1996
DOI: 10.1016/s0014-3057(96)00076-6
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New photoresponsive (meth)acrylate (co)polymers containing azobenzene pendant sidegroups with carboxylic and dimethylamino substituents—I. Synthesis and characterization of the monomers

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Cited by 21 publications
(13 citation statements)
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“…They were rather low indicating that they were oligomers. It is consistent with literature data for similar materials [50][51][52][53]. During synthesis, the high content of the initator was used (10% by weight towards monomers).…”
Section: Atomic Force Microscopysupporting
confidence: 89%
“…They were rather low indicating that they were oligomers. It is consistent with literature data for similar materials [50][51][52][53]. During synthesis, the high content of the initator was used (10% by weight towards monomers).…”
Section: Atomic Force Microscopysupporting
confidence: 89%
“…The monomer M6AzCOONa was prepared by alkalized process of 6-[4-(4-carboxylphenylazo)phenoxyl]hexyl methacrylate (M6AzCOOH), which was synthesized according to published references [45,46]. Typically, M6AzCOOH (4.1 g, 0.01 mol) was dissolved in THF (50 mL) using 5 wt% NaOH aqueous solution to adjust to pH ¼ 9.…”
Section: Synthesismentioning
confidence: 99%
“…MAzoA-0 was synthesized according to a literature procedure. 37 The desired azo monomers with an easily cross-linkable substituent (MAzoS-n, n ¼ 0, 2, 6, 10) were then readily prepared through the coupling reaction between MAzoA-n and N-hydroxysuccinimide, using DCC as the catalyst. All the intermediates and azo monomers could be obtained in quite good yields, typically ranging from 55% to almost quantitative yields, and their purity was satisfactory, as determined with both thin layer chromatography and 1 H NMR.…”
Section: Azo Monomers With An Easily Cross-linkable Substituentmentioning
confidence: 99%