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filingDate 2002-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6d02a20018ee80f17ce4810a507f84d
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publicationDate 2003-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-03045551-A1
titleOfInvention Organometallic transition metal compound, biscyclopentadienyl ligand system, catalyst system and preparation of polyolefins
abstract Organometallic transition metal compounds of the formula (I) where M1 is an element of group 3, 4, 5 or 6 of the Periodic Table of the Elements or the lanthanides; X are identical or different and are each halogen, hydrogen,C¿1?-C20-alkyl, C2-C20-alkenyl, C6-C22-aryl, alkylaryl or arylalkyl having from 1 to 10 carbon atoms in the alkyl part and from 6 to 22 carbon atoms in the aryl part, -OR?5 or -NR5R6¿, where two radicals X may also be joined to one another or two radicals X may together form a substituted or unsubstituted diene ligand, in particular a 1,3-diene ligand; where R?5 and R6¿ are each C¿1?-C10-alkyl, C6-C15-aryl, alkylaryl, arylalkyl, fluoroalkyl or fluoroaryl each having from 1 to 10 carbon atoms in the alkyl radical and from 6 to 22 carbon atoms in the aryl radical; n is a natural number from 1 to 4 which is equal to the oxidation number of M?1¿ minus 2; R1 is a C¿2?-C40 radical which is branched in the α position; R?2¿ is hydrogen or a C¿1?-C40 radical which may be branched or unbranched in the α position; R?3, R3a and R3b¿ are identical or different and are each hydrogen or a C¿1?-C40 radical, where at least one of the radicals R?3, R3a, R3b¿ is not hydrogen; R4 is a substituted or unsubstituted C¿6?-C40-aryl radical or C2-C40-heteroaromatic radical containing at least one heteroatom selected from the group consisting of O, N, S and P; T is a divalent C1-C40 group which together with the cyclopen tadienyl ring forms a further saturated or unsaturated ring system having a ring size of from 5 to 12 atoms, where T may contain the heteroatoms Si, Ge, N, P, O or S withing the ring system fused onto the cyclopentadienyl ring; and Z is a bridge consisting of a divalent atom or a divalent group, can be used in catalyst systems for preparing polyolefins by polymerization or copolymerization of at least one olefin. Biscyclopentadienyl ligand systems which have such a substitution pattern and can be used for preparing these organometallic transition metal compounds are also provided.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID91801671
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID995
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128634897
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID137329449
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21951273
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID45080817
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127473533
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID246318013
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127754314
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID245426783
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID453
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID227275485
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7044
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127791592
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID136902
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128463586
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID245957644
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128093170
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128096360
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128620786

Total number of triples: 333.