» Articles » PMID: 30675936

Harnessing Brightness in Naphthalene Diimides

Overview
Journal Chemistry
Specialty Chemistry
Date 2019 Jan 25
PMID 30675936
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

The development of brightly emissive compounds is of great research and commercial interest, with established and emerging applications across chemistry, biology, physics, medicine and engineering. Among the many types of molecules available, naphthalene diimides have been widely used for both fundamental photophysical studies and in practical applications that utilise fluorescence as an information readout. The monomeric naphthalene diimide is weakly fluorescent, however through various methods of core-derivatisation, it can be developed to be highly fluorescent and further functionalised to add utility. In this review, we highlight recent advances made in naphthalene diimide chemistry that have led to development of molecules with improved optical properties, and the design strategies utilised to produce bright fluorescence emission as small molecules or in supramolecular architectures.

Citing Articles

Synthesis and characterization of 1,2,3,4-naphthalene and anthracene diimides.

Bass A, Castellanos D, Calicdan X, Cao D Beilstein J Org Chem. 2024; 20:1767-1772.

PMID: 39076299 PMC: 11285063. DOI: 10.3762/bjoc.20.155.


Synthesis, characterization, and photophysical and fluorescence sensor behaviors of a new water-soluble double-bridged naphthalene diimide appended cyclotriphosphazene.

Tumay S, Yesilot S Turk J Chem. 2024; 47(5):1296-1306.

PMID: 38173741 PMC: 10760813. DOI: 10.55730/1300-0527.3613.


Fluorescent naphthalimide boronates as theranostics: structural investigations, confocal fluorescence and multiphoton fluorescence lifetime imaging microscopy in living cells.

Green M, Ge H, Flower S, Pourzand C, Botchway S, Wang H RSC Chem Biol. 2023; 4(12):1082-1095.

PMID: 38033726 PMC: 10685793. DOI: 10.1039/d3cb00112a.


Solvent-dependent fluorescence behaviour of imide-fused []phenacenes ( = 3, 5, 7).

Nose K, Yoshioka K, Yamaji M, Tani F, Goto K, Okamoto H RSC Adv. 2023; 13(6):4096-4101.

PMID: 36756556 PMC: 9890965. DOI: 10.1039/d2ra07771j.


A New 'Off-On' System Based on Core-Substituted Naphthalene Diimide with Dimethylamine for Reversible Acid-Base Sensing.

More V, Nadimetla D, Zalmi G, Gawade V, Jadhav R, Mane Y ChemistryOpen. 2022; 11(6):e202200060.

PMID: 35678482 PMC: 9179010. DOI: 10.1002/open.202200060.