Effect of Protonation on the Spectral–Luminescent and Photochemical Properties of a Bis(styrylbenzoquinoline) Dyad with the Naphthylene Framework and of Corresponding Dibenzoquinolylcyclobutane

• Published in: High energy chemistry Vol. 57; no. 5; pp. 396 - 403
• Main Authors: Budyka, M. F., Li, V. M., Potashova, N. I., Gavrishova, T. N., Kozlovskii, V. I., Sulimenkov, I. V.
• Format: Journal Article
• Language: English
• Published: Moscow Pleiades Publishing 01-10-2023; Springer Nature B.V
• Subjects: Absorption spectra; Chemistry; Chemistry and Materials Science; Cyclobutane; Energy transfer; Hydroxynaphthoic acid; Nitrogen atoms; Photochemistry; Photochromism; Physical Chemistry; Protonation; Quinoline; Ring opening; protonated form; styrylbenzoquinoline; diarylethylene; cyclobutane; fluorescence; energy transfer; photoisomerization; [2+2] photocycloaddition; biphotochromic dyad
• ISSN: 0018-1439; 1608-3148
• DOI: 10.1134/S0018143923050028

The photophysical and photochemical properties of the protonated forms of both covalently bound biphotochromic dyad D44N containing two styrylbenzo[f]quinoline (SBQ) photochromes and corresponding cyclobutane CB44N containing two benzo[f]quinoline (BQ) substituents have been studied. CB44N is formed from D44N as a result of a reversible [2+2] photocycloaddition (PCA) reaction. The dyad and cyclobutane contain the 3-hydroxy-2-naphthoic acid (NA) moiety as a bridging group. It has been shown that the protonation of nitrogen atoms in the SBQ and BQ groups leads to bathochromic shifts in the absorption spectra and bathofloral shifts in the fluorescence spectra of the dyad and cyclobutane. In the protonated dyad, the quantum yield of the PCA reaction decreases, presumably due to the Coulomb repulsion, which prevents the cations of the protonated SBQ photochromes from approaching each other. In protonated cyclobutane, the quantum yield of the reverse four-membered ring opening reaction (retro-PCA), on the contrary, increases due to the absence of a competitive process of energy transfer from BQ to NA, which was previously observed in neutral cyclobutane.