Contrasting reactivity of B-Cl and B-H bonds at [Ni(IMes)2] to form unsupported Ni-boryls

被引：0

作者：

Audsley, Gabrielle ^{[1
]}

Carpentier, Ambre ^{[2
]}

Pecharman, Anne-Frederique ^{[3
]}

Wright, James ^{[1
]}

Roseveare, Thomas M. ^{[4
]}

Clark, Ewan R. ^{[5
]}

Macgregor, Stuart A. ^{[2
]}

Riddlestone, Ian M. ^{[1
]}

机构：

[1] Univ Surrey, Sch Chem & Chem Engn, Guildford GU2 7XH, England

[2] Heriot Watt Univ, Inst Chem Sci, Edinburgh EH14 4AS, Scotland

[3] Univ Bath, Dept Chem, Bath BA2 7AY, England

[4] Univ Sheffield, Dept Chem, Sheffield S3 7HF, England

[5] Univ Kent, Sch Phys Sci, Canterbury CT2 7NH, England

来源：

CHEMICAL COMMUNICATIONS | 2024年 / 60卷 / 07期

关键词：

D O I：

10.1039/d3cc05369e

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

[Ni(IMes)(2)] reacts with chloroboranes via oxidative addition to form rare unsupported Ni-boryls. In contrast, the oxidative addition of hydridoboranes is not observed and products from competing reaction pathways are identified. Computational studies relate these differences to the mechanism of oxidative addition: B-Cl activation proceeds via nucleophilic displacement of Cl-, while B-H activation would entail high energy concerted bond cleavage.

引用

页码：874 / 877

页数：4

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