The tetrachloroferrates of the 2,2':6',2' ':6' ',6-trioxytriphenylamine (TOT.+.FeCl4-) and 2,2':6',2' '-dioxytriphenylamine (DOT.+.FeCl4-) radical cations were prepared, and their structures, magnetic properties, and the relationship between them were investigated. The TOT.+ moiety had a highly planar structure and packed as a dimer surrounded by tetrachroferrates, which also formed a dimer structure. The magnetic properties of TOT.+.FeCl4- were characterized by strong (2J/kB = approximately -1.3 x 103 K, H = -2JS1/2.S1/2) and weak (2J/kB = -1.76 K, H = -2JS5/2.S5/2) antiferromagnetic interactions due to the (TOT.+)2 and (FeCl4-)2 structures, respectively. DOT.+ had a twisted form and no dimer formation was observed between the DOT.+'s and FeCl4-'s. Instead, short contacts between the DOT.+ and chlorine atoms and between the DOT.+'s producing a DOT.+ chain were observed. The magnetic properties of DOT.+.FeCl4- were characterized by a 3D magnetic phase transition to an antiferromagnet with TN = approximately 8 K.
Magnetic Interaction of Tri- and Di-oxytriphenylamine Radical Cation FeCl(4) Salts. Publishing Authors By Initials
Magnetic Interaction of Tri- and Di-oxytriphenylamine Radical Cation FeCl(4) Salts. Journal Published:
PUBLICATION TYPE: Journal Article
Journal: Inorganic chemistry
VOLUME: 46
Page Numbers: 10153-7
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ISSN: 0020-1669
DAY: 31
MONTH: 10
YEAR: 2007
Magnetic Interaction of Tri- and Di-oxytriphenylamine Radical Cation FeCl(4) Salts. Information
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LANGUAGE: eng
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AFFILIATION: Departments of Chemistry and Materials Science, Graduate School of Science, Osaka City University, Sugimoto, Sumiyoshi-ku, Osaka 558-8585, Japan.
Country: United States
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MEDLINETA: Inorg Chem
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