4.6 Article

Metal-Free Synthesis and Photophysical Behaviour of Thermally Stable Blue Fluorescent Styryl-cored Biaryls by Ring Transformation of alpha-pyranone

Journal

JOURNAL OF MOLECULAR STRUCTURE
Volume 1250, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molstruc.2021.131622

Keywords

Stilbenes; Nucleophile-induced; Fluorescent; Thermal stability; Positive solvatochromism

Funding

  1. CSIR New Delhi [02/ (0330) /17-EMR-II]

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A simple and convenient nucleophile-induced synthetic route was developed for the construction of thermally stable fluorescent functionalized stilbenes from alpha-pyranones and aryl ketones. The nucleophile-induced base encourage synthetic protocol was performed under mild conditions, resulting in high yields of products with amazing emission properties and good thermal stability. The synthesized products also exhibited interesting positive solva-tochromism in different solvents based on variation in polarity.
A simple yet convenient nucleophile-induced synthetic route for the construction of thermally stable fluorescent functionalized stilbenes from alpha-pyranones and aryl ketones has been delineated. The nucleophile-induced base encourage synthetic protocol was performed under mild conditions without harming the environment and products were achieved in good yields. The synthesized stilbenes showed amazing emission properties and good thermal stability. Synthesized products displayed interesting positive solva-tochromism in different solvents based on variation in polarity. (C) 2021 Published by Elsevier B.V.

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