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• W2062454010 abstract "Analogue reaction systems of selenate reductase, which reduces substrate in the overall enzymatic reaction SeO42- + 2H+ + 2e- → SeO32- + H2O, have been developed using bis(dithiolene) complexes of MoIV and WIV. On the basis of the results of EXAFS analysis of the oxidized and reduced enzyme, the minimal reaction MoIVOH + SeO42- → MoVIO(OH) + SeO32- is probable. The square pyramidal complexes [M(OMe)(S2C2Me2)2]1- (M = Mo, W) were prepared as structural analogues of the reduced enzyme site. The systems, [ML(S2C2Me2)2]1-/SeO42- (L = OMe, OPh, SC6H2-2,4,6-Pri3) in acetonitrile, cleanly reduce selenate to selenite in second-order reactions whose negative entropies of activation implicate associative transition states. Rate constants at 298 K are in the 10-2−10-4 M-1 s-1 range with ΔS⧧ = −12 to −34 eu. When rate constants are compared with previous data for the reduction of (CH2)4SO, Ph3AsO, and nitrate by oxygen atom transfer, reactivity trends dependent on the metal, axial ligand L, and substrate are identified. As in all other cases of substrate reduction by oxo transfer, the kinetic metal effect k2W > k2Mo holds. A proposal from primary sequence alignments suggesting that a conserved Asp residue is a likely ligand in the type II enzymes in the DMSO reductase family has been pursued by synthesis of the [MoIV(O2CR)(S2C2Me2)2]1- (R = Ph, But) complexes. The species display symmetrical η2-carboxylate binding and distorted trigonal prismatic stereochemistry. They serve as possible structural analogues of the reduced sites of nitrate, selenate, and perchlorate reductases under the proposed aspartate coordination. Carboxylate binding has been crystallographically demonstrated for one nitrate reductase, but not for the other two enzymes." @default.
• W2062454010 created "2016-06-24" @default.
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• W2062454010 date "2006-03-10" @default.
• W2062454010 modified "2023-10-14" @default.
• W2062454010 title "Analogue Reaction Systems of Selenate Reductase" @default.
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• W2062454010 doi "https://doi.org/10.1021/ic0521630" @default.
• W2062454010 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16562954" @default.
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