ALKOXY-SUBSTITUTED LIQUID-CRYSTALLINE AROMATIC COPOLYESTERS .4. SYNTHESIS AND PROPERTIES OF MAIN-CHAIN COPOLYESTERS DERIVED FROM 2,5-BIS(PENTYLOXY)TEREPHTHALOYL DICHLORIDE AND TRANS-1,4-DIHYDROXYCYCLOHEXANE
G. Kossmehl et B. Lundt, ALKOXY-SUBSTITUTED LIQUID-CRYSTALLINE AROMATIC COPOLYESTERS .4. SYNTHESIS AND PROPERTIES OF MAIN-CHAIN COPOLYESTERS DERIVED FROM 2,5-BIS(PENTYLOXY)TEREPHTHALOYL DICHLORIDE AND TRANS-1,4-DIHYDROXYCYCLOHEXANE, Polymer bulletin, 34(5-6), 1995, pp. 503-508
Rigid rod copolyesters derived from 2,5-bis(pentyloxy)terephthaloyl di
chloride (3), 4,4'-dihy-droxybiphenyl (4) and trans-1,4-dihydroxycyclo
hexane (5) were synthesized and their thermal behavior analysed. The s
tructures were characterized by H-1-NMR, GPC and elemental analyses; t
heir thermal behavior was studied by DSC measurements, microscopy unde
r polarized light and thermogravimetric analyses. The composition of t
he copolyesters with 30, 50 and 70 mol % 5 was not as expected, due to
the differing reactivities of the diols 4 and 5 during the polyconden
sation. This led to the existence of two species of polyesters from on
e reaction mixture. The higher the content of 5 in the polymer, the lo
wer the molecular weight. By increasing the amount of 5, the thermal s
tabilities and melting points decrease drastically, whereas the solubi
lity increases. The copolyesters a-g show only a low ability to form f
ibres which are brittle and break very easily.