Source:http://linkedlifedata.com/resource/pubmed/id/20095641
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2010-2-8
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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.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1520-510X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1743-9
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pubmed:year |
2010
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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.
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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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