Claims
- 1. A process for the preparation of poly4-[(4-cardanyl)azo]benzoic acid comprising subjecting 4-[(4-cardanyl)azo]benzoic acid to polymerisation by any known polycondensation technique using thionyl chloride and pyridine.
- 2. A process for the preparation of poly4-[(4-acryloylcardanyl)azo]benzoic acid comprising subjecting 4-[(4-acryloylcardanyl)azo]benzoic acid to polymerisation by any known free radical polymerisation technique.
- 3. A process for the preparation of the cationic polymer of formula V of 4-[(4-cardanyl)azo]benzoic acid comprising subjecting the monomer to polymerisation by cationic mechanism in the presence of borontrifluoroetherate in dichloroethane at 100° C. to obtain the said cationic polymer polymerised through the side chain unsaturation.
- 4. A process as for the preparation of 4-[(4-cardanyl)azo]benzoic acid and 4-[(4acryloylcardanyl)azo]benzoic acid and their polymers poly 4-[(4-cardanyl)azo] benzoic acid and poly4-[(4-acryloylcardanyl)azo] benzoic acid comprising a process for the cationic polymerisation of 4-[(4-cardanyl)azo]benzoic acid comprising (a) diazotising p-amino benzoic acid by known methods, adding a solution of cardanol in an organic solvent drop wise to the diazonium salt solution and crystallising it from an organic solvent, polymerising the novel monomer 4-[(4-cardanyl)azo]benzoic acid thus obtained by known polycondensation technique using thionyl chloride and pyridine to give poly4-[(4-cardanyl)azo]benzoic acid, (b) reacting 4-[(4-cardanyl)azo]benzoic acid with acryloyl chloride to get the acrylic derivative 4-[(4acryloylcardanyl)azo]benzoic acid, (c) polymerising said acryloyl derivative by known free radical polymerisation technique to give poly4-[(4-acryloylcardanyl)azo]benzoic acid or (d) polymerising 4-[(4-cardanyl)azo] benzoic acid by cationic mechanism using borontrifluoroetherate in dichloroethane at 100° C. to get the cationic polymer of 4-[(4-cardanyl)azo]benzoic acid polymerised through the side chain unsaturation (e) and if desired converting the polymers obtained above to cross linked polymer films with azobenzene mesogens in network structures by cross linking the polymers under controlled heating at a rate of 5-10° C. per minute to a temperature of 150-180° C. and annealing at this temperature for 1-2 hours and (f) dissolving the polymer in solvents selected from tetrahydrofuran, dimethyl acetamide, dimethyl formamide and evaporating the solvent off by exposing the glass plate in a vacuum oven and raising the temperature to 150-180° C. and annealing at this temperature for 1-1½ hours whereby cross linked films exhibiting liquid crystalline phase behaviour.
Parent Case Info
This Application is divisional of application Ser. No. 10/212,589 filed Aug. 5, 2002, which is a division of Ser. No. 09/538,642 filed Mar. 30, 2000 now abandoned.
US Referenced Citations (5)
Number |
Name |
Date |
Kind |
2317585 |
Caplan |
Apr 1943 |
A |
2502436 |
Dawson et al. |
Jul 1950 |
A |
2496151 |
Dawson et al. |
Aug 1950 |
A |
2571091 |
Wasserman et al. |
Aug 1951 |
A |
6229054 |
Dai et al. |
May 2001 |
B1 |
Foreign Referenced Citations (1)
Number |
Date |
Country |
662509 |
Aug 1949 |
GB |
Non-Patent Literature Citations (2)
Entry |
Macromolecules (1993), 26(25), 7103-5 (Author Saminathan, Muthusamy et al.) “Synthesis and Characterization of Main-Chain Liquid Crystaline Polymers Containing a p-Phenyleneazo Group”. |
Macromol. New Front., Proc.IUPAC Int.Symp.Adv.Polym.Sci.Technol. (1998), vol. 1, 256-259 (Author Saminathan M. et al) “Liquid crystal side chain polymers with azobenzene mesogen”. |