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作 者:CHEN Mu-juan ZHOU Song-gen LI Mei LEI Chun-yan XIAO Rui JIANG La-sheng
机构地区:[1]School of Chemistry and Environment, South China Normal University, Guangzhou 510006, P.R.China
出 处:《Chemical Research in Chinese Universities》2013年第6期1094-1097,共4页高等学校化学研究(英文版)
基 金:National Natural Science Foundation of China,the Natural Science Foundation of Guangdong Province of China
摘 要:Two charged donor-acceptor [2]catenanes were synthesized by the cyclization of the π-acceptor 1,1 '-[1, 4-phenylenebis-(methylene)]bis(4,4'-bipyridinium)bis(hexafluorophosphate)(2) and bis(bromomethyl)benzene with the templates of the π-donor phenylene-diacetylene crown ethers la and lb in the yields of 31%, 35%, respectively. The mass spectra, 1H and 13C NMR spectra confirm that the phenylene-diacetylene crown ethers, with a nonaromatic ~r-system, successfully template the cyclization of CBPQT4+. The X-ray crystallography analysis shows that the CBPQT4+ ring encircles around the phenylene motif of the crown ethers, leaving the 1,3-butadiyne fragment out of the cavity of CBPQT4+ ring. The mechanically interlocked structure of [2]catenanes was stabilized by the cooperative effects of π-stacking and hydrogen bonding interactions.Two charged donor-acceptor [2]catenanes were synthesized by the cyclization of the π-acceptor 1,1 '-[1, 4-phenylenebis-(methylene)]bis(4,4'-bipyridinium)bis(hexafluorophosphate)(2) and bis(bromomethyl)benzene with the templates of the π-donor phenylene-diacetylene crown ethers la and lb in the yields of 31%, 35%, respectively. The mass spectra, 1H and 13C NMR spectra confirm that the phenylene-diacetylene crown ethers, with a nonaromatic ~r-system, successfully template the cyclization of CBPQT4+. The X-ray crystallography analysis shows that the CBPQT4+ ring encircles around the phenylene motif of the crown ethers, leaving the 1,3-butadiyne fragment out of the cavity of CBPQT4+ ring. The mechanically interlocked structure of [2]catenanes was stabilized by the cooperative effects of π-stacking and hydrogen bonding interactions.
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