Hydrogen bonding influence of 1,10-phenanthroline on five-coordinate high-spin imidazole-ligated iron(II) porphyrinates.
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ABSTRACT: The influence of a hydrogen bond to the coordinated imidazole on the geometric and electronic structure of iron has been further studied in new complexes of five-coordinate high-spin imidazole-ligated iron(II) porphyrinates. With 1,10-phenanthroline (1,10-phen) as the hydrogen-bond acceptor, several new octaethylporphyrin dianion (OEP) and meso-tetraphenylporphyrin dianion (TPP) derivatives have been synthesized and characterized by X-ray crystallography and Mössbauer spectroscopy. In all three new structures, the porphyrin molecules and 1,10-phenanthroline molecules have been found with a ratio of 1:1. All the porphyrin derivatives are five-coordinate 2-methylimidazole-ligated iron(II) species. 1,10-Phenanthroline is hydrogen bonded to the coordinated imidazole to form two unequal hydroge
SUBMITTER: Hu C
PROVIDER: S-EPMC2630385 | biostudies-literature | 2008 Oct
REPOSITORIES: biostudies-literature
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