Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5402020 | Journal of Luminescence | 2011 | 5 Pages |
A thermoresponsive poly(NIPAM-co-dye) copolymer with covalently attached D-Ï-A type dye was prepared by typical radical copolymerization. Software was used to calculate the electron density distribution of the push-pull, intramolecular charge transfer (ICT) operating in donor-Ï-conjugation-acceptor (D-Ï-A) configurations of dye monomer 3. It can be constructed an acid/base-induced molecular switch by modulation of intramolecular charge transfer with protonation/deprotonation. The lower critical solution temperature (LCST) behavior was investigated by means of UV-vis spectroscopy that allows the measurement of the phase transition from 25 to 40 °C in aqueous solution. The poly(NIPAM-co-dye) copolymer also exhibited color change when used an acid/base-induced molecular switch via control of intramolecular charge transfer (ICT). The morphology of the internal microstructure of the poly(NIPAM-co-dye) hydrogel was observed by scanning electron microscopy (SEM). The reversible switch could be obtained by thermal and acid/base stimuli.
⺠A thermoresponsive poly(NIPAM-co-dye) copolymer was prepared by radical polymerization. ⺠The LCST behavior of the copolymer was investigated by UV-vis spectroscopy that allows the measurement of the phase transition from 25 to 40 °C in aqueous solution. ⺠The copolymer also exhibited color change when used an acid/base-induced molecular switch via control of intramolecular charge transfer. ⺠The reversible switch of the copolymer could be obtained by thermal and acid/base stimuli.