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μ-Bis(diphenylphosphanyl)borato-κ(2) P:P′-bis[dicarbonyl(η(5)-cyclopentadienyl)iron(II)] tetrachloridoferrate(III) chloroform solvate
The title compound, [Fe(2)(C(5)H(5))(2)(C(24)H(22)BP(2))(CO)(4)][FeCl(4)]·CHCl(3), is an oxidation product of CpFe(CO)(2)PPh(2)BH(3). One pair of phenyl rings attached to the two different P atoms are almost parallel, as are the other pair [dihedral angles = 8.7 (5) and 8.9 (5)°]. The planes of the...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961392/ https://www.ncbi.nlm.nih.gov/pubmed/21202516 http://dx.doi.org/10.1107/S1600536808014931 |
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author | Dornhaus, Franz Lerner, Hans-Wolfram Bolte, Michael |
author_facet | Dornhaus, Franz Lerner, Hans-Wolfram Bolte, Michael |
author_sort | Dornhaus, Franz |
collection | PubMed |
description | The title compound, [Fe(2)(C(5)H(5))(2)(C(24)H(22)BP(2))(CO)(4)][FeCl(4)]·CHCl(3), is an oxidation product of CpFe(CO)(2)PPh(2)BH(3). One pair of phenyl rings attached to the two different P atoms are almost parallel, as are the other pair [dihedral angles = 8.7 (5) and 8.9 (5)°]. The planes of the two cyclopentadienyl rings are inclined by 26.8 (7)° with respect to each other. The carbonyl groups at each Fe atom are almost perpendicular [C—Fe—C = 92.6 (6) and 94.3 (5)°]. |
format | Text |
id | pubmed-2961392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29613922010-12-30 μ-Bis(diphenylphosphanyl)borato-κ(2) P:P′-bis[dicarbonyl(η(5)-cyclopentadienyl)iron(II)] tetrachloridoferrate(III) chloroform solvate Dornhaus, Franz Lerner, Hans-Wolfram Bolte, Michael Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers The title compound, [Fe(2)(C(5)H(5))(2)(C(24)H(22)BP(2))(CO)(4)][FeCl(4)]·CHCl(3), is an oxidation product of CpFe(CO)(2)PPh(2)BH(3). One pair of phenyl rings attached to the two different P atoms are almost parallel, as are the other pair [dihedral angles = 8.7 (5) and 8.9 (5)°]. The planes of the two cyclopentadienyl rings are inclined by 26.8 (7)° with respect to each other. The carbonyl groups at each Fe atom are almost perpendicular [C—Fe—C = 92.6 (6) and 94.3 (5)°]. International Union of Crystallography 2008-05-21 /pmc/articles/PMC2961392/ /pubmed/21202516 http://dx.doi.org/10.1107/S1600536808014931 Text en © Dornhaus et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Metal-Organic Papers Dornhaus, Franz Lerner, Hans-Wolfram Bolte, Michael μ-Bis(diphenylphosphanyl)borato-κ(2) P:P′-bis[dicarbonyl(η(5)-cyclopentadienyl)iron(II)] tetrachloridoferrate(III) chloroform solvate |
title | μ-Bis(diphenylphosphanyl)borato-κ(2)
P:P′-bis[dicarbonyl(η(5)-cyclopentadienyl)iron(II)] tetrachloridoferrate(III) chloroform solvate |
title_full | μ-Bis(diphenylphosphanyl)borato-κ(2)
P:P′-bis[dicarbonyl(η(5)-cyclopentadienyl)iron(II)] tetrachloridoferrate(III) chloroform solvate |
title_fullStr | μ-Bis(diphenylphosphanyl)borato-κ(2)
P:P′-bis[dicarbonyl(η(5)-cyclopentadienyl)iron(II)] tetrachloridoferrate(III) chloroform solvate |
title_full_unstemmed | μ-Bis(diphenylphosphanyl)borato-κ(2)
P:P′-bis[dicarbonyl(η(5)-cyclopentadienyl)iron(II)] tetrachloridoferrate(III) chloroform solvate |
title_short | μ-Bis(diphenylphosphanyl)borato-κ(2)
P:P′-bis[dicarbonyl(η(5)-cyclopentadienyl)iron(II)] tetrachloridoferrate(III) chloroform solvate |
title_sort | μ-bis(diphenylphosphanyl)borato-κ(2)
p:p′-bis[dicarbonyl(η(5)-cyclopentadienyl)iron(ii)] tetrachloridoferrate(iii) chloroform solvate |
topic | Metal-Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961392/ https://www.ncbi.nlm.nih.gov/pubmed/21202516 http://dx.doi.org/10.1107/S1600536808014931 |
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