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Journal ArticleDOI

Solvent dependence of the inhibition of intramolecular charge-transfer in N-substituted 1,8-naphthalimide derivatives as dye lasers

TLDR
In this article, an intramolecular charge transfer (CT) was used to inhibit the fluorescence and laser emission in the derivatives with an amino terminal group in the side chain, and a high lasing efficiency in the green-blue zone of the spectrum was obtained with a N 2 pulsed laser.
About
This article is published in Journal of Luminescence.The article was published on 1996-05-01. It has received 155 citations till now. The article focuses on the topics: Dye laser & Lasing threshold.

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Citations
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Journal ArticleDOI

Photophysics and Biological Applications of the Environment-Sensitive Fluorophore 6-N,N-Dimethylamino-2,3-naphthalimide

TL;DR: A new environment-sensitive fluorophore, 6-N,N-dimethylamino-2,3-naphthalimide (6DMN), which exhibits valuable fluorescent properties as a biological probe with emission in the 500-600 nm range and a marked response to changes in the environment polarity.
Journal ArticleDOI

Synthesis and properties of fluorescent 1,8-naphthalimide dyes for application in liquid crystal displays

TL;DR: A series of highly fluorescent 1,8-naphthalimide derivatives having an N-allylamino group at position 4 of the aromatic structure have been synthesized, and some of their properties for application in liquid crystal displays have been determined.
Journal ArticleDOI

Synthesis and photophysical properties of 1,8-naphthalimide-labelled PAMAM as PET sensors of protons and of transition metal ions

TL;DR: In this paper, a 4-N,N-dimethylaminoethylene-1,8-naphthalimide (PAMAM) was synthesized with designed fluorescent intensity and high sensitiveness to the presence of protons or transition metal cations.
Journal ArticleDOI

The design, synthesis and photophysical properties of two novel 1,8-naphthalimide fluorescent pH sensors based on PET and ICT

TL;DR: In this paper, the photophysical properties of two novel, yellow-green emitting pH chemosensors, namely a 1,8-naphthalimide dye and its condensed heterocyclic derivative, as a function of pH were investigated in water/ethanol.
References
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Book

Modern Molecular Photochemistry

TL;DR: In this paper, the authors bring students up to date with the advances in this field -the development of the theory of photoreactions, the utilization of photoresceptors in synthetic sequences, and the advancement of powerful laser techniques to study the mechanisms of the photoreaction.
Journal ArticleDOI

Photoinduced electron transfer

TL;DR: In this article, the relative importance of factors influencing the efficiency and rates of photo-excited state induced electron transfer is discussed. But the focus of this paper is not on the details of photosynthesis, but rather on recent developments in model systems.
Journal ArticleDOI

The proton-transfer laser. Gain spectrum and amplification of spontaneous emission of 3-hydroxyflavone

TL;DR: In this article, a systeme laser ideal a 4 niveaux, mettant en jeu 4 especes electroniques moleculaires differentes (laser chimique ''photoinduit»), calculated du coefficient de gain (10-15).
Journal ArticleDOI

Switching between charge- and proton-transfer emission in the excited state of a substituted 3-hydroxyflavone

TL;DR: Anomalous fluorescence behavior was reported for the 4′- N, N -dimethylamino derivatives of 3-hydroxy- and 3-methoxy-flavone as mentioned in this paper.
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