| US 7,592,404 B2 | ||
| Half metallocene catalyst and process for preparing syndiotactic styren polymer using the same | ||
| Young-jo Kim, Daejeon (Korea, Republic of); Doh-yeon Park, Daejeon (Korea, Republic of); You-mi Jeong, Daejeon (Korea, Republic of); and Min-hyung Lee, Daejeon (Korea, Republic of) | ||
| Assigned to LG Chem, Ltd., (Korea, Republic of) | ||
| Filed on Nov. 08, 2005, as Appl. No. 11/268,848. | ||
| Prior Publication US 2007/0105710 A1, May 10, 2007 | ||
| Int. Cl. C08F 4/642 (2006.01); C07F 7/28 (2006.01); C08F 12/08 (2006.01) | ||
| U.S. Cl. 526—160 [526/127; 526/161; 526/347.2; 526/943; 556/11; 556/20; 556/43; 556/52] | 18 Claims |

1. A half metallocene catalyst represented by the formula 1, 2 or 3:
![]() wherein, M1, M2 and M3 are transition metals independently selected from the group consisting of atoms in Groups 3, 4, 5, 6, 7, 8, 9, 10 of the Periodic
Table, and Each of L1, L2 and L3 is a cycloalkanedienyl ligand represented by the formula 4, 5, 6, 7 or 8:
![]() wherein, R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12, and R13 are independently hydrogen atom, halogen, alkyl, C3-20 cycloalkyl, C2-20 oalkenyl, alkylsilyl, haloalkyl, alkoxy, alkylsiloxy, amino, alkoxyallcyl, thioalkoxyalkyl, alkylsiloxyalkyl, aminoalkyl,
alkylphosphinoalkyl, aryl, arylalkyl, alkylaryl, arylsilyl, arylalkylsilyl, haloaryl, aryloxy, aryloxoalkyl, thioaryloxoalkyl,
aryloxoaryl, arylsiloxy, arylalkylsiloxy, arylsiloxalkyl, arylsiloxoaryl, arylamino, arylaminoalkyl, arylaminoaryl or arylphosphinoalkyl
group (here, the alkyl group is c1-20 hydrocarbon group having straight or branch structure and the aryl group is C6-40 aromatic or heteroaromatic group) and each of m and n is an integer of 1 or more;
X1, X2, and X3, which are σ-ligand functional groups, are independently hydrogen atom, halogen, alkyl, C3-20 cycloalkyl, alkylsilyl, C2-20 alkenyl, alkoxy, alkenyloxy, thioalkoxy, alkylsiloxy, amide, alkoxyalcohol, alcoholamine, aryl, alkylaryl, arylalkyl, arylsilyl,
haloaryl, aryloxy, arylalkoxy, thioaryloxy, arylalkylsiloxy, arylamide, arylalkylamide, aryloxoalcohol, alcohoarylamine, or
arylaminoaryloxy group (here, the alkyl group is c1-20 hydrocarbon group having straight or branch structure and the aryl group is C6-40 aromatic or hetero aromatic group);
A1, A2, A3, A4, A5 and A6 are functional groups bounded to a central metal and are independently oxygen atom or sulfur atom;
D1, D2, D3, D4, D5 and D6 are a carbon atom, respectively;
E1, E2, E3, E4, E5, E6, E7, E8, E9, E10, E11, and E12 are independently hydrogen atom, halogen, alkyl, C3-20 cycloalkyl, C2-20 alkenyl, alkylsilyl, haloalkyl, alkoxy, alkylsiloxy, amino, alkoxyalkyl, thioalkoxyalkyl, alkylsiloxyalkyl, aminoalkyl, alkylphosphinoalkyl,
aryl, arylalkyl, alkylaryl, arylsilyl, arylalkylsilyl, haloaryl, aryloxy, aryloxoalkyl, thioaryloxoalkyl, aryloxoaryl, arylsiloxy,
arylalkylsiloxy, arylsiloxalkyl, arylsiloxoaryl, arylamino, arylaminoalkyl, arylaminoaryl or arylphosphinoalkyl group (here,
the alkyl group is c1-20 hydrocarbon group having straight or branch structure and the aryl group is C6-40 aromatic or heteroaromatic group), wherein all of E1, E2, E3, E4, E5, and E6 are not simultaneously hydrogen atom, all of E7, E8, E9, and E10 are not simultaneously hydrogen atom, and all of E11 and E12 are not simultaneously hydrogen atom;
Q1, Q2 and Q3 are independently nitrogen or phosphorous; and
Z1, Z2 and Z3 are independently hydrogen atom, alkyl, C3-20 cycloalkyl, C2-20 alkenyl, alkylsilyl, haloalkyl, alkoxyalkyl, thioalkoxyalkyl, alkylsiloxyalkyl, aminoalkyl, alkylphosphinoalkyl, aryl, arylalkyl,
alkylaryl, arylsilyl, arylalkylsilyl, haloaryl, aryloxoalkyl, thioaryloxoalkyl, aryloxoaryl, arylsiloxy, arylalkylsiloxy,
arylsiloxalkyl, arylsiloxoaryl, arylamino, arylaminoalkyl, arylaminoaryl or arylphosphinoalkyl group (here, the alkyl group
is a C1-20 hydrocarbon group having the straight or branch structure and the aryl group is a C6-40 aromatic or heteroaromatic group).
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