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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
45
pubmed:dateCreated
2003-11-5
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.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Nov
pubmed:issn
0002-7863
pubmed:author
pubmed:issnType
Print
pubmed:day
12
pubmed:volume
125
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
13831-5
pubmed:year
2003
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.
pubmed:affiliation
Department of Chemistry, University of California, Irvine, California 92697-2025, USA. wevans@uci.edu
pubmed:publicationType
Journal Article