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硼次酞菁的拟卤化物。

Pseudohalides of boron subphthalocyanine.

机构信息

Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College Street, Toronto, Ontario, M5S 3E5, Canada.

出版信息

J Org Chem. 2012 Mar 2;77(5):2531-6. doi: 10.1021/jo202365x. Epub 2012 Feb 16.

DOI:10.1021/jo202365x
PMID:22316112
Abstract

The synthesis and study of a series of pseudohalides of boron subphthalocyanine (BsubPc) are reported. Each pseudohalide has been compared to the more common chloride and bromide of BsubPc, and we have found that most react slower under standard phenoxylation and hydrolysis conditions. Three pseudohalides (TsO-BsubPc, MsO-BsubPc, and BsO-BsubPc) do not hydrolyze at all even after prolonged periods of time in the presence of water. Single crystals of TsO-, MsO-, and ClsO-BsubPc were obtained, and their structures were unambiguously determined.

摘要

报道了一系列硼次酞菁(BsubPc)类假卤化物的合成与研究。将每种假卤化物与更为常见的 BsubPc 氯化物和溴化物进行了比较,发现大多数在标准苯氧基化和水解条件下反应更慢。三种假卤化物(TsO-BsubPc、MsO-BsubPc 和 BsO-BsubPc)即使在水中存在很长时间也根本不会水解。获得了 TsO-、MsO-和 ClsO-BsubPc 的单晶,并明确确定了它们的结构。

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引用本文的文献

1
Ring Opening Reactions through C-O Bond Cleavage Uniquely Adding Chemical Functionality to Boron Subphthalocyanine.通过碳-氧键断裂的开环反应为硼代亚酞菁独特地引入化学官能团。
Molecules. 2015 Oct 7;20(10):18237-45. doi: 10.3390/molecules201018237.