Silyliumylidene Ion Stabilized by Two σ‐Donating Ni(0)‐ and Pd(0)‐Fragments

Author:

Takahashi Shintaro1ORCID,Kazama Yugo2,Nakata Norio2,Baceiredo Antoine1,Hashizume Daisuke3,Saffon‐Merceron Nathalie4,Branchadell Vicenç5,Kato Tsuyoshi1ORCID

Affiliation:

1. Laboratoire Hétérochimie Fondamentale et Appliquée (UMR 5069) Université de Toulouse, CNRS 118 route de Narbonne F-31062 Toulouse France

2. Department of Chemistry Graduate School of Science and Engineering Saitama University Shimo-okubo, Sakura-ku Saitama 338-8570 Japan

3. RIKEN Center for Emergent Matter Science (CEMS) 2-1 Hirosawa Wako Saitama 351-0198 Japan

4. Institut de Chimie de Toulouse UAR 2599) UPS CNRS ICT UAR2599 118 route de Narbonne F-31062 Toulouse France

5. Departament de Química Universitat Autònoma de Barcelona 08193 Bellaterra Spain

Abstract

AbstractA silyliumylidene ion 2 stabilized by two σ‐donating Ni(0)‐ and Pd(0)‐fragments was successfully synthesized. Due to the σ‐donation of M→Si interactions, 2 presents a pyramidalized cationic silicon center with a localized lone pair. The additional coordination of basic Pd(0) fragment to the mono‐Ni(0)‐stabilized silyliumylidene 1 results in a higher HOMO level and an unchanged HOMO‐LUMO gap and thus, 2 remains highly reactive. Interestingly, the coordination mode at the Si center is closely related to the nature of M‐ligands. Indeed, the donor/donor‐stabilized silyliumylidene ion 2 has been transformed into a donor/acceptor‐stabilized ion 13, featuring a trigonal planar Si center with a vacant orbital, just via a ligand exchange reaction from PCy3/NHC toward PMe3.

Funder

Agence Nationale de la Recherche

Japan Society for the Promotion of Science

Saitama University

Agencia Estatal de Investigación

Publisher

Wiley

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