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Interactions of Rh(III)−Dihydrido−Bis(phosphine) Complexes with Semicarbazones
Interaction of cis,trans,cis-[Rh(H)2(PR3)2(acetone)2]PF6 complexes (R = aryl or R3 = Ph2Me, Ph2Et) under H2 with E-semicarbazones gives the Rh(III)−dihydrido−bis(phosphine)−semicarbazone species cis,trans-[Rh(H)2(PR3)2{R‘(R‘ ‘)CNN(H)CONH2}]PF6, where R‘ and R‘ ‘ are Ph, Et, or Me. The complexes ar...
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Published in: | Inorganic chemistry 2005-03, Vol.44 (5), p.1482-1491 |
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container_title | Inorganic chemistry |
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creator | Ezhova, Maria B. Patrick, Brian O. Sereviratne, Kapila N. James, Brian R. Waller, Francis J. Ford, Michael E. |
description | Interaction of cis,trans,cis-[Rh(H)2(PR3)2(acetone)2]PF6 complexes (R = aryl or R3 = Ph2Me, Ph2Et) under H2 with E-semicarbazones gives the Rh(III)−dihydrido−bis(phosphine)−semicarbazone species cis,trans-[Rh(H)2(PR3)2{R‘(R‘ ‘)CNN(H)CONH2}]PF6, where R‘ and R‘ ‘ are Ph, Et, or Me. The complexes are generally characterized by elemental analysis, 31P{1H} NMR, 1H NMR, and IR spectroscopies, and MS. X-ray analysis of three PPh3 complexes reveals chelation of E-semicarbazones by the imine-N atom and the carbonyl-O atom. In contrast, the corresponding reaction of [Rh(H)2(PPhMe2)2(acetone)2]PF6 with acetophenone semicarbazone gives the ortho-metalated-semicarbazone species cis-[RhH(PPhMe2)2{o-C6H4(Me)CN−N(H)CONH2}]PF6. The X-ray structure of E-propiophenone semicarbazone is also reported. Rhodium-catalyzed, homogeneous hydrogenation of semicarbazones was not observed even at 40 atm H2. |
doi_str_mv | 10.1021/ic0489185 |
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The complexes are generally characterized by elemental analysis, 31P{1H} NMR, 1H NMR, and IR spectroscopies, and MS. X-ray analysis of three PPh3 complexes reveals chelation of E-semicarbazones by the imine-N atom and the carbonyl-O atom. In contrast, the corresponding reaction of [Rh(H)2(PPhMe2)2(acetone)2]PF6 with acetophenone semicarbazone gives the ortho-metalated-semicarbazone species cis-[RhH(PPhMe2)2{o-C6H4(Me)CN−N(H)CONH2}]PF6. The X-ray structure of E-propiophenone semicarbazone is also reported. Rhodium-catalyzed, homogeneous hydrogenation of semicarbazones was not observed even at 40 atm H2.</description><identifier>ISSN: 0020-1669</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/ic0489185</identifier><identifier>PMID: 15732990</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Inorganic chemistry, 2005-03, Vol.44 (5), p.1482-1491</ispartof><rights>Copyright © 2005 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a313t-f708b56917d259a6b5375d50b950fc4adbc8aa9b3ac2cdb6bcc07ba92836c7843</citedby><cites>FETCH-LOGICAL-a313t-f708b56917d259a6b5375d50b950fc4adbc8aa9b3ac2cdb6bcc07ba92836c7843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15732990$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ezhova, Maria B.</creatorcontrib><creatorcontrib>Patrick, Brian O.</creatorcontrib><creatorcontrib>Sereviratne, Kapila N.</creatorcontrib><creatorcontrib>James, Brian R.</creatorcontrib><creatorcontrib>Waller, Francis J.</creatorcontrib><creatorcontrib>Ford, Michael E.</creatorcontrib><title>Interactions of Rh(III)−Dihydrido−Bis(phosphine) Complexes with Semicarbazones</title><title>Inorganic chemistry</title><addtitle>Inorg. Chem</addtitle><description>Interaction of cis,trans,cis-[Rh(H)2(PR3)2(acetone)2]PF6 complexes (R = aryl or R3 = Ph2Me, Ph2Et) under H2 with E-semicarbazones gives the Rh(III)−dihydrido−bis(phosphine)−semicarbazone species cis,trans-[Rh(H)2(PR3)2{R‘(R‘ ‘)CNN(H)CONH2}]PF6, where R‘ and R‘ ‘ are Ph, Et, or Me. The complexes are generally characterized by elemental analysis, 31P{1H} NMR, 1H NMR, and IR spectroscopies, and MS. X-ray analysis of three PPh3 complexes reveals chelation of E-semicarbazones by the imine-N atom and the carbonyl-O atom. In contrast, the corresponding reaction of [Rh(H)2(PPhMe2)2(acetone)2]PF6 with acetophenone semicarbazone gives the ortho-metalated-semicarbazone species cis-[RhH(PPhMe2)2{o-C6H4(Me)CN−N(H)CONH2}]PF6. The X-ray structure of E-propiophenone semicarbazone is also reported. 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Chem</addtitle><date>2005-03-07</date><risdate>2005</risdate><volume>44</volume><issue>5</issue><spage>1482</spage><epage>1491</epage><pages>1482-1491</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>Interaction of cis,trans,cis-[Rh(H)2(PR3)2(acetone)2]PF6 complexes (R = aryl or R3 = Ph2Me, Ph2Et) under H2 with E-semicarbazones gives the Rh(III)−dihydrido−bis(phosphine)−semicarbazone species cis,trans-[Rh(H)2(PR3)2{R‘(R‘ ‘)CNN(H)CONH2}]PF6, where R‘ and R‘ ‘ are Ph, Et, or Me. The complexes are generally characterized by elemental analysis, 31P{1H} NMR, 1H NMR, and IR spectroscopies, and MS. X-ray analysis of three PPh3 complexes reveals chelation of E-semicarbazones by the imine-N atom and the carbonyl-O atom. In contrast, the corresponding reaction of [Rh(H)2(PPhMe2)2(acetone)2]PF6 with acetophenone semicarbazone gives the ortho-metalated-semicarbazone species cis-[RhH(PPhMe2)2{o-C6H4(Me)CN−N(H)CONH2}]PF6. The X-ray structure of E-propiophenone semicarbazone is also reported. Rhodium-catalyzed, homogeneous hydrogenation of semicarbazones was not observed even at 40 atm H2.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>15732990</pmid><doi>10.1021/ic0489185</doi><tpages>10</tpages></addata></record> |
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title | Interactions of Rh(III)−Dihydrido−Bis(phosphine) Complexes with Semicarbazones |
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