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具有超分子组装两面性的氟环环己烷:轴向单、二和三烷基取代以及具有三轴 C-F 键赋予极性的环己烷的合成和固态结构。

Janus faced fluorocyclohexanes for supramolecular assembly: synthesis and solid state structures of equatorial mono-, di- and tri alkylated cyclohexanes and with tri-axial C-F bonds to impart polarity.

机构信息

University of St Andrews, School of Chemistry, North Haugh, St Andrews, Fife, KY16 9ST, UK.

University of Campinas, Chemistry Institute, Monteiro Lobato Street, Campinas, Sao Paulo, Brazil, 13083-862.

出版信息

Chem Commun (Camb). 2022 Jul 14;58(57):7968-7971. doi: 10.1039/d2cc03010a.

Abstract

Concise and general synthesis protocols are reported to generate all- mono-, di- and tri-alkylated cyclohexanes where a single fluorine is located on the remaining carbons of the ring. The alkyl groups are positioned to lie equatorially and to have triaxial C-F bonds imparting polarity to these ring systems. Intermolecular electrostatic interactions in the solid-state structure of the trialkylated systems are explored and the resultant supramolecular order opens up prospects for design in soft materials.

摘要

有报道称,通过简洁通用的合成方案可以制得所有单、二和三烷基取代环己烷,其中一个氟原子位于环上剩余的碳原子上。这些烷基基团位于环己烷的赤道位置,具有三轴 C-F 键,使这些环系具有极性。三烷基取代体系在固态结构中的分子间静电相互作用得到了研究,所得超分子有序性为软材料的设计开辟了前景。

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