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Pleated polymeric foldamers driven by donor–acceptor interaction and conjugated radical cation dimerization 被引量:1
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作者 Yun-Chang Zhang Lan Chen +3 位作者 Hui Wang Ya-Ming Zhou Dan-Wei Zhang Zhan-Ting Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2016年第6期817-821,共5页
Two naphthalene(NP) and bipyridinium(BIPY^2+) alternately incorporated polymers P1 and P2 have been prepared through the formation of dynamic hydrazone bonds. The polymers formed NP–BIPY^2+donor–acceptor inter... Two naphthalene(NP) and bipyridinium(BIPY^2+) alternately incorporated polymers P1 and P2 have been prepared through the formation of dynamic hydrazone bonds. The polymers formed NP–BIPY^2+donor–acceptor interaction-induced pleated secondary structure. Upon reducing the BIPY^2+units to radical cation BIPY+, intramolecular dimerization of the BIPY+units induced the backbones to afford another pleated secondary structure. Adding electron-rich macrocyclic polyether bis-1,5-dinaphtho[38]crown-10 or electron-deficient cyclobis(paraquat-p-phenylene) cyclophane did not break the first foldamer by complexing the BIPY^2+or NP units of the polymers, whereas the di(radical cationic)ring of the second cyclophane could break the second foldamer by forming threading complexes with the BIPY+units of the polymers. 展开更多
关键词 FOLDAMER Donor–acceptor interaction conjugated radical cation dimerization BIPYRIDINIUM Dynamic covalent chemistry
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