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Journal ArticleDOI

Excited state proton-transfer spectroscopy of 3-hydroxyflavone and quercetin

TLDR
In this article, the double minimum hydrogen-bonding potential of 3-hydroxyflavone and quercetin at room temperature in solution has been used to explain the luminescence of these molecules at 77 K in 2-methylbutane rigid matrix.
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This article is published in Chemical Physics Letters.The article was published on 1979-12-15. It has received 561 citations till now. The article focuses on the topics: Excited state & Proton transport.

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Citations
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Advanced Organic Optoelectronic Materials: Harnessing Excited-State Intramolecular Proton Transfer (ESIPT) Process

TL;DR: Recent studies on advanced ESIPT molecules and their optoelectronic applications are surveyed, particularly focusing on chemical sensors, fluorescence imaging, proton transfer lasers, and organic light-emitting diodes (OLEDs).
Journal ArticleDOI

Excited-state proton transfer reactions II. Intramolecular reactions

TL;DR: In this paper, the intrinsic processes and mechanisms of proton transfer in relation to the nature of the intramolecular hydrogen bond ring are reviewed. But the authors focus on the intrinsic process and not the mechanisms of transfer.
Journal ArticleDOI

Analytical separation and detection methods for flavonoids.

TL;DR: Special attention will be devoted to the use of tandem-mass spectrometric (MS/MS) techniques for the characterization of several important sub-classes of flavonoids, and to the potential of combined diode-array UV (DAD UV), tandem-MS and nuclear magnetic resonance (NMR) detection for unambiguous identification.
Journal ArticleDOI

Excited-state proton coupled charge transfer modulated by molecular structure and media polarization

TL;DR: With knowledge of the mechanisms of these processes, desired rates and directions can be achieved, and thus the multiple emission spectral features can be harnessed.
Journal ArticleDOI

Imidazole-based excited-state intramolecular proton-transfer materials: synthesis and amplified spontaneous emission from a large single crystal.

TL;DR: It was deduced that the four phenyl groups substituted into the imidazole ring of HPI and HPI-Ac allowed the crystals free from concentration quenching of fluorescence by limiting the excessive tight-stacking responsible for intermolecular vibrational coupling and relevant nonradiative relaxation.
References
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Journal ArticleDOI

Phenomenology of solvent matrix spectroscopic effects

TL;DR: In this paper, the Born-Oppenhelmer approach was applied to various molecular potentials in accordance with the Born Oppenhelmers approach developed in an earlier paper, including Morse vibrational, repulsive, double-bond torsional, double minimum, and pseudo-Jahn-Teller.
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Intermolecular perturbation of molecular potentials

TL;DR: In this paper, the solvent cage concept of photochemistry is translated into spectroscopic language by an extension of the Born-Oppenheimer approximation, and the intermolecular perturbation term is taken as the barrier to viscous flow, added to the intramolecular potential.
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Relaxation processes in excited molecular systems

TL;DR: In addition to vibrational relaxation, an excited molecular system may undergo various relaxation processes that occur on the nanosecond time scale as discussed by the authors, and the effects of polarity, temperature, and viscosity of the medium are examined.
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