Publicacións (54)

2022

  1. Erratum: Lead(ii) supramolecular structures formed through a cooperative influence of the hydrazinecarbothioamide derived and ancillary ligands (CrystEngComm, (2022) 24 (368–378) DOI: 10.1039/D1CE01251G)

    CrystEngComm

  2. The tetrel bonding role in supramolecular aggregation of lead(II) acetate and a thiosemicarbazide derivative

    Acta crystallographica Section B, Structural science, crystal engineering and materials, Vol. 78, pp. 685-694

  3. Supramolecular aggregation of lead(II) perchlorate and a thiosemicarbazide derivative linked by a myriad of non-covalent interactions

    Inorganica Chimica Acta, Vol. 538

  4. Multicomponent Solids of DL-2-Hydroxy-2-phenylacetic Acid and Pyridinecarboxamides

    Crystals, Vol. 12, Núm. 2

  5. Lead(ii) supramolecular structures formed through a cooperative influence of the hydrazinecarbothioamide derived and ancillary ligands

    CrystEngComm, Vol. 24, Núm. 2, pp. 368-378

  6. Experimental and Theoretical Evidence of a Pb⋅⋅⋅Pb Ditetrel Bond Without a σ-Hole

    ChemPhysChem, Vol. 23, Núm. 14

  7. Copper(I) derivatives of 4-benzoylpyridine thiosemicarbazone and 3-formylpyridine-N-methylthiosemicarbazone with triphenylphosphine as a co-ligand

    Journal of the Indian Chemical Society, Vol. 99, Núm. 1

  8. Copper(I) Derivative of Pyridine-3-carbaldehyde-N-ethylthiosemicarbazone and Triphenylphosphine—First Case of Crystal Structure Study

    Journal of Chemical Crystallography, Vol. 52, Núm. 2, pp. 233-241

2021

  1. Weak interactions in cocrystals of isoniazid with glycolic and mandelic acids

    Crystals, Vol. 11, Núm. 4

  2. Supramolecular, spectroscopic and computational analysis of weak interactions in some thiosemicarbazones derived from 5-acetylbarbituric acid

    Journal of Molecular Structure, Vol. 1245

2020

  1. Synthesis, structures, and novel antimicrobial activity of silver(I) halide complexes of imidazolidine-2-thiones

    Polyhedron, Vol. 175

  2. Structural basis and effect of copper(II) complexes with 4-oxo-thiazolidine ligands on DNA binding and nuclease activity

    Journal of Inorganic Biochemistry, Vol. 203

  3. Recurrent motifs in pharmaceutical cocrystals involving glycolic acid: X-ray characterization, Hirshfeld surface analysis and DFT calculations

    CrystEngComm, Vol. 22, Núm. 40, pp. 6674-6689

2019

  1. Synthesis of 2-acetylpyridine-N-substituted thiosemicarbazonates of copper(ii) with high antimicrobial activity against methicillin resistant S. aureus, K. pneumoniae 1 and C. albicans

    New Journal of Chemistry, Vol. 43, Núm. 29, pp. 11727-11742

  2. Silver derivatives of multi-donor heterocyclic thioamides as antimicrobial/anticancer agents: Unusual bio-activity against methicillin resistant: S. aureus, S. epidermidis, and E. faecalis and human bone cancer MG63 cell line

    RSC Advances, Vol. 9, Núm. 27, pp. 15470-15487

  3. Design and synthesis of methyl 2-{[4-phenyl-5-(pyridin-2-yl)-4H-1,2,4-Triazol-3-yl]sulfanyl}acetate (phpy2NS) as a ligand for complexes of Group 12 elements: Structural assessment and hydrogenbonded supramolecular assembly analysis1

    Acta Crystallographica Section C: Structural Chemistry, Vol. 75, Núm. 7, pp. 891-903

2018

  1. Corrigendum to “Synthesis of 5-nitro-salicylaldehyde-N-substituted thiosemicarbazonates of copper(II): Molecular structures, spectroscopy, ESI-mass studies and antimicrobial activity” [Inorg. Chim. Acta 461 (2017) 248–260](S0020169317302116)(10.1016/j.ica.2017.02.032)

    Inorganica Chimica Acta

  2. Synthesis, structures and antimicrobial activity of copper derivatives of N -substituted imidazolidine-2-thiones: Unusual bio-activity against Staphylococcus epidermidis and Enterococcus faecalis

    New Journal of Chemistry, Vol. 42, Núm. 12, pp. 9886-9900

  3. Quasi-aromatic Möbius Metal Chelates

    Inorganic Chemistry, Vol. 57, Núm. 8, pp. 4395-4408

  4. Multicomponent Supramolecular Assemblies of Melamine and α-Hydroxycarboxylic Acids: Understanding the Hydrogen Bonding Patterns and Their Physicochemical Consequences

    Crystal Growth and Design, Vol. 18, Núm. 11, pp. 6786-6800