Highly Active Iron Catalyst for Ammonia Borane Dehydrocoupling at Room Temperature

Highly Active Iron Catalyst for Ammonia Borane Dehydrocoupling at Room Temperature
复制标题

DOI:
10.1021/acscatal.5b02406
复制
发表时间:
2015-12-01
期刊:
影响因子:
12.9
通讯作者:
Schneidert, Sven
Schneidert, Sven
中科院分区:
化学1区
文献类型:
--
作者:
Glueer, Arne;Foerster, Moritz;Schneidert, Sven

文献摘要

被引文献

相似文献

铁配合物[FeH(CO)(PNP)](PNP = N-(CH(2)CH(2)PiPr(2))(2))是一种室温下高活性的氨硼烷脱氢偶联催化剂。在释放1当量的H-2时获得主要线性的聚氨基硼烷。机理研究表明,氢释放和B-N偶联都是金属催化的,并通过游离氨基硼烷进行。催化剂失活的原因是与氨基硼烷重排形成的游离BH 3反应。重要的是,用简单胺捕获硼烷允许观察到TON,这对于明确定义的贱金属催化剂是前所未有的。
The iron complex [FeH(CO) (PNP)] (PNP = N-(CH(2)CH(2)PiPr(2))(2)) is a highly active catalyst for ammonia borane dehydrocoupling at room temperature. Mainly linear polyaminoborane is obtained upon release of 1 equiv of H-2. Mechanistic studies suggest that both hydrogen release and B-N coupling are metal-catalyzed and proceed via free aminoborane. Catalyst deactivation results from reaction with free BH3 that is formed by aminoborane rearrangement. Importantly, borane trapping with a simple amine allows for the observation of a TON that is unprecedented for a well-defined base metal catalyst.