Relevant bibliographies by topics / Dithiocarbamates

Academic literature on the topic 'Dithiocarbamates'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 September 2023

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Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Journal articles on the topic "Dithiocarbamates":

1

Halimehjani, Azim Ziyaei, Reza Mohtasham, Abbas Shockravi, and Jürgen Martens. "Multicomponent synthesis of dithiocarbamates starting from vinyl sulfones/sulfoxides and their use in polymerization reactions." RSC Advances 6, no. 79 (2016): 75223–26. http://dx.doi.org/10.1039/c6ra15616a.

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2

Maurya, Chandan, and Sangeeta Bajpai. "Biological Applications of Metal Complexes of Dithiocarbamates." Journal of Applied Science and Education (JASE) 2, no. 1 (March 1, 2022): 1–16. http://dx.doi.org/10.54060/jase/002.01.002.

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Dithiocarbamates are organosulphur ligands and form chelate compounds with metals. Their uses are reported in the field of accelerating vulcanization, pesticide, material science, organic synthesis, etc. Recent research demonstrated the potential of metal complexes of these ligands as good antifungal, antibacterial, and antitumor agents. Dithiocarbamate complexes have also been reported to use as a plasmonic sensor, as an inhibitor of proteasome, and for antioxidant and antileishmanial activity. This brief review presents the biological activities of metal complexes of dithiocarbamate.
3

Pedras, M. Soledade, and Francis I. Okanga. "Metabolism of analogs of the phytoalexin brassinin by plant pathogenic fungi." Canadian Journal of Chemistry 78, no. 3 (March 1, 2000): 338–46. http://dx.doi.org/10.1139/v00-024.

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he metabolism of analogs of the cruciferous phytoalexin brassinin by the phytopathogenic fungi Phoma lingam (Tode ex Fr.) "virulent" and "avirulent" groups (sexual stage Leptosphaeria maculans (Desm.) Ces. et de Not.) and Alternaria brassicae (Berk.) Sacc. is reported. It was established that each pathogen detoxified methyl tryptamine dithiocarbamate, although yielding different metabolic products. While the biotransformation by virulent P. lingam proceeded to yield methyl 3a-hydroxy-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-1(2H)-yl carbodithioate and indole-3-acetic acid as final products, avirulent P. lingam yielded indole-3-carboxylic acid via Nb-acetyltryptamine, and A. brassicae yielded Nb-acetyltryptamine, as final products. Furthermore, to establish the importance of the dithiocarbamate group in antifungal activity against P. lingam and A. brassicae, carbamates were compared with dithiocarbamates and it was established that carbamates were devoid of antifungal activity. These products, contrary to methyl tryptamine dithiocarbamate, showed no inhibitory activity against either pathogen.Key words: Alternaria brassicae, brassinin, carbamates, detoxification, dithiocarbamates, Leptosphaeria maculans, Phoma lingam, phytoalexins.
4

Oliveira, Johny Wysllas de Freitas, Hugo Alexandre Oliveira Rocha, Wendy Marina Toscano Queiroz de Medeiros, and Marcelo Sousa Silva. "Application of Dithiocarbamates as Potential New Antitrypanosomatids-Drugs: Approach Chemistry, Functional and Biological." Molecules 24, no. 15 (August 1, 2019): 2806. http://dx.doi.org/10.3390/molecules24152806.

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Dithiocarbamates represent a class of compounds that were evaluated in different biomedical applications because of their chemical versatility. For this reason, several pharmacological activities have already been attributed to these compounds, such as antiparasitic, antiviral, antifungal activities, among others. Therefore, compounds that are based on dithiocarbamates have been evaluated in different in vivo and in vitro models as potential new antimicrobials. Thus, the purpose of this review is to present the possibilities of using dithiocarbamate compounds as potential new antitrypanosomatids-drugs, which could be used for the pharmacological control of Chagas disease, leishmaniasis, and African trypanosomiasis.
5

Tella, Toluwani, Carolina H. Pohl, and Ayansina Ayangbenro. "A review of the therapeutic properties of dithiocarbamates." F1000Research 11 (February 28, 2022): 243. http://dx.doi.org/10.12688/f1000research.109553.1.

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The persistence of infectious diseases that continue to plague the world, as well as the formation of harmful substances within the human body, such as free radicals and reactive oxygen species (ROS) have sparked new research. Thus, the need for innovative approaches for developing new or modification of existing therapeutic agents. The design of biologically important metal complexes of dithiocarbamates (DTCs) has been made possible by recent advancements in innovative research. Dithiocarbamates are reduced thiuram disulfides with excellent complexing capabilities and have various applications. They are potent and work in tandem with the core metal ions of coordinating compounds to produce synergistic effects. Dithiocarbamates have many uses, including as antidotes for metal poisoning, cisplatin or carboplatin toxicity, and clinical trials for cancer, Lyme disease, human immunodeficiency virus and antibiotics. They exert anti-oxidant effect in cells. The understanding of the mechanisms of action of this therapeutic agent is important in drug repurposing. This review highlights the protective and therapeutic properties of dithiocarbamate compounds in biological systems.
6

Ahmad, Jimmy, Fiona N. F. How, Siti Nadiah Abdul Halim, Mukesh M. Jotani, See Mun Lee, and Edward R. T. Tiekink. "A new structural motif for cadmium dithiocarbamates: crystal structures and Hirshfeld surface analyses of homoleptic zinc and cadmium morpholine dithiocarbamates." Zeitschrift für Kristallographie - Crystalline Materials 234, no. 5 (May 27, 2019): 341–49. http://dx.doi.org/10.1515/zkri-2018-2141.

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Abstract The crystal and molecular structures of two homoleptic morpholine-derived dithiocarbamates of zinc, binuclear {Zn[S2CN(CH2CH2)2O)2]2}2 (1), and cadmium, one-dimensional coordination polymer {Cd[S2CN(CH2CH2)2O)2]2}2 (2), are described. In 1, a centrosymmetric binuclear molecule is found as there are equal numbers of chelating and bidentate bridging dithiocarbamate ligands; weak transannular Zn···S interactions are found within the resultant eight-membered {···SCSZn}2 ring which has the form of a chair. The resultant 4+1 S5 donor set is highly distorted with the geometry tending towards a square-pyramid. By contrast, a square-planar geometry is found in centrosymmetric 2 defined by symmetrically chelating dithiocarbamate ligands. The presence of Cd···S secondary bonding in the crystal of 2 leads to a distorted 4+2 S6 octahedron and a linear coordination polymer, which is unprecedented in the structural chemistry of cadmium dithiocarbamates. The analyses of the Hirshfeld surfaces for 1 and 2 show the dominance of H···H, S···H/H···S and O···H/H···O contacts to the surface, i.e. contributing around 90 and 80%, respectively.
7

Begum, B., A. Sarker, AKM Lutfor Rahman, and NC Bhoumik. "Synthesis and characterization of mixed ligand catecholato-bis (diamine-mono-dithiocarbamato) vanadium (IV) complexes." Bangladesh Journal of Scientific and Industrial Research 52, no. 2 (June 13, 2017): 89–96. http://dx.doi.org/10.3329/bjsir.v52i2.32913.

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Diamine-mono-dithiocarbamates are mono-basic bidentate ligand forming stable complexes with transition metals. Mixed ligand catecholato-bis (diamine-mono-dithiocarbamato) vanadium (IV) complexes were synthesized and characterized using FT-IR, UV-visible and 1H-NMR spectroscopic techniques. The formation of vanadium complexes was con?rmed by the disappearance of ?S-H band in the complexes which was present in the ligands and incidence of ?V-S and ?V-O band in FT-IR spectra of the complexes. The mono-dithiocarbamate with one uncoordinated ?NH/NH2 group was indicated by the presence of ?N-H vibrational band in both the ligands and complexes. In the 1H-NMR spectra, the peak for –SH proton of ligands disappeared in the complexes suggest the formation of [VL2Cat] complex. Non-electrolytic nature of the synthesized complexes was established by their low molar conductance values. The +4 oxidation state of vanadium was con?rmed by the electronic spectra of the complexes. On the basis of all physico-chemical data, a six-coordinated octahedral structure has been suggested for catecholato-bis (diamine-mono-dithiocarbamato) vanadium (IV) complexes.Bangladesh J. Sci. Ind. Res. 52(2), 89-96, 2017
8

Versloot, P., J. G. Haasnoot, J. Reedijk, M. van Duin, and J. Put. "Sulfur Vulcanization of Simple Model Olefins, Part IV: Vulcanizations of 2,3-Dimethyl-2-Butene with TMTD and Activated Zinc Dithiocarbamate/Xanthate Accelerators at Different Temperatures." Rubber Chemistry and Technology 68, no. 4 (September 1, 1995): 563–72. http://dx.doi.org/10.5254/1.3538757.

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Abstract The mechanism of the accelerated sulfur vulcanization of rubber was studied by the use of 2,3-dimethyl-2-butene (C6H12, TME) as a simple, low-molecular model alkene. Treatment of TME with a mixture of ZnO, S8 and the classical accelerator TMTD at temperatures above 100°C yields a mixture of addition products ((C6H11—Sn—C6H11) ). In the temperature range of 50 up to 100 °C only intermediate products, C6H11—Sn—S(S)CN(CH3)2 are obtained. Room temperature vulcanization is feasible using highly reactive accelerators, such as xanthate derivatives. These derivatives result in formation of the crosslink precursors which are converted to the actual crosslink in the presence of zinc dithiocarbamates. The addition of (secondary) amines enhances the solubility of the dithiocarbamates, and therefore the reactivity of the xanthate/zinc dithiocarbamate combination.
9

Dogheim, Salwa M., Sohair A. Gad Alla, Ashraf M. El-Marsafy, and Safaa M. Fahmy. "Monitoring Pesticide Residues in Egyptian Fruits and Vegetables in 1995." Journal of AOAC INTERNATIONAL 82, no. 4 (July 1, 1999): 948–55. http://dx.doi.org/10.1093/jaoac/82.4.948.

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Abstract Organophosphorus, dithiocarbamates, and some synthetic pyrethroids pesticides, which are commonly used in Egypt for pest control, were monitored, as well as persistent organochlorines, which had been prohibited from use several years ago. Fruit and vegetable samples (397) were collected from 8 local markets and examined for 52 pesticides. Of all analyzed samples, 42.8% contained detectable residues, of which 1.76% exceeded their maximum residue limits (MRLs). The rates of contamination with the different pesticides were 0-86%. However, violation rates among contaminated products were very low, ranging from 0 to 4.6%. In general, organochlorine pesticide residues were not detected in most samples. Dithiocarbamate residues were found in 70.4% of 98 samples analyzed for dithiocarbamates, but only one grape sample had residues exceeding the MRL established by the Codex Committee on Pesticide Residues.
10

Bala, Veenu. "Dithiocarbamates." Synlett 25, no. 05 (January 23, 2014): 746–47. http://dx.doi.org/10.1055/s-0033-1340637.

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You might also be interested in the extended bibliographies on the topic 'Dithiocarbamates' for particular source types:
Journal articles Dissertations / Theses Books

Dissertations / Theses on the topic "Dithiocarbamates":

1

McMaster, Claire. "Radical mediated reactions of dithiocarbamates." Thesis, University of Birmingham, 2013. http://etheses.bham.ac.uk//id/eprint/3886/.

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Chapter one reviews the use of acyl radicals and the various functional groups from which they have been derived. The earlier work on the use of dithiocarbamates as a source of acyl radicals has been progressed. Systems with the potential to follow either a 6-exo or competing 7-endo cyclisation pathway have been made. Chapter two is about the radical mediated reduction of the dithiocarbamate group. Previously reported dithiocarbamate group transfer reactions are reviewed along with existing methods for the reductive removal of the dtihiocarbamate and related xanthate groups. The development of conditions for a general method of the reduction is reported, with various examples being shown. Chapter three begins with a review of the synthesis of a range of twisted amides. The formation of a twisted amide precursor, containing a dithiocarbamate groups is reported. The attempts to form the bicyclic twisted amide, by used of carabamoyl radicals generated from dithiocarbamates are described. Chapter four discusses previous attempts at the synthesis of the natural occurring compound stemofoline. The attempted formation of the dithiocarbamate containing precursor for a 7-endo-trig cyclisation, 5-exo-trig transannular cyclisation, group transfer reaction to give the azatricyclic system, analogous to the tricyclic core of stemofoline is discussed.
2

Cox, Michael Jason. "Zinc, cadmium and mercury 1,1-dithiolates /." Title page, abstract and contents only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09phc8775.pdf.

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3

Ahmed, Mohammed A. K. "Synthesis and physical investigation of tellurium dithiocarbamates." Thesis, Aston University, 1985. http://publications.aston.ac.uk/11726/.

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4

Exarchos, George. "Reactions between metal sulfur chelate complexes and class B metal centres." Thesis, King's College London (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312991.

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5

Fiddy, J. M. "A Moessbauer effect study of iron(III) dithiocarbamates." Thesis, University of Liverpool, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233819.

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6

Roe, Stephen Mark. "Structural studies of main group metal carboxylates and dithiocarbamates." Thesis, University of Warwick, 1989. http://wrap.warwick.ac.uk/56212/.

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The work contained in this thesis describes the crystal structures of a number of tin(IV) and tellurium(IV) carboxylates and dithiocarbamates. The results show the regularity at which these types of compounds form secondary bonds (weak interactions), and the effect of the lone pair of tellurium(IV) on the geometries formed. The area has been studied through the determination of the following crystal structures: i) monocarboxylates: Ph3SnOCOCH2Cl, Ph3SnOCOCHCh, Ph3SnOCOCCh.MeOH. Ph3SnOCOCCh and Ph3TeOCOCCh. ii) dicarboxulates : Ph2Sn(OCOCH3)2, Ph2Sn(OCOCH2CI)2 and Ph2Te(OCOCCI3)2 iii) dithiocarbamates : Ph2Te(S2CNEt2)2, Ph2Te(S2CN(Et)(Ph))2 and Ph2Te(S2CNPh2)2 In addition to these, six hydrolysis products of Ph3SnOCOCCh are reponed. These com- pounds show the varied results that are obtained from the facile dearylation of the organotin com- pound by a strong organic acid in the presence of water. The following structures are reported: Ph2 Sn(OH)(OCOCCh), {[Pb2Sn(OCOCCh)hOh (two isomers), [(PbSn))(Oh(OCOCCh)sh, [PhSn(O)(OCOCCh)]6 and [(Ph 2 Sn)2(OH)(OCOCCh)3h.
7

Duffour, Jacqueline. "Résidus des dithiocarbamates et de l'éthylènethiourée : aspects toxicologiques et analytiques." Montpellier 1, 1991. http://www.theses.fr/1991MON13511.

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Boisdé, Frédéric. "Sur la mise au point de dosages immunoenzymatiques de pesticides et de leurs dérivés : le cas des dithiocarbamates et de l'éthylènethiourée." Brest, 2003. http://www.theses.fr/2002BRES2038.

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La méthode officielle utilisée à ce jour pour le dosage des résidus de dithiocarbamates consiste en une hydrolyse acide des échantillons puis, après distillation, d'un dosage spectrophotométrique du disulfure de carbone (CS2) libéré. Ce procédé présente de nombreuses limites comme une faible reproductibilité, un seuil de détection inadapté à certains dosages et une absence de spécificité. Les méthodes classiques de dosage (chromatographies gazeuse et liquide) sont elles sensibles et spécifiques, mais nécessitent un matériel coûteux, manipulé par un personnel qualifié. De ce fait, les méthodes de dosage immunoenzymatique qui permettent, en outre, de traiter plusieurs échantillons simultanément sont apparues comme une alternative pertinente aux techniques habituellement utilisées. Nos travaux décrivent, dans un premier temps, la synthèse de molécules dont la structure est identique à celle des pesticides que l'on cherche à doser. Elles possèdent en plus un bras de liaison, généralement constitué d'un enchaînement plus ou moins long de méthylènes, fonctionnalisé à son extrémité par un acide carboxylique. Ces haptènes peuvent ainsi être couplés à la surface de protéines porteuses (BSA, Ova) par la formation de liaison amide avec leurs restes lysyles. Dans un second temps, ces différents conjugués haptènes-protéine sont utilisés soit comme immunogènes pour la production d'anticorps spécifiques des pesticides considérés ou soit comme traceurs lors de tests ELISA compétitifs pour la mise au point des dosages proprement dits. Cette étude nous a permis de développer complètement une méthode de dosage immunoenzymatique du thirame et d'obtenir des anticorps reconnaissant de manière compétitive les éthylène-bis-dithiocarbamates et un produit issu de leur dégradation, l'éthylènethiourée, reconnue comme cancérogène
To date, the official method to be used for the measurement of dithiocarbamates residues is to first carry out an acid hydrolysis of the samples and, after distillation, to quantify the released carbone disulfure (CS2) by spectrophotometry. But, this procedure is spoilt with many drawbacks, e. G. Low reproducibility, detection threshold unsuited for certain quantifications and lack of specificity. On the other hand, the classical quantification techniques, i. E. GC and HPLC, are sensitive and specific, but require a high-cost equipment and qualified operator(s). This is why enzyme immunoassays that, in addition, allow one to process several samples at the same time have sounded as a relevant alternative to the usual techniques. We first report on the synthesis of molecules whose structure is alike that of the pesticides to be quantified. The additional arm they carry, usually, consists of a more or less long chain of methylenes and ends with a carboxylic acid function. These haptens can be linked to the surface of carrier proteins, BSA and Ova, through an amide bond with lysyl residues. Then, in a second step, these various hapten-protein conjugates were used as either immunogens for production of specific antibodies for the pesticides of interest, or tracers in competitive ELISA assays for the development of quantification protocols. This study allowed us to both develop a complete enzyme immunoassay for thirame measurement and get competitive antibodies for ethylene-bis-dithiocarbamates and one of their by-products, ethylenethiourea, known as being carcinogenic
9

Stephens, Alan Nicholas. "Niobium dithiocarbamates : structural and solution studies in relation to a bridged-dinitrogen complex." Thesis, University of Sussex, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.236255.

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Xu, Ximing. "Arylamines N-acétyltransférases : liaison du cofacteur, mécanisme catalytique et inhibition par les dithiocarbamates." Paris 7, 2014. http://www.theses.fr/2014PA077091.

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Les principaux objectifs de cette thèse visent à mieux comprendre les relations structure/fonction de la famille de arylamine N-acétyltransférases (NAT) et comment ces enzymes peuvent être inhibées par un groupe important de pesticides: thiocarbamates. Afin d'obtenir de nouvelles informations sur les mécanismes moléculaires qui régissent la fixation de la AcCoA aux NAT, la première partie de mon travail a été consacrée à la détermination de la structure cristalline d'une isoforme NAT de Mesorhizobium loti ((RHILO) NAT1) en complexe avec CoA. La deuxième partie de mon travail a consisté à comprendre le rôle d'une position structuralement conservée au sein du motif conservé (Pro-Phe/Tyr-Glu-Asn ou PF/YEN) dans le site actif des NAT. L'isoforme (RHILO) NAT1 a été utilisée comme modèle pour comprendre le rôle de cette position conservée. Parallèlement aux études structure/fonction, la troisième partie de ma thèse a été consacrée à l'identification des thiocarbamates (principalement des pesticides) capables inhiber les NAT humaines et par conséquent le métabolisme d'autres pesticides via des mécanisme d'interaction «pesticide-pesticide». La plupart des travaux a reposé sur des approches moléculaires (expression d'enzymes recombinantes, cinétique enzymatique, mutagenèse dirigée, détermination de structure 3D, modélisation moléculaire) et des approches cellulaires (exposition des kératinocytes humains en culture à des amines aromatiques et des pesticides de type thiocarbamate, détection de métabolites dans des échantillons biologiques)
The main goals of this thesis aimed at better understanding structure/function relationships in the family of arylamine N-acetyltransferases (NAT) enzymes and how theses enzymes could be inhibited by an important group of pesticides: thiocarbamates. In order to get further insights into the molecular mechanisms that govern the binding of the AcCoA to NAT enzymes, the first part of my work was devoted to the determination of the crystal structure of a NAT isoform of Mesorhizobium loti ((RHILO)NAT1) in complex with CoA. The second part of my work consisted in understanding the role of a structurally conserved position present in a conserved motif (Pro-Phe/Tyr-Glu-Asn or PF/YEN) in the active site of NAT enzymes. (RHILO)NAT1 isoform was used as a model to decipher the role of this conserved position. In parallel to the structure/function studies, a third part of my thesis was devoted to the identification of thiocarbamates chemicals (mainly pesticides) that could inhibit human NAT enzymes and subsequently the metabolism of other pesticides through « pesticide-pesticide » interactions. Most of the work relied on molecular (recombinant enzyme expression, enzyme kinetics, site directed mutagenesis, crystal structure determination, molecular modelling) and cellular approaches (exposure of cultured human keratinocytes to aromatic amine and thiocarbamate pesticides, detection of metabolites in biological samples)
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Books on the topic "Dithiocarbamates":

1

Ahmed, Mohammed Amin Karim. Synthesis and physical investigation of tellurium dithiocarbamates. Birmingham: University of Aston. Department of Chemistry, 1985.

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2

F, Hepp Aloysius, and United States. National Aeronautics and Space Administration., eds. One-step synthesis of dithiocarbamates from metal powders. [Washington, DC]: National Aeronautics and Space Administration, 1993.

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F, Hepp Aloysius, and United States. National Aeronautics and Space Administration., eds. One-step synthesis of dithiocarbamates from metal powders. [Washington, DC]: National Aeronautics and Space Administration, 1993.

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F, Hepp Aloysius, and United States. National Aeronautics and Space Administration., eds. One-step synthesis of dithiocarbamates from metal powders. [Washington, DC]: National Aeronautics and Space Administration, 1993.

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Roe, Stephen Mark. Structural studies of main group metal carboxylates and dithiocarbamates. [s.l.]: typescript, 1989.

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6

M, Engel Tina, and Environmental Monitoring and Support Laboratory (Cincinnati, Ohio), eds. Determination of dithiocarbamate pesticides in wastewaters. Cincinnati, Ohio: U.S. Environmental Protection Agency, Environmental Monitoring and Support Laboratory, 1985.

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International Program on Chemical Safety., United Nations Environment Programme, International Labour Organisation, and World Health Organization, eds. Dithiocarbamate pesticides, ethylenethiourea, and propylenethiourea: A general introduction. Geneva: World Health Organization, 1988.

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Gessner, Peter K. Disulfiram and its metabolite diethyldithiocarbamate: Pharmacology and status in the treatment of alcoholism, HIV infections, AIDS and heavy metal toxicity. London: Chapman & Hall, 1992.

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One-step synthesis of dithiocarbamates from metal powders. [Washington, DC]: National Aeronautics and Space Administration, 1993.

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Parker, Philip M. The 2007 Import and Export Market for Thiocarbamates and Dithiocarbamates in China. ICON Group International, Inc., 2006.

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Book chapters on the topic "Dithiocarbamates":

1

Baghat, Khaled, and János Mink. "Vibrational Spectra of Metal Dithiocarbamates." In Progress in Fourier Transform Spectroscopy, 213–15. Vienna: Springer Vienna, 1997. http://dx.doi.org/10.1007/978-3-7091-6840-0_36.

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Hogarth, Graeme. "Transition Metal Dithiocarbamates: 1978-2003." In Progress in Inorganic Chemistry, 71–561. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471725587.ch2.

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Foss, Olav, and John J. Pitha. "Xanthates and Dithiocarbamates of Selenium(II) and Tellurium(II)." In Inorganic Syntheses, 91–93. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132357.ch32.

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Malepu, Vidyasagar, Christy D. Petruczok, TuTrinh Tran, Tianxi Zhang, Mahesh Thopasridharan, and Devon A. Shipp. "RAFT Polymerization of Vinyl Acetate, Styrene and Acrylates UsingN,N-Dithiocarbamates." In ACS Symposium Series, 37–47. Washington, DC: American Chemical Society, 2009. http://dx.doi.org/10.1021/bk-2009-1024.ch003.

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Onuska, Francis I. "Mass Spectrometry of Carbamates, Thiocarbamates, Dithiocarbamates, Urea, Thiourea, and Carboxanilide Pesticides." In Mass Spectrometry in Environmental Sciences, 367–404. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2361-7_17.

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Eybl, V., D. Kotyzová, J. Koutenský, D. Waitzová, and M. M. Jones. "The Influence of Some Dithiocarbamates on Oxidative Drug Metabolism: Interaction with Cadmium." In Mechanisms and Models in Toxicology, 209–12. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72558-6_33.

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Miller, Philip W. "Production and Reaction of [11C]Carbon Disulfide for the Synthesis of [11C]Dithiocarbamates." In Radiochemical Syntheses, 177–83. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118834114.ch18.

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Papadopoulou-Mourkidou, Euphemia, Emmanuil Nikolaos Papadakis, and Zisis Vryzas. "Application of Microwave-Assisted Extraction for the Analysis of Dithiocarbamates in Food Matrices." In Pesticide Protocols, 319–29. Totowa, NJ: Humana Press, 2006. http://dx.doi.org/10.1385/1-59259-929-x:319.

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Maia, Luisa B., and José J. G. Moura. "Detection of Nitric Oxide by Electron Paramagnetic Resonance Spectroscopy: Spin-Trapping with Iron-Dithiocarbamates." In Methods in Molecular Biology, 81–102. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3600-7_8.

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Mathes, Roger A., H. S. Booth, and R. D. Kirk. "Ammonium Dithiocarbamate." In Inorganic Syntheses, 48–50. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132340.ch12.

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Conference papers on the topic "Dithiocarbamates":

1

Farina, Y., M. Sanuddin, B. M. Yamin, Abarrul Ikram, Agus Purwanto, Sutiarso, Anne Zulfia, Sunit Hendrana, and Zeily Nurachman. "Structure of Biologically Active Organotin(IV) Dithiocarbamates." In NEUTRON AND X-RAY SCATTERING 2007: The International Conference. AIP, 2008. http://dx.doi.org/10.1063/1.2906071.

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Zavyalova, Ludmila V., Sergey V. Svechnikov, and Vladimir G. Tchoni. "Photodetectors of slit and sandwich types based on CdS and CdS1-xSex films obtained using MOCVD method from dithiocarbamates." In Photonics West '97, edited by Gail J. Brown and Manijeh Razeghi. SPIE, 1997. http://dx.doi.org/10.1117/12.271194.

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Muthalib, Amirah Faizah Abdul, and Ibrahim Baba. "New mono-organotin (IV) dithiocarbamate complexes." In THE 2014 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2014 Postgraduate Colloquium. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4895202.

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Zhang, Yi, Yan Luo, Jian-Qian Hu, Tao Zhang, and Yun-Yun Xu. "Tribological Performances and Mechanism of Bismuth Dialkyl-Dithiocarbamate Additive." In STLE/ASME 2008 International Joint Tribology Conference. ASMEDC, 2008. http://dx.doi.org/10.1115/ijtc2008-71016.

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Abstract:
A four-ball tester was used to evaluate the tribological performance of bismuth diamyl-dithiocarbamate in mineral oil, and compared with same types of metal additives. The results show that it exhibits better load-carrying capacities than said organic metal additives. The surface analytical tools such as X-ray photoelectron spectrometer (XPS) and Scanning electron microscopy (SEM) were used to investigate the topography, the compositions contents and the depth profile of some typical elements on the rubbing surface of worn scar. Smooth topography of worn scar further confirms that the additive showed good antiwear capacities, the results of XPS indicated that tribochemical mixed protective films consists of bismuth compounds, sulfides, sulphates and metal oxides, which contribute to improve the tribological properties of lubricants. Particularly, a larger number of bismuth containing compounds play an important role in improving extreme pressure properties of oils.
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Muliadi and Muhammad Nurdin. "Terbium piperidine dithiocarbamate with 2.2’ dimethyl-1.10 phenanthroline co-ligand." In 5TH INTERNATIONAL CONFERENCE ON ELECTRICAL, ELECTRONIC, COMMUNICATION AND CONTROL ENGINEERING (ICEECC 2021). AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0137981.

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Zhang, Yi, Yan Luo, Jian-Qiang Hu, Tao Zhang, and Yun-Yun Xu. "Study on Antioxidation Properties of the Complex of Dithiocarbamate With Tolutriazole Antioxidant." In ASME/STLE 2007 International Joint Tribology Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/ijtc2007-44020.

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Abstract:
The antioxidation properties of methylene bis(di-n-butyldithiocarbamate) (V 7723) - and tolutriazole derivative (V 887) - containing poly-a-olefin (PAO)-derived lubricants were evaluated by differential scanning calorimetry (DSC) and modified penn state micro-oxidation test (PMOT). DSC test measures incipient oxidation temperature (OT) and oxidation induction time (IT) of the lubricant at high temperatures and the oxidation stability of oil weight loss is measured by PMOT test. DSC test shows that OT and IT of V 7723-containing PAO were improved significantly by V 887 addition. PMOT test indicates that when combining with V 7723 antioxidants, V 887 can also effectively reduce the increase in weight loss of PAO. In addition, FTIR results from PMOT test confirm that addition of V 887 can significantly enhance the oxidation induction time of oils. These results suggest that the V 7723 shows a good oxidative synergism with V 887 antioxidant.
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Jamaluddin, Nur Amirah, and Ibrahim Baba. "Synthesis and structural characterization of new dithiocarbamate complexes from Sb(III) and Bi(III)." In THE 2013 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2013 Postgraduate Colloquium. AIP Publishing LLC, 2013. http://dx.doi.org/10.1063/1.4858751.

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Henckens, Anja, Laurence J. Lutsen, Dirk Vanderzande, Martin Knipper, Jean Manca, Tom Aernouts, and Jef Poortmans. "Synthesis of PTV vis the dithiocarbamate route: a new precursor route toward conjugated polymers." In Photonics Europe, edited by Paul L. Heremans, Michele Muccini, and Hans Hofstraat. SPIE, 2004. http://dx.doi.org/10.1117/12.545734.

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Li, Chuangang, Xiaohong Shu, Yuhong Zhen, Yuanyuan Li, Sa Deng, Qin Zhou, and Molin Li. "Notice of Retraction: The Protective Effects of Pyrrolidine Dithiocarbamate on Cisplatin-Induced Nephrotoxicity in Mice." In 2011 5th International Conference on Bioinformatics and Biomedical Engineering. IEEE, 2011. http://dx.doi.org/10.1109/icbbe.2011.5780444.

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Hsu, Shih-Chieh. "Research on the detection of dithiocarbamate pesticides by using surface-enhanced Raman spectroscopy (Conference Presentation)." In Label-free Biomedical Imaging and Sensing (LBIS) 2023, edited by Natan T. Shaked and Oliver Hayden. SPIE, 2023. http://dx.doi.org/10.1117/12.2665506.

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To the bibliography