1,2,3-Triazolylidene ruthenium(ii)-cyclometalated complexes and olefin selective hydrogenation catalysisElectronic supplementary information (ESI) available. CCDC 1028679-1028683. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c4dt03156c

Silver( i ) 1,2,3-triazol-5-ylidenes [(RCH 2 C 2 N 2 (NMe)Ph) 2 Ag][AgCl 2 ] (R = Ph 3a , C 6 H 2 iPr 3 3b , C 6 H 2 Me 3 3c ) and [(PhCH 2 C 2 N 2 (NMe)R) 2 Ag][AgCl 2 ] (R = C 6 H 4 Me 3d , C 6 H 4 CF 3 3e ) were synthesized and subsequently treated with RuHCl(PPh 3 ) 3 and RuHCl(H 2 )(PCy 3 ) 2 ....

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description Silver( i ) 1,2,3-triazol-5-ylidenes [(RCH 2 C 2 N 2 (NMe)Ph) 2 Ag][AgCl 2 ] (R = Ph 3a , C 6 H 2 iPr 3 3b , C 6 H 2 Me 3 3c ) and [(PhCH 2 C 2 N 2 (NMe)R) 2 Ag][AgCl 2 ] (R = C 6 H 4 Me 3d , C 6 H 4 CF 3 3e ) were synthesized and subsequently treated with RuHCl(PPh 3 ) 3 and RuHCl(H 2 )(PCy 3 ) 2 . The reaction of 3a with RuHCl(PPh 3 ) 3 gave RuHCl(PPh 3 ) 2 (PhCH 2 C 2 N 2 (NMe)Ph) ( 4a 1 ) as the minor product and the cyclometalated complex RuCl(PPh 3 ) 2 (PhCH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 4a 2 ) as the major product. However, similar reaction with 3b selectively formed the cyclometalated complex RuCl(PPh 3 ) 2 ((C 6 H 2 iPr 3 )CH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 4b 2 ). Similarly the silver( i ) triazolylidenes 3a and 3b were reacted with RuHCl(H 2 )(PCy 3 ) 2 ; gave RuHCl(PCy 3 ) 2 (PhCH 2 C 2 N 2 (NMe)Ph) ( 5a 1 ), RuCl(PCy 3 ) 2 (PhCH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 5a 2 ) and RuCl(PCy 3 ) 2 ((C 6 H 2 iPr 3 )CH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 5b 2 ), respectively. Species 3c , 3d and 3e resulted in the cyclometalated complexes ( 5c 2 , 5d 2 and 5e 2 ) as the major products as well as the ruthenium-hydride complexes ( 5c 1 , 5d 1 and 5e 1 ) as the minor products. The cyclometalated species are derived from the ruthenium-hydride complexes via C(sp 2 )-H activation. These Ru-complexes were shown to act as hydrogenation catalyst precursors for olefinic substrates including those containing a variety of functional groups. Silver( i ) 1,2,3-triazol-5-ylidenes [(RCH 2 C 2 N 2 (NMe)Ph) 2 Ag][AgCl 2 ] (R = Ph 3a , C 6 H 2 iPr 3 3b , C 6 H 2 Me 3 3c ) and [(PhCH 2 C 2 N 2 (NMe)R) 2 Ag][AgCl 2 ] (R = C 6 H 4 Me 3d , C 6 H 4 CF 3 3e ) were synthesized and subsequently treated with RuHCl(PPh 3 ) 3 and RuHCl(H 2 )(PCy 3 ) 2 to give cyclometallated and Ru-hydride species as the major and minor products, respectively.
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CCDC 1028679-1028683. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c4dt03156c</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Bagh, Bidraha ; McKinty, Adam M ; Lough, Alan J ; Stephan, Douglas W</creator><creatorcontrib>Bagh, Bidraha ; McKinty, Adam M ; Lough, Alan J ; Stephan, Douglas W</creatorcontrib><description>Silver( i ) 1,2,3-triazol-5-ylidenes [(RCH 2 C 2 N 2 (NMe)Ph) 2 Ag][AgCl 2 ] (R = Ph 3a , C 6 H 2 iPr 3 3b , C 6 H 2 Me 3 3c ) and [(PhCH 2 C 2 N 2 (NMe)R) 2 Ag][AgCl 2 ] (R = C 6 H 4 Me 3d , C 6 H 4 CF 3 3e ) were synthesized and subsequently treated with RuHCl(PPh 3 ) 3 and RuHCl(H 2 )(PCy 3 ) 2 . The reaction of 3a with RuHCl(PPh 3 ) 3 gave RuHCl(PPh 3 ) 2 (PhCH 2 C 2 N 2 (NMe)Ph) ( 4a 1 ) as the minor product and the cyclometalated complex RuCl(PPh 3 ) 2 (PhCH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 4a 2 ) as the major product. However, similar reaction with 3b selectively formed the cyclometalated complex RuCl(PPh 3 ) 2 ((C 6 H 2 iPr 3 )CH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 4b 2 ). Similarly the silver( i ) triazolylidenes 3a and 3b were reacted with RuHCl(H 2 )(PCy 3 ) 2 ; gave RuHCl(PCy 3 ) 2 (PhCH 2 C 2 N 2 (NMe)Ph) ( 5a 1 ), RuCl(PCy 3 ) 2 (PhCH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 5a 2 ) and RuCl(PCy 3 ) 2 ((C 6 H 2 iPr 3 )CH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 5b 2 ), respectively. Species 3c , 3d and 3e resulted in the cyclometalated complexes ( 5c 2 , 5d 2 and 5e 2 ) as the major products as well as the ruthenium-hydride complexes ( 5c 1 , 5d 1 and 5e 1 ) as the minor products. The cyclometalated species are derived from the ruthenium-hydride complexes via C(sp 2 )-H activation. These Ru-complexes were shown to act as hydrogenation catalyst precursors for olefinic substrates including those containing a variety of functional groups. Silver( i ) 1,2,3-triazol-5-ylidenes [(RCH 2 C 2 N 2 (NMe)Ph) 2 Ag][AgCl 2 ] (R = Ph 3a , C 6 H 2 iPr 3 3b , C 6 H 2 Me 3 3c ) and [(PhCH 2 C 2 N 2 (NMe)R) 2 Ag][AgCl 2 ] (R = C 6 H 4 Me 3d , C 6 H 4 CF 3 3e ) were synthesized and subsequently treated with RuHCl(PPh 3 ) 3 and RuHCl(H 2 )(PCy 3 ) 2 to give cyclometallated and Ru-hydride species as the major and minor products, respectively.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/c4dt03156c</identifier><language>eng</language><creationdate>2015-01</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Bagh, Bidraha</creatorcontrib><creatorcontrib>McKinty, Adam M</creatorcontrib><creatorcontrib>Lough, Alan J</creatorcontrib><creatorcontrib>Stephan, Douglas W</creatorcontrib><title>1,2,3-Triazolylidene ruthenium(ii)-cyclometalated complexes and olefin selective hydrogenation catalysisElectronic supplementary information (ESI) available. CCDC 1028679-1028683. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c4dt03156c</title><description>Silver( i ) 1,2,3-triazol-5-ylidenes [(RCH 2 C 2 N 2 (NMe)Ph) 2 Ag][AgCl 2 ] (R = Ph 3a , C 6 H 2 iPr 3 3b , C 6 H 2 Me 3 3c ) and [(PhCH 2 C 2 N 2 (NMe)R) 2 Ag][AgCl 2 ] (R = C 6 H 4 Me 3d , C 6 H 4 CF 3 3e ) were synthesized and subsequently treated with RuHCl(PPh 3 ) 3 and RuHCl(H 2 )(PCy 3 ) 2 . The reaction of 3a with RuHCl(PPh 3 ) 3 gave RuHCl(PPh 3 ) 2 (PhCH 2 C 2 N 2 (NMe)Ph) ( 4a 1 ) as the minor product and the cyclometalated complex RuCl(PPh 3 ) 2 (PhCH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 4a 2 ) as the major product. However, similar reaction with 3b selectively formed the cyclometalated complex RuCl(PPh 3 ) 2 ((C 6 H 2 iPr 3 )CH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 4b 2 ). Similarly the silver( i ) triazolylidenes 3a and 3b were reacted with RuHCl(H 2 )(PCy 3 ) 2 ; gave RuHCl(PCy 3 ) 2 (PhCH 2 C 2 N 2 (NMe)Ph) ( 5a 1 ), RuCl(PCy 3 ) 2 (PhCH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 5a 2 ) and RuCl(PCy 3 ) 2 ((C 6 H 2 iPr 3 )CH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 5b 2 ), respectively. Species 3c , 3d and 3e resulted in the cyclometalated complexes ( 5c 2 , 5d 2 and 5e 2 ) as the major products as well as the ruthenium-hydride complexes ( 5c 1 , 5d 1 and 5e 1 ) as the minor products. The cyclometalated species are derived from the ruthenium-hydride complexes via C(sp 2 )-H activation. These Ru-complexes were shown to act as hydrogenation catalyst precursors for olefinic substrates including those containing a variety of functional groups. Silver( i ) 1,2,3-triazol-5-ylidenes [(RCH 2 C 2 N 2 (NMe)Ph) 2 Ag][AgCl 2 ] (R = Ph 3a , C 6 H 2 iPr 3 3b , C 6 H 2 Me 3 3c ) and [(PhCH 2 C 2 N 2 (NMe)R) 2 Ag][AgCl 2 ] (R = C 6 H 4 Me 3d , C 6 H 4 CF 3 3e ) were synthesized and subsequently treated with RuHCl(PPh 3 ) 3 and RuHCl(H 2 )(PCy 3 ) 2 to give cyclometallated and Ru-hydride species as the major and minor products, respectively.</description><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFUD1PwzAUDAgkSmFhR3psrdQUx-4na9qITgx0r4z90hg5dmS7FeHXYyiiAxJM96S7d3fvJclNRoYZYfN7MZKBsGw8EadJJxtNp-mcstHZz0wnF8ml96-EUErGtHPSzQZ0wNK1U_zd6lYriQbB7UKFRu3qnlL9VLRC2xoD1zygBGHrRuMbeuBGgtVYKgMeNYqg9ghVK53douFBWQOCx7XWK7_85J01SoDfNdGgRhO4a0GZ0rr6oO4tn1d94HuuNH_ROIQ8X-SQETqbTOfpF87YEArrQLjWR2ttt443VXSVMSmaQb4qIPI2XuAAj6mHlFgUYfG0eoDfL7tKzkuuPV5_Yze5LZbr_DF1Xmwap-pYd3OUs__5u7_4TSNL9gE0U4ri</recordid><startdate>20150128</startdate><enddate>20150128</enddate><creator>Bagh, Bidraha</creator><creator>McKinty, Adam M</creator><creator>Lough, Alan J</creator><creator>Stephan, Douglas W</creator><scope/></search><sort><creationdate>20150128</creationdate><title>1,2,3-Triazolylidene ruthenium(ii)-cyclometalated complexes and olefin selective hydrogenation catalysisElectronic supplementary information (ESI) available. CCDC 1028679-1028683. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c4dt03156c</title><author>Bagh, Bidraha ; McKinty, Adam M ; Lough, Alan J ; Stephan, Douglas W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c4dt03156c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bagh, Bidraha</creatorcontrib><creatorcontrib>McKinty, Adam M</creatorcontrib><creatorcontrib>Lough, Alan J</creatorcontrib><creatorcontrib>Stephan, Douglas W</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bagh, Bidraha</au><au>McKinty, Adam M</au><au>Lough, Alan J</au><au>Stephan, Douglas W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1,2,3-Triazolylidene ruthenium(ii)-cyclometalated complexes and olefin selective hydrogenation catalysisElectronic supplementary information (ESI) available. CCDC 1028679-1028683. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c4dt03156c</atitle><date>2015-01-28</date><risdate>2015</risdate><volume>44</volume><issue>6</issue><spage>2712</spage><epage>2723</epage><pages>2712-2723</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>Silver( i ) 1,2,3-triazol-5-ylidenes [(RCH 2 C 2 N 2 (NMe)Ph) 2 Ag][AgCl 2 ] (R = Ph 3a , C 6 H 2 iPr 3 3b , C 6 H 2 Me 3 3c ) and [(PhCH 2 C 2 N 2 (NMe)R) 2 Ag][AgCl 2 ] (R = C 6 H 4 Me 3d , C 6 H 4 CF 3 3e ) were synthesized and subsequently treated with RuHCl(PPh 3 ) 3 and RuHCl(H 2 )(PCy 3 ) 2 . The reaction of 3a with RuHCl(PPh 3 ) 3 gave RuHCl(PPh 3 ) 2 (PhCH 2 C 2 N 2 (NMe)Ph) ( 4a 1 ) as the minor product and the cyclometalated complex RuCl(PPh 3 ) 2 (PhCH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 4a 2 ) as the major product. However, similar reaction with 3b selectively formed the cyclometalated complex RuCl(PPh 3 ) 2 ((C 6 H 2 iPr 3 )CH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 4b 2 ). Similarly the silver( i ) triazolylidenes 3a and 3b were reacted with RuHCl(H 2 )(PCy 3 ) 2 ; gave RuHCl(PCy 3 ) 2 (PhCH 2 C 2 N 2 (NMe)Ph) ( 5a 1 ), RuCl(PCy 3 ) 2 (PhCH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 5a 2 ) and RuCl(PCy 3 ) 2 ((C 6 H 2 iPr 3 )CH 2 C 2 N 2 (NMe)C 6 H 4 ) ( 5b 2 ), respectively. Species 3c , 3d and 3e resulted in the cyclometalated complexes ( 5c 2 , 5d 2 and 5e 2 ) as the major products as well as the ruthenium-hydride complexes ( 5c 1 , 5d 1 and 5e 1 ) as the minor products. The cyclometalated species are derived from the ruthenium-hydride complexes via C(sp 2 )-H activation. These Ru-complexes were shown to act as hydrogenation catalyst precursors for olefinic substrates including those containing a variety of functional groups. Silver( i ) 1,2,3-triazol-5-ylidenes [(RCH 2 C 2 N 2 (NMe)Ph) 2 Ag][AgCl 2 ] (R = Ph 3a , C 6 H 2 iPr 3 3b , C 6 H 2 Me 3 3c ) and [(PhCH 2 C 2 N 2 (NMe)R) 2 Ag][AgCl 2 ] (R = C 6 H 4 Me 3d , C 6 H 4 CF 3 3e ) were synthesized and subsequently treated with RuHCl(PPh 3 ) 3 and RuHCl(H 2 )(PCy 3 ) 2 to give cyclometallated and Ru-hydride species as the major and minor products, respectively.</abstract><doi>10.1039/c4dt03156c</doi><tpages>12</tpages></addata></record>
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title 1,2,3-Triazolylidene ruthenium(ii)-cyclometalated complexes and olefin selective hydrogenation catalysisElectronic supplementary information (ESI) available. CCDC 1028679-1028683. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c4dt03156c
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