IMIDO TRANSITION METAL COMPLEX METATHESIS CATALYSTS
An olefin metathesis catalyst system and process for the metathesis polymerization of cyclic olefins, such as dicyclopendatiene, an disclosed. The catalyst system comprises the reaction product of: (a) an imido transition metal halide complex of formula (I) wherein Ar is C6-20 aryl, preferably pheny...
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description | An olefin metathesis catalyst system and process for the metathesis polymerization of cyclic olefins, such as dicyclopendatiene, an disclosed. The catalyst system comprises the reaction product of: (a) an imido transition metal halide complex of formula (I) wherein Ar is C6-20 aryl, preferably phenyl; M is a transition metal selected from the second and third rows of groups 5, 6, 7 and 8 of the Periodic Table and including for example niobium, tantalum, molybdenum, tungsten rhenium, ruthenium or osmium, preferably tungsten or molybdenum; R is independently halide, C1-20 alkyl, C1-12 alkoxy, C1-12 haloalkyl, C6-20 aryl, C6-20 aryloxy, cyano or combinations thereof; L is independently a complexing ligand selected from carbonyl, C1-12 alkoxy, C1-12 haloalkoxy C1-12 alkyl ethers, including C1-12 alkylnitriles, C5-20 pyridines, C3-36 tri(hydrocarbyl)phosphines, X is independently halide, x is 2 to 4; r is independently 0 to 5; 7 is 0 to 3, preferably 0 or 1; and x + y = 3, 4 or 5; and (b) a biphenol of formula (II) in which each Ar represents an aromatic ring-containing moiety having at least one hydroxyl group attached to an aromatic ring; each R is independently selected from C1 - 12 alkyl, aryl, halide, mono-, di or trihalo methyl, cyano and alkoxy or together form an alkylene; each n is independently 0-4; and m is independently 1-4; and the catalyst system further includes a co-catalyst. |
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The catalyst system comprises the reaction product of: (a) an imido transition metal halide complex of formula (I) wherein Ar is C6-20 aryl, preferably phenyl; M is a transition metal selected from the second and third rows of groups 5, 6, 7 and 8 of the Periodic Table and including for example niobium, tantalum, molybdenum, tungsten rhenium, ruthenium or osmium, preferably tungsten or molybdenum; R is independently halide, C1-20 alkyl, C1-12 alkoxy, C1-12 haloalkyl, C6-20 aryl, C6-20 aryloxy, cyano or combinations thereof; L is independently a complexing ligand selected from carbonyl, C1-12 alkoxy, C1-12 haloalkoxy C1-12 alkyl ethers, including C1-12 alkylnitriles, C5-20 pyridines, C3-36 tri(hydrocarbyl)phosphines, X is independently halide, x is 2 to 4; r is independently 0 to 5; 7 is 0 to 3, preferably 0 or 1; and x + y = 3, 4 or 5; and (b) a biphenol of formula (II) in which each Ar represents an aromatic ring-containing moiety having at least one hydroxyl group attached to an aromatic ring; each R is independently selected from C1 - 12 alkyl, aryl, halide, mono-, di or trihalo methyl, cyano and alkoxy or together form an alkylene; each n is independently 0-4; and m is independently 1-4; and the catalyst system further includes a co-catalyst.</description><edition>6</edition><language>eng ; fre</language><subject>CHEMISTRY ; COMPOSITIONS BASED THEREON ; MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS ; MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS ; METALLURGY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><creationdate>2005</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=20050118&DB=EPODOC&CC=CA&NR=2167722C$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20050118&DB=EPODOC&CC=CA&NR=2167722C$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KELSEY, DONALD ROSS</creatorcontrib><title>IMIDO TRANSITION METAL COMPLEX METATHESIS CATALYSTS</title><description>An olefin metathesis catalyst system and process for the metathesis polymerization of cyclic olefins, such as dicyclopendatiene, an disclosed. The catalyst system comprises the reaction product of: (a) an imido transition metal halide complex of formula (I) wherein Ar is C6-20 aryl, preferably phenyl; M is a transition metal selected from the second and third rows of groups 5, 6, 7 and 8 of the Periodic Table and including for example niobium, tantalum, molybdenum, tungsten rhenium, ruthenium or osmium, preferably tungsten or molybdenum; R is independently halide, C1-20 alkyl, C1-12 alkoxy, C1-12 haloalkyl, C6-20 aryl, C6-20 aryloxy, cyano or combinations thereof; L is independently a complexing ligand selected from carbonyl, C1-12 alkoxy, C1-12 haloalkoxy C1-12 alkyl ethers, including C1-12 alkylnitriles, C5-20 pyridines, C3-36 tri(hydrocarbyl)phosphines, X is independently halide, x is 2 to 4; r is independently 0 to 5; 7 is 0 to 3, preferably 0 or 1; and x + y = 3, 4 or 5; and (b) a biphenol of formula (II) in which each Ar represents an aromatic ring-containing moiety having at least one hydroxyl group attached to an aromatic ring; each R is independently selected from C1 - 12 alkyl, aryl, halide, mono-, di or trihalo methyl, cyano and alkoxy or together form an alkylene; each n is independently 0-4; and m is independently 1-4; and the catalyst system further includes a co-catalyst.</description><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</subject><subject>METALLURGY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2005</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDD29PV08VcICXL0C_YM8fT3U_B1DXH0UXD29w3wcY0A80I8XIM9gxWcHYESkcEhwTwMrGmJOcWpvFCam0HezTXE2UM3tSA_PrW4IDE5NS-1JN7Z0cjQzNzcyMjZmLAKACr3Jo0</recordid><startdate>20050118</startdate><enddate>20050118</enddate><creator>KELSEY, DONALD ROSS</creator><scope>EVB</scope></search><sort><creationdate>20050118</creationdate><title>IMIDO TRANSITION METAL COMPLEX METATHESIS CATALYSTS</title><author>KELSEY, DONALD ROSS</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CA2167722C3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre</language><creationdate>2005</creationdate><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</topic><topic>METALLURGY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><toplevel>online_resources</toplevel><creatorcontrib>KELSEY, DONALD ROSS</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KELSEY, DONALD ROSS</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>IMIDO TRANSITION METAL COMPLEX METATHESIS CATALYSTS</title><date>2005-01-18</date><risdate>2005</risdate><abstract>An olefin metathesis catalyst system and process for the metathesis polymerization of cyclic olefins, such as dicyclopendatiene, an disclosed. The catalyst system comprises the reaction product of: (a) an imido transition metal halide complex of formula (I) wherein Ar is C6-20 aryl, preferably phenyl; M is a transition metal selected from the second and third rows of groups 5, 6, 7 and 8 of the Periodic Table and including for example niobium, tantalum, molybdenum, tungsten rhenium, ruthenium or osmium, preferably tungsten or molybdenum; R is independently halide, C1-20 alkyl, C1-12 alkoxy, C1-12 haloalkyl, C6-20 aryl, C6-20 aryloxy, cyano or combinations thereof; L is independently a complexing ligand selected from carbonyl, C1-12 alkoxy, C1-12 haloalkoxy C1-12 alkyl ethers, including C1-12 alkylnitriles, C5-20 pyridines, C3-36 tri(hydrocarbyl)phosphines, X is independently halide, x is 2 to 4; r is independently 0 to 5; 7 is 0 to 3, preferably 0 or 1; and x + y = 3, 4 or 5; and (b) a biphenol of formula (II) in which each Ar represents an aromatic ring-containing moiety having at least one hydroxyl group attached to an aromatic ring; each R is independently selected from C1 - 12 alkyl, aryl, halide, mono-, di or trihalo methyl, cyano and alkoxy or together form an alkylene; each n is independently 0-4; and m is independently 1-4; and the catalyst system further includes a co-catalyst.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY COMPOSITIONS BASED THEREON MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS METALLURGY ORGANIC MACROMOLECULAR COMPOUNDS THEIR PREPARATION OR CHEMICAL WORKING-UP |
title | IMIDO TRANSITION METAL COMPLEX METATHESIS CATALYSTS |
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