http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7473813-B2

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filingDate 2006-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c4fd5be864d70e61bcd08271f22dab7e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_caafc411cf79d290ae507bffdec904f1
publicationDate 2009-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7473813-B2
titleOfInvention Process for the preparation of substituted fluorenes
abstract Methods for the preparation of fluorenyl-type ligand structures and substituted fluorenyl groups which may be employed in metallocene-type olefin polymerization catalysts. There is provided a 2,2′-dihalogen-diphenylmethylene having a methylene bridge connecting a pair of phenyl groups. Each phenyl group has a halogen on a proximal carbon atom relative to the methylene bridge. The halogenated diphenylmethylene is reacted with a coupling agent comprising a Group 2 or 12 transition metal in the presence of a nickel or palladium-based catalyst to remove the halogen atoms from the phenyl groups and couple the phenyl groups at the proximal carbon atoms to produce a fluorene ligand structure. The coupling agent may be zinc, cadmium or magnesium and the catalyst may be a monophosphene nickel complex. The halogenated diphenylmethylene may be an unsubstituted ligand structure or a monosubstituted or disubstituted ligand structure. The halogenated diphenylmethylene may be monosubstituted with a tertiary butyl group or may be a dialkyl diphenylmethylene having alkyl substituents at the directly distal positions of the phenyl groups relative to the methylene bridge.
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID245007822
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID137296887
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID162230198
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID137296886
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID139260712
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426105894
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID139260711
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454904100
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450233954
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID139260710
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID248036984
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6853
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419531804
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15604
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID139260705
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457959620
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID139260704
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457959619
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID241
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457959361
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6451240
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457959347
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID158366952
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457959346
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID247467751
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426483572
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID139260718
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457959729
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID81219
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452950996
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129709093
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID243727294
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23968
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454904843
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID248726334
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457959710
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID243161048
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID935

Total number of triples: 361.