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.
Publié dans: | Organometallics. - 1998. - 42(2023), 23 vom: 11. Dez., Seite 3328-3333 |
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Auteur principal: | |
Autres auteurs: | , , , , , |
Format: | Article en ligne |
Langue: | English |
Publié: |
2023
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Accès à la collection: | Organometallics |
Sujets: | Journal Article |
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 |
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Description: | Date Revised 16.10.2024 published: Electronic-eCollection Citation Status PubMed-not-MEDLINE |
ISSN: | 0276-7333 |
DOI: | 10.1021/acs.organomet.3c00361 |