Search Results - "Longo, R.L."

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  1. 1

    CCFOM and CCFDF models to interpret infrared intensities: A comparative study by Rusu, V.H., Ramos, M.N., Longo, R.L.

    Published in Journal of molecular structure (03-05-2011)
    “…MP2/aug-cc-pVTZ and MP2/6-311++G(3d,3p) calculations were employed to compare infrared intensity parameters of the AX diatomic molecules with A = H, Li, Na and…”
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    Journal Article
  2. 2

    Theoretical and experimental photophysical studies of the tris(4,4,4-trifluoro-1-(1-naphthyl)-1,3-butanedionate) (2,2′-bipiridyl)-europium(III) by Vila Nova, S.P., Batista, H.J., Alves, S., de Mello Donegá, C., Longo, R.L., de Sá, G.F., Thompson, L.C.

    Published in Journal of luminescence (01-05-2006)
    “…The complexes tris(4,4,4-Trifluoro-1-(1-naphthyl)-1,3-butanedionate) (2,2′-bipiridyl) Ln(III), Ln(tan) 3bipy, where Ln(III)=Eu 3+ and Gd 3+ have been…”
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  3. 3
  4. 4

    Spectroscopic properties and design of highly luminescent lanthanide coordination complexes by de Sá, G.F, Malta, O.L, de Mello Donegá, C, Simas, A.M, Longo, R.L, Santa-Cruz, P.A, da Silva, E.F

    Published in Coordination chemistry reviews (2000)
    “…In this paper recent advances in the development of efficient light conversion molecular devices (LCMD) based on lanthanide complexes are reviewed, with…”
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  5. 5

    Emission quantum yield of europium (III) mixed complexes with thenoyltrifluoroacetonate and some aromatic ligands by e Silva, F.R.G., Menezes, J.F.S., Rocha, G.B., Alves, S., Brito, H.F., Longo, R.L., Malta, O.L.

    Published in Journal of alloys and compounds (24-05-2000)
    “…We report the experimental determination and theoretical calculation of the 4f–4f emission quantum yield ( q) and 5D 0 excited state lifetime in the Eu (TTA)…”
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  6. 6

    Synthesis of Mansonone F Based on the Regioselective Hydrolysis of a Hydroquinone Diacetate by Nunes, Ruth L, Bieber, Lothar W, Longo, Ricardo L

    “…The synthesis of mansonone F (1), an antimicrobial sesquiterpenequinone, is described. Starting from 2,5-dimethyl-1,4-naphthoquinone (5), the corresponding…”
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  7. 7

    A molecular orbital analysis of the DNA bases by Leão, M.B.C., Longo, R.L., Pavão, A.C.

    Published in Journal of molecular structure. Theochem (01-11-1999)
    “…The carcinogen–DNA interaction can be described as an electron transfer from the DNA (HOMO) to the carcinogen (LUMO). To get a description of the DNA's HOMO,…”
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