PREPARATION AND STRUCTURAL CHARACTERIZATION OF AN ENANTIOMERICALLY PURE, C-2-SYMMETRICAL, SINGLE-COMPONENT ZIEGLER-NATTA ALPHA-OLEFIN POLYMERIZATION CATALYST

Citation
Jp. Mitchell et al., PREPARATION AND STRUCTURAL CHARACTERIZATION OF AN ENANTIOMERICALLY PURE, C-2-SYMMETRICAL, SINGLE-COMPONENT ZIEGLER-NATTA ALPHA-OLEFIN POLYMERIZATION CATALYST, Journal of the American Chemical Society, 118(5), 1996, pp. 1045-1053
Citations number
58
Categorie Soggetti
Chemistry
ISSN journal
00027863
Volume
118
Issue
5
Year of publication
1996
Pages
1045 - 1053
Database
ISI
SICI code
0002-7863(1996)118:5<1045:PASCOA>2.0.ZU;2-A
Abstract
A new linked bis(cyclopentadienyl) ligand, {(C5H3-2-SiMe(3)-4-CMe(3))( 2)Si(OC10H6C10H6O)} (BnBpH(2)), has been designed to coordinate to tra nsition metals tp afford a single enantiomeric C-2-symmetric ansa-meta llocene. The syntheses of its dipotassium salt and (BnBp)YCl(THF) are described. Steric interactions between the 3- and 3'-methine positions of the 1,1'-binaphth-2,2'-diolate rings of the chiral linker with the alpha-trimethylsilyl substituents on the cyclopentadienyl rings force enantioselective metalation of this ligand, Thus, coordination to ytt rium occurs in an entirely diastereoselective manner: the ligand prepa red from (R)-(+)-1,1'-bi-2-naphthol directs formation of the (S)-yttro cene, (R,S)-(BnBp)YCl(THF), while that from (S)-(-)-1,1'-bi-2-naphthol directs formation of the (R)-yttrocene, (S,R)-(BnBp)YCl(THF). Removal of coordinated tetrahydrofuran allows the preparation of (BnBp)YCH(Si Me(3))(2). Treatment of rac-(BnBp)YCH(SiMe(3))(2) with H-2 yields a ki netic mixture of both heterochiral and homochiral dimers (e.g. (R,S)-( BnBp)Y(mu(2)-H)(2)-(S,R)-(BnBp) and (R,S)-(BnBp)Y(mu(2)-H)(2)-(R,S)-Y( BnBp), respectively). Over several hours this mixture undergoes conver sion to the pure homochiral dimers. As anticipated, hydrogenolysis of enantiopure (BnBp)YCH(SiMe(3))(2) (e.g. R,S-(BnBp)YCH(SiMe(3))(2)) aff ords directly only enantiopure homochiral dimer (e.g. (R,S)-(BnBp)Y(mu (2)-H)(2)-(R,S)-Y(BnBp)). The hydride, generated in situ from (R,S)-(B nBp)YCH(SiMe(3))(2), polymerizes 1-pentene to highly isotactic poly-1- pentene (M(n) = 119 000, PDI = 1.44, mmmm >95%). The much higher solub ility of the enantiopure homochiral dimers was used to grow crystals o f the racemate at the interface of layered solutions of the pure optic al isomers. rac-(BnBp)Y(mu(2)-H)(2)(BnBp) crystallizes in the centrosy mmetric space group P (1) over bar (#2) with a = 11.925(4) Angstrom, b = 19.461(8) Angstrom, c = 23.814(10) Angstrom, and alpha = 82.80(3)de grees, beta = 84.64(4)degrees, gamma = 81.30(3)degrees, with a volume of 5404(4) Angstrom(3) and Z = 2.