Effect of bulky substituents in the donor and acceptor terminal groups on solvatochromism of Brooker's merocyanine
Author:
Affiliation:
1. Institute of Organic Chemistry
2. National Academy of Sciences of Ukraine
3. 5 Murmanska St.
4. 02094 Kyiv
5. Ukraine
Abstract
Comparison of spectral properties of stilbazolium dyes in various solvents has exposed the influence of electrophilic and nucleophilic solvation on their solvatochromism.
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C9NJ00831D
Reference34 articles.
1. Color and Constitution. XI.1 Anhydronium Bases of p-Hydroxystyryl Dyes as Solvent Polarity Indicators
2. Solvatochromism of a typical merocyanine: stilbazolium betaine and its 2,6-di-tert-butyl derivative
3. On the solvatochromic reversal of merocyanine dyes. Part 1. The UV–VIS spectroscopic behaviour of vinylogous γ-pyridones
4. Solute-solvent and solvent-solvent interactions in the preferential solvation of Brooker's merocyanine in binary solvent mixtures
5. Preferential solvation of Brooker’s merocyanine in binary solvent mixtures composed of formamides and hydroxylic solvents
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