Literature DB >> 18461586

An Hg2+-gated chiral molecular switch created by using binaphthalene molecules with two anthracene units and two 1,3-dithiole-2-thione (1,3-dithiole-2-one) units.

Cheng Wang1, Deqing Zhang, Guanxin Zhang, Junfeng Xiang, Daoben Zhu.   

Abstract

By integrating the features of anthracene, 1,3-dithiole-2-thione, and binaphthalene units, (S)-1 and its analogue (S)-2, which contains two 1,3-dithiole-2-one units instead of 1,3-dithiole-2-thione, were studied for creating a new molecular regulation system and building a gated chiral molecular switch. The results show that the photodimerization is controlled by the remote functional-group transformation of C=S into C=O, thus providing an elegant example of molecular regulation. The photodimerization of two anthracene units induces circular dichroism (CD) spectral variation. Overall, the CD spectrum can be remotely modulated by Hg2+ in (S)-1, which leads to an Hg2+-gated chiral molecular switch.

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Year:  2008        PMID: 18461586     DOI: 10.1002/chem.200800216

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Toward unidirectional switches: 2-(2-Hydroxyphenyl)pyridine and 2-(2-methoxyphenyl)pyridine derivatives as pH-triggered pivots.

Authors:  Christina Tepper; Gebhard Haberhauer
Journal:  Beilstein J Org Chem       Date:  2012-06-29       Impact factor: 2.883

  1 in total

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