Abstract
Systematic NMR/UV-Vis analysis of Brooker’s merocyanine dyes reveals solvent polarity governs electronic structure and spectroscopy. Absorption maxima and ¹⁵N NMR shifts correlate with ET(30), probing zwitterionic/ vinylogous amide. Substituent and solvent effects modulate these interactions, directly linking colour changes to electronic structure for rational design of environment-sensitive probes.
Supplementary materials
Title
2025-05-20-ChemRxiv-ESI
Description
Detailed spectroscopic data; NMR and UV/Vis spectra data of the reported compounds.
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