Preparation and Reactivity of Metal-Containing Monomers 53. Synthesis and Stability of a Cluster Monomer
(μ-H)Os3(μ-OCNMe2)(CO)9PPh2CH2CH=CH2 in Solution
Full article
| Общее |
Language:
Английский,
Genre:
Full article,
Status:
Published,
Source type:
Translated
|
| Journal |
Russian Chemical Bulletin
ISSN: 1066-5285
, E-ISSN: 1573-9171
|
| Output data |
Year: 2000,
Volume: 49,
Number: 8,
Pages: 1448-1453
Pages count
: 6
DOI:
10.1007/BF02495095
|
| Tags |
1H and 31P NMR spectroscopy, Allyldiphenylphosphine, Carbamoyl ligand, Carbonyl(phosphine)osmium, Cluster monomers, Isomerization, Osmium clusters |
| Authors |
Ershova V.A.
,
Golovin A.V.
,
Sheludyakova L.A.
,
Semyannikov P.P.
,
Pomogailo S.I.
,
Pomogailo A.D.
|
| Affiliations |
| 1 |
Nikolaev Institute of Inorganic Chemistry SB RAS
|
| 2 |
Institute of Problems of Chemical Physics RAS
|
|
The stability of the complex (μ-H)Os3(μ-OCNMe2)(CO)9PPh2CH2CH=CH2 (1), which contains a free unsaturated functional group in the terminal ligand PPh2CH2CH=CH2, with respect to isomerization, chelation of the ligand, and other transformations in solutions was examined. No transformations of complex1 were observed in the course of synthesis from (μ-H)Os3(μ-OCNMe2)(CO)9NMe3 or upon heating in solution. Complex1 as well as complexes (μ-H)Os3(μ-OCNMe2)(CO)9PHPh2 and (μ-H)Os3(μ-OCNMe2)(CO)9PPh3, which were formed as admixtures, were isolated in the solid state and identified by1H,1H-{31P}, and1H-{1H} NMR, IR, and Raman spectroscopy and mass spectrometry.