Synthesis and J-Dimer Formation of Tetrapyrazinoporphyrazines with Different Functional Groups for Potential Biomolecular Probe Applications.
aggregation
fluorescence
oligonucleotide probes
phthalocyanines
self-assembly
Journal
ChemPlusChem
ISSN: 2192-6506
Titre abrégé: Chempluschem
Pays: Germany
ID NLM: 101580948
Informations de publication
Date de publication:
03 2020
03 2020
Historique:
received:
17
01
2020
revised:
18
02
2020
entrez:
19
3
2020
pubmed:
19
3
2020
medline:
4
2
2021
Statut:
ppublish
Résumé
Though tetrapyrazinoporphyrazines (TPyzPzs) are generally presented as universal dark quenchers for oligonucleotide probes, the availability of TPyzPzs bearing different functional groups suitable for attachment to 3', and 5' ends or intrastrand positions remains rather limited. Therefore, a synthetic route to hexa(bis(2-methoxyethyl)amino) or hexa(diethylamino) TPyzPzs functionalized by an azide, hydroxy, or carboxy group or their combinations was developed. Studies of self-assembly into J-dimers in nonpolar solvents and their stability upon titration with pyridine (association constants, K
Identifiants
pubmed: 32187858
doi: 10.1002/cplu.202000026
doi:
Substances chimiques
Azides
0
Coordination Complexes
0
Fluorescent Dyes
0
Ligands
0
Porphyrins
0
Pyridines
0
Solvents
0
pyridine
NH9L3PP67S
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
527-537Informations de copyright
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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