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1. AU1997027573 - UV curable high index vinyl esters

Note: Texte fondé sur des processus automatiques de reconnaissance optique de caractères. Seule la version PDF a une valeur juridique

[ EN ]
WO 97/44372 I'CT/Λ I 197/00310
1
UV CURABLE HIGH INDEX VINYL ESTERS
The present invention relates to the manufacture of plastic optical articles such as video dises and ophthalmic lenses,
The most widely used plastic ophthalmic lens material is polymerised diethylene glycol bis (allyl carbonate), This polymer has proved a satisfactory material for the manufacture of ophthalmic lenses because of a combination of features, including excellent transmission, resistance to discolouration, high strength and high impact resistance, The material has a reasonable abrasion resistance and can be coated to improve that resistance.
Lenses formed from polymers including divinyl benzene are generally brittle and have a high yellowness index.
In Australian Patent Application 81216/87, the entire disclosure of which is incorporated herein by reference, applicant describes a cross-linkable casting composition including at least polyoxyalkylene glycol diacrylate or dimethacrylate and at least one poly functional unsaturated cross-linking agent. Whilst the lenses produced from the prior art compositions provide advances in the art, difficulties may be encountered in certain applications. For example, difficulties may be encountered in some patients in fitting lenses made from such compositions. Eye discomfort, including eye fatigue problems, may be encountered. Moreover, such lenses have been found to be cosmetically unattractive.
Further, in Australian Patent Application 75160/91, the entire disclosure of which is incorporated herein by reference, applicant describes a polyoxyalkylene glycol diacrylate or dimethacrylate; a monomer including a recurring unit derived from at least ^ne radical-polymerisable bisphenol monomer capable of forming a homopolymer having a high refractive index of more than 1.55; and a urethane monomer having 2 to 6 terminal groups selected from a group comprising acrylic and methacrylic groups.
Japanese Patent Application 63-309509 to Showa Denko KK discloses the formation of a prepolymer of divinyl benzene and a polythiol compound which may be used in the formation of optical materials with high refractive indexes, Japanese Patent Application 63-19498 to Mitsubishi Gas discloses a high WO 97/44372 I*CT/AU97/00310
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refractive index composition of divinyl benzene and a thiol compound. However optical lenses produced thereby exhibit unacceptable strain characteristics and core times.
However, there remains a need in the prior art for optical articles of very high refractive indexes, very low densities and excellent colour, that still retain excellent mechanical properties.
Accordingly, it is an object of the present invention to overcome, or at least alleviate, one or more of the difficulties related to the prior art.
Accordingly, the present invention provides a cross-linkable polymeric casting composition including an effective amount of
a divinyl ester monomer of a bicyclic or polycyclic compound; and optionally a minor amount of
a di- or polythio compound.
The inclusion of the bicyclic monomer may provide an increase in rigidity, (and thus hardness) and glass transition temperature (Tg). The cross-linkable polymeric casting composition is U.V, curable. This may provide a significant decrease in cure time, e.g. from approximately 6 hours to approximately 1 hour.
The optical article formed from the casting composition of the present invention may exhibit a refractive index in the high to very high refractive index range.
The divinyl ester cyclic monomer may be a divinyl ester of an alkoxylated bisphenol C or bisphenol S, or mixtures thereof,
The bicyclic or polycyclic monomer may be selected from compounds having the formula
WO 97/44372 I'C’T/Λ 097/00310
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wharain
G is selactad from the group consisting of
wherein M is selected from the group consisting of a bond,— S“ , — S— methyleneand — CH 2 — -S — CH 2 — o
Ri, R 2, R 3and R 4 are independently selected from the group consisting of hydrogen and alkyl of 1 to 6 carbon atoms,
n is an integer having a value of 0 to 10,
Y is hydrogen or a halogen, preferably fluorine, chlorine or bromine, and J is a unsaturated terminal group particularly an allyl group or group of — C — C— CH
formula 1 K,5
wherein R 5 is hydrogen or to C 6 alkyl. Most preferably R 6 is hydrogen or methyl.
o
II
Preferably M is a bond, S or methylen
o II
when  M is a bond G has the formula 
Preferably G is a bisphenol S, naphthalene or bisphenol fluorene derivative.
Particularly preferred bicyclic or polycyclic monomers may be selected from one or more of the followi ng:
An bisphenol S divinyl ester of the formula
a naphthalene-based ethoxylated divinyl ester of the formula
a bisphenol fluorene diglycidyl allylic monomer of the formula
and
a bisphenol S diallyl ether of the formula
The divinyl ester cyclic monomers may be formed by reacting a di- or poly-epoxide monomer of a bisphenol compound with an acrylic or methacrylic acid. Suitable di-epoxide monomers are as follows:
wherein G is selected from one or more of the following
372 I'CIVAU'; 7/00310
o
M is selected from the group consisting of a bond, •s II-methylene and o
R 1 ( R 2, R 3, R 4 and R s are independently selected from the group ing of hydrogen and alkyl of 1 to 6 carbon atoms,
n is an integer having a value of 0 to 8,
Y is hydrogen or a halogen, preferably fluorine, chlorine or bromine; A di- or polyepoxide of a bisphenol monomer is preferred.
The di- or polyepoxide bisphenol monomer may be a di- or polyepoxide of nol A or bisphenol S, or mixtures thereof,
The cyclic monomer may be present in amounts of from approximately 100% by weight, preferably approximately 5 to 80% by weight, more bly approximately 10 to 70% by weight, based on the total weight of the composition,
The di- or polythiol compound, when present, may be of any suitable di-, tri- or tetra polythiol compound may be used. A tri- or tetra-polythiol is ed. The thiol may be selected from one or more of the following:
O 97AM372 I‘CT/AUi)7/00310
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(a) Pentaerythritol Tetrakis (3-mercapto-propionate) [PTMP]
C(CH2 O C CH2CH2SH)4
O
(b) Trimethylolpropane Tris (3-mercaptopropionate) [TTMP]
CH3CH2C(CH2 O C CH2CH2SH)3
O
(c) 4-mercaptomethyl-3,6-dithia-1,8-octanedithiol [MDO]
CH2SH
CHSCH2CH2SH
CH2SCH2CH2S
(d) Pentaerythritol Tetrakis (3-mercaptoacetate) [PTMA]
C(CH2 O C CH2SH)4
O
(e) Trimethylolpropane Tris (3-mercaptoacetate) [TTMA]
CH3CH2C(CH2 O C CH2SH)3
O
(f) 4-t-butyl-1 ,2-benzenedithiol
(g) 2-mercaptoethylsulfide
HSCH 2CH 2SCH 2CH 2SH
(h) 4,4'-thiodibenzenethiol
9744372                                                                                      I*CT/AU97/00310
edithiol
Dimercaptoacetate
H 2COOCCH 2-S
H 2COOCCH 2-SH
Dimercaptopropionate Ethylene bis(3-Mercaptopropionate) H2COOCCH2-CH2-SH
H2COOCCH2-CH2-SH
ylene Glycol Dimercaptoacetates
ylene Glycol Di(3-Mercaptopropionates)
CH -CH 2OOCCH 2-CH 2— SH
O CH 2 CH 2OOCCH 2-CH 2— S
2 5 (mercaptomethyl)-1 ,4-dithiane
0 3 6 ia-1 ,8-octanedithiol
iol compound may preferably be present in amounts of from 5 to 30% by weight, more preferably approximately 10 to 20% by on the total weight of the casting composition.
oss-linkable polymeric casting composition may further include a g agent. The inclusion of a strain-reducing agent provides a reduction in strain evident in optical articles produced therefrom, together with a significant decrease in cure time, e.g. from approximately 6 hours to approximately 1 hour,
The strain reducing agent may be an epoxidised monomer or oligomer. The strain reducing agent should exhibit optical transparency, in use,
The epoxidised monomer may function as a diluent for the bisphenol monomer which may exhibit very poor solubility, The epoxidised monomer or oligomer may fall into one or more of the following classes: internal, terminal, mono-functional, di-functional, tri-functional, tetra-functional, aliphatic, aromatic, cyclic, structurally simple, structurally complex, esters, ethers, amines. An epoxidised soybean material may be used. The epoxidised monomer or oligomer may be selected from one or more of the following
1) Epoxidised soybean oil - Triglycerides of a mixture of epoxidised a) oleic acid, b) linoleic acid, c) linolinic acid
a)
b)
CH 3(CH 2) 3CH 2CH-CHCH 2CH-CHCH2(CH2)6COOH
o o
c)
2) Propylene Oxide
Q CH 2— CH— CH 3
3) Hexanediol diglycidyl ether (HDGE)
CH 2-CH— CH 2— O— (CH 2) 6-O— CH 2— CH-CH 2
)          1,2 epoxy butane
C ΛH 2-CH-CH 2— CH 3
)          Bisphenol fluorene diglycidyl ether (BPGF.)
) Epolight 100MF
)         AK-601
8)          MY 721
The epoxidised monomer may be present in a sufficient amount to render the bisphenol monomer soluble or dispersible in the monomer mix. The secondary epoxidised monomer may be present in amounts of from approximately 0.001% to 2.5% by weight, preferably 0.01% to 1%, more preferably approximately 0.05% to 0.4%, based on the total weight of the casting composition.
The crosslinkable polymeric casting composition according to the present invention may be utilised in the preparation of an optical article. The optical article may be characterised by having an increased hardness relative to known prior art articles. The optical article may exhibit a high to very high refractive index, excellent colour and low density. Surprisingly, the cross-linkable polymeric casimg composition may exhibit a reduced cure time of for example from approximately 6 nours to approximately 1 hour.
By the term "high refractive index", as used herein, we mean a polymer having a refractive index of at least approximately 1.55, preferably 1.57. By the term "very high refractive index" as used herein, we mean a polymer having a refractive index of approximately 1.59 or above, preferably 1.60 or above.
By "low density", as used herein, we mean a density
in the range of approximately 1.15 to 1.25 g cm· 3.
The cross-linkable polymeric casting composition may optionally further include a polymerisable comonomer.
The polymerisable comonomer may be selected to improve the properties and/or processability of the cross-linkable polymeric casting composition. The polymerisable comonomer may be an unsaturated comonomer. The polymerisable comonomer may be selected from any suitable type, e.g. methacrylates, acrylates, vinyls, vinyl ethers, allyls, epoxides, and the like.
The polymerisable comonomer may preferably be selected from one or more ol vinyls, allylics, polyoxyalkylene glycol di-, tri-, tetra- and higher acrylates or methacrylates, polymerisable bisphenol monomers capable of forming a homopolymer having a high ref.r-.etive index of more than 1.55, urethane monomers having 2 to 6 terminal acrylic or methacrylic groups, fluorene diacrylates or dimethacrylates, and thiodiacrylate or dimethacrylate monomers. Where a vinyl comonomer is included, the vinyl comonomer may be selected from styrene, substituted styrenes, 3,9-divinyl-2,4,8,10-tetraoxaspiro[5.5]undecane (DTU), and mixtures thereof. The vinyl comonomers may be present in amounts of from approximately 1 to 40% by weight, preferably approximately 5 to 30% by weight, based on the total weight of the casting composition.
Where a thiodiacrylate or dimethacrylate is included, the thiodiacrylate or dimethacrylates may be selected frem bis(4-methacryloylthioethyl)sulfide (BMTES) and bis(4-methacryloylthiophenyl)sulfide (BMTS). The thiodiacrylate or dimethacrylate may be present in amounts of from approximately 1 to 40% by weight, preferably approximately 5 to 20% by weight, based on the total weight of the casting composition.
Where a fluorene diacrylate or methacrylate is included, the fluorene diacrylate or dimethacrylate monomer may be selected from a bisphenol fluorene dihydroxy acrylate (BFHA) or a bisphenol fluorene dimethacrylate (BFMA) or mixtures thereof.
The fluorene diacrylate or dimethacrylate monomer may be present in amounts of from approximately 1 to 35% by weight, preferably approximately 1 to 20% by weight.
The polyoxy alkylene glycol diacrylate or dimethacrylate compound according to the present invention, when present, may include ethylene oxide or propylene oxide repeating units in its backbone. A polyethylene glycol dimethacrylate is preferred. Suitable materials include dimethylacrylates where the number of repeating ethylene oxide groups is between 4 and 14.
The polyoxy alkylene glycol diacrylate or dimethacryiate component may be present in amounts of from approximately 1% by weight to 40% by weight, preferably approximately 5% to 20% by weight, based on the total weight of the casting composition.
The high index bisphenol monomer component in the cross-linkable casting composition when present may be selected from: dimethacryiate and diacrylate esters of bisphenol A; dimethacryiate and diacrylate esters of 4,4'bishydroxy-ethoxy-bisphenol A and the like.
Preferred high index bisphenol compounds include bisphenol A ethoxylated dimethacrylate and tetra brominated bisphenol A ethoxylated dimethacrylates.
The high index bisphenol monomer may be present in amounts of from approximately 1 to 40% by weight, preferably 5 to 25% by weight based on the total weight of the casting composition.
In a further aspect of the present invention the cross-linkable polymeric casting composition may further include at least one unsaturated cross-linking monomer having 3 or more polymerizable groups per molecule (polyfunctional).
The poly functional unsaturated cross-linking monomer according to the 1100 present invention may bf a tri- or tetra- functional vinyl, an acrylic or methacrylic monomer. The cross-linking monomer may be a short chain monomer for example trimethylol propane trimethacrylate, pentaerythritol triacrylate or tetracrylate, or the like.
An ethoxylated trimethylol propane triacrylate has also been found to be 1155 suitable.
The poly functional unsaturated cross-linking monomer may be present in amounts of from 0 to approximately 40% by weight, preferably approximately 5 to 20% by weight based on the total weight of the casting composition.
The c^ss-linkable casting composition according to the present invention 2200 may include a polymerisation initiator. The polymerisation initiator may be a ultraviolet (U.V.) cationic or radical initiator. A long wavelength UV initiator is preferred.
A range of long wavelength photoinitiators available commercially can be used, depending on sample thickness, type of U.V. lamp used and the absorption wavelength of the monomer mix.
The UV photoinitiator may be selected from the following:
TPO Lucirin LR 8728 2,4,6-trimethylbenzoyldiphenylphosphine oxide
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Irgacure 907 (2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropane-1-one)
Irgacure 184 (hydroxycyclohexyl) phenyl ketone
Irgacure 369 (2-benzyl-2-N-dimethylamino-1-(4-morpholinophenyl)-1-butanone)
Lucirin BDK; Irgacure 651 (Benzyl Dimethyl Ketal)
Vicure 30 2-(carbamoylazo)-substituted
WB 4744 2-n-propoxy-9H-thioxanthen-9-one
Quantacure EPD Ethyl 4*(dimothylamino)benzoate
A mixture of two or more of the above may also be used.
The UV photoinitiator may be present in any suitable amounts in the crosslinking casting composition, The UV photoinitiator may be present in amounts of from approximately 0.05% to 0,25% by weight, preferably approximately 0,20% to 0.25% by weight, based on the total weight of the casting composition.
The source of ultraviolet radiation may be of any suitable type. Any commercial UV curing system may be used. We have used a Fusion System with microwave driven lamps. A number of fusion bulbs with different output Spectra may be considered.
One source we have found satisfactory is a 10 inch, 300 watt/inch mercury lamp. This means that fully cured lenses can be manufactured, if desired, in about 5 to 10 minutes,
Typically 2 -4 passes under the U.V. completes the cure.
Other additives may be present which are conventionally used in casting compositions such as inhibitors, dyes, UV stabilisers and materials capable of modifying refractive index. Mould release agents can be added but they are in general not required with the compositions used in the method of the present invention. Such additives may include:
UV Absorbers including
• Ciba Geigy Tinuvin P - 2(2'-hydroxy-5'methyl phenyl) benzotriazole
• Cyanamid Cyasorb UV 531 -2-hydroxy-4-n-octoxybenzo-phenone
• Cyanamid Cyasorb UV5411-2(2-hydroxy-5-t-octylphenyl)-benzotriazole · Cyanamid UV 2098 - 2 hydroxy-4-(2-acryloyloxyethoxy)-benzophenone • National Starch and Chemicals Permasorb MA - 2 hydroxy-4-(2 hydroxy-3-methacry!oxy)propoxy benzophenone
• Cyanamid UV24 -°,2'-dihydroxy-4-methoxybenzophenone
•       BASF  UVINUL 400 - 2,4 dihydroxy-benzophenone 
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• BASF UVINUL D-40 « 2,2' »dihydroxy-4 ,4' dimethoxy·* benzophenone
• BASF UVINUL D-50 - 2,2', 4,4' tetrahydroxy benzophenone
• BASF UVINUL D-35-ethyl-2«cyano-3,3-diphenyl acrylate
• BASF UVINUL N-539-2-ethexyl-2-cyano-3,3-diphenyl acrylate
· Ciba Geigy Tinuvin 213
Hinderejlamine light stabilisers (HALS), including
• Ciba Geigy Tinuvin 765/292 - bis (1,2,2,6,6-penta-methyl-4-piperidyl)-sebacate
• Ciba Geigy 770 - bis (2,2,6,6-tetramethyl-4- piperidinyl) sebacate Antioxidants including
• Ciba Geigy Irganox 245 - triethylene glycol-bis-3-(3-tertbutyl-4-hydroxy-5-methyl phenyl)propionate
• Irganox 1010 -2,2-bis[[3-[3,4-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-1-oxopropoxy]methyl]-1,3-propanediyl 3,5-bis(1,1 -dimethyl ethyl)-4-hydroxy benzene propanoate
• Irganox 1076 - octadecyl 3-(3',5'-di-tert-butyl(-4'- hydroxyphenyl) propionate Anticolourina agents including
• 9, 10 dihydro-9-oxa-10-phosphaphenanthrene-1 -oxide
Cure modifiers including
· Dodecyl mercaptan
• Butyl mercaptan
• Thiophenol
• Nitroso compounds such as Q1301 from Wako
• Nofmer from Nippon Oils and Fats
Other monomeric additives can be present in amounts up to 10% by weight as viscosity modifiers, and include monomers such as methacrylic acid, vinyl silanes, and other functional monomers. Other monomeric additives may be included to improve processing and/or material properties, these include:
• methacrylic acid, maleic anhydride, acrylic acid
· adhesion promoters/modifiers such as Sartomer 9008, Sartomer 9013, Sartomer 9015 etc.
•       dye-enhancing, pH-adjusting monomers like Alcolac SIPOMER 2MIM
•       a charge-reducing cationic monomer to render the material more antistatic, example Sipomer Q5-80 or Q9-75
In a further aspect of the present invention there is provided a polymeric article formed from a cross linkable casting composition including an effective amount of
a divinyl ester monomer of a bisphenol compound; and
a di- or polythio compound.
The polymeric article may be an optical article. The optical article may provide characteristics equal to or greater than those achievable with articles made from diethylene glycol bis(allyl carbonate) but with a considerably reduced cure time and substantially Increased throughout. The optical article may be further characterised by having rec jd weight and/or thickness relative to the prior art, high tg, very low Yellowness Index and low density, whilst retaining good abrasion resistance and impact resistance,
The overall refractive index may be in the high to very high refractive index range of approximately 1.58 to 1 ,70, preferably 1.59 to 1.65.
The optical articles prepared by the method of this invention include camera lenses, ophthalmic lenses and video dises.
The casting composition may be formed into a suitable article by mixing In a convenient vessel the components making up the material, and then adding the curing catalyst and/or photo-initiator. The mixed material is then degassed or filtered. As the curing time is substantially reduced the casting process may be undertaken on a continuous or semi-continuous basis.
The present invention will now be more fully described with reference to the accompanying examples, It should be understood, however, that the description following is illustrative only and should not be taken In any way as a restriction on the generality of the invention described above.
EXAMPLE 1
Background
The diglycidyl ether of bisphenol-S EBPS-300 with a structure (I) was supplied by Japan Chemical Company, The converted product may then be used in the formulation of the cross-linkable polymeric casting composition according to the present invention to improve the hardness and impact strength.
acrylic acid
benzyl dimethylamlne
Materials
EBPS-300 (Japan Chemical Company, EEW=255), acrylic acid (Fluka, 99%), benzyl dimethyl amine (Pacific Anchor Chemical Corporation, Amicure BPMA),
Experimental
In a 500 ml round flask, 144 g acrylic acid (2 mol) and 2,7 g of benzyl dimethyl amine (0.02 mole) were stirred at 50°C, 51 g (0.2 mole) EBPS-300 solid was added by small portions during 2 hours. After another nine hours of stirring at 50°C, the FTIR showed that the epoxy group was fully converted into an acrylate. After cooling down, the product mixture was precipitated into 1 litre water. After drying, the product was dissolved in ethyl acetate (50 ml) first, then precipitated into 500 ml of petroleum ether (60 to 80°C). The product was dissolved in acetone (50 ml) and precipitated into 1 litre of 0.1 M NaOH, 1 litre of 0.1 M HCI and 1 litre of distilled water successively. The final product was dried under vacuum at room temperature of two days. The yield of the product (II) was 54 g (83%). The product was a clear plastic like solid (slightly yellow), It could be molten at 60°C. The FTIR spectrum of the product showed the conversion of the epoxy groups into acrylate was complete (Figure 1).
Discussion
The 915 cm '1 peak in the infrared spectrum in Figure 1 was associated with the oxirane group, it is the characteristic peak of epoxy resins. During conversion the peak at 915 cm "1 gradually decreased till the whole peak disappeared. At the same time a band at 1723, which is due to the carbonyl group of the ester formation gradually increased (Figure 1).
Conclusions
50 grams of the acrylated diglycidyl ether of bisphenol-S was obtained for formulation investigation. The monomer is miscible with a standard polymeric lens formulation and is UV curable. A lens was cast with 10% acrylated diglycidyl ether of bisphenol-S in a standard polymeric lens formulation. The hardness of this lens was 50% harder than a standard plastic lens,
EXAMPLE 2
THE CONVERSION OF NAPHTHALENE-BASED EPOXY RESIN INTO AN
ACRYLATE MONOMER
Background
The naphthalene-based epoxy resin (Epiclon HP-4032D) with a structure of (I) was supplied by Dainippon Ink Chemical Industry Company, The converted product may then be used in the UV curable formulation to improve the rigidity of the lens materials.
acrylic acid
benzyl dimethyl amin
Materials
Epiclon HP-4032D (Dainippon Ink Chemical Industry Company, EEW-141, white solid), acrylic acid (Fluka, 99%), benzyl dimethyl amine (Pacific Anchor Chemical Corporation, Amicure BPMA), Acetone was dried over magnesium sulphate for two hours before use,
Experimental
In a 1 litre three neck round bottom flask equipped with a condenser and a magnetic stirrer, 110 g acrylic acid (1.52 mol, 100% excess), and 5,14 g of benzyl dimethyl amine (0.038 mole) were stirred at 50°C. 108 g Epiclon HP-40320 (0.76 mole epoxy groups) dissolved in 250 ml acetone was dropped in slowly during two hours through a pressure balanced dropping funnel. The reaction was carried out under nitrogen protection. After 18 hours of refluxing, the FTIR showed that the epoxy group was fully converted into acrylate. The product mixture was poured into 1 litre water. After 30 minutes standing, a viscous liquid was obtained at the bottom of the solution. The viscous liquid was further washed by water (3 x 1000 ml), 0.1 M NaOH aqueous solution (500 ml), water (1000 ml), 0.1 M HCI (2 x 500 ml) successively. The viscous liquid was dissolved into 500 ml ethyl acetate, and dried over anhydrous magnesium sulphate for 1 hour. The solvent was removed by rotary evaporator, The final product was dried under vacuum at room temperature for two days. The yield of the product (II) was 104 g (66%). The product was a viscous honey-like liquid (slightly yellow). The FTIR spectrum of the product showed the conversion of the epoxy groups into acrylate was complete (Figure 1).
Properties of Monomer
Discussion
The 912 cm-1 peak in the infrared spectrum (Figure 2) was associated with the oxirane group, it is the characteristic peak of epoxy resins. After conversion the peak at 912 cm-1 disappeared completely. At the same time a band at 1724 cm-1 , which is due to the carbonyl group of the ester formation was observed. The band at 3450 cm-1 is due to the hydroxy group in the product (Figure 1).
Conclusions
100 grams of the acrylated naphthalene-based epoxy resin was obtained for formulation investigation. This monomer can be polymerised by both heat and UV curing method.
EXAMPLE 3
THE CONVERSION OF BISPHENOL FLUORENE DIGLYCIDYL ETHER iBPGE
INTO ALLYLIC MONOMER
The following reaction was carried out to convert bisphenol fluorene diglycidyl ether (BPGE) (III) into its allylic monomer, so that the converted allyl type monomer can be used in thiol-ene reactions.
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Synthetic Method
276 g of bisphenol fluorene diglycidyl ether (0.6 mol) and 409 ml alcohol (6 mol, excess) was dissolved into 800 ml toluene (dried over anhydrous magnesium sulphate) at 70°C. The solution was then cooled down. Cooling with ice-bath, 6 ml boron trifluoride etherate was injected in by 1 ml portions, the temperature of the solution was controlled between 0 to 5°C. After 30 minutes stirring the ice bath was removed, the temperature was allowed to rise to room temperature (25°C). Stirring at room temperature for two hours, the solution changed from cloudy to clear colourless. Both thin layer chromatography and infrared spectrum indicated the completion of the reaction at this stage. After further 5 hours stirring at room temperature, the solvent and excess allyl alcohol was removed by rotary evaporator under vacuum. Dissolved into 1 litre toluene, the solution was allowed to pass a silica gel column (10 cm in diameter, 5 cm in height). Removal of the solvent gate 240 g colourless, honey like liquid (IV). Yield = 70%.
Properties of Monomer
Discussion
Both the thin layer chromatography and infrared-spectrum (Figure 3b) indicated the disappearance of starting material. In the IR spectrum, the peaks at 910 and 864 cm-1 which are associated with epoxide group disappeared, new peaks at 1651 (CH2=CH-) and 3431 (OH) cm-1 were observed. 1H-NMR spectrum (Figure 3a) confirmed the formation of the allyl monomer.
This monomer can be cured by heat with 3% of TX29 as initiator MDO was UV curable. The stoichiometrical formulation of allylic bisphenol fluorene with the conversion of double bonds and thiol groups were complete.
Conclusions
This monomer is a colourless viscous liquid, it is possible to be used in lens formulation. Refractive index of this monomer is 1.60.
EXAMPLE 4
SYNTHESIS OF DIALLYL ETHER OF 4,4'-SULFONYLDIPHENOL
Introduction
In order to obtain a rigid monomer the diallyl ether of 4,4'-sulfonyldiphenol was synthesised.
Synthetic Method
25 g 4,4'-sulfonyldiphenol sulfone (0.1 mol, V) was dissolved Into 200 ml DMSO with 12 g NaOH (0.3 mol). The mixture was heated to 65 to 70°C, with stirring and N 2 protection, then 19 ml (0.22 mol, 10% excess) allyl bromide was added slowly during 1 hour. After 6 more hours reaction at 70°C, the reaction mixture was poured into 1 litre water. On standing overnight, a lot of solid was formed. The solid was collected by filtration, washed twice with water and recrystallised from acetone/water mixture solvent twice. After drying 27 g of white crystalline solid were obtained (Vl)(yield=82%).
Properties of Monomer
Discussion
Both 1H-NMR (Figure 4b) and Infrared spectra (Figure 4a) confirmed the chemical structure of the product.
Conclusion
This crystalline solid is white in solid state, it is possible to be used in lens material formulation in term of colour. Refractive index of this compound is 1.61 WO 97/44372 1*CT/AU97/00310
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as predicted by Expode computer software. Formulations with pdythiols can be cured by UV irradiation,
EXAMPLE 5
A cross-linkable casting composition having the following components was prepared
Percent
• PTMP (pentaerythritol tetrakis (3-mercapto-propionate) 27 • Bisphenol S ethoxylated divinyl ester (Example 1) 70 • Epolight 100 MF 0.4 · Nofmer-MSD (2,4-diphenyl-4-methyl-1-pentene) 2.6 The monomer mix was prepared in a beaker together with 0.2% TPO Lucirin long wavelength U.V. initiator.
The casting material was used to fill the space between a pair of glass moulds separated by a plastic gasket at their periphery and held together by a clip. The mould was then passed 4 times under a U.V. lamp. Cure time was 1 hour.
Finally, it is to be understood that various other modifications and/or alterations may be made without departing from the spirit of the present invention as outlined herein.