Syntheses, Crystal and Electronic Structures of Rhodium and Iridium Pyridine Di-Imine Complexes with O- and S-Donor Ligands: (Hydroxido, Methoxido and Thiolato)

被引:2
作者
Stephan, Michel [1 ]
Voelker, Max [1 ]
Schreyer, Matthias [1 ]
Burger, Peter [1 ]
机构
[1] Univ Hamburg, Inst Inorgan & Appl Chem, Dept Chem, Martin Luther King Pl 6, D-20146 Hamburg, Germany
来源
CHEMISTRY-SWITZERLAND | 2023年 / 5卷 / 03期
关键词
metal-ligand d & pi; -p & pi; -interaction; Ir-O; S bond dissociation enthalpies; DFT; P/LNO-CCSD(T) calculations; oxidation state analysis; metal-ligand charge transfer; non-innocent ligand; pyridine di-imine ligand; FITTING BASIS-SETS; POLYMERIZATION CATALYSTS; REDUCTIVE ELIMINATION; DENSITY FUNCTIONALS; QUANTUM-CHEMISTRY; ACCURATE; BOND; ACTIVATION; METHYL; ENERGIES;
D O I
10.3390/chemistry5030133
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The syntheses of new neutral square-planar pyridine di-imine rhodium and iridium complexes with O- and S-donor (OH, OR, SH, SMe and SPh) ligands along with analogous cationic compounds are reported. Their crystal and electronic structures are investigated in detail with a focus on the non-innocence/innocence of the PDI ligand. The oxidation states of the metal centers were analyzed by a variety of experimental (XPS and XAS) and theoretical (LOBA, EOS and OSLO) methods. The dp-pp interaction between the metal centers and the p-donor ligands was investigated by theoretical methods and revealed the partial multiple-bond character of the M-O,S bonds. Experimental support is provided by a sizable barrier for the rotation about the Ir-S bond in the methyl thiolato complex and confirmed by DFT and LNO-CCSD(T) calculations. This was corroborated by the high Ir-O and Ir-S bond dissociation enthalpies calculated at the PNO-CCSD(T) level.
引用
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页码:1961 / 1989
页数:29
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