About: Synthesis and Oxidation of TriarylamineDerivatives Bearing Hydrogen-Bonding Groups

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_13/w
Subject	Note
Title	Synthesis and Oxidation of TriarylamineDerivatives Bearing Hydrogen-Bonding Groups
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_13/101021jo070318a/m/print http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_13/101021jo070318a/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_13/101021jo070318a/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_13/101021jo070318a/authorship/2
Author	Lahti Paul M. Murata Hidenori
Abstract	Hydrogen-bonding triarylamines, 4-(N,N-bis(4-methoxyphenyl)amino)benzoic acid (TPA1), 5-(N,N-bis(4-methoxyphenyl)amino)isophthalic acid (TPA2), and N-(4-(1H-benzimidazol-2-yl)phenyl)-N,N-bis(4-methoxyphenyl)amine(BImTPA), were synthesized as radical cation precursors.TPA1 and TPA2 are readily p-doped by AgSbF6 to givehighly persistent radical cations. Poor solid-state spin yieldsof the radical cation from BImTPA may be due to spindelocalization.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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