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Synthesis,Characterization, and Theoretical Investigation of Two‐Coordinate Palladium(0) and Platinum(0) Complexes Utilizing π‐Accepting Carbenes
Authors:Dr. Sudipta Roy  Dr. Kartik Chandra Mondal  Dipl.‐Chem. Jann Meyer  Dipl.‐Chem. Benedikt Niepötter  Christian Köhler  Dr. Regine Herbst‐Irmer  Prof. Dr. Dietmar Stalke  Dr. Birger Dittrich  Dr. Diego M. Andrada  Prof. Dr. Gernot Frenking  Prof. Dr. Herbert W. Roesky
Affiliation:1. Institut für Anorganische Chemie, Georg‐August‐Universit?t, Tammannstrasse 4, 37077‐G?ttingen (Germany);2. Institut für Anorganische und Angewandte Chemie, Universit?t Hamburg, Martin‐Luther‐King‐Platz 6, Raum AC 15c (Erdgeschoss), 20146 Hamburg (Germany);3. Fachbereich Chemie, Philipps‐Universit?t Marburg, Hans‐Meerwein‐Strasse 35032 Marburg (Germany)
Abstract:
An elegant general synthesis route for the preparation of two coordinate palladium(0) and platinum(0) complexes was developed by reacting commercially available tetrakis(triphenylphosphine)palladium/platinum with π‐accepting cyclic alkyl(amino) carbenes (cAACs). The complexes are characterized by NMR spectroscopy, mass spectrometry, and single‐crystal X‐ray diffraction. The palladium complexes exhibit sharp color changes (crystallochromism) from dark maroon to bright green if the C‐Pd‐C bond angle is sharpened by approximately 6°, which is chemically feasible by elimination of one lattice THF solvent molecule. The analogous dark orange‐colored platinum complexes are more rigid and thus do not show this phenomenon. Additionally, [(cAAC)2Pd/Pt] complexes can be quasi‐reversibly oxidized to their corresponding [(cAAC)2Pd/Pt]+ cations, as evidenced by cyclic voltammetry measurements. The bonding and stability are studied by theoretical calculations.
Keywords:carbenes  crystallochromism  density functional calculations  palladium  platinum
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