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Synthetic routes to methylpalladium(II) and dimethylpalladium(II) chemistry and the synthesis of new nitrogen donor ligand systems
Convenient and widely applicable synthetic routes to methylhalogenopalladium(II), PdXMe(L{sub 2}), and dimethylpalladium(II) complexes, PdMe{sub 2}(L{sub 2}), have been developed, including complexes of triphenylphosphine and a wide range of bidentate nitrogen donor ligands. These routes involve eit...
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Published in: | Organometallics 1990-01, Vol.9 (1), p.210-220 |
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description | Convenient and widely applicable synthetic routes to methylhalogenopalladium(II), PdXMe(L{sub 2}), and dimethylpalladium(II) complexes, PdMe{sub 2}(L{sub 2}), have been developed, including complexes of triphenylphosphine and a wide range of bidentate nitrogen donor ligands. These routes involve either the generation of Pd{sup II}Me{sub n} species at low temperature from methyllithium reagents and trans-PdCl{sub 2}(SMe{sub 2}){sub 2} followed by addition of ligand, PdIMe(2,2{prime}-bipyridyl) being synthesized through the oxidative-addition reactivity of Pd{sub 2}(dba){sub 3}(CHCl{sub 3}) or the facile synthesis of complexes with the reagents (PdIMe(SMe{sub 2})){sub 2} and (PdMe{sub 2}(pyridazine)){sub n} in organic solvents at ambient temperature. These reagents are particularly suitable for ligands sensitive to MeLi reagents, and (PdIMe(SMe{sub 2})){sub 2} is also a suitable substrate for the synthesis of chloro and bromo complexes, PdXMe(L{sub 2}), including PPh{sub 3} complexes. Several new nitrogen donor bidentate ligands are described, containing 1-methylimidazol-2-yl (mim) and pyridin-2-yl (py) groups in (mim){sub 2}C=CH{sub 2} and (py)(mim)C=CH{sub 2} as relatives of planar ligands such as 2,2{prime}-bipyridyl and mim, py, and pyrazol-1-yl (pz) groups in (py)(mim)CH{sub 2}, (py)(mim)CHMe, (mim){sub 2}CH{sub 2}, (mim){sub 2}CHMe, and (pz)(mim)CH{sub 2} as relatives of ligands such as (py){sub 2}CH{sub 2} and (pz){sub 2}CH{sub 2}. Methylpalladium(II) complexes of unsymmetrical bidentate ligands exhibit isomerism; e.g., isomers of PdIMe{l brace}(py)(mim)C=O{r brace} occur in the ratio 9:1, where the dominant isomer has the pyridine ring trans to methyl. |
doi_str_mv | 10.1021/om00115a033 |
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These routes involve either the generation of Pd{sup II}Me{sub n} species at low temperature from methyllithium reagents and trans-PdCl{sub 2}(SMe{sub 2}){sub 2} followed by addition of ligand, PdIMe(2,2{prime}-bipyridyl) being synthesized through the oxidative-addition reactivity of Pd{sub 2}(dba){sub 3}(CHCl{sub 3}) or the facile synthesis of complexes with the reagents (PdIMe(SMe{sub 2})){sub 2} and (PdMe{sub 2}(pyridazine)){sub n} in organic solvents at ambient temperature. These reagents are particularly suitable for ligands sensitive to MeLi reagents, and (PdIMe(SMe{sub 2})){sub 2} is also a suitable substrate for the synthesis of chloro and bromo complexes, PdXMe(L{sub 2}), including PPh{sub 3} complexes. Several new nitrogen donor bidentate ligands are described, containing 1-methylimidazol-2-yl (mim) and pyridin-2-yl (py) groups in (mim){sub 2}C=CH{sub 2} and (py)(mim)C=CH{sub 2} as relatives of planar ligands such as 2,2{prime}-bipyridyl and mim, py, and pyrazol-1-yl (pz) groups in (py)(mim)CH{sub 2}, (py)(mim)CHMe, (mim){sub 2}CH{sub 2}, (mim){sub 2}CHMe, and (pz)(mim)CH{sub 2} as relatives of ligands such as (py){sub 2}CH{sub 2} and (pz){sub 2}CH{sub 2}. Methylpalladium(II) complexes of unsymmetrical bidentate ligands exhibit isomerism; e.g., isomers of PdIMe{l brace}(py)(mim)C=O{r brace} occur in the ratio 9:1, where the dominant isomer has the pyridine ring trans to methyl.</description><identifier>ISSN: 0276-7333</identifier><identifier>EISSN: 1520-6041</identifier><identifier>DOI: 10.1021/om00115a033</identifier><identifier>CODEN: ORGND7</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>CATALYSIS ; Chemistry ; COMPLEXES ; DATA ; DATA ANALYSIS ; ELEMENTS ; Exact sciences and technology ; EXPERIMENTAL DATA ; INFORMATION ; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY ; LIGANDS ; MEASURING INSTRUMENTS ; MEASURING METHODS ; NITROGEN ; NONMETALS ; NUMERICAL DATA ; Organic chemistry ; ORGANIC COMPOUNDS ; ORGANOMETALLIC COMPOUNDS ; Organometalloidal and organometallic compounds ; PALLADIUM COMPLEXES ; Preparations and properties ; SYNTHESIS ; TRANSITION ELEMENT COMPLEXES 400200 -- Inorganic, Organic, & Physical Chemistry ; Transition metals derivatives</subject><ispartof>Organometallics, 1990-01, Vol.9 (1), p.210-220</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a357t-3fb3c84d0cf6d1b2bd990116d94a6ad2fbf4b44042de09cbbab34307a9175d9c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/om00115a033$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/om00115a033$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,780,784,885,4024,27064,27923,27924,27925,56766,56816</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6741304$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/6654579$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Byers, Peter K</creatorcontrib><creatorcontrib>Canty, Allan J</creatorcontrib><title>Synthetic routes to methylpalladium(II) and dimethylpalladium(II) chemistry and the synthesis of new nitrogen donor ligand systems</title><title>Organometallics</title><addtitle>Organometallics</addtitle><description>Convenient and widely applicable synthetic routes to methylhalogenopalladium(II), PdXMe(L{sub 2}), and dimethylpalladium(II) complexes, PdMe{sub 2}(L{sub 2}), have been developed, including complexes of triphenylphosphine and a wide range of bidentate nitrogen donor ligands. These routes involve either the generation of Pd{sup II}Me{sub n} species at low temperature from methyllithium reagents and trans-PdCl{sub 2}(SMe{sub 2}){sub 2} followed by addition of ligand, PdIMe(2,2{prime}-bipyridyl) being synthesized through the oxidative-addition reactivity of Pd{sub 2}(dba){sub 3}(CHCl{sub 3}) or the facile synthesis of complexes with the reagents (PdIMe(SMe{sub 2})){sub 2} and (PdMe{sub 2}(pyridazine)){sub n} in organic solvents at ambient temperature. These reagents are particularly suitable for ligands sensitive to MeLi reagents, and (PdIMe(SMe{sub 2})){sub 2} is also a suitable substrate for the synthesis of chloro and bromo complexes, PdXMe(L{sub 2}), including PPh{sub 3} complexes. Several new nitrogen donor bidentate ligands are described, containing 1-methylimidazol-2-yl (mim) and pyridin-2-yl (py) groups in (mim){sub 2}C=CH{sub 2} and (py)(mim)C=CH{sub 2} as relatives of planar ligands such as 2,2{prime}-bipyridyl and mim, py, and pyrazol-1-yl (pz) groups in (py)(mim)CH{sub 2}, (py)(mim)CHMe, (mim){sub 2}CH{sub 2}, (mim){sub 2}CHMe, and (pz)(mim)CH{sub 2} as relatives of ligands such as (py){sub 2}CH{sub 2} and (pz){sub 2}CH{sub 2}. Methylpalladium(II) complexes of unsymmetrical bidentate ligands exhibit isomerism; e.g., isomers of PdIMe{l brace}(py)(mim)C=O{r brace} occur in the ratio 9:1, where the dominant isomer has the pyridine ring trans to methyl.</description><subject>CATALYSIS</subject><subject>Chemistry</subject><subject>COMPLEXES</subject><subject>DATA</subject><subject>DATA ANALYSIS</subject><subject>ELEMENTS</subject><subject>Exact sciences and technology</subject><subject>EXPERIMENTAL DATA</subject><subject>INFORMATION</subject><subject>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</subject><subject>LIGANDS</subject><subject>MEASURING INSTRUMENTS</subject><subject>MEASURING METHODS</subject><subject>NITROGEN</subject><subject>NONMETALS</subject><subject>NUMERICAL DATA</subject><subject>Organic chemistry</subject><subject>ORGANIC COMPOUNDS</subject><subject>ORGANOMETALLIC COMPOUNDS</subject><subject>Organometalloidal and organometallic compounds</subject><subject>PALLADIUM COMPLEXES</subject><subject>Preparations and properties</subject><subject>SYNTHESIS</subject><subject>TRANSITION ELEMENT COMPLEXES 400200 -- Inorganic, Organic, & Physical Chemistry</subject><subject>Transition metals derivatives</subject><issn>0276-7333</issn><issn>1520-6041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNpt0E9LHDEYBvBQWuhWe_ILBClUKdMmk0zSOYp_2oUtFVbPIZNk3NiZZMmbxc7VT250RDx4yuH9vQ9vHoQOKPlOSU1_xJEQShtNGHuHFrSpSSUIp-_RgtRSVJIx9hF9ArglhAjJ6gW6X08hb1z2Bqe4yw5wjnh0eTMNWz0M2vrdeLRcHmMdLLb-rYnZuNFDTtOTKWEYnjLBA449Du4OB59TvHEB2xhiwoO_eaQwQXYj7KMPvR7AfX5-99D1xfnV6e9q9ffX8vRkVWnWyFyxvmPmJ7fE9MLSru5s25bPCttyLbSt-67nHeeE19aR1nSd7hhnROqWysa2hu2hwzk3QvYKjM_ObEwMwZmshGh4I9uCvs3IpAiQXK-2yY86TYoS9dixetVx0V9mvdVg9NAnHYyHlxUhOWWEF1bNrNTk_r-MdfpXCJONurpcq-bsYlWvL_8oUfzX2WsD6jbuUii9vHnAA413mbs</recordid><startdate>19900101</startdate><enddate>19900101</enddate><creator>Byers, Peter K</creator><creator>Canty, Allan J</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>19900101</creationdate><title>Synthetic routes to methylpalladium(II) and dimethylpalladium(II) chemistry and the synthesis of new nitrogen donor ligand systems</title><author>Byers, Peter K ; Canty, Allan J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a357t-3fb3c84d0cf6d1b2bd990116d94a6ad2fbf4b44042de09cbbab34307a9175d9c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>CATALYSIS</topic><topic>Chemistry</topic><topic>COMPLEXES</topic><topic>DATA</topic><topic>DATA ANALYSIS</topic><topic>ELEMENTS</topic><topic>Exact sciences and technology</topic><topic>EXPERIMENTAL DATA</topic><topic>INFORMATION</topic><topic>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</topic><topic>LIGANDS</topic><topic>MEASURING INSTRUMENTS</topic><topic>MEASURING METHODS</topic><topic>NITROGEN</topic><topic>NONMETALS</topic><topic>NUMERICAL DATA</topic><topic>Organic chemistry</topic><topic>ORGANIC COMPOUNDS</topic><topic>ORGANOMETALLIC COMPOUNDS</topic><topic>Organometalloidal and organometallic compounds</topic><topic>PALLADIUM COMPLEXES</topic><topic>Preparations and properties</topic><topic>SYNTHESIS</topic><topic>TRANSITION ELEMENT COMPLEXES 400200 -- Inorganic, Organic, & Physical Chemistry</topic><topic>Transition metals derivatives</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Byers, Peter K</creatorcontrib><creatorcontrib>Canty, Allan J</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Organometallics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Byers, Peter K</au><au>Canty, Allan J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthetic routes to methylpalladium(II) and dimethylpalladium(II) chemistry and the synthesis of new nitrogen donor ligand systems</atitle><jtitle>Organometallics</jtitle><addtitle>Organometallics</addtitle><date>1990-01-01</date><risdate>1990</risdate><volume>9</volume><issue>1</issue><spage>210</spage><epage>220</epage><pages>210-220</pages><issn>0276-7333</issn><eissn>1520-6041</eissn><coden>ORGND7</coden><abstract>Convenient and widely applicable synthetic routes to methylhalogenopalladium(II), PdXMe(L{sub 2}), and dimethylpalladium(II) complexes, PdMe{sub 2}(L{sub 2}), have been developed, including complexes of triphenylphosphine and a wide range of bidentate nitrogen donor ligands. These routes involve either the generation of Pd{sup II}Me{sub n} species at low temperature from methyllithium reagents and trans-PdCl{sub 2}(SMe{sub 2}){sub 2} followed by addition of ligand, PdIMe(2,2{prime}-bipyridyl) being synthesized through the oxidative-addition reactivity of Pd{sub 2}(dba){sub 3}(CHCl{sub 3}) or the facile synthesis of complexes with the reagents (PdIMe(SMe{sub 2})){sub 2} and (PdMe{sub 2}(pyridazine)){sub n} in organic solvents at ambient temperature. These reagents are particularly suitable for ligands sensitive to MeLi reagents, and (PdIMe(SMe{sub 2})){sub 2} is also a suitable substrate for the synthesis of chloro and bromo complexes, PdXMe(L{sub 2}), including PPh{sub 3} complexes. Several new nitrogen donor bidentate ligands are described, containing 1-methylimidazol-2-yl (mim) and pyridin-2-yl (py) groups in (mim){sub 2}C=CH{sub 2} and (py)(mim)C=CH{sub 2} as relatives of planar ligands such as 2,2{prime}-bipyridyl and mim, py, and pyrazol-1-yl (pz) groups in (py)(mim)CH{sub 2}, (py)(mim)CHMe, (mim){sub 2}CH{sub 2}, (mim){sub 2}CHMe, and (pz)(mim)CH{sub 2} as relatives of ligands such as (py){sub 2}CH{sub 2} and (pz){sub 2}CH{sub 2}. Methylpalladium(II) complexes of unsymmetrical bidentate ligands exhibit isomerism; e.g., isomers of PdIMe{l brace}(py)(mim)C=O{r brace} occur in the ratio 9:1, where the dominant isomer has the pyridine ring trans to methyl.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/om00115a033</doi><tpages>11</tpages></addata></record> |
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subjects | CATALYSIS Chemistry COMPLEXES DATA DATA ANALYSIS ELEMENTS Exact sciences and technology EXPERIMENTAL DATA INFORMATION INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY LIGANDS MEASURING INSTRUMENTS MEASURING METHODS NITROGEN NONMETALS NUMERICAL DATA Organic chemistry ORGANIC COMPOUNDS ORGANOMETALLIC COMPOUNDS Organometalloidal and organometallic compounds PALLADIUM COMPLEXES Preparations and properties SYNTHESIS TRANSITION ELEMENT COMPLEXES 400200 -- Inorganic, Organic, & Physical Chemistry Transition metals derivatives |
title | Synthetic routes to methylpalladium(II) and dimethylpalladium(II) chemistry and the synthesis of new nitrogen donor ligand systems |
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