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张力双磷桥连联芳基和紫精的合成与物理性质

Synthesis and Physical Properties of Strained Doubly Phosphorus-Bridged Biaryls and Viologens.

作者信息

Greulich Tobias W, Yamaguchi Eriko, Doerenkamp Carsten, Lübbesmeyer Maximilian, Daniliuc Constantin G, Fukazawa Aiko, Eckert Hellmut, Yamaguchi Shigehiro, Studer Armido

机构信息

Westfälische Wilhelms Universität, Organisch-Chemisches Institut, Corrensstrasse 40, 48149, Münster, Germany.

Department of Chemistry, Graduate School of Science and Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Furo, Chikusa, Nagoya, 464-8602, Japan.

出版信息

Chemistry. 2017 May 2;23(25):6029-6033. doi: 10.1002/chem.201605272. Epub 2017 Feb 23.

Abstract

New P/N-containing π-electron systems comprising fully planar biaryl arrays are synthesized by multiple radical phosphanylation. The biaryl moiety in these highly strained planar π-systems is rigidified by double P-bridging. The electronic properties of the core biaryl entity are varied by introducing N-donor substituents or by installing N-atoms within the π-system, thereby moving to the viologen core structure. The electrochemical and photophysical properties of these compounds are discussed and compared with those of related systems.

摘要

通过多次自由基膦酰化反应合成了包含完全平面联芳基阵列的新型含磷氮π电子体系。这些高度应变的平面π体系中的联芳基部分通过双磷桥连而刚性化。通过引入氮供体取代基或在π体系中引入氮原子来改变核心联芳基实体的电子性质,从而转向紫精核心结构。讨论了这些化合物的电化学和光物理性质,并与相关体系的性质进行了比较。

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