Triple Emission of 5'-( para -R-Phenylene)vinylene-2-(2'-hydroxyphenyl)benzoxazole ( PVHBO ). Part II: Emission from Anions

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Vol. 126; no. 7; pp. 1062 - 1075
• Main Authors: Hurley, Joseph J M, Meisner, Quinton J, Guo, Peijun, Schaller, Richard D, Gosztola, David J, Wiederrecht, Gary P, Zhu, Lei
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 24-02-2022
• Subjects: Absorption; Anions; Dyes and pigments; Energy; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Quantum mechanics
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/acs.jpca.1c10167

This paper is the second part of a study on the effects of a substituted 5'-phenylenevinylene (PV) functionality on the emission properties of 2-(2'-hydroxyphenyl)benzoxazole (HBO)─a dye that is known for excited-state intramolecular proton transfer. The topical compounds are referred to as
s, each of which is a structural fusion of HBO and a 4-hydroxy-4'-R-stilbene fluorophore that occurs at the hydroxyphenyl moiety. Therefore, the resulting fusion fluorophore manifests the properties of one component or the other, as governed by its interactions with the environment. In part I (the preceding paper),
s are divided into two groups depending on whether the R substituent is electron-donating/neutral (group I) or electron-withdrawing (group II). The difference in absorption and emission properties between groups I and II is explained based on observations from spectroscopic experiments (both steady-state and time-resolved) and quantum chemical calculations. In the current paper, the same set of tools is applied to characterize the photophysical properties of the conjugate bases─that is, the anions─of
s. The emission energy of the anion of any group I compound, where the R substituent is either electron-donating or neutral, is situated between those of the neutral enol and keto forms. The emission of the anion of any given group II compound, on the other hand, has a lower energy than both the enol and keto emissions. The frontier molecular orbitals (i.e., HOMO, LUMO, and LUMO + 1) of a
localized on either HBO or stilbenoid are impacted by the substituent R and the solvent/additive differently, which leads to the differences in the optical properties of group I and II
s in both neutral and anion forms.