Ketimine synthesis in the coordination sphere of thallium (I)
- Fernández, E.J. 1
- Laguna, A. 2
- Lasanta, T. 1
- López-de-Luzuriaga, J.M. 1
- Montiel, M. 1
- Elena Olmos, M. 1
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1
Universidad de La Rioja
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2
Instituto de Nanociencia y Materiales de Aragón
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ISSN: 0020-1693
Year of publication: 2011
Volume: 363
Issue: 9
Pages: 1965-1969
Type: Article
More publications in: Inorganica Chimica Acta
Metrics
JCR (Journal Impact Factor)
- Year 2011
- Journal Impact Factor: 1.846
- Journal Impact Factor without self cites: 1.631
- Article influence score: 0.393
- Best Quartile: Q3
- Area: CHEMISTRY, INORGANIC & NUCLEAR Quartile: Q3 Rank in area: 23/44 (Ranking edition: SCIE)
SCImago Journal Rank
- Year 2011
- SJR Journal Impact: 0.626
- Best Quartile: Q2
- Area: Inorganic Chemistry Quartile: Q2 Rank in area: 32/69
- Area: Physical and Theoretical Chemistry Quartile: Q2 Rank in area: 75/167
- Area: Materials Chemistry Quartile: Q2 Rank in area: 72/290
Scopus CiteScore
- Year 2011
- CiteScore of the Journal : 3.3
- Area: Materials Chemistry Percentile: 81
- Area: Inorganic Chemistry Percentile: 63
- Area: Physical and Theoretical Chemistry Percentile: 60
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Abstract
[AuTl(C6F5)2(en)] (en = ethylenediamine) reacts with cyclic ketones as cyclopentanone (Cy5{double bond, long}O), cyclohexanone (Cy6{double bond, long}O) or cycloheptanone (Cy7{double bond, long}O) in 1:1 or 1:2 molar ratio leading to products of stoichiometry [AuTl(C6F5)2{Cyx{double bond, long}N(CH2)2NH2}] (x = 5 1, 6 2 or 7 3), or [AuTl(C6F5)2{Cyx{double bond, long}N(CH2)2N{double bond, long}Cyx}] (x = 5 4, 6 5 or 7 6). Addition of ethylenediamine to the ketimine complexes in chloroform regenerates [AuTl(C6F5)2(en)], the starting material, and the free ketimines, as their NMR and mass spectra evidenced. The ketimine complexes display luminescence in solid state at room temperature and at 77 K at higher wavelengths than the diamine starting product (505 nm). The excited states responsible for this behaviour are assigned to orbitals due to the gold-thallium interactions. © 2009 Elsevier B.V. All rights reserved.