1993
DOI: 10.1080/02678299308027769
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Unusual phase behaviour of a new liquid-crystalline side group polymer

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Cited by 24 publications
(18 citation statements)
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“…The transition temperatures appear strongly dependent on the polymerization degree, the glass (Tg), the smectic-nematic (T SM ) and the nematic-isotropic transition temperatures (Ti) of the series diminishing with the decrease of chain length (Figure 7). In particular, the Ti and T SM values of Star(M6A)-2 to Star(M6A)-24 increase from 124 to 150 C and from 78 to 94 C (Table 1) approaching the maximum values of 152 and 97 C, respectively, found for poly(M6A) with M w ¼ 74;000, obtained by AIBN-initiated free radical polymerization [16]. Interestingly, Star(M6A)-8 and Star(M6A)-24 show higher Tg than the corresponding linear derivative, this finding being attributable to the stiffness of aromatic core, which limits the free movements of one chain end, thus favoring the macromolecules to increase the extent of interchromophore interactions with respect to the related linear sample.…”
Section: Thermal Properties and Polarized Optical Microscopy Charactementioning
confidence: 74%
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“…The transition temperatures appear strongly dependent on the polymerization degree, the glass (Tg), the smectic-nematic (T SM ) and the nematic-isotropic transition temperatures (Ti) of the series diminishing with the decrease of chain length (Figure 7). In particular, the Ti and T SM values of Star(M6A)-2 to Star(M6A)-24 increase from 124 to 150 C and from 78 to 94 C (Table 1) approaching the maximum values of 152 and 97 C, respectively, found for poly(M6A) with M w ¼ 74;000, obtained by AIBN-initiated free radical polymerization [16]. Interestingly, Star(M6A)-8 and Star(M6A)-24 show higher Tg than the corresponding linear derivative, this finding being attributable to the stiffness of aromatic core, which limits the free movements of one chain end, thus favoring the macromolecules to increase the extent of interchromophore interactions with respect to the related linear sample.…”
Section: Thermal Properties and Polarized Optical Microscopy Charactementioning
confidence: 74%
“…The monomer 4-x-methacryloyloxy-hexyloxy-4 0 -ethoxyazobenzene (M6A) was synthesized as previously reported [16]. THF was purified and dried according to the reported procedures [17] and stored under nitrogen.…”
Section: Methodsmentioning
confidence: 99%
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“…4-Alkoxy-4'-hydroxyazobenzenes 2 were obtained from 4-acetamidophenol 1 using standard methods of *Author for correspondence; e-mail: bubnov@fzu.cz alkylation, diazotation and coupling (using phenol or o-cresol) [16]. Mesogenic phenols 3 were obtained by esterification of 2 with 4-methoxycarbonyloxybenzoic acid chloride in dry pyridine followed by ammonolysis by 30% ammonia solution at room temperature for 3 h in a mixture of ethanol and acetone (1/1).…”
Section: Synthesismentioning
confidence: 99%