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1.
Org Biomol Chem ; 18(18): 3475-3480, 2020 05 13.
Artigo em Inglês | MEDLINE | ID: mdl-32329760

RESUMO

An investigation into the self-assembly of two 4-amino- and a 4-bromo-1,8-naphthalimide (Nap) based structures (1-3) possessing an appended glycan unit, from protic polar media, is presented. The results demonstrate the formation of complex hierarchical luminescent aggregates, wherein the morphologies, sizes and spherical structures were highly dependent on both the media and the Nap structure. Upon cleaving the native glycosidic bond, using an enzyme, the structure/morphology of the self-assembly of 3 in buffered solution was significantly transformed.

2.
Chem Commun (Camb) ; 56(17): 2562-2565, 2020 Feb 28.
Artigo em Inglês | MEDLINE | ID: mdl-32011616

RESUMO

The 4-amino-1,8-naphthalimide-Tröger's base fluorophore, TBNap-TPy, adorned with phenyl-terpyridine moiety was synthesised and assessed for its aggregation-induced emission (AIE) behaviour. TBNap-TPy was further employed as a fluorescent sensor for the discriminative sensing of π-electron-deficient nitroaromatic; the TBNap-TPy displaying the largest fluorescence quenching with high selectivity for picric acid, a harmful environmental pollutant widely used in the dye industries.

3.
Chem Commun (Camb) ; 55(81): 12140-12143, 2019 Oct 08.
Artigo em Inglês | MEDLINE | ID: mdl-31531424

RESUMO

The 4-amino-1,8-naphthalimide Tröger's base functionalized triazine covalent organic polymer TB-TZ-COP was synthesised and employed as a "turn-on" fluorescent and a colorimetric sensor for the discriminative sensing of volatile organic compounds; the TB-TZ-COP displaying the largest fluorescent enhancement and high sensitivity for 1,4-dioxane, a harmful environmental pollutant classified as a Group 2B carcinogen.

4.
Org Biomol Chem ; 17(8): 2287, 2019 02 20.
Artigo em Inglês | MEDLINE | ID: mdl-30702731

RESUMO

Correction for 'Glycosylated naphthalimides and naphthalimide Tröger's bases as fluorescent aggregation probes for Con A' by Elena Calatrava-Pérez et al., Org. Biomol. Chem., 2019, DOI: 10.1039/c8ob02980f.

5.
Org Biomol Chem ; 17(8): 2116-2125, 2019 02 20.
Artigo em Inglês | MEDLINE | ID: mdl-30629076

RESUMO

Herein we report the synthesis of fluorescent, glycosylated 4-amino-1,8-naphthalimide (Nap) 1, and the related 1,8-naphthalimides Tröger's bases (TBNap) 2 and 3, from 1,8-naphthalic anhydride precursors, the α-mannosides being introduced through the use of CuAAC mediated 'click' chemistry. We investigate the photophysical properties of these probes in buffered solution and demonstrate their ability to function as fluorescent probes for Concanavalin A (Con A) lectin. We show that both the Nap and TBNap structures self-assemble in solution. The formation of the resulting supramolecular structures is driven by head-to-tail π-π stacking and extended hydrogen bonding interactions of the Nap and the triazole moieties. These interactions give rise to spherical nano-structures (ca. 260 nm and 100 nm, for 1 and 3, respectively), which interact with the Con-A protein, the interaction being probed by using both luminescent and Scanning Electron Microscopy imaging as well as dynamic light scattering measurements. Finally, we show that these supramolecular assembles can be used as luminescent imaging agents, through confocal fluorescence imaging of HeLa cells of the per-acetylated version 2.

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