Theoretical Studies on Metal−Metal Interaction, Excited States, and Spectroscopic Properties of Binuclear Au−Au, Au−Rh, and Rh−Rh Complexes with Diphosphine Ligands: Buildup of Complexity from Monomers to Dimers

Abstract

To understand their photocatalytic activity and application in luminescent materials, a series of gold and rhodium phosphine complexes (mononuclear [Au(I)(PH(3))(2)](+) (1) and [Rh(I)(CNH)(2)(PH(3))(2)](+) (2); homobinuclear [Au(I)(2)(PH(2)CH(2)PH(2))(2)](2+) (3) and [Rh(I)(2)(CNH)(4)(PH(2)CH(2)PH(2))(2)](2+) (4); heterobinuclear [Au(I)Rh(I)(CNH)(2)(PH(2)CH(2)PH(2))(2)](2+) (5), [Au(I)Rh(I)(CNH)(2)(PH(2)NHPH(2))(2)Cl(2)] (6), and [Au(I)Rh(I)(CNH)(2)(PH(2)NHPH(2))(2)](2+) (7); and oxidized derivatives [Au(II)Rh(II)(CNH)(2)(PH(2)CH(2)PH(2))(2)](4+) (8), [Au(II)Rh(II)(CNH)(2)(PH(2)NHPH(2))(2)Cl(3)](+) (9), and [Au(II)Rh(II)(CNH)(2)(PH(2)NHPH(2))(2)](4+) (10)) were investigated using ab initio methods and density functional theory. With the use of the MP2 method, the M-M' distances in 3-7 were estimated to be in the range of 2.76-3.02 A, implying the existence of weak metal-metal interaction. This is further evident in the stretching frequencies and bond orders of M-M'. The two-electron oxidation from 5-7 to their respective partners 8-10 was shown to mainly occur in the gold-rhodium centers. Experimental absorption spectra were well reproduced by our time-dependent density functional theory calculations. The metal-metal interaction results in a large shift of d(z(2)) --> p(z) transition absorptions in binuclear complexes relative to mononuclear analogues and concomitantly produces a low-lying excited state that is responsible for increasing visible-light photocatalytic activities. Upon excitation, the metal-centered transition and the metal-to-metal charge transfer strengthen the metal-metal interaction in triplet excited states for 3-6, while the promotion of electrons into the sigma*(d(z(2))) orbital weakens the interaction in 9.