Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10569612 | Coordination Chemistry Reviews | 2013 | 17 Pages |
Abstract
⺠Negative correlations between FeX and XO stretching frequencies establish backbonding in XO adducts (X = C, N, O) of heme proteins. ⺠For Fe(II)CO adducts, donation from the trans axial ligand decreases νCO, with little change in νFeC, and shifts the backbonding correlation. ⺠For Fe(III)NO, Fe(II)NO and Fe(II)O2, dz2-dxz orbital mixing produces positive νFeX/νXO correlations, as the trans donation increases. ⺠For Fe(II)NO and Fe(II)O2, negative or positive correlations are induced by H-bonding to the outer or inner XO atom. ⺠Fe(III)NO adducts do not support distal H-bonds, but do support lone pair donor interactions. Strong donors interact with N, bending the FeNO.
Keywords
CH2Cl2HRPCTBNOSCCOSGCCCPYC-13-(5′-hydroxymethyl-2′-furyl)-1-benzylindazoleDMFCooAN-methylimidazoleH-NOXBackbondingBjFixLHTMCHSWMbP450norCPOTrpDFTQM/MMArginineArgHomohighest occupied molecular orbitalbenzeneTryptophanDioxygendimethylformamideDichloromethaneRamanResonance RamanSANOScytochrome c oxidaseCytochrome c peroxidaseSoluble guanylate cyclasePhthalocyanineInfraredcarbon monoxideSperm Whale myoglobinDensity functional theoryNitrophorinNitric oxidenitric oxide synthaseHemeHemoglobinHorseradish peroxidaseProteinH-bondHydrogen bondChloroperoxidase
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Thomas G. Spiro, Alexandra V. Soldatova, Gurusamy Balakrishnan,