Double donation in trigonal planar iron–carbodiphosphorane complexes – a concise study on their spectroscopic and electronic properties†
Nis-Julian H. Kneusels,Jörn E. Münzer,Kimon Flosdorf,Dandan Jiang,Bernhard Neumüller,Lili Zhao,Andreas Eichhöfer,Istemi Kuzu
Dalton Transactions Pub Date : 02/05/2020 00:00:00 , DOI:10.1039/C9DT04725E
Abstract

We present the syntheses of trigonal planar coordinated Fe(II) carbodiphosphorane (CDPR) complexes, starting from iron(II)-bis(trimethylsilylamide) [Fe{N(SiMe3)2}2] and hexaphenyl-(CDPPh) and sym-dimethyltetraphenyl-carbodiphosphoranes (CDPMe), respectively. Both complexes [CDPPh-Fe{N(SiMe3)2}2] (1) and [CDPMe-Fe{N(SiMe3)2}2] (2) were examined in solution and in the solid state. 1 shows a dissociation equilibrium in solution which we monitored by variable temperature 1H-NMR spectroscopy. Magnetic measurements of 1 and 2 yielded a high spin configuration (S = 2) for both complexes. Quantum chemical calculations were performed to analyze the bonding situation in compound 1.

Graphical abstract: Double donation in trigonal planar iron–carbodiphosphorane complexes – a concise study on their spectroscopic and electronic properties