Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes

Mathieu, R. ; Poilblanc, R. ; Lemoine, P. ; Gross, M.

Amsterdam : Elsevier
ISSN:
0022-328X
Source:
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
Topics:
Chemistry and Pharmacology
Type of Medium:
Electronic Resource
URL:
_version_ 1798291057622908928
autor Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
autorsonst Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
book_url http://linkinghub.elsevier.com/retrieve/pii/S0022-328X(00)94326-2
datenlieferant nat_lic_papers
fussnote The electrochemical behaviour of thio and phosphido complexes of iron(I): Fe"2XY(CO)"6""nL"n (X = Y = SR, PR"2 and X = SR, Y = PR"2, L = PR"3) has been studied on platinum and mercury electrodes, in organic solvent. These complexes are reduced in a two-electron irreversible process. A large difference is observed between their oxidation potentials on mercury and platinum electrodes; this is ascribed to the formation of a mercury complex in which mercury is inserted into the metalmetal bond. In oxidation on platinum electrodes, two mono-electronic waves are observed. The influece of the ligand basicity on the cathodic E"1"2 values is discussed. A parallel shift is observed between the E"1"2 and the IR ν(CO) of the totally symmetrical mode. Chemical oxidation of the complexes shows that the dications cannot be isolated, and leads to isolation of the following species: [FeP(CH"3)"2(CO)"3]"2AgNO"3, [FeSCH"3(CO)"2P(CH"3)"3]"2(NO"3)"2, {[FeSCH"3(CO)"2P(CH"3)"3]"2F} PF"6, where NO"3^- and F^- act as ligands.
hauptsatz hsatz_simple
identnr NLZ174962479
issn 0022-328X
journal_name Journal of Organometallic Chemistry
materialart 1
package_name Elsevier
publikationsort Amsterdam
publisher Elsevier
reference 165 (1979), S. 243-252
search_space articles
shingle_author_1 Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
shingle_author_2 Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
shingle_author_3 Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
shingle_author_4 Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
shingle_catch_all_1 Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
0022-328X
0022328X
Elsevier
shingle_catch_all_2 Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
0022-328X
0022328X
Elsevier
shingle_catch_all_3 Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
0022-328X
0022328X
Elsevier
shingle_catch_all_4 Mathieu, R.
Poilblanc, R.
Lemoine, P.
Gross, M.
Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
0022-328X
0022328X
Elsevier
shingle_title_1 Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
shingle_title_2 Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
shingle_title_3 Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
shingle_title_4 Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
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source_archive Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
timestamp 2024-05-06T08:26:34.682Z
titel Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
titel_suche Electrochemical behaviour and chemical oxidation study of the thio- and phosphido-bridge binuclear iron complexes
The electrochemical behaviour of thio and phosphido complexes of iron(I): Fe"2XY(CO)"6""nL"n (X = Y = SR, PR"2 and X = SR, Y = PR"2, L = PR"3) has been studied on platinum and mercury electrodes, in organic solvent. These complexes are reduced in a two-electron irreversible process. A large difference is observed between their oxidation potentials on mercury and platinum electrodes; this is ascribed to the formation of a mercury complex in which mercury is inserted into the metalmetal bond. In oxidation on platinum electrodes, two mono-electronic waves are observed. The influece of the ligand basicity on the cathodic E"1"2 values is discussed. A parallel shift is observed between the E"1"2 and the IR ν(CO) of the totally symmetrical mode. Chemical oxidation of the complexes shows that the dications cannot be isolated, and leads to isolation of the following species: [FeP(CH"3)"2(CO)"3]"2AgNO"3, [FeSCH"3(CO)"2P(CH"3)"3]"2(NO"3)"2, {[FeSCH"3(CO)"2P(CH"3)"3]"2F} PF"6, where NO"3^- and F^- act as ligands.
topic V
uid nat_lic_papers_NLZ174962479