Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9776482 | Synthetic Metals | 2005 | 4 Pages |
Abstract
New organic functional anions that includes the ferrocenyl group, CpFeCp-CONHCH2SO3â and Fe(Cp-CONHCH2SO3â)2, are prepared as tetraphenylphosphonium (PPh4) salts. They reacted with (TTF)3(BF4)2 to give TTF monocation salts. The X-ray analyses indicate that for all salts TTF forms a dimer which is separated by the relatively larger anions. The oxidation reaction of (PPh4)(CpFeCp-CONHCH2SO3) with I2 gave the Zwitter-ion, CpFe+Cp-CONHCH2SO3â, which shows a Curie-Weiss behavior (C = 0.800 emu·K/mol, θ = â1.13 K) with weak antiferromagnetic interaction. This magnetic moment is found to be attributed to the ferrocenyl radical.
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Physical Sciences and Engineering
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Authors
Keigo Furuta, Hiroki Akutsu, Jun-ichi Yamada, Shin'ichi Nakatsuji,