1th no loss 1n darken~ng or fad1ng speeds relat1ve to Example 1.
Sim11?rly 1n Example 22 a grey pret1nted lens darkens to a blue/grey ,~ w1th a work1ng range of 38/9 and aga1n no loss 1n darkening and fad1ng speeds relat1ve to Example 1. A w1de range of pret1nts can be obta1ned by convent10nal use of any of the commerc1ally ava11able lens "
dyes.
"
: ;' ;~ ' ' ' ' ~
" ' ' . "
', '' '~
.
13C~
. ~.~., A spiro-oxazine compound selected from Examples l to 20 was incorporated into a plastic host material to prepare a laminated structure, such as could be utilized in a roof light for motor vehicles. A mixture of the sprio-oxazine compounds of E~amples l and 5 2 was dissolved in chloroform, together with polyvinylbutyral. The solution was sprayed onto a glass sheet to give a thin, uniform, coating. The sprayed glass sheet was then laminated to a second glass sheet using a polyvinyl butyral sheet as an interlayer and subjected to autoclaving in a conventional manner, the sprayed surface of the 10 first glass sheet being the surface which contacts the polyvinyl butyral sheet.
On exposure to actinic radiation the laminate turned deep blue and there was a corresponding reduction in the light transmitted through the laminate. The edges of the laminate were sealed to prevent undue degradation of the photochromic material in that vicinity.
The optical properties of the roof light were as follows:
COLOUR PURPLE/BLUE
B.IVT 82 D.IVT lO.9 RANGE AT A MAX 82/2.4 IOD 1.53 T88 (sec) 4 ~ ODG-l 95 From these results it can be seen that the photochromic roof light exhibited optical properties comparable to the ophthalmic lens prepared using the photochromic materials according to the invention.
Those skilled in the art will realise that ophthalmic lenses and vehical roof lights are merely illustrative of the many photochromic articles that can be made with these spiro-oxazines. Architectural windows, vehical windows and filters are ~ust some of the other appl~cations for these materials.
The range at ~max gives the bleached and darkened trans~issions at the point of maximum absorption of the chromophore, and allows the calculation of induced optical density (IOD):
IOD = loglo BT
DT
The high IOD's of the spiro-oxazines of the invention ranging from 0.76 to 2.6 demonstrate the very dense colouring of the samples.
These results contrast markedly with the values of induced optical density of 0.29 and 0.23 obtained with the chromophores of Comparative Examples l and 2.
An ~ndication of the speed of the photochromic response can be obtained by comparing the time required for the lens, in its darkening phase, to cover 88% of its total available transmission range (Tgg) The Table shows all the compounds of the invention exh~bit fast rates of darkening as indicated by T88 less than 60 secs, generally less than 30 secs.
Comparison of the speed at which lenses fade from the darkened state is obtained by comparing % ODG - 1 values, This gives the percentage of the induced optical density range recovered after one minute's fading. The higher the value of % ODG-l, the faster is the fading rate of the lens. A fast fading rate would be shown by % ODG-l greater than 50~; the results in the Table ind1cate that all compounds of the invention exhibit a % ODG-l value greater than 50, in general greater than 70~.
..
~" 130~Z71 We have also found that lenses in accordance with the present invention exhibit good fatigue resistance.
, ! .
... .
~ . ., ~ `' ? ' ~ ~ .,"1 -. . , i , ~ ~ ' :~ , , ~` 131~S;~ il . ,~
. _ . .
co ~ ~ In C~ _ cn a 0 O ~ D
~o C~
~ ~ ~ 0 0 -- ~
,.
N ~ 1~
1-- a:~ ~ ~ cn 0 ~ ~ ~
C~
O ~ 0 ~ ~D
0 ~ ~
~ I
_ 1 ~3~S~i - ~-`. . ~ ' _. _ ~ ~, ~. _ C~l , C ~
_ J ~ a~ ~ ~ . _ a~
~ C~
~o ~ ~ ~ o ~ ~
~ _ U ~ C~ o _ C~ ' ~ U~ CO ~ N ~ CO
~ ~ In ~ O
c ~ ~ ~ n _ , ~
U~
.~ _ C~
e _ ~ C~
~ C2 o ~ J ~
~I LL~I
U~ ~ O C~
~ CL ~ C~
~ O ~ ~ ~ ~ ~ O
. ' ., :, ~ - ` ' .
, 3~5271 .
L~
~, ~ ~ ~, ,~
O x~ _ ~ u:~ O~ ~ ~ r~
c~ o cn o ~C ~ Ln ~ d o X _ o -, oo o C~.
CO o ,' CO
O O ~ O cr~
~ N
c~ I ~ I~
J LLJ N
~ ~ ~ ~ ~ ? ~
~ ~ O d' o ~ U~
,~
. ~`
~ ~ ,` -- o ~ C~l U'~
CL ~
oo Z
z ~
~o~ o ~
130SZ7~
EXAMPLES ZI and 22 Lenses made as described in Example l were modified by pretinting with "SOLA" fast tint brown and "SOLA" fast tint grey, respectively, supplied by Yorkshire Chemicals to produce lenses having a brown pretint (Example 21) or a grey pretint (Example 22).
The optical properties of the lenses were as follows:
Example 21 22 PRETINT BROWN GREY
lS B.IVT(~) 31 38 D.IVT(~) 9 9 Range at A max 37/2.5 44/1.6 lOD 1.17 1.44 T88 (secs) 6 6 ,~, ~OOG-l 65 69 from the results above 1t w111 be seen that 1n Example 21 a brown pre-t1nted 1ens shows an IVT range of 31/9 and darkens to a grey brown - w1th no loss 1n darken~ng or fad1ng speeds relat1ve to Example 1.
Sim11?rly 1n Example 22 a grey pret1nted lens darkens to a blue/grey ,~ w1th a work1ng range of 38/9 and aga1n no loss 1n darkening and fad1ng speeds relat1ve to Example 1. A w1de range of pret1nts can be obta1ned by convent10nal use of any of the commerc1ally ava11able lens "
dyes.
"
: ;' ;~ ' ' ' ' ~
" ' ' . "
', '' '~
.
13C~
. ~.~., A spiro-oxazine compound selected from Examples l to 20 was incorporated into a plastic host material to prepare a laminated structure, such as could be utilized in a roof light for motor vehicles. A mixture of the sprio-oxazine compounds of E~amples l and 5 2 was dissolved in chloroform, together with polyvinylbutyral. The solution was sprayed onto a glass sheet to give a thin, uniform, coating. The sprayed glass sheet was then laminated to a second glass sheet using a polyvinyl butyral sheet as an interlayer and subjected to autoclaving in a conventional manner, the sprayed surface of the 10 first glass sheet being the surface which contacts the polyvinyl butyral sheet.
On exposure to actinic radiation the laminate turned deep blue and there was a corresponding reduction in the light transmitted through the laminate. The edges of the laminate were sealed to prevent undue degradation of the photochromic material in that vicinity.
The optical properties of the roof light were as follows:
COLOUR PURPLE/BLUE
B.IVT 82 D.IVT lO.9 RANGE AT A MAX 82/2.4 IOD 1.53 T88 (sec) 4 ~ ODG-l 95 From these results it can be seen that the photochromic roof light exhibited optical properties comparable to the ophthalmic lens prepared using the photochromic materials according to the invention.
Those skilled in the art will realise that ophthalmic lenses and vehical roof lights are merely illustrative of the many photochromic articles that can be made with these spiro-oxazines. Architectural windows, vehical windows and filters are ~ust some of the other appl~cations for these materials.
Claims (38)
1. A plastic organic photochromic article comprising a plastics host material having a photochromic compound incorporated therein or applied thereto, the article exhibiting the following properties, measured at Air Mass 2 at 25°C:
(a) an integrated visible transmission in the faded state (B.IVT) ranging from 90 to 25X, (b) an integrated visible transmission in the darkened state (D.IVT) ranging from 1 to 50X, (c) the rate of darkening of the article when it is exposed to actinic radiation is such that 88X of the darkening range is achieved in 30 seconds or less, i.e. T88 ? 30 secs, (d) the rate of fading of the article from its fully darkened condition is such that more than 60X of the optical density range is recovered in 60 seconds, i.e. X ODG-1 ? 60X, and (e) the induced optical density of the article, i.e. the change in the optical density of the article, in moving from the faded state (B.IVT) to the darkened state (D.IVT), is greater than 0.45.
wherein the photochromic compound incorporated in or applied to the plastics host material is a photochromic compound of the general formula (I):
(I) wherein n is an integer of 1 to 4, and m is 1, 2 or 3, each of R1 and R2 independently represents (i) a hydrogen atom or an amine functionality of general formula -NR'R'', wherein each of R' and R'' independently represents a hydrogen atom or an alkyl, cycloalkyl or phenyl group or a substituted derivative thereof, or an amine functionality which is a cycloheteroalkyl ring or a substituted cycloheteroalkyl ring which ring includes one or more heteroatoms, (ii) d group of formula -R, -OR, -SR, -COR, or -COOR wherein R
represents H, alkyl, aryl or heteroaryl, (iii) -Hal, -CH2Hal, -CH(Hal)2 , -C(Hal)3 wherein Hal represents halogen, or (iv) -NO2, -CN, -SCN, with the proviso that ring A is always substituted at the 6' position by a group R2 which is an amine-functionality as defined above;
R4-represents -H, alkyl, alkenyl, phenyl, phenylalkyl, mono-, di- or tri-substituted phenyl or alkoxy, each of R5 and R6 independently represents -H, alkyl, alkenyl, phenyl, phenylalkyl such as benzyl, mono-, di- or tri-substituted phenyl, or R5 and R6 together represent an alicyclic ring including spiro carbons, norbornane, and adamantane, R3 represents a hydrogen atom, or an alkyl, aryl or heteroaryl group, R7 is as defined for R1 and R2 above, or is a ring system fused to ring A, which ring system may incorporate aromatic and/or alicyclic rings, the said ring system optionally carrying one or more substituents R8, the substituent R8 being as defined above for R1 and R2, and Ring B may optionally contain one or more ring nitrogen atoms.
(a) an integrated visible transmission in the faded state (B.IVT) ranging from 90 to 25X, (b) an integrated visible transmission in the darkened state (D.IVT) ranging from 1 to 50X, (c) the rate of darkening of the article when it is exposed to actinic radiation is such that 88X of the darkening range is achieved in 30 seconds or less, i.e. T88 ? 30 secs, (d) the rate of fading of the article from its fully darkened condition is such that more than 60X of the optical density range is recovered in 60 seconds, i.e. X ODG-1 ? 60X, and (e) the induced optical density of the article, i.e. the change in the optical density of the article, in moving from the faded state (B.IVT) to the darkened state (D.IVT), is greater than 0.45.
wherein the photochromic compound incorporated in or applied to the plastics host material is a photochromic compound of the general formula (I):
(I) wherein n is an integer of 1 to 4, and m is 1, 2 or 3, each of R1 and R2 independently represents (i) a hydrogen atom or an amine functionality of general formula -NR'R'', wherein each of R' and R'' independently represents a hydrogen atom or an alkyl, cycloalkyl or phenyl group or a substituted derivative thereof, or an amine functionality which is a cycloheteroalkyl ring or a substituted cycloheteroalkyl ring which ring includes one or more heteroatoms, (ii) d group of formula -R, -OR, -SR, -COR, or -COOR wherein R
represents H, alkyl, aryl or heteroaryl, (iii) -Hal, -CH2Hal, -CH(Hal)2 , -C(Hal)3 wherein Hal represents halogen, or (iv) -NO2, -CN, -SCN, with the proviso that ring A is always substituted at the 6' position by a group R2 which is an amine-functionality as defined above;
R4-represents -H, alkyl, alkenyl, phenyl, phenylalkyl, mono-, di- or tri-substituted phenyl or alkoxy, each of R5 and R6 independently represents -H, alkyl, alkenyl, phenyl, phenylalkyl such as benzyl, mono-, di- or tri-substituted phenyl, or R5 and R6 together represent an alicyclic ring including spiro carbons, norbornane, and adamantane, R3 represents a hydrogen atom, or an alkyl, aryl or heteroaryl group, R7 is as defined for R1 and R2 above, or is a ring system fused to ring A, which ring system may incorporate aromatic and/or alicyclic rings, the said ring system optionally carrying one or more substituents R8, the substituent R8 being as defined above for R1 and R2, and Ring B may optionally contain one or more ring nitrogen atoms.
2. A photochromic article according to Claim 1, having incorporated therein or applied thereto a photochromic compound of the general formula (II) (II) wherein each of R1, R9 and R10 independently represents (i) a hydrogen atom or an amine functionality of general formula -NR'R'' , where each of R' and R'' independently represents a hydrogen atom or an alkyl, cycloalkyl or phenyl group or a substituted derivative thereof, or an amine functionality which is a cycloheteroalkyl ring or a substituted cycloheteroalkyl ring, which ring includes one or more heteroatoms, (ii) a group of formula -R, -OR, -SR, -COR, or -COOR wherein R
represents H, alkyl, aryl or heteroaryl, (iii) -Hal, -CH2Hal, -CH(Hal)2, -C(Hal)3 wherein Hal represents halogen, or (iv) -NO2, -CN, -SCN: with the proviso that the group (R9)p always includes an amine-functionality as defined above at the 6'-position, n is an integer of 1 to 4, p is 1 or 2, q is 1, 2 or 3, and =X- and =Y- each independently represents or wherein R10 is as defined above, and R3, R4, R5 and R6 are as defined in claim 1 for formula (I).
represents H, alkyl, aryl or heteroaryl, (iii) -Hal, -CH2Hal, -CH(Hal)2, -C(Hal)3 wherein Hal represents halogen, or (iv) -NO2, -CN, -SCN: with the proviso that the group (R9)p always includes an amine-functionality as defined above at the 6'-position, n is an integer of 1 to 4, p is 1 or 2, q is 1, 2 or 3, and =X- and =Y- each independently represents or wherein R10 is as defined above, and R3, R4, R5 and R6 are as defined in claim 1 for formula (I).
3. A photochromic article according to Claim 2, wherein the photochromic compound of general formula (II) is one in which n is 1 and R1 is a hydrogen atom, or a 5- alkoxy substituent, or a 5-halogen substituent; R3 is a hydrogen atom; each of R4, R5 and R6 is an alkyl group; p is 1 and R9 is a 6'- piperidino, 6'-morpholino, 6'-N-methylpiperazino, 6'-N-phenylpiperazino, 6'-tetrahydroisoquinolino, 6'-indolino, 6'-thiomorpholino, 6'-homopiperidino, 6'-(1,2,3,4,4a,9a-hexahydrocarbazolino, or 6' aziridino substituent; q is 1 and R10 is a hydrogen atom or an 9'-alkoxy substituent; X is -CH= or -N= located in the 7' position; and Y is -CH= or -N=.
4. A photochromic article according to claim 1, which exhibits an integrated visible transmission in the darkened state (D.IVT) within the range 4 to 30%.
5. A photochromic article according to claim 3, wherein the photochromic confound of general formula (II) is one in which R1 is a 5-methoxy substituent, or a 5-chloro substituent.
6. A photochromic article according to claim 3, wherein the photochromic compound of general formula (II) is one in which each of R4, R5 and R6 is a methyl group.
7. A photochromic article according to claim 3, wherein the photochromic compound of general formula (II) is one in which R10 is a 9'-methoxy substituent.
8. A photochromic article according to Claim 2 , wherein the photochromic spiro-oxazine compound is 6'-indolino-1,3,3-trimethylspiro[indoline-2,3'-3H-naphtho[2,1-b][1,4]oxazine].
9. A photochromic article according to Claim 2 , wherein the photochromic spiro-oxazine compound is 1,3,3-Trimethyl-6'-piperidinospiro[indoline-2,3'-3H-naphtho[2,1-b][1,4]
oxazine].
oxazine].
10. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 9'-Methoxy-1,3,3-trimethyl-6'-piperidinospiro[indoline-2,3-3H-naphtho [2,1-b][1,4]oxazine].
11. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 5-Methoxy-1,3,3-trimethyl-6'-piperidinospiro[indoline-2,3'-3H-naphtho [2,1-b][1,4]oxazine].
12. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 1,3,3-Trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphtho[2,1-b][1,4]oxazine].
13. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 5-Methoxy-1,3,3-trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphtho [2,1-b][1,4]oxazine].
14. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 9'-Methoxy-1,3,3-trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphtho [2,1-b][1,4]oxazine].
15. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 5-Chloro-1,3,3-trimethyl-6'-morpholinospiro[indoline-2,3'-3H-naphtha [2.1-b][1,4]oxazine].
16. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 1,3,3-Trimethyl-6'-thiomorpholinospiro[indoline-2,3'-3H-naphtho[2,1-b][1,4]oxazine].
17. A photochromic article according to Claim 2 , wherein the photochromic spiro-oxazine compound is 1,3,3-Trimethyl-6'-(N-methylpiperazino)spiro[indoline-2,3'-3H-naphtho [2,1-b][1,4]oxazine].
18. A photochromic article according to Claim 2 , wherein the photochromic spiro-oxazine compound is 1,3,3-Trimethyl-6'-(N-phenylpiperazino)spiro[indoline-2,3'-3H-naphtho [2,1-b][1,4-oxazine].
19. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 6'-(1,2,3,4-Tetrahydroisoquinolino)-1,3,3-trimethylspiro[indoline-2,3'-3H-naphtho [2,1-b][1,4]oxazine].
20. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 6'-Homopiperidino-1,3,3-trimethylspiro[indoline-2,3'-3H-naphtho[1,2-b][1,4]oxazine].
21. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 6'-Aziridino-1,3,3-trimethylspiro[indoline-2,3'-3H-naphtho[2,1-b][1,4]oxazine].
22. A photochromic article according to Claim 1, wherein the photochromic spiro-oxazine compound is 6'-Dimethylamino-1,3,3-trimethylspiro[indoline-2,3'-3H-naphtho[2,1-b][1,4]oxazine].
23. A photochromic article according to Claim 1, wherein the photochromic spiro-oxazine compound is 6'-Dimethylamino-1,3,3-trimethylspiro[indoline-2,3'-3H-benzo[1,4]oxazine].
24. A photochromic article according to Claim 1, wherein the photochromic spiro-oxazine compound is 6'-Diethylamino-1,3,3-trimethylspiro[indoline-2,3'-3H-benzo[1,4]oxazine].
25. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 6'-indolino-1,3,3-trimethylspiro[indoline-2,3'-3H-pyrido[3,2-f][1,4]benzooxazine].
26, A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 1,3,3-Trimethyl-6'-piperidinospiro[7-azaindoline-2,3'-3H-naphtho[2,1-b][1,4]oxazine].
27. A photochromic article according to Claim 2, wherein the photochromic spiro-oxazine compound is 6'-indolino-1,3,3-trimethylspiro[7-azaindoline-2,3'-3H-naphtho[2,1-b][1,4]oxazine].
28. A photochromic article according to Claim 1, wherein the plastics host material is an optically clear plastics selected from polyacrylates, poly(alkylacrylates), cellulose acetate, cellulose triacetate, cellulose acetate propionate, cellulose acetate butyrate, poly(vinyl acetate), poly(vinyl alcohol), polyurethanes, polycarbonates, polyethylene terephthalate, polystyrene, poly(styrene-methyl-methacrylate) copolymers, poly(styreneacrylonitrile) copolymers, and polyvinylbutyral.
29. A photochromic article according to claim 28, wherein the poly(alkylacrylate) is polymethylmethacrylate.
30. A photochromic article according to claim 1, wherein the plastics host material is an optically clear plastics which is a polymer of polyol(allyl carbonate) monomers.
31. A photochromic article according to Claim 1, wherein the plastics host material is an optically clear polymer or copolymer of a methacrylate or acrylate of a linear or branched aliphatic or aromatic liquid polyol.
32. A photochromic article according to Claim 31, wherein the plastics host material is a polymer or copolymer of triethylene glycol dimethacrylate, ethylene glycol dimethacrylate, 1,3-butyleneglycol dimethacrylate or trimetholpropane trimethacrylate.
33. A photochromic article according to Claim 18, wherein the plastics host material is a polymer or copolymer of diethylene glycol bis (allyl carbonate).
34. A photochromic article according to Claim 1, 2 or 3, wherein the amount of spiro-oxazine compound incorporated in the article is 0.05 to 5% by weight, based on the volume of the polymer host material.
A photochromic article according to Claim 1 which is in the form of an optical lens.
36. A lens according to Claim 35 which is an ophthalmic lens.
37. A photochromic article according to Claim 1, the said article being incorporated in a window pane.
38. A photochromic article according to Claim 37 in the form of a vehicle roof light.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8,610,709 | 1986-05-01 | ||
| GB868610709A GB8610709D0 (en) | 1986-05-01 | 1986-05-01 | Photochromic lenses |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1305271C true CA1305271C (en) | 1992-07-14 |
Family
ID=10597204
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000536229A Expired - Fee Related CA1305271C (en) | 1986-05-01 | 1987-05-01 | Photochromic articles |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4913544A (en) |
| EP (1) | EP0245020B1 (en) |
| JP (1) | JP2690305B2 (en) |
| KR (1) | KR940007779B1 (en) |
| AR (1) | AR246355A1 (en) |
| AT (1) | ATE68053T1 (en) |
| AU (1) | AU605763B2 (en) |
| BR (1) | BR8702162A (en) |
| CA (1) | CA1305271C (en) |
| DE (1) | DE3773426D1 (en) |
| ES (1) | ES2027292T3 (en) |
| FI (1) | FI90560C (en) |
| GB (1) | GB8610709D0 (en) |
| GR (1) | GR3003252T3 (en) |
| ZA (1) | ZA873011B (en) |
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1986
- 1986-05-01 GB GB868610709A patent/GB8610709D0/en active Pending
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1987
- 1987-04-24 AU AU71966/87A patent/AU605763B2/en not_active Expired
- 1987-04-27 ZA ZA873011A patent/ZA873011B/en unknown
- 1987-04-27 FI FI871826A patent/FI90560C/en not_active IP Right Cessation
- 1987-04-29 AT AT87303819T patent/ATE68053T1/en not_active IP Right Cessation
- 1987-04-29 ES ES198787303819T patent/ES2027292T3/en not_active Expired - Lifetime
- 1987-04-29 DE DE8787303819T patent/DE3773426D1/en not_active Expired - Lifetime
- 1987-04-29 EP EP87303819A patent/EP0245020B1/en not_active Expired - Lifetime
- 1987-04-30 KR KR1019870004209A patent/KR940007779B1/en not_active IP Right Cessation
- 1987-04-30 AR AR87307432A patent/AR246355A1/en active
- 1987-04-30 BR BR8702162A patent/BR8702162A/en not_active IP Right Cessation
- 1987-04-30 JP JP62104851A patent/JP2690305B2/en not_active Expired - Lifetime
- 1987-05-01 US US07/044,715 patent/US4913544A/en not_active Expired - Lifetime
- 1987-05-01 CA CA000536229A patent/CA1305271C/en not_active Expired - Fee Related
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1991
- 1991-12-02 GR GR91401880T patent/GR3003252T3/en unknown
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| ES2027292T3 (en) | 1992-06-01 |
| FI90560C (en) | 1994-02-25 |
| GR3003252T3 (en) | 1993-02-17 |
| FI871826A (en) | 1987-11-02 |
| BR8702162A (en) | 1988-02-09 |
| FI871826A0 (en) | 1987-04-27 |
| EP0245020B1 (en) | 1991-10-02 |
| AU7196687A (en) | 1987-11-05 |
| DE3773426D1 (en) | 1991-11-07 |
| ATE68053T1 (en) | 1991-10-15 |
| AR246355A1 (en) | 1994-07-29 |
| KR940007779B1 (en) | 1994-08-25 |
| AU605763B2 (en) | 1991-01-24 |
| ZA873011B (en) | 1988-02-24 |
| GB8610709D0 (en) | 1986-06-04 |
| EP0245020A3 (en) | 1988-08-03 |
| EP0245020A2 (en) | 1987-11-11 |
| JPS62288830A (en) | 1987-12-15 |
| KR870011492A (en) | 1987-12-23 |
| FI90560B (en) | 1993-11-15 |
| JP2690305B2 (en) | 1997-12-10 |
| US4913544A (en) | 1990-04-03 |
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