Well‐defined cyclic‐polymers (cyclic‐PAzoMMAs), bearing side‐chain phenylazo naphthalene chromophore, were successfully synthesized by the combination of atom transfer radical polymerization (ATRP) and copper(I)‐catalyzed azide/alkyne cycloaddition “click” reaction, as verified by GPC, 1H NMR, FTIR, and MALDI‐TOF mass spectrometry. The cyclic‐PAzoMMA showed higher glass transition temperatures than the linear‐PAzoMMA with the same molecular weight. Interestingly, the cyclic‐PAzoMMA exhibited deeper modulation depth (M.D.) induced by SRG, larger value of the photoinduced birefringence, increased fluorescence emission, and longer fluorescence lifetime in comparison with its linear counterpart. 相似文献
The association within one molecule ofcalix[4]arene and crown ether moieties leads toligands with new complexing properties. In particular,calix[4]arene bis(crown-6) and some of itsderivatives have been shown to be highly selectiveextractants for caesium ions. This review presents thebackground of the study and the results of crystalstructure determinations and molecular modellingcalculations performed during the investigation of twomolecular families, the bis(crown ether) and theazobenzocrown derivatives of calix[4]arene. 相似文献
An innovative heterojunction is fabricated between two sides of a
freestanding thin film of HCl-doped polyaniline (PANI) derivative
containing azobenzene side-chain, which is synthesized through an
N-alkyl-substituted reaction. Of the film, the side with being
irradiated by UV light during preparation is represented as `A
side'; the other side without being irradiated is represented as
`N side'. The electrical properties of the heterojunction are
measured and the rectifying effect is observed in the
{current--voltage} characteristic curves with the values of
rectifying ratio (γ) being 20 at ±0.06 V at T= 77K
and 4 at ±0.02V at T=300 K separately. 相似文献
Poly(N‐isopropylacrylamide)‐block‐poly{6‐[4‐(4‐methylphenyl‐azo) phenoxy] hexylacrylate} (PNIPAM‐b‐PAzoM) was synthesized by successive reversible addition‐fragmentation chain transfer (RAFT) polymerization. In H2O/THF mixture, amphiphilic PNIPAM‐b‐PAzoM self‐assembles into giant micro‐vesicles. Upon irradiation of light at 365 nm, fusion of the vesicles was observed directly under an optical microscope. The real‐time fusion process is presented and the derivation is preliminarily due to the perturbation by the photoinduced trans‐to‐cis isomerization of azobenzene units in the vesicles.