Improving PCM in Protic Media: Markov State Models for TD-DFT Calculations

Predicting the optical properties of dyes in protic media requires accounting for specific solute-solvent interactions, which go beyond polarizable continuum models (PCM). We introduce a workflow that combines molecular dynamics simulations, time-lagged independent component analysis, and Markov State Models (MSM) to identify key macrostates and system configurations relevant to model electronic excitations using time-dependent density functional theory (TD-DFT) with only H-bonded solvent molecules in the explicit input. This MSM(PCM)TD-DFT approach shows that just a few thermally accessible, nonoptimized geometries could be more representative of the experimental spectra than optimized structures. By testing this approach on two compounds, including one with a transition with strong charge-transfer character, we show that MSM(PCM)TD-DFT is a promising way to understand these kinds of systems in a cost-effective way.

Authors

Institutions

Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2026-07-02
DOI
https://doi.org/10.1021/acs.jctc.6c00705
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Improving PCM in Protic Media: Markov State Models for TD-DFT Calculations

D. Mariano A. Vera, N. Rodríguez, Carlos A. Chesta
Journal of Chemical Theory and Computation
Spectroscopy and Quantum Chemical Studies
article

Improving PCM in Protic Media: Markov State Models for TD-DFT Calculations

D. Mariano A. Vera, N. Rodríguez, Carlos A. Chesta
article en

Abstract

Predicting the optical properties of dyes in protic media requires accounting for specific solute-solvent interactions, which go beyond polarizable continuum models (PCM). We introduce a workflow that combines molecular dynamics simulations, time-lagged independent component analysis, and Markov State Models (MSM) to identify key macrostates and system configurations relevant to model electronic excitations using time-dependent density functional theory (TD-DFT) with only H-bonded solvent molecules in the explicit input. This MSM(PCM)TD-DFT approach shows that just a few thermally accessible, nonoptimized geometries could be more representative of the experimental spectra than optimized structures. By testing this approach on two compounds, including one with a transition with strong charge-transfer character, we show that MSM(PCM)TD-DFT is a promising way to understand these kinds of systems in a cost-effective way.

Journal of Chemical Theory and Computation
Universidad Nacional de Río Cuarto (AR), Exact Sciences (United States) (US), Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (AR), Centro Científico Tecnológico - Tucumán (AR), Instituto de Química y Fisicoquímica Biológicas (AR), Instituto de Biotecnología y Biología Molecular (AR), Fundación Ciencias Exactas y Naturales (AR)
Ministerio de Ciencia, Tecnología e Innovación Productiva, Fondo Nacional de Desarrollo Científico y Tecnológico
Openalex Percentile: Top 8%
Spectroscopy and Quantum Chemical Studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.