Fluorinated silicon phthalocyanines and naphthalocyanines for electrophoretic display
View Patent ↗This invention relates to stable colorants of high extinction coefficient and high solubility or dispersibility for an electrophoretic, magnetophoretic or electromagnetophoretic display. More particularly, it relates to stable colorants for a microcup-based electrophoretic or electromagnetophoretic display the cells of which are filled with charged and/or magnetic particles dispersed in a halogenated, preferably a fluorinated, solvent. The use of the stable colorants allows the display to be of superior contrast ratio and longevity, and suitable for high-quality imagery applications.
1. An electrophoretic display comprising:
a) two electrode plates;
b) an array of display cells filled with an electrophoretic fluid comprising charged pigment particles dispersed in a fluorinated solvent or solvent mixture wherein the fluorinated solvent or solvent mixture is colored by a fluorinated silicon phthalocyanine or silicon naphthalocyanine compound represented by the following formulas:
wherein each n is individually 0-4 for silicon phthalocyanine (I) or 0-6 for silicon naphthalocyanine (II);
R 1 is independently R f -A-, alkyl, heteroalkyl, aryl, heteroaryl, heteroalkylaryl, alkylheteroaryl, heteroarylalkyl, arylheteroalkyl, R′O—, R′S—, R′R″N—, R′CO—, R′OCO—, R′COO—, R′CONR″—, R′R″NCO—, R′NHCONR″—, R′SO 2 NR″—, or R′R″NSO 2 —; or a halogenated derivative of alkyl, heteroalkyl, aryl, heteroaryl, heteroalkylaryl, alkylheteroaryl, heteroarylalkyl, arylheteroalkyl, R′O—, R′S—, R′R″N—, R′CO—, R′OCO—, R′COO—, R′CONR″—, R′R″NCO—, R′NHCONR″—, R′SO 2 NR′—, or R′R″NSO 2 —; wherein R′ and R″ are independently hydrogen, R f , alkyl, heteroalkyl, aryl, heteroaryl, heterarylalkyl, arylheteralkyl, heteroalkylaryl, or alkylheteroaryl;
A is a single bond, —CH 2 O—, —CH 2 CH 2 O—, or —CO—;
Z is O or NR′ wherein R′ is defined as above;
R 2 is hydrogen, R f —B—, alkyl, heteroalkyl, a halogenated derivative of alkyl, a halogenated derivative of heteroalkyl, or SiR 3 R 4 R 5 , wherein R 3 , R 4 , and R 5 are independently an alkyl or fluoroalkyl group of 1 to 20 carbon atoms or alkoxy or fluoralkoxy of 2 to 40 carbon atoms;
B is a single bond, —CH 2 —, or —CH 2 CH 2 —;
R f is a fluorinated polymeric or oligomeric moiety having a molecular weight of 100-100,000 and is prepared from one or more types of fluorinated monomers; provided that the substituents, R 1 , R 2 , R 3 , R 4 , R 5 , R f , Z and n are so selected that the total fluorine content of the fluorinated silicon phthalocyanine or silicon napthalocyanine compound is at least 20% by weight,
and said charged pigment particles in the electrophoretic fluid are capable of moving towards one or the other electrode plate depending on the voltage difference imposed between the two electrode plates.
2. The electrophoretic display of claim 1 , wherein the total fluorine content of said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is at least 30% by weight.
3. The electrophoretic display of claim 2 , wherein the total fluorine content is at least 50% by weight.
4. The electrophoretic display of claim 1 , wherein R f in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is prepared from one or more types of the fluorinated monomers selected from the group consisting of epoxide, hydrofuran, cyclolactone, cyclolactam, acrylate, methacrylate, styrene, vinylether and vinylalkane.
5. The electrophoretic display of claim 1 , wherein A in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is —CH 2 O—, —CH 2 CH 2 O—, or —CO—.
6. The electrophoretic display of claim 1 , wherein B in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is —CH 2 —.
7. The electrophoretic display of claim 1 , wherein n in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is 0-2.
8. The electrophoretic display of claim 1 , wherein R 1 in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is an alkyl, fluoroalkyl, alkoxy, or fluoralkoxy group having from 1 to 20 carbon atoms.
9. The electrophoretic display of claim 8 , wherein R 1 in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is an alkyl, fluoroalkyl, alkoxy, or fluoralkoxy group having 1 to 12 carbon atoms.
10. The electrophoretic display of claim 1 , wherein Z in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is oxygen.
11. The electrophoretic display of claim 1 , wherein R 2 in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is hydrogen,
R f —CH 2 —, alkyl, fluoroalkyl, or —SiR 3 R 4 R 5 , wherein R 3 , R 4 and R 5 are indep alkyl group, a fluorinated alkyl of 6 to 12 carbon atoms, or a fluorinated alkoxy of 6 to 18 carbon atoms.
12. The electrophoretic display of claim 11 , wherein R 2 is —SiR 3 R 4 R 5 in which one, two or all three of R 3 , R 4 and R 5 are methyl.
13. The electrophoretic display of claim 11 , wherein the fluoroalkyl is —(CH 2 ) 2 (CF 2 ) 5 CF 3 or —(CH 2 ) 2 (CF 2 ) 7 CF 3 .
14. The electrophoretic display of claim 11 , wherein the fluoroalkoxy is —OCH 2 (CF 2 ) 12 CF 3 or —CH 2 (CF 2 ) 6 CF 3 .
15. The electrophoretic display of claim 1 , wherein R f in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound is a fluorinated polymer or oligomer having a molecular weight of 200-20,000.
16. The electrophoretic display of claim 15 , wherein R f is a fluorinated polymer or oligomer having a molecular weight of 400-10,000.
17. The electrophoretic display of claim 15 , wherein R f is perfluoropolyether or hydrofluoropolyether.
18. The electrophoretic display of claim 15 , wherein R f is poly(chlorotrifluoroethylene).
19. The electrophoretic display of claim 15 , wherein R f is a polymeric chain derived from fluorinated epoxides.
20. The electrophoretic display of claim 19 , wherein R f is —CF(CF 3 )[OCF 2 CF(CF 3 )] n F.
21. The electrophoretic display of claim 1 , wherein in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound n is 0, Z is oxygen and R 2 is —CH 2 CF(CF 3 )[OCF 2 CF(CF 3 )] n F.
22. The electrophoretic display of claim 1 , wherein in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound n is 0, Z is oxygen and R 2 is —SiR 3 R 4 R 5 , in which R 3 is —(CH 2 ) 2 (CF 2 ) 7 CF 3 and R 4 and R 5 are both —OCH 2 (CF 2 ) 12 CF 3 .
23. The electrophoretic display of claim 1 , wherein in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound n is 0, Z is oxygen and R 2 is —SiR 3 R 4 R 5 , in which R 3 , R 4 and R 5 are all —(CH 2 ) 2 (CF 2 ) 5 CF 3 .
24. The electrophoretic display of claim 1 , wherein in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound, n is 1, R 1 is n-C 8 F 17 , Z is oxygen, and R 2 is hydrogen.
25. The electrophoretic display of claim 1 wherein in said fluorinated silicon phthalocyanine or silicon naphthalocyanine compound n is 1, R 1 is n-C 8 F 17 , Z is oxygen, and R 2 is —SiR 3 R 4 R 5 , in which R 3 and R 4 both methyl and R 5 is —(CH 2 ) 2 (CF 2 ) 7 CF 3 .