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Organotin(IV) Dithiocarbamate Complexes: Chemistry and Biological Activity [PDF]

open access: yesMolecules, 2018
Significant attention has been given to organotin(IV) dithiocabamate compounds in recent times. This is due to their ability to stabilize specific stereochemistry in their complexes, and their diverse application in agriculture, biology, catalysis and as
Jerry O. Adeyemi, Damian C. Onwudiwe
doaj   +8 more sources

Organotin (IV) Dithiocarbamate Compounds as Anticancer Agents: A Review of Syntheses and Cytotoxicity Studies [PDF]

open access: yesMolecules, 2023
Organotin (IV) dithiocarbamate has recently received attention as a therapeutic agent among organotin (IV) compounds. The individual properties of the organotin (IV) and dithiocarbamate moieties in the hybrid complex form a synergy of action that ...
Nurul Amalina Abd Aziz   +4 more
doaj   +2 more sources

Cellular Basis of Organotin(IV) Derivatives as Anticancer Metallodrugs: A Review [PDF]

open access: yesFrontiers in Chemistry, 2021
Organotin(IV) compounds have wide applications in industrial and agricultural fields owing to their ability to act as poly(vinyl chloride) stabilizers and catalytic agents as well as their medicinal properties.
Sharifah Nadhira Syed Annuar   +3 more
doaj   +2 more sources

Series of Organotin(IV) Compounds with Different Dithiocarbamate Ligands Induced Cytotoxicity, Apoptosis and Cell Cycle Arrest on Jurkat E6.1, T Acute Lymphoblastic Leukemia Cells [PDF]

open access: yesMolecules, 2023
The discovery of cisplatin has influenced scientists to study the anticancer properties of other metal complexes. Organotin(IV) dithiocarbamate compounds are gaining attention as anticancer agents due to their potent cytotoxic properties on cancer cells.
Nur Rasyiqin Rasli   +3 more
doaj   +2 more sources

New Organotin (IV) Compounds Derived from Dehydroacetic Acid and Thiosemicarbazides: Synthesis, Rational Design, Cytotoxic Evaluation, and Molecular Docking Simulation [PDF]

open access: yesBioinorganic Chemistry and Applications, 2023
Organotin complexes were prepared through a one-pot reaction with three components by reacting thiosemicarbazide or 4-methyl-3-thiosemicarbazide or 4-phenylthiosemicarbazide, dehydroacetic acid (DHA) and dibutyl, diphenyl, dicyclohexyl, and bis ...
Elizabeth Gómez   +11 more
doaj   +2 more sources

Synthesis of Telmisartan Organotin(IV) Complexes and their use as Carbon Dioxide Capture Media [PDF]

open access: yesMolecules, 2019
Novel, porous, highly aromatic organotin(IV) frameworks were successfully synthesized by the condensation of telmisartan and an appropriate tin(IV) chloride. The structures of the synthesized organotin(IV) complexes were elucidated by elemental analysis,
Angham G. Hadi   +5 more
doaj   +2 more sources

Photostabilization of Poly(vinyl chloride) by Organotin(IV) Compounds against Photodegradation [PDF]

open access: yesMolecules, 2019
Poly(vinyl chloride) (PVC), a polymer widely used in common household and industrial materials, undergoes photodegradation upon ultraviolet irradiation, leading to undesirable physicochemical properties and a reduced lifetime.
Angham G. Hadi   +6 more
doaj   +2 more sources

ORGANOTIN(IV) DERIVATIVES OF AZOLES

open access: yesMain Group Metal Chemistry, 1999
AbstractFor Abstract see ChemInform Abstract in Full Text.
Pettinari, Claudio
doaj   +2 more sources

Synthesis, Characterization and In Vitro Antibacterial Studies of Organotin(IV) Complexes with 2-Hydroxyacetophenone-2-methylphenylthiosemicarbazone (H2dampt) [PDF]

open access: yesBioinorganic Chemistry and Applications, 2012
Five new organotin(IV) complexes of 2-hydroxyacetophenone-2-methylphenylthiosemicarbazone [H2dampt, (1)] with formula [RSnCl𝑛−1(dampt)] (where R=Me, 𝑛=2 (2); R=Bu, 𝑛=2 (3); R=Ph, 𝑛=2 (4); R=Me2, 𝑛=1 (5); R=Ph2, 𝑛=1 (6)) have been synthesized by direct ...
M. A. Salam   +4 more
doaj   +2 more sources

Organotin(IV) Alkoxides, Siloxides, and Related Stannoxanes. Characterisation and Thermogravimetric Studies [PDF]

open access: yesChemistryOpen
A series of C,O‐chelated organotin(IV) alkoxides, L2PhSnOtBu (4), L2PhSnOMe (6), L2Sn(OtBu)2 (11), and siloxides L2PhSnOSiPh3 (3), L2Sn(OSiPh3)2 (10) (L=[2‐(CH2O)2CH]C6H4), was prepared by salt elimination reactions. They were obtained from the organotin(
Vlad Penciu   +3 more
doaj   +2 more sources

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