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José S. Casas

Researcher at University of Santiago de Compostela

Publications -  250
Citations -  4959

José S. Casas is an academic researcher from University of Santiago de Compostela. The author has contributed to research in topics: Crystal structure & Ligand. The author has an hindex of 32, co-authored 250 publications receiving 4777 citations.

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Main group metal complexes of semicarbazones and thiosemicarbazones. A structural review

TL;DR: The structural aspects of the complexes formed by thiosemicarbazones and semicarazones (TSCs) with the metallic elements of Groups 12, 13, 14 and 15 are surveyed up to 1998.
Book

Lead : chemistry, analytical aspects, environmental impact and health effects

TL;DR: This chapter discusses the historical importance, occurrence, isolation, properties and applications of lead, as well as analytical procedures for the lead determination in biological and environmental samples.
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Symmetrisation, isomerism and structural studies on novel phenylmercury( II ) thiosemicarbazonates: correlation of the energy barrier to rotation of the amino group with the bonding parameters of the thioamide group

TL;DR: In this article, the reaction of phenylmercury(II) acetate with a series of alkyl, aryl and heterocyclic thiosemicarbazones in ethanol formed novel phenylmerscury derivatives of stoichiometry, characterised with the help of analytical data, physical properties, IR, far-IR, multinuclear NMR (1H, 13C, 199Hg) spectroscopy and X-ray crystallography of complexes 1, 5 and 6.
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Coordination modes of 5-pyrazolones : A solid-state overview

TL;DR: In this article, the coordination modes of 5-pyrazolones are reviewed in light of the available X-ray diffraction studies of their complexes, and the coordination behavior of the molecules without any donor atoms other than those associated with the pyrazolone ring is discussed.
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New Pd(II) and Pt(II) complexes with N,S-chelated pyrazolonate ligands: molecular and supramolecular structure and preliminary study of their in vitro antitumoral activity.

TL;DR: The in vitro antitumoral assays performed with two HL ligands and their metal complexes showed significant cytostatic activity for the latter, with the most active [ML2] derivative being about sixteen times more active than cis-DDP against the cisplatinum-resistant cell line A2780cisR.