Open AccessSpectroscopic and Computational Investigations of a Mononuclear Manganese(IV)-Oxo Complex Reveal Electronic Structure Contributions to Reactivity
Author(s) -
Domenick F. Leto,
Allyssa A. Massie,
Derek B. Rice,
Timothy A. Jackson
Publication year - 2016
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.6b08661
Subject(s) - chemistry , excited state , reactivity (psychology) , hydrogen atom , density functional theory , ligand (biochemistry) , ligand field theory , ground state , electronic structure , computational chemistry , atomic physics , crystallography , ion , physics , medicine , biochemistry , alkyl , alternative medicine , organic chemistry , receptor , pathology
The mononuclear Mn(IV)-oxo complex [Mn IV (O)(N4py)] 2+ , where N4py is the pentadentate ligand N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine, has been proposed to attack C-H bonds by an excited-state reactivity pattern [ Cho, K.-B.; Shaik, S.; Nam, W. J. Phys. Chem. Lett. 2012 , 3 , 2851 - 2856 (DOI: 10.1021/jz301241z )]. In this model, a 4 E excited state is utilized to provide a lower-energy barrier for hydrogen-atom transfer. This proposal is intriguing, as it offers both a rationale for the relatively high hydrogen-atom-transfer reactivity of [Mn IV (O)(N4py)] 2+ and a guideline for creating more reactive complexes through ligand modification. Here we employ a combination of electronic absorption and variable-temperature magnetic circular dichroism (MCD) spectroscopy to experimentally evaluate this excited-state reactivity model. Using these spectroscopic methods, in conjunction with time-dependent density functional theory (TD-DFT) and complete-active space self-consistent-field calculations (CASSCF), we define the ligand-field and charge-transfer excited states of [Mn IV (O)(N4py)] 2+ . Through a graphical analysis of the signs of the experimental C-term MCD signals, we unambiguously assign a low-energy MCD feature of [Mn IV (O)(N4py)] 2+ as the 4 E excited state predicted to be involved in hydrogen-atom-transfer reactivity. The CASSCF calculations predict enhanced Mn III -oxyl character on the excited-state 4 E surface, consistent with previous DFT calculations. Potential-energy surfaces, developed using the CASSCF methods, are used to determine how the energies and wave functions of the ground and excited states evolved as a function of Mn═O distance. The unique insights into ground- and excited-state electronic structure offered by these spectroscopic and computational studies are harmonized with a thermodynamic model of hydrogen-atom-transfer reactivity, which predicts a correlation between transition-state barriers and driving force.