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Heterometallic Borole Complexes of Iron and Gold
The first heterometallic borole complexes of Fe and Au have been prepared by reaction of [HFe{η5-(1-phenylborole)}(CO)2]- (1) with [AuCl(PPh3)] in CH2Cl2, and the crystal structure of [(OC)2{η5-(1-phenylborole)}Fe{Au(PPh3)}2] (2) reveals an interesting orientation of the borole ligand. This complex...
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Published in: | Organometallics 1998-05, Vol.17 (11), p.2177-2182 |
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container_issue | 11 |
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container_title | Organometallics |
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creator | Braunstein, Pierre Herberich, Gerhard E. Neuschütz, Mark Schmidt, Martin U. Englert, Ulli Lecante, Pierre Mosset, Alain |
description | The first heterometallic borole complexes of Fe and Au have been prepared by reaction of [HFe{η5-(1-phenylborole)}(CO)2]- (1) with [AuCl(PPh3)] in CH2Cl2, and the crystal structure of [(OC)2{η5-(1-phenylborole)}Fe{Au(PPh3)}2] (2) reveals an interesting orientation of the borole ligand. This complex reacts with [AuCl(PPh3)]/TIPF6 in CH2Cl2 to give the new cationic FeAu3 cluster [(OC)2{η5-(1-phenylborole)}Fe{Au(PPh3)}3]PF6 (4) which has a tetrahedral metal core, as established by a wide angle X-ray scattering study. |
doi_str_mv | 10.1021/om9703189 |
format | article |
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This complex reacts with [AuCl(PPh3)]/TIPF6 in CH2Cl2 to give the new cationic FeAu3 cluster [(OC)2{η5-(1-phenylborole)}Fe{Au(PPh3)}3]PF6 (4) which has a tetrahedral metal core, as established by a wide angle X-ray scattering study.</description><identifier>ISSN: 0276-7333</identifier><identifier>EISSN: 1520-6041</identifier><identifier>DOI: 10.1021/om9703189</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Organometallics, 1998-05, Vol.17 (11), p.2177-2182</ispartof><rights>Copyright © 1998 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a361t-9e7e0bd968b94b1100c3478628d0c22cf498afe1a2a3308521de3d9f37271063</citedby><cites>FETCH-LOGICAL-a361t-9e7e0bd968b94b1100c3478628d0c22cf498afe1a2a3308521de3d9f37271063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Braunstein, Pierre</creatorcontrib><creatorcontrib>Herberich, Gerhard E.</creatorcontrib><creatorcontrib>Neuschütz, Mark</creatorcontrib><creatorcontrib>Schmidt, Martin U.</creatorcontrib><creatorcontrib>Englert, Ulli</creatorcontrib><creatorcontrib>Lecante, Pierre</creatorcontrib><creatorcontrib>Mosset, Alain</creatorcontrib><title>Heterometallic Borole Complexes of Iron and Gold</title><title>Organometallics</title><addtitle>Organometallics</addtitle><description>The first heterometallic borole complexes of Fe and Au have been prepared by reaction of [HFe{η5-(1-phenylborole)}(CO)2]- (1) with [AuCl(PPh3)] in CH2Cl2, and the crystal structure of [(OC)2{η5-(1-phenylborole)}Fe{Au(PPh3)}2] (2) reveals an interesting orientation of the borole ligand. This complex reacts with [AuCl(PPh3)]/TIPF6 in CH2Cl2 to give the new cationic FeAu3 cluster [(OC)2{η5-(1-phenylborole)}Fe{Au(PPh3)}3]PF6 (4) which has a tetrahedral metal core, as established by a wide angle X-ray scattering study.</description><issn>0276-7333</issn><issn>1520-6041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNptz01Lw0AUheFBFKzVhf8gGxcuovfOTWYySy32AwoKBrfDNLmB1KRTZiLUf2-k0pWrs3k48Apxi_CAIPHR90YDYWHOxARzCamCDM_FBKRWqSaiS3EV4xYAlCY5EbDkgYPveXBd11bJsw--42Tm-33HB46Jb5JV8LvE7epk4bv6Wlw0rot887dTUc5fytkyXb8uVrOndepI4ZAa1gyb2qhiY7INIkBFmS6ULGqopKyazBSuYXTSEUGRS6yZatOQlhpB0VTcH2-r4GMM3Nh9aHsXvi2C_S21p9LRpkfbxoEPJ-jCpx0jdW7Lt3dLH_PSoAGrR3939K6Kduu_wm4M-ef3B3-8Xqo</recordid><startdate>19980525</startdate><enddate>19980525</enddate><creator>Braunstein, Pierre</creator><creator>Herberich, Gerhard E.</creator><creator>Neuschütz, Mark</creator><creator>Schmidt, Martin U.</creator><creator>Englert, Ulli</creator><creator>Lecante, Pierre</creator><creator>Mosset, Alain</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19980525</creationdate><title>Heterometallic Borole Complexes of Iron and Gold</title><author>Braunstein, Pierre ; Herberich, Gerhard E. ; Neuschütz, Mark ; Schmidt, Martin U. ; Englert, Ulli ; Lecante, Pierre ; Mosset, Alain</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a361t-9e7e0bd968b94b1100c3478628d0c22cf498afe1a2a3308521de3d9f37271063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Braunstein, Pierre</creatorcontrib><creatorcontrib>Herberich, Gerhard E.</creatorcontrib><creatorcontrib>Neuschütz, Mark</creatorcontrib><creatorcontrib>Schmidt, Martin U.</creatorcontrib><creatorcontrib>Englert, Ulli</creatorcontrib><creatorcontrib>Lecante, Pierre</creatorcontrib><creatorcontrib>Mosset, Alain</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Organometallics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Braunstein, Pierre</au><au>Herberich, Gerhard E.</au><au>Neuschütz, Mark</au><au>Schmidt, Martin U.</au><au>Englert, Ulli</au><au>Lecante, Pierre</au><au>Mosset, Alain</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterometallic Borole Complexes of Iron and Gold</atitle><jtitle>Organometallics</jtitle><addtitle>Organometallics</addtitle><date>1998-05-25</date><risdate>1998</risdate><volume>17</volume><issue>11</issue><spage>2177</spage><epage>2182</epage><pages>2177-2182</pages><issn>0276-7333</issn><eissn>1520-6041</eissn><abstract>The first heterometallic borole complexes of Fe and Au have been prepared by reaction of [HFe{η5-(1-phenylborole)}(CO)2]- (1) with [AuCl(PPh3)] in CH2Cl2, and the crystal structure of [(OC)2{η5-(1-phenylborole)}Fe{Au(PPh3)}2] (2) reveals an interesting orientation of the borole ligand. This complex reacts with [AuCl(PPh3)]/TIPF6 in CH2Cl2 to give the new cationic FeAu3 cluster [(OC)2{η5-(1-phenylborole)}Fe{Au(PPh3)}3]PF6 (4) which has a tetrahedral metal core, as established by a wide angle X-ray scattering study.</abstract><pub>American Chemical Society</pub><doi>10.1021/om9703189</doi><tpages>6</tpages></addata></record> |
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title | Heterometallic Borole Complexes of Iron and Gold |
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