1994
DOI: 10.1002/masy.19940770136
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Hybrid thermotropic liquid‐crystalline block copolymers

Abstract: A new approach to the preparation of two classes of block copolymers containing liquid‐crystalline segments is reported. Copolymers 1 and 2 are constituted by polytetrahydrofuran and side‐chain liquid‐crystalline polymethacrylate blocks, whereas block copolymers 3 consist of polystyrene and main‐chain liquid‐crystalline polyester blocks. The synthetic procedures leading to copolymers 1‐3 are extremely versatile and can be used to prepare a great variety of block copolymer architectures. In both copolymer class… Show more

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Cited by 21 publications
(16 citation statements)
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“…The interface was observed to be very well defined, about 2.5 f 1 nm thick. The same effect was observed for block copolymers with main chain components by Galli et al [57] (see Fig. Therefore, only a minor reduction of the A HcI compared to homopolymer has been recorded and attributed to the interface (see section size effects above) [52, 531. Similar results were reported by Finkelmann [33] and van der Velde [6 11.…”
Section: Interaction Between Morphology and Lc Phase Structuresupporting
confidence: 68%
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“…The interface was observed to be very well defined, about 2.5 f 1 nm thick. The same effect was observed for block copolymers with main chain components by Galli et al [57] (see Fig. Therefore, only a minor reduction of the A HcI compared to homopolymer has been recorded and attributed to the interface (see section size effects above) [52, 531. Similar results were reported by Finkelmann [33] and van der Velde [6 11.…”
Section: Interaction Between Morphology and Lc Phase Structuresupporting
confidence: 68%
“…Only statistical statements concerning the structure of the block copolymers can be made without extensive SEC investigations and a subsequent cleavage of the segmented block polymers in the individual polymer blocks [57]. However, the polymers obtained are insoluble in common organic solvents in most cases.…”
Section: Lc Main Chain Block Copolymersmentioning
confidence: 99%
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“…The carboxylic acid function brings about these side reactions, which compete with the grafting reaction. This explains the rapid gel formation in entry (6). The use of tert-butyl ester instead of carboxylic acid function, as the site of grafting reaction, rather precludes gel formation.…”
Section: Chemical Modification Methodsmentioning
confidence: 91%