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Weakly Bonded Lewis Base Adducts of Plumbocene and Stannocene: A Synthetic and Calculational Study
The coordination of [(η-Cp)2Pb] and [(η-Cp)2Sn] by bidentate Lewis-base ligands gives the first examples of adducts of neutral p-block metallocenes. Ab initio MO calculations of [(η-Cp)2Pb·TMEDA] (1) (TMEDA = (Me2NCH2)2), [Cp2Pb·4,4‘-Me2bipy] (2) (4,4‘-Me2bipy = 4,4‘-dimethylbipyridine), and the new...
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Published in: | Organometallics 1998-07, Vol.17 (15), p.3176-3181 |
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container_end_page | 3181 |
container_issue | 15 |
container_start_page | 3176 |
container_title | Organometallics |
container_volume | 17 |
creator | Armstrong, David R Beswick, Michael A Cromhout, Natalie L Harmer, Christopher N Moncrieff, David Russell, Christopher A Raithby, Paul R Steiner, Alexander Wheatley, Andrew E. H Wright, Dominic S |
description | The coordination of [(η-Cp)2Pb] and [(η-Cp)2Sn] by bidentate Lewis-base ligands gives the first examples of adducts of neutral p-block metallocenes. Ab initio MO calculations of [(η-Cp)2Pb·TMEDA] (1) (TMEDA = (Me2NCH2)2), [Cp2Pb·4,4‘-Me2bipy] (2) (4,4‘-Me2bipy = 4,4‘-dimethylbipyridine), and the new complex [(η-Cp)2Sn·TMEDA] (3) confirm that despite the presence of longer Pb−N and Sn−N bonds in the solid-state structures of the TMEDA adducts, the association of TMEDA with the metallocenes is more favorable than with 4,4‘-Me2bipy. This finding is a consequence of the greater reorganization energy of 4,4‘-Me2bipy compared to TMEDA. The low association energies of these species can be rationalized in terms of metal lone pair/ligand lone pair repulsion. |
doi_str_mv | 10.1021/om980077k |
format | article |
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The low association energies of these species can be rationalized in terms of metal lone pair/ligand lone pair repulsion.</description><identifier>ISSN: 0276-7333</identifier><identifier>EISSN: 1520-6041</identifier><identifier>DOI: 10.1021/om980077k</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Organometallics, 1998-07, Vol.17 (15), p.3176-3181</ispartof><rights>Copyright © 1998 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a387t-427c4e4523636bfa47abc236c680c602d7e14156767c25ac98d6292daf126c1a3</citedby><cites>FETCH-LOGICAL-a387t-427c4e4523636bfa47abc236c680c602d7e14156767c25ac98d6292daf126c1a3</cites></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>Armstrong, David R</creatorcontrib><creatorcontrib>Beswick, Michael A</creatorcontrib><creatorcontrib>Cromhout, Natalie L</creatorcontrib><creatorcontrib>Harmer, Christopher N</creatorcontrib><creatorcontrib>Moncrieff, David</creatorcontrib><creatorcontrib>Russell, Christopher A</creatorcontrib><creatorcontrib>Raithby, Paul R</creatorcontrib><creatorcontrib>Steiner, Alexander</creatorcontrib><creatorcontrib>Wheatley, Andrew E. 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H</creatorcontrib><creatorcontrib>Wright, Dominic S</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Organometallics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Armstrong, David R</au><au>Beswick, Michael A</au><au>Cromhout, Natalie L</au><au>Harmer, Christopher N</au><au>Moncrieff, David</au><au>Russell, Christopher A</au><au>Raithby, Paul R</au><au>Steiner, Alexander</au><au>Wheatley, Andrew E. H</au><au>Wright, Dominic S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Weakly Bonded Lewis Base Adducts of Plumbocene and Stannocene: A Synthetic and Calculational Study</atitle><jtitle>Organometallics</jtitle><addtitle>Organometallics</addtitle><date>1998-07-20</date><risdate>1998</risdate><volume>17</volume><issue>15</issue><spage>3176</spage><epage>3181</epage><pages>3176-3181</pages><issn>0276-7333</issn><eissn>1520-6041</eissn><abstract>The coordination of [(η-Cp)2Pb] and [(η-Cp)2Sn] by bidentate Lewis-base ligands gives the first examples of adducts of neutral p-block metallocenes. Ab initio MO calculations of [(η-Cp)2Pb·TMEDA] (1) (TMEDA = (Me2NCH2)2), [Cp2Pb·4,4‘-Me2bipy] (2) (4,4‘-Me2bipy = 4,4‘-dimethylbipyridine), and the new complex [(η-Cp)2Sn·TMEDA] (3) confirm that despite the presence of longer Pb−N and Sn−N bonds in the solid-state structures of the TMEDA adducts, the association of TMEDA with the metallocenes is more favorable than with 4,4‘-Me2bipy. This finding is a consequence of the greater reorganization energy of 4,4‘-Me2bipy compared to TMEDA. The low association energies of these species can be rationalized in terms of metal lone pair/ligand lone pair repulsion.</abstract><pub>American Chemical Society</pub><doi>10.1021/om980077k</doi><tpages>6</tpages></addata></record> |
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title | Weakly Bonded Lewis Base Adducts of Plumbocene and Stannocene: A Synthetic and Calculational Study |
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