Michael R. Dooley
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Michael R. Dooley has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
- Shubham Vyas
Department of Chemistry, Colorado School of Mines, 1012 14th Street, Golden, Colorado 80401, USA
4 shared publications Benjamin E. Payton
Department of Chemistry, Colorado School of Mines, 1012 14th Street, Golden, Colorado 80401, United States
1 shared publication- Brian G. Trewyn
Department of Chemistry, Colorado School of Mines, 1500 Illinois Street, Golden, Colorado 80401, United States
1 shared publication Fiona Odei
Department of Chemistry, Colorado School of Mines, 1012 14th Street, Golden, Colorado 80401, United States
1 shared publicationFrank R. A. Schrama
Department of Chemistry, Colorado School of Mines, Golden, CO 80401, USA
1 shared publicationMikayla A. Hudak
Department of Chemistry, Colorado School of Mines, 1012 14th Street, Golden, Colorado 80401, United States
1 shared publication
Latest Publications
- Open Access
- 21 October 2026
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 28 (40) , 25271-25283
Explicit microsolvation as a “conformational chaperone” for openCOSMO-RS solvation energy predictions
Conformational sampling with implicit solvation models can incorrectly favor intramolecular bonding. Explicit solvation during sampling can act as a conformational chaperone disrupting these bonds and improving COSMO-RS solvation energy predictions.
- 21 October 2026
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 28 (40) , 25271-25283
Open AccessExplicit microsolvation as a “conformational chaperone” for openCOSMO-RS solvation energy predictions
Conformational sampling with implicit solvation models can incorrectly favor intramolecular bonding. Explicit solvation during sampling can act as a conformational chaperone disrupting these bonds and improving COSMO-RS solvation energy predictions.
- Open Access
- 12 February 2025
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 27 (14) , 6867-6874
Role of explicit solvation and level of theory in predicting the aqueous reduction potential of carbonate radical anion by DFT
Explicit solvation and dispersion corrections required for accurate energies for ion and radical forms of carbonate with DFT.
- 12 February 2025
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 27 (14) , 6867-6874
Open AccessRole of explicit solvation and level of theory in predicting the aqueous reduction potential of carbonate radical anion by DFT
Explicit solvation and dispersion corrections required for accurate energies for ion and radical forms of carbonate with DFT.
- 10 October 2024
- Published by American Chemical Society (ACS) in ACS ES&T Air
- Vol. 1 (11) , 1352-1361
Atmospheric Oxidation of PFAS by Hydroxyl Radical: A Density Functional Theory Study
- 10 October 2024
- Published by American Chemical Society (ACS) in ACS ES&T Air
- Vol. 1 (11) , 1352-1361
Atmospheric Oxidation of PFAS by Hydroxyl Radical: A Density Functional Theory Study
- Open Access
- 5 July 2024
- Published by Royal Society of Chemistry (RSC) in RSC Applied Interfaces
- Vol. 1 (5) , 833-845
Light-driven interfaces for PFAS detection and destruction
Due to exposure risks and health concerns, global limitations on per- and polyfluoroalkyl substances (PFAS) have become increasingly restrictive. Light-driven technologies can potentially destroy and detect PFAS, addressing these limitations.
- 5 July 2024
- Published by Royal Society of Chemistry (RSC) in RSC Applied Interfaces
- Vol. 1 (5) , 833-845
Open AccessLight-driven interfaces for PFAS detection and destruction
Due to exposure risks and health concerns, global limitations on per- and polyfluoroalkyl substances (PFAS) have become increasingly restrictive. Light-driven technologies can potentially destroy and detect PFAS, addressing these limitations.