This study focuses on the hydrolysis of terbufos, an organophosphorus pesticide. Combining GC-MS and wet chemistry methods, di-tert-butyl disulfide and formaldehyde were identified and quantified as major degradation products. Diethyl dithiophosphate was also indirectly identified as a degradation product under alkaline conditions. Hydrolysis rate constants of terbufos under homogeneous conditions were comparable to those of phorate and show relative insensitivity to pH under slightly acidic to neutral pH conditions, as the observed rate constants varied only in the range of (4.5-5.0) x 10(-6) s(-1) between pH 5.7 and 9.4; neutral hydrolysis is thus the most dominant hydrolysis pathway of terbufos in ambient waters. The mechanisms for terbufos hydrolysis and the formation of the major products and their temporal profiles are discussed. To assess the environmental impact of degradation products of this widely used pesticide, Microtox was used to analyze the toxicity of terbufos and two of its degradation products: diethyl dithiophosphate and di-tert-butyl disulfide; the EC(50) of terbufos was found to be >17 microM, whereas the EC(50) of di-tert-butyl disulfide was 1.3 microM.
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http://dx.doi.org/10.1021/jf010339k | DOI Listing |
Angew Chem Int Ed Engl
May 2024
Anorganisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 276, 69120, Heidelberg, Germany.
A mononuclear, T-shaped palladium(I) d metalloradical (3), stabilized by a bulky carbazole-based PNP-ligand, was obtained by reduction of palladium chloride or thermal Pd-C bond homolysis of the corresponding neopentyl complex. Pressurizing with CO gave the Pd(I) carbonyl complex, which was structurally characterized by X-ray diffraction. Delocalization of the unpaired electron to the carbonyl carbon was detected by EPR spectroscopy and theoretically modeled by DFT and ab initio methods.
View Article and Find Full Text PDFInorg Chem
October 2023
Laboratory for Advanced Materials, Faculty of Natural Sciences, Comenius University, Ilkovičova 8, 84104 Bratislava, Slovakia.
Currently, two approaches dominate the large-scale production of MoS: liquid-phase exfoliation, referred to as the top-down approach, and bottom-up colloidal synthesis from molecular precursors. Known colloidal synthesis approaches utilize toxic precursors. Here, an alternative green route for the bottom-up synthesis of MoS nanoflakes (NFs) is described.
View Article and Find Full Text PDFMolecules
October 2022
G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, 49 Tropinina Str., 603137 Nizhny Novgorod, Russia.
A series of binuclear triphenylantimony(V) bis-catecholato complexes - of the type (Cat)PhSb-linker-SbPh(Cat) was prepared by a reaction of the corresponding mononuclear catecholates (Cat)SbPh with a neutral bidentate donor linker ligands pyrazine (Pyr), 4,4'-dipyridyl (Bipy), bis-(pyridine-4-yl)-disulfide (PySSPy), and diazobicyclo[2,2,2]octane (DABCO) in a dry toluene: Cat = 3,6-di-tert-butyl-catecholate (3,6-DBCat), linker = Pyr (); PySSPy (); Bipy (); DABCO (); Cat = 3,5-di-tert-butyl-catecholate (3,5-DBCat), linker = Bipy (); DABCO (); Cat = 4,5-(piperazine-1,4-diyl)-3,6-di-tert-butylcatecholate (pip-3,6-DBCat), linker = Bipy (); DABCO (); Cat = 4,5-dichloro-3,6-di-tert-butylcatecholate (4,5-Cl-3,6-DBCat), linker = Bipy (); DABCO (); and Cat = 4,5-dimethoxy-3,6-di-tert-butylcatecholate (4,5-(MeO)-3,6-DBCat), linker = Bipy (). The same reaction of (4,5-Cl-3,6-DBCat)SbPh with DABCO in an open atmosphere results in a formation of 1D coordination polymer {[(4,5-Cl-3,6-DBCat)SbPh·HO]·DABCO} (). Bis-catecholate complex PhSb(Cat-Spiro-Cat)SbPh reacts with Bipy as 1:1 yielding a rare macrocyclic tetranuclear compound {PhSb(Cat-Spiro-Cat)SbPh∙(Bipy)} ().
View Article and Find Full Text PDFMolecules
June 2022
Department of Chemistry, Astrakhan State Technical University, 16 Tatisheva Str., 414056 Astrakhan, Russia.
Natural or synthetic antioxidants with biomimetic fragments protect the functional and structural integrity of biological molecules at a minimum concentration, and may be used as potential chemotherapeutic agents. This paper is devoted to in silico and in vitro evaluation of the antioxidant and cytotoxic properties of synthetic analogues of natural compounds-aromatic oligosulfides. The antiradical and SOD-protective activity of oligosulfides was demonstrated in the reaction with O generated in enzymatic and non-enzymatic systems.
View Article and Find Full Text PDFDalton Trans
February 2021
School of Integrative Engineering, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul, 06974, Republic of Korea.
The chemical transformation from zinc oxide (ZnO) to zinc sulphide (ZnS), using di-tert-butyl disulphide (TBDS) as a highly reactive sulphur precursor, is demonstrated herein. Through anion exchange, we investigate the phase and morphological changes associated with the nanoparticle (NP) transformation of ZnO to ZnS using TBDS. The Zn-O-S alloy was not formed through the anion exchange reaction, only the ZnO and ZnS phases were detected.
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