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Journal ArticleDOI

A new fluoroionophore derived from 4-amino-N-methyl-1,8-naphthalimide

Frédéric Cosnard, +1 more
- 30 Apr 1998 - 
- Vol. 39, Iss: 18, pp 2751-2754
TLDR
In this paper, a new azacrown ether derived from 1,8-naphthalimide was prepared by a two-step reaction from 4-bromo-1,8 naphthalic anhydride.
About
This article is published in Tetrahedron Letters.The article was published on 1998-04-30. It has received 78 citations till now. The article focuses on the topics: Ether.

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Citations
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Journal ArticleDOI

A copolymer of 4-N,N-dimethylaminoethylene-N-allyl-1,8-naphthalimide with methylmethacrylate as a selective fluorescent chemosensor in homogeneous systems for metal cations

TL;DR: In this article, the basic photophysical characteristics of two fluorophores: monomeric N,N-dimethylaminoethylene-N-allyl-1,8-naphthalimide and methylmethacrylate based copolymer are described both in the absence and presence of Fe2+, Pb2+, Zn2+ and Ni2+ cations.
Journal ArticleDOI

Fluorescent and colorimetric chemosensors for cations based on 1,8-naphthalimide derivatives: design principles and optical signalling mechanisms

TL;DR: In this article, the application of 1,8-naphthalimide derivatives as the photoactive units for the design of optical chemosensors for metal cations and protons with different mechanisms of analyte binding signal transduction and different receptors is discussed.
Journal ArticleDOI

Synthesis and spectroscopic characterization of 4-butoxyethoxy-N-octadecyl-1,8-naphthalimide as a new fluorescent probe for the determination of proteins.

TL;DR: Fluorescence data revealed that the fluorescence quenching of BSA by BON was likely the result of the formation of the BON-BSA complex, indicating that the hydrogen bonds and hydrophobic interactions played a dominant role in the binding of BON to BSA.
Journal ArticleDOI

Fluorescent 4-(2,2,6,6-tetramethylpiperidin-4-ylamino)-1,8-naphthalimide pH chemosensor based on photoinduced electron transfer

TL;DR: Two isomeric 2,2,6,6-tetramethylpiperidinyl-4-amino-1,8-naphthalimides 5 and 7 were configured as fluorophore-spacer-receptor systems as discussed by the authors.
Journal ArticleDOI

Synthesis and energy-transfer properties of fluorescence sensing bichromophoric system based on Rhodamine 6G and 1,8-naphthalimide

TL;DR: In this article, a bichromophoric system based on Rhodamine 6G and 1,8-naphthalimide was designed as a wavelength-shifting FRET chromophore.
References
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Journal ArticleDOI

Ion-responsive fluorescent compounds. 4. Effect of cation binding on the photophysical properties of a coumarin linked to monoaza- and diaza-crown ethers

TL;DR: In this paper, the photophysical changes upon complexation with alkali and alkaline-earth metal cations can be described in terms of enhancement of the intramolecular charge transfer in the coumarin dye.
Journal ArticleDOI

The UV–visible absorption and fluorescence of some substituted 1,8-naphthalimides and naphthalic anhydrides

Abstract: A number of substituted 1,8-naphthalimides and naphthalic anhydrides have been prepared and their absorption and fluorescence properties in absolute ethanol have been determined. In the absence of an alkylamino substituent in the naphthalene ring, the compounds are colourless and weakly fluorescent. In the presence of such a substituent they become yellow and frequently fluoresce strongly with quantum yields of the order of 0.8.
Journal ArticleDOI

Heterocycles as Structural Units in New Optical Brighteners

TL;DR: In this article, the syntheses, properties, and applications of new optical brighteners are described with references to patent literature, and they are used in detergents, textiles, paper, plastics, and paints.
Journal ArticleDOI

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

TL;DR: 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.
Journal Article

Preclinical evaluation of LU 79553: a novel bis-naphthalimide with potent antitumor activity.

TL;DR: The excellent activity of this compound in such a wide variety of tumor types suggests LU 79553 merits further investigation in clinical trials, and further studies were conducted to examine its antitumor activity in human xenograft models.
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