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首页> 外文期刊>International journal of nanoscience >SUPRAMOLECULAR CHIRALITY OF THE LANGMUIR-BLODGETT FILMS OF AN ACHIRAL 2-(HEPTADECYL)PHENANTHRO[9, 10-d]IMIDAZOLE
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SUPRAMOLECULAR CHIRALITY OF THE LANGMUIR-BLODGETT FILMS OF AN ACHIRAL 2-(HEPTADECYL)PHENANTHRO[9, 10-d]IMIDAZOLE

机译:非手性2-(庚基)苯并[9,10-d]咪唑的朗缪尔-布洛杰德膜的超分子手性

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摘要

A novel amphiphilic compound, 2-(heptadecyl)phenanthro[9, 10-d]imidazole (PhImC17), was synthesized and its assembly at the air/water interface was investigated. It has been found that although the compound was achiral, it can form a chiral Langmuir-Blodgett film through the interfacial organization. The larger aromatic ring of the compound, which caused the cooperative arrangement of the chromophore in the assembled ultrathin film, was suggested to play an important role in forming such supramolecular chirality. A comparison between the supramolecular chirality of the PhImC17 film with that of previously published 2-heptadecyl-naphtha[2, 3]imidazole film was performed and a further insight into the supramolecular chirality of the system from achiral molecules was proposed.
机译:合成了一种新型的两亲化合物2-(十七烷基)菲[9,10-d]咪唑(PhImC17),并研究了其在空气/水界面的组装情况。已经发现尽管该化合物是非手性的,但是它可以通过界面组织形成手性的Langmuir-Blodgett膜。化合物的较大芳环导致组装的超薄膜中生色团的协同排列,被认为在形成这种超分子手性中起重要作用。进行了PhImC17膜的超分子手性与以前发表的2-十七烷基-石脑油[2,3]咪唑膜的超分子手性之间的比较,并提出了从非手性分子对系统的超分子手性的进一步认识。

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