Heterotrimetallic tetrathiomolybdate and tetrathiotungstate complexes of rhodium(I) and copper(I) with Rh-Mo(W)-Cu interactions.

The Rh ··· M ··· Cu bonding orbital of heterotrimetallic RhMCu represents a 7c-2e bond. TDDFT studies of the electronic spectra showed that the main band of the electronic spectrum is assigned to the ν (Rh→M) electron transfer transition. The correlations of Δδ (P) and 1 J (Rh-P) for phosphite complexes, with respect to QALE model electronic parameters χ d , π p and E ar , has succeeded in the assessment of the σ and π effects on NMR spectral parameters. [Display omitted] • The Rh ··· M ··· Cu bonding orbital of heterotrimetallic RhMCu represents a 7c-2e bond. • The main band of the UV-vis spectra is assigned to ν (Rh → Mo/W) transition. • ν (Rh → Mo/W) is a well defined electronic parameter for phosphites. The synthesis and characterization of the monoanionic heterotrimetallic (d 8 ··· d 0 ··· d 10) complexes [L 2 Rh(μ-S) 2 M(μ-S) 2 CuCl]− (L = P(OPh) 3 , P(O- o -Tol) 3 (P(O- o -CH 3 C 6 H 4) 3), P(OMe) 3 , P(OEt) 3 , P(O i Pr) 3 ; L 2 = COD (1,5-cyclooctadiene), cis -dppen (cis -Ph 2 PCH = CHPPh 2); M = Mo, W) is presented. The complex (NEt 4)[(cis -dppen)Rh(μ-S) 2 W(μ-S) 2 CuCl] was characterized by X-ray diffraction analysis. The detailed DFT study of the electronic structure of the complexes with P(OMe) 3 and COD ligands has revealed the existence of extended electron delocalization over the atom-sharing (spiro) four-membered rings system Rh(μ-S) 2 M(μ-S) 2 Cu and the possibility of electronic communication between the terminal metal centers. The electronic spectra of the complexes with P(OMe) 3 ligands were studied with TDDFT calculations and the main absorption band in the visible region was assigned to ν (Rh → Mo/W) electron transfer transition. The ν (Rh → Mo/W) transition was found to correlate linearly with Tolman's electronic parameter of the phosphite ligands, making it an electronic parameter for the ligands studied. Finally, the study of the dependence of Δδ(31P) and 1 J (Rh-P) of the phosphite complexes, with respect to the QALE model electronic parameters χ d , π p and E ar , has succeeded in the assessment of the σ and π effects on these NMR spectral parameters. [ABSTRACT FROM AUTHOR]