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Synthesis and characterization of tetraphenylammonium salts

The phenyl (Ph) group is a representative substituent in the field of organic chemistry as benzene (the parent molecule) is of fundamental importance. Simple Ph-substituted compounds of common chemical elements are well known. However, extensive structural characterization of tetraphenylammonium (Ph...

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Detalles Bibliográficos
Autores principales: Fujita, Hikaru, Sasamoto, Ozora, Kobayashi, Shiori, Kitamura, Masanori, Kunishima, Munetaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085870/
https://www.ncbi.nlm.nih.gov/pubmed/35534487
http://dx.doi.org/10.1038/s41467-022-30282-y
Descripción
Sumario:The phenyl (Ph) group is a representative substituent in the field of organic chemistry as benzene (the parent molecule) is of fundamental importance. Simple Ph-substituted compounds of common chemical elements are well known. However, extensive structural characterization of tetraphenylammonium (Ph(4)N(+)) salts has not been reported. Herein, the synthesis of Ph(4)N(+) salts and their characterization data including the (1)H and (13)C nuclear magnetic resonance (NMR) spectra and the single-crystal X-ray structure have been presented. An intermolecular radical coupling reaction between an aryl radical and a triarylammoniumyl radical cation was conducted to synthesize the target moieties. The Ph(4)N(+) salts described herein are the simplest tetraarylammonium (Ar(4)N(+)) salts known. The results reported herein can potentially help access the otherwise inaccessible non-bridged Ar(4)N(+) salts, a new class of rigid and sterically hindered organic cations.