Optical Behaviors and Electronic Properties of Mo2–Mo2 Mixed-Valence Complexes within or beyond the Class III Regime: Testing the Limits of the Two-State Model
journal contributionposted on 20.11.2017, 00:00 by Ying Ning Tan, Tao Cheng, Miao Meng, Yu Yu Zhang, Chun Y. Liu, Mei Fang Sun, Yu Zhang, Paul J. Low
Three symmetric Mo2 dimers [Mo2(DAniF)3](μ-E2CCE2)[Mo2(DAniF)3] (DAniF = N,N′-di(p-anisyl)formamidinate) with oxalate (E = O) or the thiolated derivatives (E = O or S) as bridging ligands have been synthesized, and the optical properties of the mixed-valence (MV) derivatives obtained by one-electron oxidation studied within the framework of the vibronic two-state model. These Mo2–Mo2 systems are effective models for testing electron transfer theories, with the δ electrons of the Mo2 fragments that are responsible for the redox and optical properties of the MV complex being well isolated from other metal d and ligand π-type orbitals. This in turn gives rise to unique, well-resolved metal to ligand (MLCT) and intervalence charge transfer (IVCT) absorption bands that permit accurate analyses based on band shape. In the series [Mo2(DAniF)3](μ-E2CCE2)[Mo2(DAniF)3], the extent of electron delocalization between the Mo2 cores increases with increasing number of sulfur atoms, E, in the bridge. Higher-energy IVCT absorption bands are observed for the more strongly coupled complex, but in contrast to the predictions from the two-state model, the IVCT band becomes more symmetric in shape as the electronic coupling constant increases beyond the Class III border and 2Hab/λ ≫ 1. Thus, the oxalate-bridged complex (E2 = O2) is situated on the Class II–III borderline, while the two thiolated species are well placed deep into Class III, where novel optical behavior can be observed. The electronic coupling matrix elements (HDA) estimated from the transition energy EIT (HDA = EIT/2, 2000–2500 cm–1) are in excellent agreement with data (Hab, 2400–3000 cm–1) calculated from the modified Mulliken–Hush expression for Class III systems. DFT calculations show that linear combinations of the δ orbitals of the Mo2 centers generate the HOMO (out-of-phase, δ−δ) and HOMO–1 (in-phase, δ + δ), with the energy difference corresponding to the EIT. This study illustrates a systematic transition from a strongly coupled MV complex near the Class II–III border, to Class III, and to systems in which the underlying ground state is better described in terms of simple delocalized electronic states rather evolving from strongly coupled diabatic states which define Class III.
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DFT calculations showCCEMo 2 dimersClass III borderligand π- type orbitalsClass III systemsClass IIIHigher-energy IVCT absorption bandsDAniFtesting electron transfer theoriestransition energy EMVHOMOMo 2 cores increasesH DAvibronic two-state modelMo 2 centersMo 2Class III RegimeMLCTintervalence charge transferMo 2 fragments