Cargando…

Phosphaalkenylidene bridged ferrocenes

The lithiation of ferrocenylphosphane Fc-PH(2) (Fc = –C(5)H(4)FeC(5)H(5)) has been reinvestigated and both Fc-PHLi and Fc-PLi(2) have been identified by NMR-spectroscopy. The lithiated phosphanides have been converted to the corresponding mono and bis(silylated) species the latter of which gave synt...

Descripción completa

Detalles Bibliográficos
Autores principales: Orthaber, Andreas, Herber, Rolfe H., Pietschnig, Rudolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Sequoia 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480635/
https://www.ncbi.nlm.nih.gov/pubmed/23162166
http://dx.doi.org/10.1016/j.jorganchem.2012.08.020
_version_ 1782247587187785728
author Orthaber, Andreas
Herber, Rolfe H.
Pietschnig, Rudolf
author_facet Orthaber, Andreas
Herber, Rolfe H.
Pietschnig, Rudolf
author_sort Orthaber, Andreas
collection PubMed
description The lithiation of ferrocenylphosphane Fc-PH(2) (Fc = –C(5)H(4)FeC(5)H(5)) has been reinvestigated and both Fc-PHLi and Fc-PLi(2) have been identified by NMR-spectroscopy. The lithiated phosphanides have been converted to the corresponding mono and bis(silylated) species the latter of which gave synthetic access to an oligomer in which three ferrocene units are symmetrically connected by phosphaalkene units. The charge distribution within this oligomer and its isomers has been analyzed using DFT calculations which indicates that the iron atom of the central metallocene unit is slightly more positive than the terminal ones. These findings are supported experimentally by Mößbauer spectroscopy and cyclic voltammetry.
format Online
Article
Text
id pubmed-3480635
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Elsevier Sequoia
record_format MEDLINE/PubMed
spelling pubmed-34806352012-11-15 Phosphaalkenylidene bridged ferrocenes Orthaber, Andreas Herber, Rolfe H. Pietschnig, Rudolf J Organomet Chem Article The lithiation of ferrocenylphosphane Fc-PH(2) (Fc = –C(5)H(4)FeC(5)H(5)) has been reinvestigated and both Fc-PHLi and Fc-PLi(2) have been identified by NMR-spectroscopy. The lithiated phosphanides have been converted to the corresponding mono and bis(silylated) species the latter of which gave synthetic access to an oligomer in which three ferrocene units are symmetrically connected by phosphaalkene units. The charge distribution within this oligomer and its isomers has been analyzed using DFT calculations which indicates that the iron atom of the central metallocene unit is slightly more positive than the terminal ones. These findings are supported experimentally by Mößbauer spectroscopy and cyclic voltammetry. Elsevier Sequoia 2012-11-15 /pmc/articles/PMC3480635/ /pubmed/23162166 http://dx.doi.org/10.1016/j.jorganchem.2012.08.020 Text en © 2012 Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/3.0/Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Orthaber, Andreas
Herber, Rolfe H.
Pietschnig, Rudolf
Phosphaalkenylidene bridged ferrocenes
title Phosphaalkenylidene bridged ferrocenes
title_full Phosphaalkenylidene bridged ferrocenes
title_fullStr Phosphaalkenylidene bridged ferrocenes
title_full_unstemmed Phosphaalkenylidene bridged ferrocenes
title_short Phosphaalkenylidene bridged ferrocenes
title_sort phosphaalkenylidene bridged ferrocenes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480635/
https://www.ncbi.nlm.nih.gov/pubmed/23162166
http://dx.doi.org/10.1016/j.jorganchem.2012.08.020
work_keys_str_mv AT orthaberandreas phosphaalkenylidenebridgedferrocenes
AT herberrolfeh phosphaalkenylidenebridgedferrocenes
AT pietschnigrudolf phosphaalkenylidenebridgedferrocenes