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Efficient Catalytic Phosphate Ester Cleavage by Binuclear Zinc(II) Pyrazolate Complexes as Functional Models of Metallophosphatases

Larysa V. PenkovaDepartment of Inorganic Chemistry, National Taras Shevchenko University, Volodymyrska str. 64, Kyiv 01033, UkraineAnna MaciągFaculty of Chemistry, University of Wrocław, 14 F. Joliot-Curie, 50-383 Wrocław, PolandE.V. Rybak-AkimovaDepartment of Chemistry, Pearson Chemistry Laboratory, Tufts University, Medford, Massachusetts 02155Matti HaukkaDepartment of Chemistry, University of Joensuu, P.O. Box 111, 80101, Joensuu, FinlandV.A. PavlenkoDepartment of Inorganic Chemistry, National Taras Shevchenko University, Volodymyrska str. 64, Kyiv 01033, UkraineTurganbay S. IskenderovKarakalpakian University, Department of Chemistry, Universitet Keshesi 1, 742012 Nukus, UzbekistanHenryk KozłowskiFaculty of Chemistry, University of Wrocław, 14 F. Joliot-Curie, 50-383 Wrocław, PolandFranc MeyerInstitut für Anorganische Chemie, Georg-August-Universität Göttingen, Tammannstr. 4, 37077 Göttingen, GermanyIgor O. FritskyDepartment of Inorganic Chemistry, National Taras Shevchenko University, Volodymyrska str. 64, Kyiv 01033, Ukraine

Inorganic Chemistryjournal2009en

ABI

Annotatsiya

A series of dizinc(II) complexes based on the pyrazolate ligands 3-[(1E)-N-hydroxyethanimidoyl]-4-methyl-1H-pyrazole-5-carboxylic acid (H(3)L(1)), (1E,1'E)-1,1'-(4-methyl-1H-pyrazole-3,5-diyl)diethanone dihydrazone (HL(2)), (E,E)-(4-methyl-1H-pyrazole-3,5-diyl)bis(methylmethanone) dioxime (H(3)L(3)), (E,E)-(4-phenyl-1H-pyrazole-3,5-diyl)bis(phenylmethanone) dioxime (H(3)L(4)), and 1H-pyrazole-3,5-dicarboxylic acid (H(3)L(5)) have been synthesized and investigated as functional models of phosphoesterases, focusing on correlations between the hydrolytic activity and molecular parameters of the bimetallic core. Speciation of the various dizinc complexes in solution has been determined potentiometrically, and the structures in the solid state have been established by X-ray crystallography. The hydrolysis of two phosphoesters, an RNA model 2-hydroxypropyl-p-nitrophenyl phosphate (HPNP) and the pesticide paraoxon-ethyl (POE), promoted by the dinuclear phosphoesterase model complexes has been investigated in DMSO/buffered water (1:1) at 50 degrees C as a function of complex concentration, substrate concentration, and pH. Drastic differences in the hydrolytic activities of [Zn(2)(HL(1))(2)](0), [Zn(2)(L(2))(2)](2+), [Zn(2)(H(2)L(3))(2)](2+), and [Zn(2)(HL(5))(2)](2-) are observed and can be attributed to molecular peculiarities. Pyrazolate-bridged dinuclear zinc(II) complexes seem to provide a sufficient number of coordination sites for both activating the substrate and generating the nucleophile, where the phosphate esters are preferentially bound in a bidentate bridging fashion (in the case of HPNP) and in a monodentate fashion (in the case of POE).

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Metal complexes synthesis and properties Synthesis and Characterization of Heterocyclic Compounds Chemical Reaction Mechanisms

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DOI: 10.1021/ic900520j

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