Solvent Dependence of Cationic-Exciplex Emission: Limitation of Solvent Polarity Functions and the Role of Hydrogen Bonding

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Vol. 124; no. 19; pp. 3730 - 3737
• Main Authors: Dinnocenzo, Joseph P, Tingson, Joshua, Young, Ralph H, Farid, Samir
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 14-05-2020
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/acs.jpca.0c01774

Conventional exciplexes are products of excited-state charge generation reactions between neutral reactants (e.g., A* + D → A•–D•+), whereas cationic exciplexes are products of charge shift reactions of cations with neutral donors (e.g., A+* + D → A•D•+). Compared herein is the solvent-dependent fluorescence of a cationic exciplex with extant data for conventional exciplexes. Although linear correlations of conventional exciplex emission maxima with the Lippert–Mataga solvent polarity function are well documented in low to moderate polarity solvents, the correlations are often poor in more polar solvents. A number of such plots in moderate to high polarity solvents show a strong curvature. Intriguingly, for these same cases, plots of emission maxima versus the solvent dielectric constant (ε) are remarkably linear. Interestingly, emission maxima for the cationic exciplex of 1 + in nitrile and alcohol solvents also correlate linearly with ε. The solvent dependency for cationic exciplex emission maxima on ε is ca 1/3 of that for conventional exciplexes, which is ascribed to solvent stabilization of both the excited state and the ground state for cationic exciplexes. Differences in exciplex emissions between nitrile and alcohol solvents for 1 + are attributed to hydrogen bonding, with larger differences in higher hydrogen-bond acidity solvents.