| Literature DB >> 27862749 |
Yasuhiro Ohki1,2, Yuki Shimizu1, Ryoichi Araake1, Mizuki Tada1,3, W M C Sameera4, Jun-Ichi Ito5, Hisao Nishiyama5.
Abstract
A square-planar Co4 amide cluster, Co4 {N(SiMe3 )2 }4 (2), and an octahedral Co6 hydride cluster, Co6 H8 (Pi Pr3 )6 (4), were obtained from metathesis-type amide to hydride exchange reactions of a CoII amide complex with pinacolborane (HBpin) in the absence/presence of Pi Pr3 . The crystal structure of 4 revealed face-capping hydrides on each triangular [Co3 ] face, while the formal CoII2 CoI4 oxidation state of 4 indicated a reduction of the cobalt centers during the assembly process. Cluster 4 catalyzes the hydrosilylation of 2-cyclohexen-1-one favoring the conjugate reduction. Generation of the catalytically reactive Co cluster species was indicated by a trapping experiment with a chiral chelating agent.Entities:
Keywords: clusters; cobalt; hydride; hydrosilylation
Year: 2016 PMID: 27862749 DOI: 10.1002/anie.201608262
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336