5026-95-9Relevant articles and documents
Kinetic resolution of chiral α-olefins using optically active ansa-zirconocene polymerization catalysts
Baar, Cliff R.,Levy, Christopher J.,Min, Endy Y.-J.,Henling, Lawrence M.,Day, Michael W.,Bercaw, John E.
, p. 8216 - 8231 (2007/10/03)
A series of enantiopure C1-symmetric metallocenes, {(SiMe 2)2[η5-C5H(CHMe 2)2][η5-C5H2((S) CHMeCMe3)]}ZrCl2, (S)-2, {(SiMe2) 2[η5-C5H(CHEt2) 2][η5-C5H2((S)-CHMeCMe 3)]}ZrCl2, (S)-6, and {(SiMe2) 2[η5-C5HCy2][η5- C5H2((S)-CHMeCMe3)]}ZrCl2), (S)-7 (Cy = cyclohexyl), zirconocene dichlorides that have an enantiopure methylneopentyl substituent on the "upper" cyclopentadienyl ligand, and diastereomerically pure precatalysts, {(SiMe2) 2[η5-C5H((S)-CHMeCy)(CHMe 2)][η5-C5H3]}ZrCl2, (S)-8a and (S)-8b, which have an enantiopure, 1-cyclohexylethyl substituent on the "lower" cyclopentadienyl ligand, has been synthesized for use in the polymerization of chiral α-olefins. When activated with methylaluminoxane, these metallocenes show unprecedented activity for the polymerization of bulky racemic monomers bearing substitution at the 3- and/or 4-positions. Due to the optically pure nature of these single site catalysts, they effect kinetic resolution of racemic monomers: the polymeric product is enriched with the faster reacting enantiomer, while recovered monomer is enriched with the slower reacting enantiomer. The two components are easily separated. For most olefins surveyed, a partial kinetic resolution was achieved (s = kfaster/kslower ≈ 2), but, in one case, the polymerization of 3,4-dimethyl-1-pentene, high levels of separation were obtained (s > 15). 13C NMR spectroscopy of poly (3-methyl-1-pentene) produced with (S)-2 indicates that the polymers are highly isotactic materials. X-ray crystal structure determinations for (S)-2, {(SiMe2)2[η 5-C5H(CHMe2)2][η5- C5H2((S)-CHMeCMe3)]}Zr(SC6H 5)2, (S)-6, and (S)-7 have been used in combination with molecular mechanics calculations to examine the prevailing steric interactions expected in the diastereomeric transition states for propagation during polymerization. Precatalysts (S)-8a and (S)-8b are less selective polymerization catalysts for the kinetic resolution of 3-methyl-1-pentene than are (S)-2, (S)-6, and (S)-7.
Simple Access to Highly Enantiomerically Enriched (S)-3-Methyl-1-pentanol, (S)-3-Methyl-1-pentene, (2R,3S)-2-Deuterio-3-methyl-1-pentanol, and (2S,3S)-3-Methyl-2-pentanol from Natural L-Isoleucine
Schurig, Volker,Leyrer, Ulrich,Wistuba, Dorothee
, p. 242 - 245 (2007/10/02)
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