New 1,3,5-triphenyl-2-pyrazoline-containing 3-hydroxychromones as highly solvatofluorochromic ratiometric polarity probes

Denis A. Svechkarev; Ilya V. Bukatich; Andrey O. Doroshenko

doi:10.1016/j.jphotochem.2008.09.005

New 1,3,5-triphenyl-2-pyrazoline-containing 3-hydroxychromones as highly solvatofluorochromic ratiometric polarity probes

Denis A. Svechkarev, Ilya V. Bukatich, Andrey O. Doroshenko

Research output: Contribution to journal › Article › peer-review

23 Scopus citations

Abstract

Two novel 1,3,5-triphenyl-2-pyrazoline moiety containing derivatives of 3-hydroxychromone were synthesized and studied by ¹H NMR, absorption and fluorescence spectroscopy. The prospects of practical application of these compounds exhibiting high solvatofluorochromism into analytical chemistry and biophysics as effective ratiometric polarity probes were discussed proceeding from the data on their fluorescent properties.

Original language	English (US)
Pages (from-to)	426-431
Number of pages	6
Journal	Journal of Photochemistry and Photobiology A: Chemistry
Volume	200
Issue number	2-3
DOIs	https://doi.org/10.1016/j.jphotochem.2008.09.005
State	Published - Dec 15 2008
Externally published	Yes

Keywords

1,3,5-Triphenyl-2-pyrazoline-substituted 3-hydroxychromone
ESIPT
Multi-band fluorescence emission
Ratiometric probe
Solvatofluorochromism

ASJC Scopus subject areas

General Chemistry
General Chemical Engineering
General Physics and Astronomy

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10.1016/j.jphotochem.2008.09.005

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title = "New 1,3,5-triphenyl-2-pyrazoline-containing 3-hydroxychromones as highly solvatofluorochromic ratiometric polarity probes",

abstract = "Two novel 1,3,5-triphenyl-2-pyrazoline moiety containing derivatives of 3-hydroxychromone were synthesized and studied by 1H NMR, absorption and fluorescence spectroscopy. The prospects of practical application of these compounds exhibiting high solvatofluorochromism into analytical chemistry and biophysics as effective ratiometric polarity probes were discussed proceeding from the data on their fluorescent properties.",

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year = "2008",

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doi = "10.1016/j.jphotochem.2008.09.005",

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T1 - New 1,3,5-triphenyl-2-pyrazoline-containing 3-hydroxychromones as highly solvatofluorochromic ratiometric polarity probes

AU - Svechkarev, Denis A.

AU - Bukatich, Ilya V.

AU - Doroshenko, Andrey O.

PY - 2008/12/15

Y1 - 2008/12/15

N2 - Two novel 1,3,5-triphenyl-2-pyrazoline moiety containing derivatives of 3-hydroxychromone were synthesized and studied by 1H NMR, absorption and fluorescence spectroscopy. The prospects of practical application of these compounds exhibiting high solvatofluorochromism into analytical chemistry and biophysics as effective ratiometric polarity probes were discussed proceeding from the data on their fluorescent properties.

AB - Two novel 1,3,5-triphenyl-2-pyrazoline moiety containing derivatives of 3-hydroxychromone were synthesized and studied by 1H NMR, absorption and fluorescence spectroscopy. The prospects of practical application of these compounds exhibiting high solvatofluorochromism into analytical chemistry and biophysics as effective ratiometric polarity probes were discussed proceeding from the data on their fluorescent properties.

KW - 1,3,5-Triphenyl-2-pyrazoline-substituted 3-hydroxychromone

KW - ESIPT

KW - Multi-band fluorescence emission

KW - Ratiometric probe

KW - Solvatofluorochromism

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SN - 1010-6030

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JO - Journal of Photochemistry and Photobiology A: Chemistry

JF - Journal of Photochemistry and Photobiology A: Chemistry

IS - 2-3

ER -

New 1,3,5-triphenyl-2-pyrazoline-containing 3-hydroxychromones as highly solvatofluorochromic ratiometric polarity probes

Abstract

Keywords

ASJC Scopus subject areas

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