Electronic structure, porphyrin core distortion, and fluxional behavior of bis-ligated low-spin iron(II) porphyrinates
Electronic structure, porphyrin core distortion, and fluxional behavior of bis-ligated low-spin iron(II) porphyrinates
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DOI:
10.1021/jp963039s
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发表时间:
1997-06-05
影响因子:
2.9
通讯作者:
Trautwein, AX
中科院分区:
文献类型:
--
作者:
Grodzicki, M;Flint, H;Trautwein, AX
Three axially bis-ligated Fe(II) porphyrinates, [PFeL2], have been investigated by Mossbauer spectroscopy over the temperature range 4.2-230 EC. and in an applied field of 6 rh( Relatively large differences in the quadrupole splitting Delta E-Q were found among [TMEPFe(2-MeImH)(2)] (1), [TMPFe(N-MeIm)(2)] (2), and [OEPFe-(PMe3)(2)] (3) (1.61, 1.07, and 0.38 mm/s, respectively). Compound 3 exhibits significant line broadening above 150 K that indicates fluxional distortion and/or ligand rotation. Molecular orbital calculations in the local density approximation yield electric field gradients (efg) in good agreement with the measured quadrupole splittings, Delta E-Q, and the measured sign of the efg, The observed differences in quadrupole splittings can be ascribed to distortions (ruffling) of the porphyrin core in 1 as compared to 2 and 3 and to the differences in covalent interactions of the axial nitrogen donors of 1 and 2 and phosphorous donors of 3. The observed temperature-dependent line broadening of 3 correlates with the low calculated rotational barrier.