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rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2010-2-8
pubmed:abstractText
The reductive chemistry of U(3+) in the metallocene amidinate coordination environment of (C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr-kappa(2)N,N']U, 1, has been explored. Two equivalents of 1 react with PhSSPh and 2,2'-dithiopyridine (pySSpy) to produce (C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr-kappa(2)N,N']U(SPh), 2, and (C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr-kappa(2)N,N']U(Spy), 3, respectively. Complexes 2 and 3 can also be synthesized through insertion of (i)PrN horizontal lineC horizontal lineN(i)Pr into the methyl group in (C(5)Me(5))(2)UMe(SPh) and (C(5)Me(5))(2)UMe(Spy), 4, respectively. Complex 1 readily reduces the Cu(1+) reagents, CuBr, CuI, and CuO(2)CMe, to produce the corresponding (C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr-kappa(2)N,N']UX complexes (X = Br, 5; I, 6; O(2)CMe, 7). X-ray crystallography established complex 7 as the first f element complex containing a monodentate acetate anion. Complex 7 can also be obtained by reaction of (C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr-kappa(2)N,N']UMe with CO(2) at 80 psi. In contrast to the reactions above, 1 reduces TlC(5)H(5) with the unusual loss of (C(5)Me(5))(-) to form (C(5)Me(5))(C(5)H(5))(2)[(i)PrNC(Me)N(i)Pr-kappa(2)N,N']U, 8.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Feb
pubmed:issn
1520-510X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
49
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1743-9
pubmed:year
2010
pubmed:articleTitle
Reaction chemistry of the U(3+) metallocene amidinate (C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr]U including the isolation of a uranium complex of a monodentate acetate.
pubmed:affiliation
Department of Chemistry, University of California Irvine, California 92697-2025, USA. wevans@uci.edu
pubmed:publicationType
Journal Article