Central-metal effect on intramolecular vibrational energy transfer of M(CO)5Br (M = Mn, Re) probed by two-dimensional infrared spectroscopy. Issue 5 (17th January 2018)

• Record Type: Journal Article
• Authors: Yang, Fan; Dong, Xueqian; Feng, Minjun; Zhao, Juan; Wang, Jianping
• Is Part Of: Physical chemistry chemical physics. Volume 20:Issue 5(2018)
• Page Start: 3637
• Page End: 3647
• Publication Date: 2018-01-17
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c7cp05117d
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Central-metal effect on IVR time correlates with the vibrational coupling between the two involved modes. Abstract : Vibrational energy transfer in transition metal complexes with flexible structures in condensed phases is of central importance to catalytical chemistry processes. In this work, two molecules with different metal atoms, M(CO)5 Br (where M = Mn, Re), were used as model systems, and their axial and radial carbonyl stretching modes as infrared probes. The central-metal effect on intramolecular vibrational energy redistribution (IVR) in M(CO)5 Br was investigated in polar and nonpolar solvents. The linear infrared (IR) peak splitting between carbonyl vibrations increases as the metal atom changes from Mn to Re. The waiting-time dependent two-dimensional infrared diagonal- and off-diagonal peak amplitudes reveal a faster IVR process in Re(CO)5 Br than in Mn(CO)5 Br. With the aid of density functional theory (DFT) calculations, the central-metal effect on IVR time linearly correlates with the vibrational coupling strength between the two involved modes. In addition, the polar solvent is found to accelerate the IVR process by affecting the anharmonic vibrational potentials of a solute vibration mode.