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位阻五芳基环戊二烯基配体的钌配合物

Ruthenium complexes of sterically-hindered pentaarylcyclopentadienyl ligands.

作者信息

Asato Ryosuke, Martin Colin J, Gisbert Yohan, Abid Seifallah, Kawai Tsuyoshi, Kammerer Claire, Rapenne Gwénaël

机构信息

Division of Materials Science, Nara Institute of Science and Technology, NAIST 8916-5 Takayama-cho Ikoma Nara 630-0192 Japan

International Collaborative Laboratory for Supraphotoactive Systems, NAIST-CEMES, CNRS UPR 8011 29 rue Marvig F-31055 Toulouse Cedex 4 France.

出版信息

RSC Adv. 2021 Jun 7;11(33):20207-20215. doi: 10.1039/d1ra03875c. eCollection 2021 Jun 3.

Abstract

The synthesis of ruthenium complexes incorporating an overcrowded pentaarylcyclopentadienyl ligand has been investigated, and higher efficiency has been reached using chlorine-functionalised precursors when compared with their brominated counterparts. A new methodology for the preparation of chlorocyclopentadienes has been developed which is well adapted for highly sterically hindered compounds and works with either electron rich or poor systems.

摘要

对含有过度拥挤的五芳基环戊二烯基配体的钌配合物的合成进行了研究,与溴化前体相比,使用氯官能化前体时效率更高。已开发出一种制备氯环戊二烯的新方法,该方法非常适合空间位阻大的化合物,并且适用于富电子或贫电子体系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5fe/9033943/4553717e87fc/d1ra03875c-s1.jpg

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