US2003216248A1PendingUtilityA1
Catalyst composition and method of polymerization
Priority: Dec 4, 2000Filed: Apr 14, 2003Published: Nov 20, 2003
Est. expiryDec 4, 2020(expired)· nominal 20-yr term from priority
Inventors:John H. Oskam
C08F 110/14C07F 7/003C08F 4/65908C07F 7/00C08F 10/00C08F 110/02C08F 210/02C08F 4/65912C08F 210/16
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Claims
Abstract
This invention relates to a composition of matter comprising the catalyst compound comprising a transition metal complexed with a facially coordinating tridentate bisamide ligand. The invention is also directed to a catalyst system or a supported catalyst system comprising this compound and an activator and to a process for using the catalyst system or supported catalyst system in a process for polymerizing olefin(s).
Claims
exact text as granted — not AI-modifiedI claim:
1 . A compound represented by the following formula:
wherein
M is a group 3, 4 or 5 transition metal or a lanthanide or actinide group metal,
each X is independently an anionic leaving group,
n is the oxidation state of M,
a is 0 or 1,
m is the formal charge of the YZL ligand,
Y is a group 15 element,
Z is a group 15 element,
J is a C 1 to C 20 hydrocarbon group, a heteroatom containing group, silicon, germanium, tin, or phosphorus,
L is a group comprising a group 15 or 16 element,
R 1 and R 2 are independently a C 1 to C 20 hydrocarbon group, a heteroatom containing group, silicon, germanium, tin, or phosphorus,
R 1 and R 2 may also be interconnected to each other,
R 3 is hydrogen, a hydrocarbyl group or a heteroatom containing group,
R 4 and R 5 are independently an aryl group, a substituted aryl group, a cyclic alkyl group, a substituted cyclic alkyl group, or multiple ring system, and
R 6 and R 7 are independently absent or hydrogen, halogen, heteroatom or a hydrocarbyl group, or a heteroatom containing group.
2 . The compound of claim 1 wherein the compound has been combined with an activator selected from the group consisting of alumoxanes, modified alumoxanes, non-coordinating anions, non-coordinating group 13 metal or metalliod anions, boranes and borates.
3 . The compound of claim 1 wherein the compound has been combined with an activator selected from the group consisting of:
trimethylammonium tetraphenylborate; triethylammonium tetraphenylborate,
tripropylammonium tetraphenylborate; tri(n-butyl)ammonium tetraphenylborate,
tri(t-butyl)ammonium tetraphenylborate; N,N-dimethylanilinium tetraphenylborate,
N,N-diethylanilinium tetraphenylborate; N,N-dimethyl-(2,4,6-trimethylanilinium) tetraphenylborate; trimethylammonium tetrakis(pentafluorophenyl)borate; triethylammonium tetrakis(pentafluorophenyl)borate; tripropylammonium tetrakis(pentafluorophenyl)borate; tri(n-butyl)ammonium tetrakis(pentafluorophenyl)borate; tri(sec-butyl)ammonium tetrakis(pentafluorophenyl) borate; N,N-dimethylanilinium tetrakis(pentafluorophenyl) borate; N,N-diethylanilinium tetrakis(pentafluorophenyl) borate; N,N-dimethyl-(2,4,6-trimethylanilinium) tetrakis(pentafluorophenyl) borate, trimethylammonium tetrakis-(2,3,4,6-tetrafluorophenylborate; triethylammonium tetrakis-(2,3,4,6-tetrafluorophenyl) borate; tripropylammonium tetrakis-(2,3,4,6-tetrafluorophenyl) borate; tri(n-butyl)ammonium tetrakis-(2,3,4,6-tetrafluoro-phenyl) borate; dimethyl(t-butyl)ammonium tetrakis-(2,3,4,6-tetrafluorophenyl) borate; N,N-dimethylanilinium tetrakis-(2,3,4,6-tetrafluorophenyl) borate; N,N-diethylanilinium tetrakis-(2,3,4,6-tetrafluoro-phenyl) borate; N,N-dimethyl-(2,4,6-trimethylanilinium)tetrakis-(2,3,4,6-tetrafluorophenyl) borate; di-(i-propyl) ammonium tetrakis(pentafluorophenyl) borate; dicyclohexylammonium tetrakis pentafluorophenyl) borate; triphenylphosphonium tetrakis(pentafluorophenyl) borate; tri(o-tolyl)phosphonium tetrakis(pentafluorophenyl) borate; tri(2,6-dimethylphenyl) phosphonium tetrakis(pentafluorophenyl) borate, or mixtures thereof.
4 . The compound of claim 2 wherein the combination further comprises a support.
5 . The compound of claim 4 wherein the support comprises one or more of silica, fumed silica, alumina, silica-alumina, magnesia, titania, zirconia, magnesium chloride, montmorillonite, phyllosilicate, zeolites, talc, clays, porous acrylic polymers, nanocomposites, aerogels, spherulites, or polymeric beads.
6 . The compound of claim 1 wherein M is a group 4, 5 or 6 transition metal.
7 . The compound of claim 1 wherein each X is independently hydrogen, a hydrocarbyl group, a heteroatom or a halogen.
8 . The compound of claim 1 wherein n is 4.
9 . The compound of claim 1 wherein L is nitrogen.
10 . The compound of claim 1 wherein J is a C 1 to C 20 alkyl, aryl or aralkyl group.
11 . The compound of claim 1 wherein Y is nitrogen.
12 . The compound of claim 1 wherein Z is nitrogen.
13 . The compound of claim 1 wherein R 4 and R 5 are independently a group represented by the following formula:
wherein
R 8 to R 12 are each independently hydrogen, a C 1 to C 40 alkyl group, a heteroatom, a heteroatom containing group containing up to 40 carbon atoms, any two R groups may form a cyclic group and/or a heterocyclic group.
14 . The compound of claim 13 wherein R 9 and R 10 are methyl groups, and R 8 , R 11 and R 12 are hydrogen.
15 . The compound of claim 11 wherein R 1 and R 2 are independently a C 1 to C 20 alkyl, aryl or aralkyl group.
16 . The compound of claim 11 wherein R 6 and R 7 are absent.Join the waitlist — get patent alerts
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