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Oscar E. Piro

Researcher at National University of La Plata

Publications -  287
Citations -  4039

Oscar E. Piro is an academic researcher from National University of La Plata. The author has contributed to research in topics: Crystal structure & Molecule. The author has an hindex of 31, co-authored 276 publications receiving 3639 citations. Previous affiliations of Oscar E. Piro include National Scientific and Technical Research Council.

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A detailed experimental and theoretical study of two novel substituted trifluoromethylchromones. The influence of the bulky bromine atom on the crystal packing.

TL;DR: The CF3 group revealed a strong rotational disorder around the CCF3 bond, which could be explained in terms of four split positions with about uniform angular distribution.
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Molecular structure and single crystal EPR spectra of bis(L-Valinato)copper(II) monohydrate, Cu[H2NCH(CH3)2CHCO2]2·H2O

TL;DR: In this article, a magnetic-structural study of the title compound, Cu(L-Val)2·H2O, employing EPR spectroscopy and X-ray diffraction methods is presented.
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Structural and IR-spectroscopic characterization of magnesium acesulfamate

TL;DR: Piro, Oscar Enrique as mentioned in this paper, et al. as mentioned in this paper presented a model of the Instituto de Fisica La Plata (IFLP) in the context of the Consejo Nacional de Investigaciones Cientificas y Tecnicas.
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Reactions of 1,2,5‐thiadiazole 1,1‐dioxide derivatives with nitrogen nucleophiles. Part IV. Addition of α‐diamines

TL;DR: In this article, a new compound acenaphtho [5,6-b]-2,3-dihydropyrazine was synthesized and characterized, which was followed by cyclic voltammetry and NMR spectroscopy which, in some cases, allowed the detection of the thiadiazolidine intermediate.
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Improving the antidepressant action and the bioavailability of sertraline by co-crystallization with coumarin 3-carboxylate. Structural determination.

TL;DR: It is reasonable to conclude that the replacement of chloride anion by a large organic anion in sertraline strengthens the pharmacological action of the native drug, binding to BSA with higher activity and retaining the antimicrobial activity of the antidepressant compound.