THE REACTION OF COBALT(III) BETA-KETOENOLATES WITH TRIFLUOROACETIC-ACID

被引:11
作者
BRUNI, M
DIVERSI, P
INGROSSO, G
LUCHERINI, A
PINZINO, C
RAFFAELLI, A
机构
[1] UNIV PISA,DIPARTIMENTO CHIM & CHIM IND,I-56126 PISA,ITALY
[2] CNR,IST CHIM QUANTIST & ENERGET MOLEC,I-56126 PISA,ITALY
[3] CNR,CTR STUDIO MACROMOLEC STEREORDINATE & OTTICAMENTE,I-56126 PISA,ITALY
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1995年 / 06期
关键词
D O I
10.1039/dt9950001035
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of cobalt(III) beta-ketoenolates with trifluoroacetic acid (tfa) results in a ligand-to-metal electron-transfer process with the formation of radical species which have been detected and characterized by ESR spectroscopy. Depending upon the structure of the beta-ketoenolate ligand, the spin delocalization varies markedly, so that the radicals can be described as cationic derivatives of cobalt(III) containing a cobalt-bonded beta-ketoenolyl radical, or as cationic beta-ketoenolates of cobalt(IV). The formation of these radicals was accompanied by mononuclear high-spin cobalt(II) derivatives whose ESR spectra became observable at temperatures below 50 K. Some aspects of the chemistry behind the reaction of tris(acetylacetonato)cobalt(III) with tfa are understood through UV/VIS, IR, ESR and ion spray mass spectrometry studies. On the basis of these as well as of an ESR study of the reaction of tris(3-nitropentane-2,4 dionato)cobalt(III) with oxidants such as CoF3, ASB F-4, Tl(OCOCF3)(3) and tetracyanoethylene, a possible route to the radicals observed is discussed.
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页码:1035 / 1041
页数:7
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