Reactions of 1,1,3,3-tetramethyldisilazane with dicobalt octacarbonyl and iron pentacarbonyl. Thermal decomposition of the cobalt and iron carbonyl silazane complexes

被引:0
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作者
V. V. Semenov
E. Yu. Ladilina
S. Ya. Khorshev
N. P. Makarenko
Yu. A. Kurskii
O. A. Bochkova
机构
[1] Russian Academy of Sciences,G. A. Razuvaev Institute of Organometallic Chemistry
[2] Russian Academy of Sciences,Institute of Biochemical Physics
来源
Russian Chemical Bulletin | 1998年 / 47卷
关键词
cobalt and iron complexes; tetramethyldisilasane; dicobalt octacarbonyl; iron pentacarbonyl; tetracarbonyl cobalt hydride; cobalt carbonyl silazane complex; iron carbonylhydride silazane complex; acid-base interaction; thermal decomposition of organometallic compounds; ferromagnetic properties;
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摘要
The reaction of (HMe2Si)2NH with Co2(CO)8 gives the complex [Co2(CO)7(SiMe2)2NH2]+[Co(CO)4]−. Its thermal decomposition starts with dissociation into the “acid” HCo(CO)4 and the “base” Co2(CO)7(SiMe2)2NH. After that, the base and the initial complex decompose further under the action of HCo(CO)4. The final products of this reaction are CO, NH3, Co, volatile dimethylcyclosilazane, and a solid residue consisting of cobalt particles encapsulated into a polymethylsiloxane matrix and possessing properties of mixed para- and ferromagnetics with an ultimate specific magnetization of 64–74 G g−1. Tetramethyldisilazane reacts with iron pentacarbonyl under UV irradiation to give relatively stable 1,3-bis(tetracarbonylthydrideiron)-1,1,3,3-tetramethyldisilazane. This product contains Fe−H…N hydrogen bonds, which stabilize it against dehydrogenation and cyclization to diironcyclodisilazane. Thermal decomposition of this product was investigated.
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页码:2455 / 2462
页数:7
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