[(acridine)BCl2]+ : A Borenium Cation That Is a Strong Boron- and Carbon-Based Lewis Acid

被引：60

作者：

Clark, Ewan R. ^{[1
]}

Ingleson, Michael J. ^{[1
]}

机构：

[1] Univ Manchester, Sch Chem, Manchester M13 9PL, Lancs, England

来源：

ORGANOMETALLICS | 2013年 / 32卷 / 22期

基金：

英国工程与自然科学研究理事会;

关键词：

REACTIVITY; HYDROGEN; ACTIVATION; ION; PAIRS; CATALYSIS; ELECTROPHILES; DERIVATIVES; BORYLATION; REDUCTION;

D O I：

10.1021/om400463r

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

[(acridine)BCl2][AlCl4] was synthesized by halide abstraction from (acridine)BCl3 with AlCl3. The hydride ion affinity of the C9 position in [(acridine)BCl2](+)was calculated to be 14 kcal mol(-1) greater than that at boron. [(acridine)BCl2][AlCl4] reacts with 1 equiv of acridine to form the strained boronium cation [(acridine)(2)BCl2][AlCl4] and with P(mesityl)(3) by photoinduced one-electron transfer to form the 9,9'-biacridane moiety by radical coupling. A stable frustrated Lewis pair (FLP) was formed on combining [(acridine)BCl2][AlCl4] and 2,4,6-tri-tert-butylpyridine (TBP), which heterolytically activated H-2 at 100 degrees C. The ultimate location of the hydride from H-2 activation was the C9 position of acridine and not boron. Carbon Lewis acid based reactivity also occurred when thieno[3,2-b]thiophene was added to the [(acridine)BCl2][AlCl4]/TBP FLP or to [(acridine)(2)BCl2][AlCl4], with arylation of acridine at C9 observed for both.

引用

页码：6712 / 6717

页数：6

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