Abstract
Two-photon absorption (2PA) spectroscopy is a robust bioimaging tool that depends
on the determined cross-sections (σ2PA). The absorption of both photons occurs
simultaneously with equivalent (degenerate) or different (non-degenerate) photon
energies, D-2PA and ND-2PA, respectively. The former has been investigated experimentally
and computationally for many systems, while the latter remains relatively
unexplored computationally and limited experimentally. In this study, response theory
using time-dependent density functional theory (TD-DFT) and the 2-state model
(2SM) have been utilized to investigate σD-2PA and σND-2PA for the excitation to the
lowest energy singlet state (S1) of coumarin, coumarin 6, coumarin 120, coumarin 307,
and coumarin 343. Solvents involved were methanol (MeOH), chloroform (ClForm),
and dimethylsulfoxide (DMSO), where the latter leads to the largest σ2PA. Values of
σ2PA are largest for coumarin 6 and lowest for coumarin, which illustrates the effect of
substituents. The 2SM clarifies how the largest cross-sections correspond to molecules
with the largest transition dipole moments, μ01. In general, σD-2SM computations agree
with σD-2PA. Moreover, σND-2SM are in qualitative agreement with σND-2PA with comparable
enhancement relative to σD-2PA. Overall, σND-2PA are larger than σD-2PA where
the increase is in the range of 22% to 49%. This work aids in future investigations into
various fluorophores to understand their photophysical properties for ND-2PA.
Supplementary materials
Title
Supplementary Information for “Degenerate and Non-Degenerate Two-Photon Absorption of Coumarin Dyes”
Description
Supplementary Information
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Title
Coumarins Coordinates for “Degenerate and Non-Degenerate Two-Photon Absorption of Coumarin Dyes”
Description
xyz coordinates
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