Copper(I) and Gold(I) Complexes of Aminofunctionalized Phosphinines: Synthesis and Structural Characterization. Issue 6 (27th December 2022)

• Record Type: Journal Article
• Authors: Lin, Jinxiong; Frost, Daniel S.; Coles, Nathan T.; Weber, Manuela; Müller, Christian
• Is Part Of: Zeitschrift für anorganische und allgemeine Chemie. Volume 649:Issue 6/7(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-12-27
• Subjects: Au(I) Complexes -- Coordination Chemistry -- Cu(I) Complexes -- DFT Calculations -- Phosphinine; Chemistry, Inorganic -- Periodicals; Chemistry -- Periodicals; 540
• DOI: 10.1002/zaac.202200365
• Languages: English
• ISSNs: 0044-2313

Abstract

Abstract: A series of novel 3‐ N, N ‐dimethylaminofunctionalized phosphinines were synthesized and structurally characterized. DFT calculations showed that these aromatic phosphorus heterocycles possess stronger π‐donor and σ‐donor properties compared to the parent phosphinine C5 H5 P. With CuBr ⋅ SMe2, the corresponding complexes of the type [(phosphinine)2 CuBr]2 are formed, which show the classical terminal σ‐coordination mode of the phosphorus donor towards the Cu(I) center. Upon reaction with AuCl ⋅ SMe2, mononuclear phosphinine‐Au(I)Cl complexes could be obtained and crystallographically characterized. Moreover, the presence of a SiMe3 ‐group and a donor‐functionality provide the possibility for post‐synthetic ligand modifications. With CuCl ⋅ SMe2 the phosphinine‐based hydrochloride salts forms a rare Cu(I) complex with a Cu4 Cl4 ‐core, that contains two pairs of differently coordinating phosphinine ligands. Abstract :