Isomerization and Conformational Transformations of the N-allyl-N-methylcarbamoyl Bridging Ligand in the (μ-H)Os3{μ-OCN(Me)CH2CH=CH2}(CO) 10 Complex
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: 1998,
Volume: 47,
Number: 1,
Pages: 160-164
Pages count
: 5
DOI:
10.1007/BF02495524
|
Tags |
Allylic isomerization, Conformation, Os3 clusters, carbamoyl ligand |
Authors |
Ershova V.A.
1
,
Maksakov V.A.
1
,
Golovin A.V.
2
,
Tkachev S.V.
1
,
Sheludyakova L.A.
1
|
Affiliations |
1 |
lnstitute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences,
3 prosp. Akad. Lavrent'eva, 630090 Novosibirsk, Russian Federation
|
2 |
G. K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences,
5 prosp. Akad. Lavrent'eva, 630090 Novosibirsk, Russian Federation
|
|
Funding (2)
1
|
Russian Foundation for Basic Research
|
97-03-33046
|
2
|
Russian Foundation for Basic Research
|
97-03-33292
|
The (μ-H)Os3{μ-OCN(Me)CH2CH=CH2}(CO)10 complex containing an allylic fragment in theN,N-dialkylsubstituted carbamoyl briding ligand was synthesized. The stereo-chemical behavior of this complex in solution was investigated. As follows from the NMR spectral data, the complex undergoes reversible conformational (about the amide C−N bond) and irreversible allylic isomerization. Both conformers were isolated in the solid state by chromatography at a reduced temperature. The allylic isomerization occurs stereospecifically to produce the (μ-H)Os3{μ-OCN(Me)CH=CHMe}(CO)10 complex with thetrans-oriented olefinic hydrogen atoms.