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Updated: Sep 15, 2025

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
An NMR insight into the solvatochromic behaviour of Brooker's merocyanine dyes
Michal Afri1, Hugo E Gottlieb1, Natalia Fridman2
1Department of Chemistry, Bar-Ilan University Ramat-Gan 52900 Israel abed.saady@biu.ac.il.
Abstract:
Systematic NMR/UV-Vis analysis of Brooker's merocyanine dyes reveals solvent polarity governs electronic structure and spectroscopy. Absorption maxima 13C and 15N NMR shifts correlate with E T(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.
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