Distinguishing packing configurations of molecular dimers using excited-state absorption peaks in two-dimensional electronic spectra

Packing conformations of molecular aggregates are known to strongly influence the locations and intensities of spectral peaks. Here, we develop the third-order nonlinear spectroscopy signals for a purely electronic model of a molecular dimer, which is a prototype aggregate system. The model-which focuses on excited-state absorption (ESA) pathways in two-dimensional electronic spectra-reveals that orientational averaging leads to diagnostic ESA peak locations for H- and J-dimers. We constructed DNA-templated dimers of cyanine molecules as representative systems and used ultrabroadband two-dimensional electronic spectroscopy measurements to support the predicted signatures arising from the theoretical model. Fitting of steady-state spectra supports the assigned packing conformations. The results elucidate how ESA peaks can be diagnostic spectral signatures of packing conformation. This work lays the foundation for future studies that can include the complicating effects of vibronic states and additional electronic levels.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-05-01
DOI
https://doi.org/10.1063/5.0258934
Citations
2
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
2.49

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article

Distinguishing packing configurations of molecular dimers using excited-state absorption peaks in two-dimensional electronic spectra

Veronica R. Policht, Gissela Pascual, Paul D. Cunningham, Igor L. Medintz et al.
2 citations
The Journal of Chemical Physics
Spectroscopy and Quantum Chemical Studies
2.49
article

Distinguishing packing configurations of molecular dimers using excited-state absorption peaks in two-dimensional electronic spectra

Veronica R. Policht, Gissela Pascual, Paul D. Cunningham, Igor L. Medintz, Jeunghoon Lee, Bernard Yurke, Adam Meares, Matthew S. Barclay, Ryan D. Pensack, Paul H. Davis, Simon K. Roy, Kimihiro Susumu, Joseph S. Melinger, Divita Mathur, Lance K. Patten, Daniel B. Turner, William B. Knowlton
article en
2 citations

Abstract

Packing conformations of molecular aggregates are known to strongly influence the locations and intensities of spectral peaks. Here, we develop the third-order nonlinear spectroscopy signals for a purely electronic model of a molecular dimer, which is a prototype aggregate system. The model-which focuses on excited-state absorption (ESA) pathways in two-dimensional electronic spectra-reveals that orientational averaging leads to diagnostic ESA peak locations for H- and J-dimers. We constructed DNA-templated dimers of cyanine molecules as representative systems and used ultrabroadband two-dimensional electronic spectroscopy measurements to support the predicted signatures arising from the theoretical model. Fitting of steady-state spectra supports the assigned packing conformations. The results elucidate how ESA peaks can be diagnostic spectral signatures of packing conformation. This work lays the foundation for future studies that can include the complicating effects of vibronic states and additional electronic levels.

The Journal of Chemical PhysicsVol. 162(17)
Micron (United States) (US), Boise State University (US), United States Naval Research Laboratory (US), Optical Sciences (United States) (US), Center for Advanced Energy Studies (US), Case Western Reserve University (US)
Office of Naval Research, National Institute of General Medical Sciences, National Institute of Biomedical Imaging and Bioengineering
Openalex Percentile: Top 12%
Spectroscopy and Quantum Chemical Studies
2.49
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