Halogen substituted metallocene compounds for olefin...

Organic compounds -- part of the class 532-570 series – Organic compounds – Heavy metal containing

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C502S103000, C502S152000, C502S155000, C526S160000, C526S161000, C526S165000, C526S943000

Reexamination Certificate

active

07446216

ABSTRACT:
A metallocene compound is represented by the formula (1):in-line-formulae description="In-line Formulae" end="lead"?A2YyMXn-2in-line-formulae description="In-line Formulae" end="tail"?wherein:M is a transition metal atom having a coordination number of n selected from Group 3, 4, 5 or 6 of the Periodic Table of Elements, or a lanthanide metal atom, or actinide metal atom;each A is independently a substituted polycyclic arenyl ligand pi-bonded to M, each A ligand includes at least one halogen substituent directly bonded to an sp2carbon at a bondable ring position and, when each A is a substituted indenyl ligand and y is equal to one and the ligand includes at least one chloro, bromo or iodo substituent at the 4, 5, or 6 position of the indenyl ligand, then A also includes at least one other substituent in the indenyl ligand selected from hydrocarbyl, substituted hydrocarbyl, halogen, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, substituted germylcarbyl, or other heteroatom substituents wherein the heteroatom is bonded directly to a ring carbon of the ring structure ligand and is boron, a Group 15 atom, or a Group 16 atom, preferably boron, nitrogen, oxygen, phosphorus, or sulfur;Y is an optional bridging group containing at least one Group 13, 14, 15, or 16 element and is bonded to any single position of the ring structure of A,y is zero or 1, indicating the absence (y=0) or presence (y=1) of Y; andthe or each X is a univalent anionic ligand, or two X are joined and bound to the metal atom to form a metallocycle ring, or two X are joined to form a chelating ligand, a diene ligand, or an alkylidene ligand;provided that when y is equal to 1, then A is not 5,6-dichloroindenyl or an indenyl group having a fluoro- or chloro substituent at the 7 position and a hydrocarbyl or substituted hydrocarbyl substituent at the 4 position, and provided further that when y is equal to 0, then A is not 5,6-difluoroindenyl.

REFERENCES:
patent: 3678088 (1972-07-01), Hedberg et al.
patent: 5466766 (1995-11-01), Patsidis et al.
patent: 5504232 (1996-04-01), Winter et al.
patent: 5763542 (1998-06-01), Winter et al.
patent: 5840644 (1998-11-01), Küber et al.
patent: 5936053 (1999-08-01), Fukuoka et al.
patent: 6075171 (2000-06-01), Sullivan et al.
patent: 6087292 (2000-07-01), Winter et al.
patent: 6291699 (2001-09-01), Birmingham et al.
patent: 6399723 (2002-06-01), Burkhardt et al.
patent: 6414095 (2002-07-01), Burkhardt et al.
patent: 6465700 (2002-10-01), Sullivan et al.
patent: 6492539 (2002-12-01), Bingel et al.
patent: 6737487 (2004-05-01), Meverden
patent: 7214746 (2007-05-01), Voskoboynikov et al.
patent: 7214747 (2007-05-01), Voskoboynikov et al.
patent: 7276567 (2007-10-01), Voskoboynikov et al.
patent: 2002/0193535 (2002-12-01), Meverden et al.
patent: 2004/0260107 (2004-12-01), Oberhoff et al.
patent: 2006/0160967 (2006-07-01), Voskoboynikov et al.
patent: 2006/0160968 (2006-07-01), Voskoboynikov et al.
patent: 2007/0135593 (2007-06-01), Voskoboynikov et al.
patent: 2007/0135594 (2007-06-01), Voskoboynikov et al.
patent: 2007/0135595 (2007-06-01), Voskoboynikov et al.
patent: 2007/0135596 (2007-06-01), Voskoboynikov et al.
patent: 2007/0135597 (2007-06-01), Voskoboynikov et al.
patent: 2007/0135623 (2007-06-01), Voskoboynikov et al.
patent: 0 666 267 (1995-08-01), None
patent: 0 582 195 (2000-12-01), None
patent: 1995-216011 (1995-08-01), None
patent: 11-080183 (1999-03-01), None
patent: 1999-080183 (1999-03-01), None
patent: 91/04257 (1991-04-01), None
patent: 02/092647 (2002-11-01), None
patent: 03/000744 (2003-01-01), None
MacDowell, Denis W.H., et al., “Keto-Enol Tautomerism in the Thiophene Analogues of Naphthacen-5-one,”J. Org. Chem.1982, 47, 705-709.
McEwen, Ian, et al., “Hydrogen Bonding of Hydroxy Groups to Carbanions in Indenide and Fluorenide Derivatized Alcohols Directly Observed by UV, IR, and NMR Spectroscopy,”J. Am. Chem. Soc.1993, 115, 3989-3996.
Halterman, Ronald L., et al., “Synthesis, Characterization, and Polymerization Properties of Bis(2-menthylindenyl)zirconium Dichloride and Bis(2-methyl-4,7-dimethylindenyl)zirconium Dichloride,”Organometallics2000, 19, 5464-5470.
Ryabov, Alexey N., et al., “Zirconium Complexes with Cyclopentadienyl Ligands Involving Fused a Thiophene Fragment,”Organometallics2002, 21, 2842-2855.
Zhang, Xingwang, et al., “General Synthesis of Racemic Me2Si-Bridged Bis(indenyl) Zirconocene Complexes,”J. Am. Chem. Soc.2000, 122, 8093-8094.
Johnston, Randy F., et al., “Investigation of the Electrochemical Properties of Substituted Titanocene Dichlorides,”Electrochemica Acta1995, 40, 473-477.
Conway, Brian G., et al., “Formation and Reactivity of Halogen Derivatives of η5-Cyclopentadienyl)thallium,”Organometallics1985, 4, 688-693.
Rausch, Marvin D., et al., “The Formation of Ring-Substituted Titanocene Derivatives Containing Chloro and Carbomethoxy Substituents,”J. Organometallic Chem.1988, 358, 161-168.
Finch, William C., et al., “Substituent Effects on the Cleavage Rates of Titanocene Metallocyclobutanes,”J. Am. Chem. Soc.1988, 110, 2406-2413.
Piccolrovazzi, Nicoletta, et al., “Electronic Effects in Homogenous Indenylzirconium Ziegler-Natta Catalysts,”Organometallics1990, 9, 3098-3105.
Schmid, Michael A., et al., “Unbridged Cyclopentadienyl-Fluorenyl Complexes of Zirconium as Catalysts for Homogenous Olefin Polymerization,”J. Organometallic Chem.1995, 501, 101-106.
Siedle, et al., “Synthesis of Unsymmetrical Ansa-Fluorenyl Metallocenes,”J. Mol. Catal. A. Chem.2004, 214(2), 187-198.
Linnolahti, et al., “Theoretical Study on the Factor Controlling the Accessibility of Cationic Metal Centers in Zirconocene Polymerization Catalysts,”Macromolecules2000, 33(25), 9205-9214.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Halogen substituted metallocene compounds for olefin... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Halogen substituted metallocene compounds for olefin..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Halogen substituted metallocene compounds for olefin... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-4033790

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.