Source:http://linkedlifedata.com/resource/pubmed/id/14599223
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
45
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pubmed:dateCreated |
2003-11-5
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pubmed:abstractText |
Sterically crowded isoelectronic nf(3) (C(5)Me(5))(3)M complexes of neodymium and uranium, compounds which have unconventionally long metal ligand distances, are found to react very differently with CO as a substrate. The 4f(3) complex (C(5)Me(5))(3)Nd reacts with CO to form a nonclassical carbonium ion complex, (C(5)Me(5))(2)Nd(O(2)C(7)Me(5)), which contains a three-coordinate planar carbon. (C(5)Me(5))(3)U reacts with CO to form an even more crowded CO adduct through a reaction type never observed before for (C(5)Me(5))(3)M compounds. The rare uranium carbonyl complex, (C(5)Me(5))(3)U(CO), has nu(CO) = 1922 cm(-1) and a U-C(CO) distance of 2.485(9) A.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0002-7863
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
12
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pubmed:volume |
125
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
13831-5
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pubmed:year |
2003
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pubmed:articleTitle |
Comparative reactivity of sterically crowded nf3 (C5Me5)3Nd and (C5Me5)3U complexes with CO: formation of a nonclassical carbonium ion versus an f element metal carbonyl complex.
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pubmed:affiliation |
Department of Chemistry, University of California, Irvine, California 92697-2025, USA. wevans@uci.edu
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pubmed:publicationType |
Journal Article
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