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  4. Substrate-Gated Transformation of a Pre-Catalyst into an Iron-Hydride Intermediate [(NO)2(CO)Fe(μ-H)Fe(CO)(NO)2]− for Catalytic Dehydrogenation of Dimethylamine Borane
 
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Substrate-Gated Transformation of a Pre-Catalyst into an Iron-Hydride Intermediate [(NO)2(CO)Fe(μ-H)Fe(CO)(NO)2]− for Catalytic Dehydrogenation of Dimethylamine Borane

Journal
Inorganic Chemistry
Date Issued
2023-01-16
Author(s)
CHIEN-HONG CHEN
DOI
10.1021/acs.inorgchem.2c03278
URI
https://www.scopus.com/pages/publications/85145454427
https://scholars.csmu.edu.tw/handle/123456789/23205
Abstract
Continued efforts are made on the development of earth-abundant metal catalysts for dehydrogenation/hydrolysis of amine boranes. In this study, complex [K-18-crown-6-ether][(NO)2Fe(μ-MePyr)(μ-CO)Fe(NO)2] (3-K-crown, MePyr = 3-methylpyrazolate) was explored as a pre-catalyst for the dehydrogenation of dimethylamine borane (DMAB). Upon evolution of H2(g) from DMAB triggered by 3-K-crown, parallel conversion of 3-K-crown into [(NO)2Fe(N,N′-MePyrBH2NMe2)]− (5) and an iron-hydride intermediate [(NO)2(CO)Fe(μ-H)Fe(CO)(NO)2]− (A) was evidenced by X-ray diffraction/nuclear magnetic resonance/infrared/nuclear resonance vibrational spectroscopy experiments and supported by density functional theory calculations. Subsequent transformation of A into complex [(NO)2Fe(μ-CO)2Fe(NO)2]− (6) is synchronized with the deactivated generation of H2(g).
Type
journal article
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