Syntheses and fluxional processes of diphenyl(2-thienyl)phosphane derivatives of triosmium clusters
(2006) In European Journal of Inorganic Chemistry p.2058-2068- Abstract
- Thermal treatment of [OS3(CO)(12)] with diphenyl(2-thienyl)phosphane, Ph(2)p(C4H3S), results in the formation of [Os-3(CO)(12-x){Ph2P(C4H3S)}(x)] (x = 1-3, 1-3), but no C-H bond activation was observed. Reaction of [H2Os3(CO)(10)] with diphenyl(2-thienyl)phosphane at ambient temperature affords [HOs3(mu-H)(CO)(10){Ph2P(C4H3S}] (4), but when the same reaction is repeated at elevated temperatures, the cyclometallated species [(mu-H)Os-3(CO)(9){mu(3)-Ph(2)p(C4H2S)}] (5) and [mu-H) Os-3(CO)(8){mu 3-Ph2P(C4H2S)}(Ph2P(C4H3S)}] (6) are formed. In addition, two more products, tentatively assigned as [(mu-H)Os-3(CO)(6()mu(3)-Ph2P(C4H2S)}{mu-Ph2P(C4H3S)}{Ph2P-(C4H3S)}] (7) and [(mu-H)Os-3 (CO)(7) {mu-Ph2P(C4H2S)}]... (More)
- Thermal treatment of [OS3(CO)(12)] with diphenyl(2-thienyl)phosphane, Ph(2)p(C4H3S), results in the formation of [Os-3(CO)(12-x){Ph2P(C4H3S)}(x)] (x = 1-3, 1-3), but no C-H bond activation was observed. Reaction of [H2Os3(CO)(10)] with diphenyl(2-thienyl)phosphane at ambient temperature affords [HOs3(mu-H)(CO)(10){Ph2P(C4H3S}] (4), but when the same reaction is repeated at elevated temperatures, the cyclometallated species [(mu-H)Os-3(CO)(9){mu(3)-Ph(2)p(C4H2S)}] (5) and [mu-H) Os-3(CO)(8){mu 3-Ph2P(C4H2S)}(Ph2P(C4H3S)}] (6) are formed. In addition, two more products, tentatively assigned as [(mu-H)Os-3(CO)(6()mu(3)-Ph2P(C4H2S)}{mu-Ph2P(C4H3S)}{Ph2P-(C4H3S)}] (7) and [(mu-H)Os-3 (CO)(7) {mu-Ph2P(C4H2S)}] (4)tPh(2)P(C(4)H3(S)))(Ph2P(C4H3S))] (8) are obtained. The dynamic behaviours of 2, 5 and 6 have been studied by variable-temperature (VT) and H-1 P-31{H-1} NMR spectroscopy. The VT P-31{H-1} NMR spectra of [Os-3(CO)(10){Ph2P(C4H3S)}(2)] (2) demonstrate that a mixture of two isomers, which are in rapid exchange at room temperature, is present and that the less common cis-trans isomer, whose structure has been determined by X-ray crystallography, is favoured for this cluster. The VT H-1 NMR spectra of 5 indicate the presence of two isomers which are proposed to arise from an oscillation of the sigma,eta(2)-vinyl group of the thienyl moiety between two metal atoms. A similar fluxional process is proposed to occur in 6 and the assignment of the room-temperature structure(s) of this cluster was confirmed by H-1-Os-187 2D HMQC spectroscopy. In addition to 2, the solid-state structures of 3, 5 and 6 have been determined by X-ray crystallography. (c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/407468
- author
- Kiriakidou-Kazemifar, Nitsa LU ; Stchedroff, M ; Mottalib, M A ; Selva, S ; Monari, M and Nordlander, Ebbe LU
- organization
- publishing date
- 2006
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- hydrodesulfurisation, fluxionality, cluster, thienylphosphane
- in
- European Journal of Inorganic Chemistry
- issue
- 10
- pages
- 2058 - 2068
- publisher
- John Wiley & Sons Inc.
- external identifiers
-
- wos:000237998200018
- scopus:33646917232
- ISSN
- 1099-0682
- DOI
- 10.1002/ejic.200501141
- language
- English
- LU publication?
- yes
- id
- 916101b6-a94b-451a-a6f2-6adf35f6164b (old id 407468)
- date added to LUP
- 2016-04-01 11:34:16
- date last changed
- 2022-04-20 18:46:31
@article{916101b6-a94b-451a-a6f2-6adf35f6164b,
abstract = {{Thermal treatment of [OS3(CO)(12)] with diphenyl(2-thienyl)phosphane, Ph(2)p(C4H3S), results in the formation of [Os-3(CO)(12-x){Ph2P(C4H3S)}(x)] (x = 1-3, 1-3), but no C-H bond activation was observed. Reaction of [H2Os3(CO)(10)] with diphenyl(2-thienyl)phosphane at ambient temperature affords [HOs3(mu-H)(CO)(10){Ph2P(C4H3S}] (4), but when the same reaction is repeated at elevated temperatures, the cyclometallated species [(mu-H)Os-3(CO)(9){mu(3)-Ph(2)p(C4H2S)}] (5) and [mu-H) Os-3(CO)(8){mu 3-Ph2P(C4H2S)}(Ph2P(C4H3S)}] (6) are formed. In addition, two more products, tentatively assigned as [(mu-H)Os-3(CO)(6()mu(3)-Ph2P(C4H2S)}{mu-Ph2P(C4H3S)}{Ph2P-(C4H3S)}] (7) and [(mu-H)Os-3 (CO)(7) {mu-Ph2P(C4H2S)}] (4)tPh(2)P(C(4)H3(S)))(Ph2P(C4H3S))] (8) are obtained. The dynamic behaviours of 2, 5 and 6 have been studied by variable-temperature (VT) and H-1 P-31{H-1} NMR spectroscopy. The VT P-31{H-1} NMR spectra of [Os-3(CO)(10){Ph2P(C4H3S)}(2)] (2) demonstrate that a mixture of two isomers, which are in rapid exchange at room temperature, is present and that the less common cis-trans isomer, whose structure has been determined by X-ray crystallography, is favoured for this cluster. The VT H-1 NMR spectra of 5 indicate the presence of two isomers which are proposed to arise from an oscillation of the sigma,eta(2)-vinyl group of the thienyl moiety between two metal atoms. A similar fluxional process is proposed to occur in 6 and the assignment of the room-temperature structure(s) of this cluster was confirmed by H-1-Os-187 2D HMQC spectroscopy. In addition to 2, the solid-state structures of 3, 5 and 6 have been determined by X-ray crystallography. (c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006.}},
author = {{Kiriakidou-Kazemifar, Nitsa and Stchedroff, M and Mottalib, M A and Selva, S and Monari, M and Nordlander, Ebbe}},
issn = {{1099-0682}},
keywords = {{hydrodesulfurisation; fluxionality; cluster; thienylphosphane}},
language = {{eng}},
number = {{10}},
pages = {{2058--2068}},
publisher = {{John Wiley & Sons Inc.}},
series = {{European Journal of Inorganic Chemistry}},
title = {{Syntheses and fluxional processes of diphenyl(2-thienyl)phosphane derivatives of triosmium clusters}},
url = {{http://dx.doi.org/10.1002/ejic.200501141}},
doi = {{10.1002/ejic.200501141}},
year = {{2006}},
}