Synthesis of a pyridinium bis[citrato(2-)]oxochromate(V) complex and its ligand-exchange reactions

被引:18
作者
Cawich, CM
Ibrahim, A
Link, KL
Bumgartner, A
Patro, MD
Mahapatro, SN [1 ]
Lay, PA
Levina, A
Eaton, SS
Eaton, GR
机构
[1] Regis Coll, Dept Chem, Denver, CO 80221 USA
[2] Univ Sydney, Sch Chem, Ctr Heavy Met Res, Sydney, NSW 2006, Australia
[3] Univ Denver, Dept Chem & Biochem, Denver, CO 80208 USA
关键词
D O I
10.1021/ic034146l
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of citric acid (caH(4)) with pyridinium dichromate (PDC) in anhydrous acetone yields pyridinium bis[citrato(2-)]oxochromate(V), pyH[CrO(caH(2))(2)], as a mixed salt with the Cr(III) product. The compound persists in the solid state for months, is highly soluble in water (pH 4.0), and gives a sharp electron paramagnetic resonance (EPR) signal in solution (g(iso) = 1.9781, A(iso)(Cr) = 17.1 X 10(-4) cm(-1)), which is characteristic of d(1) Cr(V). The presence of [(CrO)-O-V(caH(2))(2)](-) in the solid state was confirmed by electrospray mass spectroscopy, X-ray absorption near-edge structure (XANES), and EPR spectroscopy. Solid-state EPR spectroscopy, XANES, and a spectrophotometric assay showed that the solid is a mixture of [(CrO)-O-V(caH(2))(2)](-) and a Cr(III)-citrate complex. The structures of the [(CrO)-O-V(caH(2))(2)](-) and [Cr-III(caH(2))(2)](-) components of the mixture were established by multiple-scattering MS analysis of the X-ray absorption fine structure data. The structure of [(CrO)-O-V(caH(2))(2)](-) is similar to that of other 2-hydroxy acid complexes with Cr=O, Cr-O(alcoholato), and Cr-O(carboxylato) bond lengths of 1.59, 1.81, and 1.90 Angstrom, respectively. The Cr(III) complex has bond lengths typical for ligands with deprotonated carboxylate and protonated alcohol donors with distances of 1.90 and 1.99 Angstrom, respectively, for the Cr-O(carboxylato) and Cr-O(alcohol) bond lengths. In aqueous solution, [CrO(caH(2))(2)](-) is short lived, but it is a convenient starting material for ligand-exchange reactions. It has been used to generate short-lived mixed-ligand Cr(V) complexes with citrate and picolinate, iminodiacetate, 2,2'-bipyridine, or 1,10-phenanthroline, which were characterized by EPR spectroscopy. The g values are between 1.971 and 1.974. For the picolinate, 2,2'-bipyridine, and 1,10-phenanthroline mixed-ligand complexes, there is hyperfine coupling (2.2 x 10(-4) to 2.4 x 10(-4) cm(-1)) to a single proton of the citrate ligand.
引用
收藏
页码:6458 / 6468
页数:11
相关论文
共 83 条
[1]  
[Anonymous], 1990, IARC MON EV CARC RIS
[2]  
AREON I, 1998, J AM CERAM SOC, V81, P222
[3]  
*AUSTR SYNCHR RES, 1996, XFIT WINDOWS95
[4]   CHELATION OF NICKEL(II) BY CITRATE - THE CRYSTAL-STRUCTURE OF A NICKEL CITRATE COMPLEX, K2[NI(C6H5O7)(H2O)2]2.4H2O [J].
BAKER, EN ;
BAKER, HM ;
ANDERSON, BF ;
REEVES, RD .
INORGANICA CHIMICA ACTA-BIOINORGANIC CHEMISTRY, 1983, 78 (06) :281-285
[5]   EPR CHARACTERIZATION OF THE CR-V INTERMEDIATES IN THE CR-VI/V OXIDATIONS OF ORGANIC SUBSTRATES AND OF RELEVANCE TO CR-INDUCED CANCERS [J].
BARRDAVID, G ;
CHARARA, M ;
CODD, R ;
FARRELL, RP ;
IRWIN, JA ;
LAY, PA ;
BRAMLEY, R ;
BRUMBY, S ;
JI, JY ;
HANSON, GR .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1995, 91 (08) :1207-1216
[6]   SUPPRESSION BY VANADIUM(IV) OF CHROMIUM(V)-MEDIATED DNA CLEAVAGE AND CHROMIUM(VI/V)-INDUCED MUTAGENESIS - SYNTHESIS AND CRYSTAL-STRUCTURE OF THE VANADIUM(IV) COMPLEX (NH4)[V(O)(HOC(ET)2COO)(OC(ET)2COO)] [J].
BARRDAVID, G ;
HAMBLEY, TW ;
IRWIN, JA ;
JUDD, RJ ;
LAY, PA ;
MARTIN, BD ;
BRAMLEY, R ;
DIXON, NE ;
HENDRY, P ;
JI, JY ;
BAKER, RSU ;
BONIN, AM .
INORGANIC CHEMISTRY, 1992, 31 (24) :4906-4908
[7]   ENGINEERING OF PROTEIN-BOUND IRON-SULFUR CLUSTERS - A TOOL FOR THE STUDY OF PROTEIN AND CLUSTER CHEMISTRY AND MECHANISM OF IRON-SULFUR ENZYMES [J].
BEINERT, H ;
KENNEDY, MC .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 186 (1-2) :5-15
[8]   CONSTRAINED AND RESTRAINED REFINEMENT IN EXAFS DATA-ANALYSIS WITH CURVED WAVE THEORY [J].
BINSTED, N ;
STRANGE, RW ;
HASNAIN, SS .
BIOCHEMISTRY, 1992, 31 (48) :12117-12125
[9]   Mechanisms of DNA damage by chromium(V) carcinogens [J].
Bose, RN ;
Fonkeng, BS ;
Moghaddas, S ;
Stroup, D .
NUCLEIC ACIDS RESEARCH, 1998, 26 (07) :1588-1596
[10]   PREPARATIONS AND CHARACTERIZATIONS OF MU-3-OXO-HEXAKIS(MU-2-CARBOXYLATOPYRIDINE-O,O)-TRIAQUATRICHROMIUM(III)PERCHLORATES [J].
BRADSHAW, JE ;
GROSSIE, DA ;
MULLICA, DF ;
PENNINGTON, DE .
INORGANICA CHIMICA ACTA, 1988, 141 (01) :41-47