Breaking Azacalix[4]arenes into Induline Derivatives
Zhongrui Chen,
Gabriel Canard,
Olivier Grauby,
Benjamin Mourot,
Olivier Siri
Affiliations
Zhongrui Chen
Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), UMR 7325 CNRS Aix-Marseille Université, Campus de Luminy, Case 913, F-13288 Marseille, France
Gabriel Canard
Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), UMR 7325 CNRS Aix-Marseille Université, Campus de Luminy, Case 913, F-13288 Marseille, France
Olivier Grauby
Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), UMR 7325 CNRS Aix-Marseille Université, Campus de Luminy, Case 913, F-13288 Marseille, France
Benjamin Mourot
Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), UMR 7325 CNRS Aix-Marseille Université, Campus de Luminy, Case 913, F-13288 Marseille, France
Olivier Siri
Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), UMR 7325 CNRS Aix-Marseille Université, Campus de Luminy, Case 913, F-13288 Marseille, France
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.