PROCESS FOR PREPARING LOW MOLECULAR WEIGHT OLEFIN POLYMERS, ORGANOMETALLIC TRANSITION METAL COMPOUNDS BISCYCLOPENTADIENYL LIGAND SYSTEMS AND CATALYST SYSTEMS
Preparation of olefin polymers with a molecular mass of 500-50,000 g/mol comprises polymerization or copolymerization of at least an olefin (A) (in solution, in suspension or in the gas phase) at -60 to 200[deg]C and 0.5-100 bar, in the presence of hydrogen and a catalyst system containing at least...
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description | Preparation of olefin polymers with a molecular mass of 500-50,000 g/mol comprises polymerization or copolymerization of at least an olefin (A) (in solution, in suspension or in the gas phase) at -60 to 200[deg]C and 0.5-100 bar, in the presence of hydrogen and a catalyst system containing at least an organo-transition metal component (I) and at least a co-catalyst system. Preparation of olefin polymers with a molecular mass of 500-50,000 g/mol comprises polymerization or copolymerization of at least an olefin (A) (in solution, in suspension or in the gas phase) of formula (Ra-CH=CH-Rb) at -60 to 200[deg]C and 0.5-100 bar, in the presence of hydrogen and a catalyst system containing at least an organo transition metallic component of formula (I) and at least a co-catalyst system. M1>elements of 3-6 groups of the periodic table of elements or lanthanide; X : organic or inorganic residue (where two of X forms a double bond residue); n : 1-4; R1>, R4>H, 1-40C organic residue (unbranched in alpha -position) or 1-40C organic residue (hybridized over sp2>-carbon); R2>, R3>1-40C organic residue; either R5>-R8>H, halo or R2>; or two of the groups R5>-R8>1-40C mono- or polycyclic ring system optionally substituted with heteroatoms of Si, Ge, N, P, O, S, Se or Te; Z : bridge between double bonded atom or a double bonded group; and either Ra, Rb : H or 1-20C hydrocarbon; and/or Ra, Rb+atoms : ring. Independent claims are also included for: (1) organo-transition metal component (I); (2) a biscyclopentadienyl ligand system of formula (II) or its double bonded isomers; (3) a catalyst system comprising at least one organo-transition metal (4) component and at least a co-catalyst system; and (5) use of biscyclopentadienyl ligand system for the manufacture of the organo-transition metal component. [Image] [Image]. |
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Preparation of olefin polymers with a molecular mass of 500-50,000 g/mol comprises polymerization or copolymerization of at least an olefin (A) (in solution, in suspension or in the gas phase) of formula (Ra-CH=CH-Rb) at -60 to 200[deg]C and 0.5-100 bar, in the presence of hydrogen and a catalyst system containing at least an organo transition metallic component of formula (I) and at least a co-catalyst system. M1>elements of 3-6 groups of the periodic table of elements or lanthanide; X : organic or inorganic residue (where two of X forms a double bond residue); n : 1-4; R1>, R4>H, 1-40C organic residue (unbranched in alpha -position) or 1-40C organic residue (hybridized over sp2>-carbon); R2>, R3>1-40C organic residue; either R5>-R8>H, halo or R2>; or two of the groups R5>-R8>1-40C mono- or polycyclic ring system optionally substituted with heteroatoms of Si, Ge, N, P, O, S, Se or Te; Z : bridge between double bonded atom or a double bonded group; and either Ra, Rb : H or 1-20C hydrocarbon; and/or Ra, Rb+atoms : ring. Independent claims are also included for: (1) organo-transition metal component (I); (2) a biscyclopentadienyl ligand system of formula (II) or its double bonded isomers; (3) a catalyst system comprising at least one organo-transition metal (4) component and at least a co-catalyst system; and (5) use of biscyclopentadienyl ligand system for the manufacture of the organo-transition metal component. [Image] [Image].</description><language>eng ; fre ; ger</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; COMPOSITIONS BASED THEREON ; HETEROCYCLIC COMPOUNDS ; MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS ; METALLURGY ; ORGANIC CHEMISTRY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><creationdate>2007</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20071031&DB=EPODOC&CC=EP&NR=1848748A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20071031&DB=EPODOC&CC=EP&NR=1848748A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>ELDER, MICHAEL J</creatorcontrib><title>PROCESS FOR PREPARING LOW MOLECULAR WEIGHT OLEFIN POLYMERS, ORGANOMETALLIC TRANSITION METAL COMPOUNDS BISCYCLOPENTADIENYL LIGAND SYSTEMS AND CATALYST SYSTEMS</title><description>Preparation of olefin polymers with a molecular mass of 500-50,000 g/mol comprises polymerization or copolymerization of at least an olefin (A) (in solution, in suspension or in the gas phase) at -60 to 200[deg]C and 0.5-100 bar, in the presence of hydrogen and a catalyst system containing at least an organo-transition metal component (I) and at least a co-catalyst system. Preparation of olefin polymers with a molecular mass of 500-50,000 g/mol comprises polymerization or copolymerization of at least an olefin (A) (in solution, in suspension or in the gas phase) of formula (Ra-CH=CH-Rb) at -60 to 200[deg]C and 0.5-100 bar, in the presence of hydrogen and a catalyst system containing at least an organo transition metallic component of formula (I) and at least a co-catalyst system. M1>elements of 3-6 groups of the periodic table of elements or lanthanide; X : organic or inorganic residue (where two of X forms a double bond residue); n : 1-4; R1>, R4>H, 1-40C organic residue (unbranched in alpha -position) or 1-40C organic residue (hybridized over sp2>-carbon); R2>, R3>1-40C organic residue; either R5>-R8>H, halo or R2>; or two of the groups R5>-R8>1-40C mono- or polycyclic ring system optionally substituted with heteroatoms of Si, Ge, N, P, O, S, Se or Te; Z : bridge between double bonded atom or a double bonded group; and either Ra, Rb : H or 1-20C hydrocarbon; and/or Ra, Rb+atoms : ring. Independent claims are also included for: (1) organo-transition metal component (I); (2) a biscyclopentadienyl ligand system of formula (II) or its double bonded isomers; (3) a catalyst system comprising at least one organo-transition metal (4) component and at least a co-catalyst system; and (5) use of biscyclopentadienyl ligand system for the manufacture of the organo-transition metal component. [Image] [Image].</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2007</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNizEKwkAQRdNYiHqHOYAWQcG062YSB2Z3lp0VSSUiayUa0Ot4V6Nob_X_f_w3Lp4hikVVaCRCiBhMJN8Cyx6cMNodmwh7pHabYNgNeQjCncOoc5DYGi8Ok2EmCykar5RIPHwYWHFBdr5W2JDazrIE9MnUhL5jYBrsGrTThE7h3a0ZtGH_4LQYnY-Xe559c1JAg8luF7m_HfK9P57yNT8OGMpqVa1XlSmXf1xe3QxE_w</recordid><startdate>20071031</startdate><enddate>20071031</enddate><creator>ELDER, MICHAEL J</creator><scope>EVB</scope></search><sort><creationdate>20071031</creationdate><title>PROCESS FOR PREPARING LOW MOLECULAR WEIGHT OLEFIN POLYMERS, ORGANOMETALLIC TRANSITION METAL COMPOUNDS BISCYCLOPENTADIENYL LIGAND SYSTEMS AND CATALYST SYSTEMS</title><author>ELDER, MICHAEL J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_EP1848748A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre ; ger</language><creationdate>2007</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><toplevel>online_resources</toplevel><creatorcontrib>ELDER, MICHAEL J</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>ELDER, MICHAEL J</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PROCESS FOR PREPARING LOW MOLECULAR WEIGHT OLEFIN POLYMERS, ORGANOMETALLIC TRANSITION METAL COMPOUNDS BISCYCLOPENTADIENYL LIGAND SYSTEMS AND CATALYST SYSTEMS</title><date>2007-10-31</date><risdate>2007</risdate><abstract>Preparation of olefin polymers with a molecular mass of 500-50,000 g/mol comprises polymerization or copolymerization of at least an olefin (A) (in solution, in suspension or in the gas phase) at -60 to 200[deg]C and 0.5-100 bar, in the presence of hydrogen and a catalyst system containing at least an organo-transition metal component (I) and at least a co-catalyst system. Preparation of olefin polymers with a molecular mass of 500-50,000 g/mol comprises polymerization or copolymerization of at least an olefin (A) (in solution, in suspension or in the gas phase) of formula (Ra-CH=CH-Rb) at -60 to 200[deg]C and 0.5-100 bar, in the presence of hydrogen and a catalyst system containing at least an organo transition metallic component of formula (I) and at least a co-catalyst system. M1>elements of 3-6 groups of the periodic table of elements or lanthanide; X : organic or inorganic residue (where two of X forms a double bond residue); n : 1-4; R1>, R4>H, 1-40C organic residue (unbranched in alpha -position) or 1-40C organic residue (hybridized over sp2>-carbon); R2>, R3>1-40C organic residue; either R5>-R8>H, halo or R2>; or two of the groups R5>-R8>1-40C mono- or polycyclic ring system optionally substituted with heteroatoms of Si, Ge, N, P, O, S, Se or Te; Z : bridge between double bonded atom or a double bonded group; and either Ra, Rb : H or 1-20C hydrocarbon; and/or Ra, Rb+atoms : ring. Independent claims are also included for: (1) organo-transition metal component (I); (2) a biscyclopentadienyl ligand system of formula (II) or its double bonded isomers; (3) a catalyst system comprising at least one organo-transition metal (4) component and at least a co-catalyst system; and (5) use of biscyclopentadienyl ligand system for the manufacture of the organo-transition metal component. [Image] [Image].</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMISTRY COMPOSITIONS BASED THEREON HETEROCYCLIC COMPOUNDS MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS METALLURGY ORGANIC CHEMISTRY ORGANIC MACROMOLECULAR COMPOUNDS THEIR PREPARATION OR CHEMICAL WORKING-UP |
title | PROCESS FOR PREPARING LOW MOLECULAR WEIGHT OLEFIN POLYMERS, ORGANOMETALLIC TRANSITION METAL COMPOUNDS BISCYCLOPENTADIENYL LIGAND SYSTEMS AND CATALYST SYSTEMS |
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