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TÍTULO: In situ photoproduction of dichlorodibenzo-p-dioxin from non-ionic triclosan isolated in solid argon  Full Text
AUTORES: Nihal Kuş; Igor Reva; Sevgi Bayarı; Rui Fausto;
PUBLICAÇÃO: 2012, FONTE: Journal of Molecular Structure, VOLUME: 1007
INDEXADO EM: CrossRef
NO MEU: ORCID
72
TÍTULO: Conformers, Infrared Spectrum and UV-Induced Photochemistry of Matrix-Isolated Furfuryl Alcohol
AUTORES: Araujo-Andrade, C; Gómez-Zavaglia, A; Reva, ID; Fausto, R;
PUBLICAÇÃO: 2012, FONTE: J. Phys. Chem. A - The Journal of Physical Chemistry A, VOLUME: 116, NÚMERO: 9
INDEXADO EM: CrossRef
NO MEU: ORCID
73
TÍTULO: Using heavy atom rare gas matrix to control the reactivity of 4-methoxybenzaldehyde: A comparison with benzaldehyde  Full Text
AUTORES: Nihal Kuş; Archna Sharma; Igor Reva; Leszek Lapinski; Rui Fausto;
PUBLICAÇÃO: 2012, FONTE: The Journal of Chemical Physics - J. Chem. Phys., VOLUME: 136, NÚMERO: 14
INDEXADO EM: CrossRef
NO MEU: ORCID
74
TÍTULO: Conformational Behavior and Tautomer Selective Photochemistry in Low Temperature Matrices: The Case of 5-(1 H -Tetrazol-1-yl)-1,2,4-triazole
AUTORES: Pagacz-Kostrzewa, M; Reva, ID; Bronisz, R; Giuliano, BM; Fausto, R; Wierzejewska, M;
PUBLICAÇÃO: 2011, FONTE: J. Phys. Chem. A - The Journal of Physical Chemistry A, VOLUME: 115, NÚMERO: 22
INDEXADO EM: CrossRef
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75
TÍTULO: Thermal and Photoinduced Control of Relative Populations of 4-Methoxybenzaldehyde ( p -Anisaldehyde) Conformers
AUTORES: Nihal Kuş; Archna Sharma; Igor Reva; Leszek Lapinski; Rui Fausto;
PUBLICAÇÃO: 2010, FONTE: J. Phys. Chem. A - The Journal of Physical Chemistry A, VOLUME: 114, NÚMERO: 29
INDEXADO EM: CrossRef
NO MEU: ORCID
76
TÍTULO: Photoisomerization and Photochemistry of Matrix-Isolated 3-Furaldehyde
AUTORES: Nihal Kuş; Igor Reva; Rui Fausto;
PUBLICAÇÃO: 2010, FONTE: J. Phys. Chem. A - The Journal of Physical Chemistry A, VOLUME: 114, NÚMERO: 47
INDEXADO EM: CrossRef
NO MEU: ORCID
77
TÍTULO: Selective IR-induced isomerization of 1,2-dichloropropane isolated in xenon matrix  Full Text
AUTORES: Adriana Olbert-Majkut; Igor D Reva; Rui Fausto;
PUBLICAÇÃO: 2008, FONTE: Chemical Physics Letters, VOLUME: 456, NÚMERO: 4-6
INDEXADO EM: CrossRef
NO MEU: ORCID
78
TÍTULO: Low-Temperature FTIR Spectroscopic and Theoretical Study on an Energetic Nitroimine:  Dinitroammeline (DNAM)
AUTORES: Simões, PN; Reva, I; Pedroso, LM; Fausto, R; Portugal, AA;
PUBLICAÇÃO: 2008, FONTE: J. Phys. Chem. A - The Journal of Physical Chemistry A, VOLUME: 112, NÚMERO: 15
INDEXADO EM: CrossRef: 8
NO MEU: ORCID
79
TÍTULO: FTIR Spectroscopic and Theoretical Study of the Photochemistry of Matrix-isolated Coumarin  Full Text
AUTORES: Nihal Kuş; Susana Breda; Igor Reva; Erol Tasal; Cemil Ogretir; Rui Fausto;
PUBLICAÇÃO: 2007, FONTE: Photochemistry and Photobiology - Photochem Photobiol, VOLUME: 83, NÚMERO: 5
INDEXADO EM: CrossRef
NO MEU: ORCID
80
TÍTULO: Matrix isolation FTIR and theoretical study of ?-pyrone photochemistryElectronic supplementary information (ESI) available: Tables S1, S2, S3, S12 and S14 provide internal coordinates used in the normal modes analysis for ?-pyrone, 2-oxa-3-oxobicyclo[2.2.0]hex-5-ene, open-ring aldehyde?ketene isomers, cyclobutadiene and 4-formyl-2-cyclobutene-1-one. Experimental infrared spectra of ?-pyrone isolated in Xe matrix are compared with the theoretical spectra in Fig. S1. Table S4 provides the assignment of infrared observed bands and the calculated vibrational frequencies, intensities and potential energy distribution for ?-pyrone monomer. Calculated vibrational frequencies, intensities and potential energy distributions for all open-ring aldehyde?ketene conformers and for 4-formyl-2-cyclobutene-1-one monomer (forms A and B) are listed in Tables S5?S11 and Table S15, respectively. Table S13 provides the assignment of infrared observed bands and the calculated vibrational frequencies, intensities and potential energy distribution for cyclobutadiene monomer. Fig. S2 presents differential spectra showing the progress of the irradiation experiments. The optimized structure for the ?-pyrone analogue of benzvalene is shown in Fig. S3. Fig. S4 illustrates the observed photochemistry of ?-pyrone in an argon matrix. See http://www.rsc.org/suppdata/cp/b3/b309660b/  Full Text
AUTORES: Breda, S; Reva, I; Lapinski, L; Fausto, R;
PUBLICAÇÃO: 2004, FONTE: Phys. Chem. Chem. Phys. - Physical Chemistry Chemical Physics, VOLUME: 6, NÚMERO: 5
INDEXADO EM: CrossRef
NO MEU: ORCID
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