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Synthesis and electronic spectra of 3‐hetaryl substituted coumarin derivatives 7‐hydroxy‐2H‐chromen‐2‐on and 9‐hydroxy‐2H‐benzo(f)chromen‐2‐on
Author(s) -
Deligeorgiev Todor,
Tsvetkova Teodora,
Ivanova Diana,
Timtcheva Iliana
Publication year - 2008
Publication title -
coloration technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.297
H-Index - 49
eISSN - 1478-4408
pISSN - 1472-3581
DOI - 10.1111/j.1478-4408.2008.00141.x
Subject(s) - coumarin , chemistry , fluorescence , ethanol , absorption (acoustics) , medicinal chemistry , stereochemistry , organic chemistry , materials science , physics , quantum mechanics , composite material
The synthesis of 3‐hetaryl substituted coumarin derivatives [7‐hydroxy‐2H‐chromen‐2‐on and 9‐hydroxy‐2H‐benzo(f)chromen‐2‐on] containing a hydroxyl group by reacting 2,4‐dihydroxybenzaldehyde and 2,4‐dihydroxynaphtaldehydes with 2‐cyanomethylbenzothiazole, 2‐cyanomethylbenzimidazole, 1‐methyl‐2‐cyanomethylbenzimidazole and 2‐cyanomethyl‐4‐phenylthiazole is presented. The absorption and steady‐state fluorescence characteristics of the synthesised 3‐hetaryl substituted 7‐hydroxy‐2H‐chromen‐2‐on and 9‐hydroxy‐2H‐benzo(f)chromen‐2‐on in a solution of ethanol and at different pH values are studied to assess their possible application as fluorescent probes for use in molecular biology and medicine.

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