4.7 Article

Solvent-free Zn (NSNO) complex-catalysed dihydroboration of nitriles

期刊

CHEMICAL COMMUNICATIONS
卷 58, 期 59, 页码 8266-8269

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cc03517k

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资金

  1. NSERC [RGPIN-2019-05958]
  2. University of Ottawa, Canada Foundation for Innovation
  3. Ontario Ministry of Economic Development and Innovation

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In this study, a new catalyst for esterification reaction was discovered, and the reaction mechanism was explored. The catalyst demonstrated high efficiency in converting nitrites to double hydroborated products.
N-donors are the most commonly employed Lewis bases in ligand-assisted catalysis. A dimeric zinc complex (Zn-1) employing a tetradentate pyridine-thioether-anitido-aryloxide NSNO ligand (L) effects the quantitative conversion of nitrites to the corresponding double hydroborated products at 1 mot% catalyst loading. Variable Time Normalization Analysis kinetic studies showed a first-order dependence with respect to the nitrite, pinacolborane and zinc and clear evidence for catalyst deactivation. A plausible ligand-assisted reaction pathway involves B-H bond activation by the aryloxide (vs. anilido) donor.

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