SYNTHESIS AND CHARACTERIZATION OF HYDROXO-BRIDGED DIIRON(III) COMPLEXES CONTAINING CARBOXYLATE OR PHOSPHATE ESTER BRIDGES - COMPARISONS TO DIIRON(III) PROTEINS

Citation
Pn. Turowski et al., SYNTHESIS AND CHARACTERIZATION OF HYDROXO-BRIDGED DIIRON(III) COMPLEXES CONTAINING CARBOXYLATE OR PHOSPHATE ESTER BRIDGES - COMPARISONS TO DIIRON(III) PROTEINS, Inorganic chemistry, 33(4), 1994, pp. 636-645
Citations number
81
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201669
Volume
33
Issue
4
Year of publication
1994
Pages
636 - 645
Database
ISI
SICI code
0020-1669(1994)33:4<636:SACOHD>2.0.ZU;2-2
Abstract
Complexes containing a phosphate- or acetate-bridged (mu-hydroxo)diiro n(III) core, such as may exist in the metalloproteins uteroferrin, bee f spleen purple acid phosphatase, or the hydroxylase component of meth ane monooxygenase, have been prepared. A general procedure is presente d for synthesizing hydroxo-bridged complexes by protonation of their o xo-bridged analogues in ether solution. As a result of protonating the bridging oxygen atom, the dimetallic core in the hydroxo-bridged comp lexes is expanded (Fe-OH = 1.95-1.97 angstrom, Fe...Fe = 3.44-3.59 ang strom, angle Fe-OH-Fe = 123-131-degrees) relative to that in the corre sponding mu-oxo complexes (Fe-O = 1.78-1.81 angstrom, Fe...Fe = 3.10-3 .33 angstrom, angle Fe-O-Fe = 120-130-degrees), with a concomitant dec rease in the magnitude of the antiferromagnetic spin exchange coupling constants (J almost-equal-to -10 to -20 cm-1) and correspondingly lar ger paramagnetic shifts (-20 to -70 ppm) in the H-1 NMR spectra. Elect ronic transitions differ considerably from those of oxo-bridged comple xes, and Mossbauer quadrupolar coupling parameters (0.25-0.40 mm/s) ar e considerably smaller in the hydroxo-bridged analogues. A new diiron( III) complex containing three bidentate bridging groups, [Fe2{O2P(OC6H 5)2}3(HBpz3)2]-(BF4), was also prepared and characterized spectroscopi cally, magnetically, and structurally. In this weakly antiferromagneti cally coupled compound (J = -0.8 cm-1), the Fe...Fe distance is 4.677( 1) angstrom. Unit cell data: [Fe2(OH)(O2CCH3)2(HBPZ3)2](ClO4).CH2Cl2, space group C5(2h)-P2(1)/n, a = 11.757(2) angstrom, b = 19.925(4) angs trom, c = 15.580(2) angstrom, beta = 92.03(1)degrees, V = 3647(2) angs trom3, Z = 4, T = -15-degrees-C; C6H5)2}2(HBPZ3)2](BF4).2CH2-Cl2.0.5(C H3CH2)2O.H2O, space group C6(2h)-C2/c, a = 21.156(4) angstrom, b = 20. 518(2) angstrom, c = 27.157(4) angstrom, beta = 104.268(7)degrees, V = 11 425(3) angstrom3, Z = 8, T = -38-degrees-C; [Fe2(OH){O2P(C6H5)2}2( HBpz3)2](BF4).2.5(CH3)2CO, space group C3(2h)-C2/m, a = 16.772(2) angs trom, b = 33.585(4) angstrom, c = 10.902(1) angstrom, beta = 105.206(8 )degrees, V = 5926(2) angstrom3, Z = 4, T = -54-degrees-C; [Fe2{O2P(OC 6H5)2}3(HBPZ3)2](BF4).CH2Cl2, space group C1i-P1BAR, a = 12.346(2) ang strom, b = 15.084(2) angstrom, c = 17.633(2) angstrom, alpha = 97.50(1 )degrees, beta = 99.02(1)degrees, gamma = 95.76(1)degrees, V = 3191(2) angstrom3, Z = 2, T = -54-degrees-C.