From Carbene-Dithiolene Zwitterion Mediated B-H Bond Activation to BH3·SMe2-Assisted Boron-Boron Bond Formation

© 2023 The Authors. Published by American Chemical Society.

Détails bibliographiques
Publié dans:Organometallics. - 1998. - 42(2023), 23 vom: 11. Dez., Seite 3328-3333
Auteur principal: Wang, Yuzhong (Auteur)
Autres auteurs: Tran, Phuong M, Lahm, Mitchell E, Wei, Pingrong, Adams, Earle R, Schaefer, Henry F 3rd, Robinson, Gregory H
Format: Article en ligne
Langue:English
Publié: 2023
Accès à la collection:Organometallics
Sujets:Journal Article
Description
Résumé:© 2023 The Authors. Published by American Chemical Society.
The 1:1 reaction of the carbene-stabilized dithiolene zwitterion 1 with BH3·SMe2 gave the dithiolene-based hydroborane 2 and the doubly hydrogen-capped CAAC species 3 via hydride-coupled reverse electron transfer processes. The mechanism of this transformation was probed computationally using density functional theory. The subsequent 2:1 reaction of 2 with 1 resulted in 4 and 3, suggesting that 1 can mediate the B-H bond activation not only for BH3 but also for monohydroboranes. In the presence of BH3·SMe2, 2 was unexpectedly converted to the corresponding diborane(4) complex 5 through a dehydrocoupling reaction at an elevated temperature
Description:Date Revised 16.10.2024
published: Electronic-eCollection
Citation Status PubMed-not-MEDLINE
ISSN:0276-7333
DOI:10.1021/acs.organomet.3c00361