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国家自然科学基金(50673095)

作品数:4 被引量:13H指数:3
相关作者:刘鸣华于微王天宇李远刚李占双更多>>
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发文基金:国家自然科学基金中国科学院知识创新工程重要方向项目国家重点基础研究发展计划更多>>
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溶剂和分子结构对席夫碱分子在有机凝胶中的荧光增强和超分子手性的影响(英文)被引量:3
2008年
研究了在有机胶凝剂中掺杂的席夫碱化合物的结构和性质.实验发现,虽然席夫碱分子单独不能在有机溶剂中形成凝胶,当其与一种胶凝剂N,N′-双十八烷基-L-Boc-谷氨酸混合时,它们在二甲基亚砜或甲苯中形成透明的有机凝胶.与相应的溶液相比,观察到在有机凝胶中的荧光增强现象,并且这一增强与席夫碱的结构有密切关系.在二甲基亚砜的有机凝胶中,观察到带有长烷基链的席夫碱具有诱导手性.表明通过凝胶的形成,胶凝剂的手性能传递到带有长链的席夫碱上.
于微李远刚王天宇刘鸣华李占双
关键词:有机凝胶胶凝剂荧光手性席夫碱
Towards a universal organogelator:A general mixing approach to fabricate various organic compounds into organogels被引量:5
2011年
Low-molecular-weight organogels(LMOG) have been attracting a surge interest in fabricating soft materials.Although the finding of the gelator molecules has been developed from serendipity to objective design,the achievement of the gelator molecules still needs good design and tedious organic synthesis.In this paper,we proposed a simple and general mixing approach to get the organogel for nearly all the organic compounds and even soluble nanoparticles without any modification.We have designed a universal gelator molecule,which forms organogels with more than 40 kinds of organic solvents from aploar to polar solvents.More interestingly,when other organic compounds or even nanomaterials,which are soluble in certain organic solvents,are mixed with this gelator molecule,they can form organogels no matter whether the individual compounds could form organogel or not.This method is applicable to nearly all kinds of soluble organic compounds and opens an efficient and universal way to fabricate gel materials.
DUAN PengFeiLI YuanGangJIANG JianWANG TianYuLIU MingHua
关键词:ORGANOGELSELF-ASSEMBLY
手性光学开关研究被引量:2
2008年
手性是自然界的普遍现象,有关超分子手性的研究由于超分子体系中分子间非共价相互作用的可调性逐渐引起了人们的研究兴趣。本文综述了手性光学开关研究的最新进展,介绍了如何设计分子体系,由手性分子制备手性光学开关;基于超分子思想,介绍了由非手性分子参与形成的手性光学开关,并最终制备出完全由非手性分子组装得到的手性光学开关。
郭培志刘鸣华赵修松
关键词:超分子手性超分子组装体
Interfacial assembly and host-guest interaction of anthracene-conjugated L-glutamate dendron with cyclodextrin at the air/water interface被引量:3
2014年
The interracial assembly of photo-induced dimerization of atypical anthracene-containing amphiphilic dendron and host-guest interaction with γ-cyclodextrin has been investigated. It has been proved that even without long alkyl chain the amphiphilic dendron could still form stable Langmuir monolayer at the air/water interface. Through the host-guest interaction,γ-cyclodextrin can be used to encapsulate two headgroups of amphiphilic dendron in the antiparallel direction. However, the formed host-guest complex was sensitive to the surface pressure. Slight compression of surface pressure led amphiphilic dendron to reassemble into nanofibers through the strong π-π stacking between headgroups. On the other hand, under in situ irradiation, the amphiphilic dendron was stabilized in the cavity of γ- cyclodextrin through headgroup dimerization and the host-guest complex further irregularly aggregated to nanoparticles. Meanwhile, γ-cyclodextrin, as a silencer, blocked the supramolecular chirality transfer. Our conclusion was demonstrated through UV/vis, FT-IR, CD spectrum and AFM images, respectively.
Long QinPeng-Fei DuanMing-Hua Liu
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