Redox-Untersuchungen an Jodboranen, XV / Redox-Studies on Iodoboranes, XV

Author:

Siebert Walter1,Schaper Klaus-Juergen1,Asgarouladi Bagher1

Affiliation:

1. Institut für Anorganische Chemie der Universität Würzburg

Abstract

Of the three diiodobenzenes the 1,3- and 1,4-isomer react with BI3 to give the corresponding bis(diiodoboryl)benzenes. Due to the electronic acceptor properties of the BI2-group the formation of the 1,3-isomer is favored over the 1,4-product. Attempts to prepare the 1,2-bis(diiodoboryl)benzene resulted in the formation of a dibenzo-1,4-diborine derivative.

Publisher

Walter de Gruyter GmbH

Subject

General Chemistry

Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Boron Triiodide;Encyclopedia of Reagents for Organic Synthesis;2009-03-15

2. Syntheses, structures, luminescence and electrochemistry of benzene- and biphenyl-centered bis- and tris-1,3,2-diazaboroles and -1,3,2-diazaborolidines;Dalton Transactions;2006

3. Boron Triiodide;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

4. Benzene-Centered Tri- and Tetrametallacarborane Sandwich Complexes;Angewandte Chemie;2000-12-15

5. Benzene-Centered Tri- and Tetrametallacarborane Sandwich Complexes;Angewandte Chemie International Edition;2000-12-15

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