Reaction pathway for the formation of binuclear samarocene hydride from monomeric alkyl samarocene derivative and the effective catalysis of samarocene hydride for the block copolymerization of ethylene with polar monomers

Citation
G. Desurmont et al., Reaction pathway for the formation of binuclear samarocene hydride from monomeric alkyl samarocene derivative and the effective catalysis of samarocene hydride for the block copolymerization of ethylene with polar monomers, ORGANOMETAL, 19(10), 2000, pp. 1811-1813
Citations number
16
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANOMETALLICS
ISSN journal
02767333 → ACNP
Volume
19
Issue
10
Year of publication
2000
Pages
1811 - 1813
Database
ISI
SICI code
0276-7333(20000515)19:10<1811:RPFTFO>2.0.ZU;2-E
Abstract
The X-ray analysis of Me2Si(C5H3-3-Me3Si)(2)SmCH(Me3Si)(2)(THF) (1) reveale d a monomeric structure, while the hydrogenated complex, [Me2Si(C5H3-3-Me3S i)(2)SmH(THF)](2), (2), exhibits binuclear mu-H structure to indicate that Me2SiCp'M-2 --> M(mu-Me2SiCp'(2))(2)M rearrangement of the eta(5)-eta(5) li gation occurs during the hydrogenation. The resulting samarocene hydride 2 exhibits high activity as an initiator for the bloch copolymerization of et hylene with polar monomers such as methyl methacrylate and epsilon-caprolac tone.