Affiliation:
1. Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), UMR 7325 CNRS Aix-Marseille Université, Campus de Luminy, Case 913, F-13288 Marseille, France
Abstract
Tetraamino-tetranitro-azacalixarene 5 is at the crossroad of two different families of compounds depending on the conditions and the agent used to reduce the NO2 groups: (1) azacalixphyrin 7 in neutral medium, or (2) phenazinium of type 8 in acidic medium. The key role of the N-substituted amino functions at the periphery is highlighted by investigating octaaminoazacalixarene as a model compound, and by using the corresponding tetrahydroxy-tetranitro-azacalixarene 15 as a precursor, which behaves differently.
Funder
Centre National de la Recherche Scientifique
Ministère de l’Enseignement supérieur et la Recherche
Subject
Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science
Reference46 articles.
1. Calixarene-based multivalent ligands;Baldini;Chem. Soc. Rev.,2007
2. Calixarene-Derived Fluorescent Probes;Kim;Chem. Rev.,2007
3. Novel Cavity Design Using Calix[n]arene Skeletons: Toward Molecular Recognition and Metal Binding;Ikeda;Chem. Rev.,1997
4. Neri, P., Sessler, J.L., and Wang, M.-X. (2016). Calixarenes and Beyond, Springer. [1st ed.]. English Edition.
5. Chemistry of Thiacalixarenes;Eur. J. Org. Chem.,2004
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1 articles.
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