Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From phosphorus-containing reactant
Reexamination Certificate
1999-11-12
2001-09-11
Truong, Duc (Department: 1711)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
From phosphorus-containing reactant
C528S176000, C528S167000, C525S532000, C525S097000, C525S210000, C525S212000, C351S159000, C264S001320
Reexamination Certificate
active
06288210
ABSTRACT:
FIELD OF THE INVENTION
The present invention is directed to melt processable, high molecular weight polyphosphonates having a high refractive index and methods of preparing the same.
BACKGROUND OF THE INVENTION
Polycarbonates are tough, rigid engineering thermoplastics. They are melt-processable and can easily be formed into optical and ophthalmic products by injection molding, instead of more time consuming and expensive casting processes. There is increasing demand for high refractive index materials for optical and opthalmic products. Polycarbonates, however, have only a limited refractive index.
Thus, there is a need for melt processable materials which have high refractive indices.
SUMMARY OF THE INVENTION
The present invention provides high molecular weight, film forming, high refractive index, melt-processable polyphosphonates. These polymers typically have lower melt processing temperatures and birefringerence than polycarbonates. These polymers may be used to form optical or ophthalmic products, such as lenses. Furthermore, the polymers of the present invention can be transferred directly from a reactor to a final mold for, for example, ophthalmic lens production, increasing the economic efficiency of the lens manufacturing process.
Another embodiment of the invention is a method of preparing the polyphosphonates of the present invention.
DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS
The present invention encompasses melt-processable phosphonate homopolymers or copolymers comprising, consisting essentially of, or consisting of units of the formula:
wherein R
1
, R
2
, and R
3
are independently O or S; at least one of R
1
, R
2
, and R
3
is S; R
4
is a linear or branched C
1
-C
4
alkyl or C
1
-C
4
haloalkyl, phenyl, chlorophenyl, p-tolyl, benzyl, biphenyl, or cyclohexyl; and R
5
is
or any combination of any of the foregoing. R
1
and R
3
are preferably O. Preferably, R
2
is S. Preferably, R
4
is phenyl. R
5
is preferably
or any combination of any of the foregoing.
Another embodiment of the present invention encompasses melt-processable phosphonate homopolymers or copolymers comprising, consisting essentially of, or consisting of units of the formula:
wherein R
6
, R
7
, and R
8
are independently O or S; R
9
is a linear or branched C
1
-C
4
alkyl or C
1
-C
4
haloalkyl, phenyl, chlorophenyl, p-tolyl, benzyl, biphenyl, or cyclohexyl; and R
10
is
Preferably, R
6
and R
8
are O.
The invention further includes an optical or ophthalmic part, preferably a lens, comprising, consisting essentially of, or consisting of melt-processable phosphonate homopolymers or copolymers comprising units of the formula:
wherein R
11
, R
12
, and R
13
independently are O or S; R
14
is a linear or branched C
1
-C
4
alkyl or C
1
-C
4
haloalkyl, phenyl, chlorophenyl, p-tolyl, benzyl, biphenyl, or cyclohexyl; and R
15
is defined as R
5
above. The optical or ophthalmic part may also be a transparent or translucent sheet comprising the melt-processable phosphonate polymers of formula III.
The polymers of the present invention can be homopolymers or copolymers, including, but not limited to, random copolymers and block copolymers. A preferred copolymer comprises a first unit having the formula
where R
16
, R
17
, and R
18
are independently O or S; R
19
is phenyl; and R
20
is
and a second unit having the formula
where R
21
, R
22
, and R
23
are independently O or S; R
24
is phenyl; and R
25
is
The number average molecular weight of a homopolymer or copolymer of the present invention is typically from about 10,000 to about 60,000 g/mol and preferably from about 15,000 to about 40,000 g/mol.
Generally, these homopolymers and copolymers have a glass transition temperature (T
g
) greater than or equal to about 120° C. Also, these polymers typically have a refractive index ranging from about 1.58 to about 1.64. These polymers are typically processable at from about 75 to about 100° C. above their glass transition temperatures.
The melt-processable phosphonate homopolymers and copolymers of the present invention may be prepared as described in Japanese Patent Publication No. 61-261321. One method of preparing these polymers is as follows. At least one phosphonic acid halide having the formula
where R
26
and R
28
are independently halogens; R
27
is O or S; and R
29
is a linear or branched C
1
-C
4
alkyl or C
1
-C
4
haloalkyl, phenyl, chlorophenyl, p-tolyl, benzyl, biphenyl, or cyclohexyl is reacted with one or more bisphenols to yield the phosphonate homopolymer or copolymer. Preferred phosphonic acid halides include phenyl phosphonic dichloride, phenyl thiophosphonic dichloride, and any combination of any of the foregoing. The phosphonic acid halide may be dissolved by mixing it in a solvent, such as methylene chloride, prior to reacting the phosphonic acid halide with the bisphenol. When preparing polymers having units of the formula I or II above, R
27
and R
29
of the phosphonic acid halide are defined as R
2
and R
4
or R
7
and R
9
above, respectively.
Suitable bisphenols include, but are not limited to, hydroquinone; resorcinol; 4,4′-dihydroxybiphenyl; 4,4′-cyclohexylidenediphenol; bisphenol A; bis(4-hydroxyphenyl)methane; 2,2-bis(2-hydroxyphenyl)propane; bis P; 4,4′-bis-S; 2,2′-bis-S; 2-hydroxyphenyl-4′-hydroxyphenyl sulfone; dihydroxydiphenyl ether; bis(4-hydroxyphenyl) sulfide; bis(2-hydroxyphenyl) sulfide; dihydroxybenzophenone; 1,5-dihydroxynaphthalene; 2,5-dihydroxynaphthalene; 2,2-bis(3,5-dimethyl-4-hydroxyphenyl) propane; thiodithiophenol; phenolphthalein; 4,4′-bis(hydroxyphenyl)phenyl phosphine oxide; &agr;,&agr;′-bis(4-hydroxy-3-methylphenyl)-1,4-diisopropylbenzene; bis E; 2,2-bis(4-hydroxy-3-methylphenyl)propane; bis(4-hydroxy-3-methylphenyl)sulfide; dihydroxydiphenylether; 1,3-bis(4-hydroxyphenoxy)benzene; phenyl HC; t-butyl HQ; 4,4′-thiobis(t-butyl cresol); 2,2′-thiobis(4-t-octylphenol); and any combination of any of the foregoing. The bisphenol may be dissolved by mixing it in a solvent, such as methylene chloride with triethylamine and 1-methyl imidazole, prior to reacting the bisphenol with the phosphonic acid halide.
The copolymer of the present invention may be prepared by reacting at least two different phosphonic acid halides having the aforementioned formula with one or more bisphenols. Alternatively, the copolymer may be prepared by reacting at least one phosphonic acid halide with at least two different bisphenols.
Optical or ophthalmic lenses may be prepared by injection or compression molding a melt-processable phosphonate polymer of the present invention into the form of a lens.
REFERENCES:
patent: 6040416 (2000-03-01), Sekharipuram et al.
Chem Abstracts; 122:56712 “Synthesis and Structural Characterization of Polyphosphate and Polyphosphonate Esters Derived from Biologically Active Diols” Carraher et al. 1993.*
115:197854 “Synthesis and Biological Charactrization of Polyphosphate and Polyphosphonate esters . . . Diols” Carraher et al. 1991.*
99:213370 “Thermal Behavior with Polypropylene” Petreus et al. 1983.*
94:192931 “Nonflammable poly (Phenylphosphonothioates” Petreus et al. 1981.*
89:11437 “Plasticized polycarbonate composition” Mark et al. 1978.*
86:17295 “Phosphorus-Containing Polyesters” Okada et al. 1977.*
84:60204 “Phosphonate polymers” Kato et al. 1976.
Bhatnagar Atul
McGrath James E.
Sekharipuram Venkat
Shobha Hosadurga K.
Darby & Darby
Truong Duc
Virginia Tech. Intellectual Properties, Inc.
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