Charge-transfer-to-solvent states provide a sensitive spectroscopic tool to probe local structure of water around solvated anions

02 September 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

This computational study characterizes charge-transfer-to-solvent (CTTS) states of aqueous thiocyanate anion using equation-of-motion coupled-cluster methods combined with electrostatic embedding quantum mechanics/molecular mechanics (QM/MM) scheme. Equilibrium sampling was carried out using classical molecular dynamics (MD) with standard force-fields and QM/MM ab initio molecular dynamics (AIMD) using DFT. The two calculations yield significantly different local structure around solvated SCN−. Because of the diffuse character of CTTS states, they are very sensitive to the local structure of solvent around the solute and its dynamic fluctuations. Owing to this sensitivity, the spectra computed using MD and AIMD based snapshots differ considerably. This sensitivity suggests that the spectroscopy exploiting CTTS transitions can provide an experimental handle for assessing the quality of force-fields and density functionals.

Keywords

QM/MM
AIMD
Anion solvation
UV Spectroscopy
Charge transfer to solvent
Molecular Dynamics

Supplementary materials

Title
Description
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Title
Charge-transfer-to-solvent states provide a sensitive spectroscopic tool to probe local structure around solute: Supplementary Information
Description
Details of protocol development for EOM-EE calculations and calculation setup.
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