Square‐Planar Anionic Pt0Complexes

Author:

Kameo Hajime1ORCID,Tanaka Yudai1,Shimoyama Yoshihiro2ORCID,Izumi Daisuke1,Matsuzaka Hiroyuki1,Nakajima Yumiko2ORCID,Lavedan Pierre3,Le Gac Arnaud4,Bourissou Didier4ORCID

Affiliation:

1. Department of Chemistry Graduate School of Science Osaka Metropolitan University Gakuen-cho, Naka-ku, Sakai Osaka 599-8531 Japan

2. Interdisciplinary Research Center for Catalytic Chemistry (IRC3) National Institute of Advanced Industrial Science and Technology (AIST) Tsukuba Ibaraki 305-8565 Japan

3. Institut de Chimie de Toulouse Université de Toulouse/CNRS UAR 2599 118 Route de Narbonne 31062 Toulouse Cedex 09 France

4. Laboratoire Hétérochimie Fondamentale et Appliquée Université Paul Sabatier/CNRS UMR 5069 118 Route de Narbonne 31062 Toulouse Cedex 09 France

Abstract

AbstractA T‐shaped Pt0complex with a diphosphine‐borane (DPB) ligand was prepared. The Pt→B interaction enhances the electrophilicity of the metal and triggers the addition of Lewis bases to give the corresponding tetracoordinate complexes. For the first time, anionic Pt0complexes are isolated and structurally authenticated. X‐ray diffraction analyses show the anionic complexes [(DPB)PtX](X=CN, Cl, Br, I) to be square‐planar. The d10configuration and Pt0oxidation state of the metal were unambiguously established by X‐ray photoelectron spectroscopy and DFT calculations. The coordination of Lewis acids as Z‐type ligands is a powerful mean to stabilize elusive electron‐rich metal complexes and achieve uncommon geometry.

Funder

Centre National de la Recherche Scientifique

Agence Nationale de la Recherche

Université Toulouse III - Paul Sabatier

Ministry of Education, Culture, Sports, Science and Technology

Iketani Science and Technology Foundation

Publisher

Wiley

Subject

General Medicine

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