6533b7dcfe1ef96bd127320b
RESEARCH PRODUCT
Structural and functional models for the dinuclear copper active site in catechol oxidases
Santiago García-grandaJose Montejo-bernardoGloria AlzuetJoaquín BorrásMarta González-álvarezsubject
chemistry.chemical_classificationbiologyStereochemistryActive sitechemistry.chemical_elementNuclear magnetic resonance spectroscopyCrystal structureMethoxideBiochemistryCopperlaw.inventionSulfonamideInorganic ChemistryCrystallographychemistry.chemical_compoundchemistrylawbiology.proteinElectron paramagnetic resonanceMonoclinic crystal systemdescription
Two new mu-methoxo-bridged dinuclear copper(II) complexes with a N-substituted sulfonamide, [Cu(mu-OMe)(L)(NH(3))](2) (1) and [Cu(mu-OMe)(L)(DMSO)](2) (2) [HL, N-2-(4-methylbenzothiazole)benzenesulfonamide], have been prepared and characterized by single-crystal X-ray difraction analyses. Compound 1 crystallizes in the monoclinic space group C(2)/c with a=22.0678(18), b=7.9134(7), c=21.1186(18)A, beta=113.788(4) degrees and Z=8. Compound 2 crystallizes in the monoclinic space group C(2)/c with a=18.0900(10), b=9.5720(10), c=24.2620(10) A, beta=98.7120(10) degrees and Z=8. In both complexes the copper atoms have square-planar environments bridged by two oxygen atoms from methoxide groups. Magnetic susceptibility measurements indicate a very strong antiferromagnetic coupling between the copper(II) ions in both complexes (2J<-1000 cm(-1)). Electronic Paramagnetic Resonance (EPR) spectra of the two complexes both in solid and in solution are silent. 13C NMR spectra of the complexes in solid state have been studied. The complexes have been evaluated as model systems for the catechol oxidase enzyme using 3,5-di-tert-butylcatechol as the test substrate. Complex 2 is slightly more active than complex 1.
year | journal | country | edition | language |
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2003-09-01 | Journal of Inorganic Biochemistry |