Issue 62, 2019

Stoichiometric reactions and catalytic dehydrogenations of amine–boranes with calcium aryloxide

Abstract

Catalysis with the main-group metal calcium conventionally relies on σ-bond metathesis to initiate the reactions. Here, we report a calcium aryloxide based on the tridentate β-diketiminato ligand, which shows transition-metal-like reactivity with dialkylamine–boranes H3B·NHR2 (R = CH3, Cy, C6H5CH2, and iPr) to afford unprecedented amine–borane coordinated complexes through Ca⋯H interactions. This calcium aryloxide was also an active catalyst in dehydrogenation of amine–boranes, and gave aminoboranes H2B[double bond, length as m-dash]NR2, as the sole product. The initiating species was a calcium amine–borane complex rather than the traditional calcium amidoborane complex formed by σ-bond metathesis.

Graphical abstract: Stoichiometric reactions and catalytic dehydrogenations of amine–boranes with calcium aryloxide

Supplementary files

Article information

Article type
Communication
Submitted
19 Jun 2019
Accepted
08 Jul 2019
First published
09 Jul 2019

Chem. Commun., 2019,55, 9152-9155

Stoichiometric reactions and catalytic dehydrogenations of amine–boranes with calcium aryloxide

X. Zheng, J. Huang, Y. Yao and X. Xu, Chem. Commun., 2019, 55, 9152 DOI: 10.1039/C9CC04698D

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