An unprecedented chromophore, based on a nitrogen fused tricyclic heterocycle, is presented. This prototype molecule can be considered a “rigidified” monomethine cyanine dye and the central core is isoelectronic to pyridine-based BODIPY analogues, such as boron difluoride dipyridylmethene. The chromophore was synthesized and its photophysical properties examined. The new molecule can be considered the starting point to develop dyes, fluorophores or dual-emission fluorescent probes with excitation window in the green region of the spectrum.

A new auspicious scaffold for small dyes and fluorophores

Volpi G.;Garino C.;Priola E.;Barolo C.
2022

Abstract

An unprecedented chromophore, based on a nitrogen fused tricyclic heterocycle, is presented. This prototype molecule can be considered a “rigidified” monomethine cyanine dye and the central core is isoelectronic to pyridine-based BODIPY analogues, such as boron difluoride dipyridylmethene. The chromophore was synthesized and its photophysical properties examined. The new molecule can be considered the starting point to develop dyes, fluorophores or dual-emission fluorescent probes with excitation window in the green region of the spectrum.
DYES AND PIGMENTS
197
109849
109853
https://www.sciencedirect.com/science/article/pii/S0143720821007154
Dual emission fluorescent probe; Green light absorber; Monomethine cyanine; pH sensitive chromophore; Small dye; Small fluorophore
Volpi G.; Garino C.; Priola E.; Barolo C.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2318/1824061
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