2009
DOI: 10.1039/b812291a
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Photoresponsive side-chain liquid crystalline polymers with an easily cross-linkable azobenzene mesogen

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Cited by 58 publications
(57 citation statements)
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“…This result indicated the full overlap of the side chains in an interdigitated packing structure, as shown in the insets of Fig. 3 [21]. In addition, the first-order reflection peak is very weak and the second-order reflection peak is the most intense.…”
Section: Resultsmentioning
confidence: 74%
“…This result indicated the full overlap of the side chains in an interdigitated packing structure, as shown in the insets of Fig. 3 [21]. In addition, the first-order reflection peak is very weak and the second-order reflection peak is the most intense.…”
Section: Resultsmentioning
confidence: 74%
“…4-((4-Hydroxy)phenylazo)benzoic acid, 4-((4--hydroxyalkyloxy)phenylazo)benzoic acid (HAzoA-m (m = 2, 6, 10)), and 4-((4-(-acryloyloxyalkyloxy))phenylazo)benzoic acid 35 (AAzoA-m (m = 2, 6, 10)) were synthesized following our previous procedure (Scheme 1). [67][68][69] All the other reagents were commercially available and used without further purification unless otherwise stated.…”
Section: Methodsmentioning
confidence: 99%
“…71 Recently, we have synthesized a series of methacrylate type azo monomers with an N-hydroxysuccinimide 25 carboxylate substituent and their homopolymers by the free radical polymerization. 68 The obtained azo polymer films proved to be crosslinkable with 1,6-hexanediamine in methanol, but such post-crosslinking process was still relatively slow (about 1 h), probably due to the rigid characteristics of poly(methacrylate) 30 type azo polymers. In addition, the resulting azo polymers had rather high Tg values (≥ 102 o C as determined by DSC at the second heating processes with a heating rate of 10 o C/min), which might prevent their fast formation of SRGs.…”
Section: Synthesis and Characterization Of Azo Polymersmentioning
confidence: 98%
“…The second route starts with a liquid crystalline polymer that contains additional functional groups. This polymer is mixed with a bi- or multi-functional crosslinking agent that can react selectively with these functional groups under defined reaction conditions, leading to network formation [1923]. This pathway has the advantage that the LC polymers can be purified and characterized before the crosslinking step.…”
Section: The Synthesis and Fabrication Of Lce Materialsmentioning
confidence: 99%