BN-Phenanthrene- and BN-Pyrene-Based Fluorescent Uridine Analogues.


Journal

Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393

Informations de publication

Date de publication:
29 Jan 2024
Historique:
medline: 29 1 2024
pubmed: 29 1 2024
entrez: 29 1 2024
Statut: aheadofprint

Résumé

Two unprecedented fluorescent nucleosides that feature BN-doped polycyclic aromatic hydrocarbons are presented. One of them, having a BN-modified phenanthrene moiety incorporated, shows blue fluorescence but suffers from poor stability under aqueous conditions. The other nucleoside comprises an internally BN-doped pyrene as the chromophore. It shows green fluorescence in various solvents and is stable under aqueous and alkaline conditions.

Identifiants

pubmed: 38285916
doi: 10.1021/acs.orglett.3c04226
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Michael Müller (M)

Julius-Maximilians-Universität Würzburg, Institute of Inorganic Chemistry, Am Hubland, 97074 Würzburg, Germany.
Julius-Maximilians-Universität Würzburg, Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Am Hubland, 97074 Würzburg, Germany.

Hermann Neitz (H)

Julius-Maximilians-Universität Würzburg, Institute of Organic Chemistry, Am Hubland, 97074 Würzburg, Germany.

Claudia Höbartner (C)

Julius-Maximilians-Universität Würzburg, Institute of Organic Chemistry, Am Hubland, 97074 Würzburg, Germany.
Julius-Maximilians-Universität Würzburg, Center for Nanosystems Chemistry (CNC), Theodor-Boveri-Weg, 97074 Würzburg, Germany.

Holger Helten (H)

Julius-Maximilians-Universität Würzburg, Institute of Inorganic Chemistry, Am Hubland, 97074 Würzburg, Germany.
Julius-Maximilians-Universität Würzburg, Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Am Hubland, 97074 Würzburg, Germany.

Classifications MeSH