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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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 |
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. |
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