OBSERVATION OF STABLE 17 e IRON(III) CYCLOPENTADIENYL RADICAL COMPLEXES
The EPR spectra of a series of mononuclear complexes <FONT FACE=Symbol>[ CpFe(dppe)SR]</FONT> PF6R = C6H5 (1), C3H7 (2),p-C6H4Br (3) and the binuclear <FONT FACE=Symbol>[ CpFe(dppe)-S-CH2CH2-S-CpFe(dppe]</FONT> (PF6)2 (4) were measured. All the paramagnetic complexes exhibit...
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Sociedad Chilena de Química
1999
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oai:scielo:S0366-164419990003000082000-10-13OBSERVATION OF STABLE 17 e IRON(III) CYCLOPENTADIENYL RADICAL COMPLEXESDIAZ,C. Iron-sulfur complexes EPR organometallicradical thiolate compounds The EPR spectra of a series of mononuclear complexes <FONT FACE=Symbol>[ CpFe(dppe)SR]</FONT> PF6R = C6H5 (1), C3H7 (2),p-C6H4Br (3) and the binuclear <FONT FACE=Symbol>[ CpFe(dppe)-S-CH2CH2-S-CpFe(dppe]</FONT> (PF6)2 (4) were measured. All the paramagnetic complexes exhibit intense signals in both solid state as well as in CH2Cl2solution. Analysis of the spectra indicates a pseudooctahedral structurefor the complexes except for complex (2) for which a tetragonaldistortion in solid state was observed. Some degree of delocalization ofthe unpaired electron for (3) and (4) was suggested. The stabilization of the radicals by the thiolate ligands is discussedinfo:eu-repo/semantics/openAccessSociedad Chilena de QuímicaBoletín de la Sociedad Chilena de Química v.44 n.3 19991999-09-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0366-16441999000300008en10.4067/S0366-16441999000300008 |
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Scielo Chile |
collection |
Scielo Chile |
language |
English |
topic |
Iron-sulfur complexes EPR organometallicradical thiolate compounds |
spellingShingle |
Iron-sulfur complexes EPR organometallicradical thiolate compounds DIAZ,C. OBSERVATION OF STABLE 17 e IRON(III) CYCLOPENTADIENYL RADICAL COMPLEXES |
description |
The EPR spectra of a series of mononuclear complexes <FONT FACE=Symbol>[ CpFe(dppe)SR]</FONT> PF6R = C6H5 (1), C3H7 (2),p-C6H4Br (3) and the binuclear <FONT FACE=Symbol>[ CpFe(dppe)-S-CH2CH2-S-CpFe(dppe]</FONT> (PF6)2 (4) were measured. All the paramagnetic complexes exhibit intense signals in both solid state as well as in CH2Cl2solution. Analysis of the spectra indicates a pseudooctahedral structurefor the complexes except for complex (2) for which a tetragonaldistortion in solid state was observed. Some degree of delocalization ofthe unpaired electron for (3) and (4) was suggested. The stabilization of the radicals by the thiolate ligands is discussed |
author |
DIAZ,C. |
author_facet |
DIAZ,C. |
author_sort |
DIAZ,C. |
title |
OBSERVATION OF STABLE 17 e IRON(III) CYCLOPENTADIENYL RADICAL COMPLEXES |
title_short |
OBSERVATION OF STABLE 17 e IRON(III) CYCLOPENTADIENYL RADICAL COMPLEXES |
title_full |
OBSERVATION OF STABLE 17 e IRON(III) CYCLOPENTADIENYL RADICAL COMPLEXES |
title_fullStr |
OBSERVATION OF STABLE 17 e IRON(III) CYCLOPENTADIENYL RADICAL COMPLEXES |
title_full_unstemmed |
OBSERVATION OF STABLE 17 e IRON(III) CYCLOPENTADIENYL RADICAL COMPLEXES |
title_sort |
observation of stable 17 e iron(iii) cyclopentadienyl radical complexes |
publisher |
Sociedad Chilena de Química |
publishDate |
1999 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0366-16441999000300008 |
work_keys_str_mv |
AT diazc observationofstable17eironiiicyclopentadienylradicalcomplexes |
_version_ |
1718438094238121984 |