Two-Dimensional Infrared Study of (13)C-Natural Abundant Vibrational Transition Reveals Intramolecular Vibrational Redistribution Rather than Fluxional Exchange in Mn(CO)5Br

The Journal of Physical Chemistry. B
Fan YangJianping Wang

Abstract

In this work, molecular-symmetry enhanced (13)CO natural abundant isotopic infrared transition was identified in Mn(CO)5Br dissolved in CCl4 by FTIR spectroscopy. Diagonal and associated off-diagonal two-dimensional IR (2D IR) peaks of the (13)CO-species were found to be spectrally separated from the all-(12)CO species, allowing a direct probe of the (13)C natural abundant ensemble. Temperature-dependent FTIR experiment showed no evidence of ligand exchange in the metal carbonyl complex. Intramolecular vibrational redistribution dynamics among the CO stretching vibrational states were extracted using population-time dependent 2D IR diagonal and off-diagonal peaks for both radial mono-(13)CO and all-(12)CO isotopomers. This work demonstrates the potential use of natural abundant isotopic molecular species as a probe for revealing equilibrium and nonequilibrium structural dynamics in condensed-phase molecular systems.

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Citations

Feb 3, 2018·The Journal of Physical Chemistry. a·James J Turner, Michael Bühl
Nov 19, 2019·The Journal of Physical Chemistry. a·Andrew J SchmitzMatthew J Tucker

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