STEREOCHEMISTRY OF COORDINATION GROUP IN AN IRON(3) DERIVATIVE OF TETRAPHENYLPORPHINE
STEREOCHEMISTRY OF COORDINATION GROUP IN AN IRON(3) DERIVATIVE OF TETRAPHENYLPORPHINE
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DOI:
10.1021/ja00985a004
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发表时间:
1967-01-01
影响因子:
15
通讯作者:
GLICK, MD
中科院分区:
文献类型:
--
作者:
HOARD, JL;COHEN, GH;GLICK, MD
The X-ray data reported by Fleischer, et al.,* for tetragonal crystals assumed to be the aquohydroxyiron-(III) derivative of tetraphenylporphine (H2OFeOHTPP) are reanalyzed to take account of (1) the probability thatthe material studied was in fact the chloroiron (III) derivative of tetraphenylporphine (ClFeTPP) and (2) orientational disorder of the molecules in the crystal that, on either chemical formulation, is of major importance in interpreting the experimental data. Chemical analysis of the original preparation prior to recrystallization supports, but does not establish, the ClFeTPP composition. The structural modelfor each formulation assigns equal probabilities for parallel and antiparallel orientation of the polar coordination group along c; independent refinement of these models yields a pair of statistically averaged molecules that have objectively indistinguishable geometries. The ClFeTPP formulation provides a rational accounting for every aspect of the experimental data and the derived results, whereas the H2OFeOHTPPformulation requires several detailed interpretations that are rather uncon-vincing. The square-pyramidal coordination group in the ClFeTPP molecule, with Fe-N= 2.049±0.009 A and Fe-Cl= 2.192±0.012 A, closelyresembles that in chlorohemin. The iron atom is displaced out-of-plane from the nitrogen atoms by 0.383±0.005 A.