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Abstract
The reactions of [Os-3(mu-CO)(CO)(9){mu(3)-eta(2)-Me3SiCCC CSiMe3}] with phosphorus donor ligands (PPh3, PEt3, P(OEt)(3), PHPh2 and a diphosphine; Ph2PCH2PPh2 (dppm)) afford carbonyl mono-substitution products [Os-3(mu-CO)(CO)(8){mu(3)-eta(2)-Me3SiC2C2SiMe3}] even in the case of the bidentate phosphine dppm. All the complexes have been characterized by IR and multinuclear NMR spectroscopy and for 2 (L = PPh3), 3 (L = PEt3), 4 (L = P(OEt)(3)) and 5 (L = eta(1)-dppm) the structures have been confirmed by single- crystal X- ray analysis. The structural analyses show that in all four clusters the substitution has occurred at one of osmium equatorial sites that is sigma- bonded to the mu(3)-eta(2)-alkyne. (C) 2009 Published by Elsevier B.V.
Original language | English |
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Pages (from-to) | 156-161 |
Number of pages | 6 |
Journal | Journal of Organometallic Chemistry |
Volume | 695 |
Issue number | 2 |
DOIs | |
Publication status | Published - 15 Jan 2010 |
Keywords
- Phosphine
- Diyne
- X-ray crystallograph
- Osmium cluster carbonyl
- Phosphite
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Dive into the research topics of 'Reaction of the diyne complex Os-3(mu-CO)(CO)(9){mu(3)-eta(2)-Me3SiCCC CSiMe3} with phosphines and phosphites: Characterization of monophosphine substituted clusters Os-3(mu-CO)(CO)(8)(PR3){mu(3)-eta(2)-Me3SiCCC CSiMe3} (PR3 = PPh3, P(OEt)(3), PEt3, PHPh2 and Ph2PCH2PPh2)'. Together they form a unique fingerprint.Projects
- 1 Finished
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Senior Fellowship - TIME RESOLVED CRYSTALLOGRAPHY
Raithby, P. (PI)
Engineering and Physical Sciences Research Council
1/12/06 → 30/11/11
Project: Research council