GLORIA MARÍA
TARDAJOS RODRÍGUEZ
Investigadora hasta 2020
MAURICIO
ALCOLEA PALAFOX
Profesor titular de universidad
Publicaciones en las que colabora con MAURICIO ALCOLEA PALAFOX (12)
2017
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Femtosecond laser reshaping yields gold nanorods with ultranarrow surface plasmon resonances
Science, Vol. 358, Núm. 6363, pp. 640-644
2010
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FT-IR and FT-Raman spectra, ab initio and density functional computations of the vibrational spectra, molecular geometry, atomic charges and some molecular properties of the biomolecule 5-iodouracil
Journal of Molecular Structure: THEOCHEM, Vol. 940, Núm. 1-3, pp. 29-44
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Quantum chemical scaling and its importance: The infrared and raman spectra of 5-bromouracil
Spectroscopy Letters, Vol. 43, Núm. 1, pp. 51-59
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Raman and infrared spectra of hydrated 2,4-dithiouracil molecule
AIP Conference Proceedings
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Raman and infrared spectra of hydrated 5-nitrouracil molecule
AIP Conference Proceedings
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Relationships observed in the structure and spectra of uracil and its 5-substituted derivatives
Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, Vol. 75, Núm. 4, pp. 1261-1269
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Simulation of a tetramer form of 5-iodouracil: The vibrational spectra and molecular structure in the isolated and in the solid state by using DFT calculations
Vibrational Spectroscopy, Vol. 52, Núm. 2, pp. 108-121
2008
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On the connection between the complexation and aggregation thermodynamics of oxyethylene nonionic surfactants
Journal of Physical Chemistry B, Vol. 112, Núm. 49, pp. 15691-15700
2007
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FT-IR, FT-Raman spectra, density functional computations of the vibrational spectra and molecular geometry of biomolecule 5-aminouracil
Chemical Physics, Vol. 340, Núm. 1-3, pp. 17-31
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Studying the transfer process of a gemini surfactant from water to β-cyclodextrin at a molecular level
Chemical Physics Letters, Vol. 446, Núm. 1-3, pp. 92-97
2006
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Unexpected binding mode of gemini surfactants and γ-cyclodextrin: DOSY as a tool for the study of complexation
Chemical Physics Letters, Vol. 432, Núm. 4-6, pp. 486-490
2002
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Study of phenothiazine and N-methyl phenothiazine by infrared, Raman, 1H-, and 13C-NMR spectroscopies
International Journal of Quantum Chemistry, Vol. 89, Núm. 3, pp. 147-171