2667-20-1Relevant articles and documents
Eosin y catalyzed difunctionalization of styrenes using O2 and CS2: A direct access to 1,3-oxathiolane-2-thiones
Yadav, Arvind K.,Yadav, Lal Dhar S.
, p. 4240 - 4244 (2016)
Visible light promoted straightforward highly regioselective synthesis of 1,3-oxathiolane-2-thiones (cyclic dithiocarbonates) starting directly from styrenes, CS2 and air (O2) is reported. The protocol utilizes eosin Y as an organophotoredox catalyst and clean resources like visible light and air (O2) as sustainable reagents at room temperature in a one-pot procedure. Additionally, the approach is advantageous in terms of step economy as it skips the prefunctionalization of styrenes to oxiranes, which has been inevitable in commonly used syntheses of 1,3-oxathiolane-2-thiones.
Synthesis, characterization, semi-empirical study, and biological activities of organotin(IV) and transition metal complexes with o -methyl carbonodithioate
Javed, Fatima,Ali, Saqib,Shah, Muhammad Wajid,Munawar, Khuram Shahzad,Shahzadi, Saira,Hameedullah,Fatima, Humaira,Ahmed, Madiha,Sharma, Saroj K.,Qanungo, Kushal
, p. 2795 - 2808 (2014)
Three transition metal and six organotin(IV) complexes have been synthesized by treating potassium o-methyl carbonodithioate with ZnCl2/CdCl2/HgCl2 and R2SnCl2/R3SnCl under stirring. The co
Synthesis and crystal structure of bis(O-methyl hydrogenato carbonodithioate)-Pb(II): structural, optical and photocatalytic studies of PbS nanoparticles from the complex
Ajibade, Peter A.,Oluwalana, Abimbola E.
, p. 3575 - 3588 (2019)
Lead(II) methyl xanthate [Pb(S2COMe)2] was synthesized and characterized by single crystal X-ray crystallography. The molecular structure showed a distorted tetrahedral geometry around Pb(II) with each monomeric unit linked with another through Pb???S interactions. The compound was used to prepare hexadecylamine capped PbS (HDA-PbS) and oleylamine capped PbS (OLA-PbS) nanoparticles. The PbS nanoparticles were indexed to the cubic PbS crystalline phase with particle sizes of 4.5–34.5 nm. The estimated optical bandgaps obtained from the tauc’s plots were 3.47 and 3.30 eV for HDA-PbS and OLA-PbS, respectively, which are blue shifted in comparison to bulk PbS. The photodegradation of methylene blue using PbS as photocatalyst shows that HDA-PbS have the best degradation efficiency of 77.70% after 240 min.
The Alkali Metal Salts of Methyl Xanthic Acid
Liebing, Phil,Schmeide, Marten,Kühling, Marcel,Witzorke, Juliane
, p. 2428 - 2434 (2020/06/17)
Methyl xanthates of the type M(SSC-OMe) (M = Li–Cs) are readily formed when carbon disulfide is reacted with the corresponding alkali metal hydroxides in methanol exposed to air, or with the alkali metal methoxides in dry methanol or THF under exclusion of air. The reactions are easily monitored by 13C NMR spectroscopy. The Na, K, Rb, and Cs salt could be isolated in high yields, while the Li salt decomposed upon attempted isolation. All compounds are readily complexed by crown ethers and form isolable 1:1 adducts, including the elusive Li salt. All products were studied by NMR (1H, 13C, and alkali metal nuclei) and IR spectroscopy, and most of them where structurally characterized by single-crystal X-ray diffraction. Li(SSC-OMe)(12c4) (12c4 = [12]crown-4) and Cs(SSC-OMe)(18c6) (18c6 = [18]crown-6) represent the first structurally characterized lithium and caesium xanthate complexes, respectively.
COMPOUNDS, THEIR PREPARATION, RELATED COMPOSITIONS, CATALYSTS, ELECTROCHEMICAL CELLS, FUEL CELLS, AND USES THEREOF
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Paragraph 0407, (2019/04/25)
In some embodiments, this application relates to inventive compounds (e.g., Formula (I), Formula (II), thiosemicarbazones and/or thiosemicarbazones and their metal (e.g., zinc, cobalt, nickel, or copper) complexes, and extended structures thereof), methods for preparation of the inventive compounds, compositions comprising the inventive compounds (e.g., anode, cathodes, catalysts (e.g., electrocatalysts), glassy carbon electrodes, carbon paste electrodes, covalently modified carbon (e.g., modified graphene)), electrochemical cells comprising compositions that comprise one or more inventive compounds, fuel cells comprising compositions that comprise one or more inventive compounds, uses of one or more inventive compounds to produce H2 (e.g., via an electrochemical cell), and uses of one or more inventive compounds to create energy from H2 (e.g., via a fuel cell). Additional embodiments of the invention are also discussed herein.
Highly efficient structurally characterised novel precatalysts: Di- and mononuclear heteroleptic Cu(i) dixanthate/xanthate-phosphine complexes for azide-alkyne cycloadditions
Anamika,Agrahari, Anand K.,Manar, Krishna K.,Yadav, Chote Lal,Tiwari, Vinod K.,Drew, Michael G. B.,Singh, Nanhai
, p. 8939 - 8949 (2019/06/17)
Novel heteroleptic dinuclear [Cu2(L)(PPh3)4] (L = 2,6-pyridinedimethyldixanthate L1 1, 1,4-benznedimethyldixanthate L2 2, 1,4-cyclohexanedixanthate L3 3) and mononuclear [Cu(L4)(PPh3)2] 4 (L4 = pipero
Important Phase Control of Indium Sulfide Nanomaterials by Choice of Indium(III) Xanthate Precursor and Thermolysis Temperature
Masikane, Siphamandla C.,McNaughter, Paul D.,Lewis, David J.,Vitorica-Yrezabal, Inigo,Doyle, Bryan P.,Carleschi, Emanuela,O'Brien, Paul,Revaprasadu, Neerish
, p. 1421 - 1432 (2019/03/07)
Four In(III) xanthate complexes, [In(S2COR)3] where R = Me, Et, iPr and sBu, respectively, were synthesized, characterized and subsequently used as single source molecular precursors via a solventless thermolysis route to obtain indium sulfide materials. By choice of precursor and reaction temperature crystalline powders of tetragonal In2S3, cubic In2S3 and cubic In2.77S4 were acquired. The phase identification and purity were conducted through examination of the experimental powder X-ray diffraction patterns relative to the simulated patterns for single X-ray crystal diffraction.
Discovery of Potent Protease-Activated Receptor 4 Antagonists with in Vivo Antithrombotic Efficacy
Miller, Michael M.,Banville, Jacques,Friends, Todd J.,Gagnon, Mark,Hangeland, Jon J.,Lavallée, Jean-Fran?ois,Martel, Alain,O'Grady, Harold,Rémillard, Roger,Ruediger, Edward,Tremblay, Fran?ois,Posy, Shana L.,Allegretto, Nick J.,Guarino, Victor R.,Harden, David G.,Harper, Timothy W.,Hartl, Karen,Josephs, Jonathan,Malmstrom, Sarah,Watson, Carol,Yang, Yanou,Zhang, Ge,Wong, Pancras,Yang, Jing,Bouvier, Michel,Seiffert, Dietmar A.,Wexler, Ruth R.,Lawrence, R. Michael,Priestley, E. Scott,Marinier, Anne
, p. 7400 - 7416 (2019/08/26)
In an effort to identify novel antithrombotics, we have investigated protease-activated receptor 4 (PAR4) antagonism by developing and evaluating a tool compound, UDM-001651, in a monkey thrombosis model. Beginning with a high-throughput screening hit, we identified an imidazothiadiazole-based PAR4 antagonist chemotype. Detailed structure-activity relationship studies enabled optimization to a potent, selective, and orally bioavailable PAR4 antagonist, UDM-001651. UDM-001651 was evaluated in a monkey thrombosis model and shown to have robust antithrombotic efficacy and no prolongation of kidney bleeding time. This combination of excellent efficacy and safety margin strongly validates PAR4 antagonism as a promising antithrombotic mechanism.
Accessing γ-Ga2S3 by solventless thermolysis of gallium xanthates: A low-temperature limit for crystalline products
Alderhami, Suliman A.,Collison, David,Lewis, David J.,McNaughter, Paul D.,O'Brien, Paul,Spencer, Ben F.,Vitorica-Yrezabal, Inigo,Whitehead, George
, p. 15605 - 15612 (2019/11/03)
Alkyl-xanthato gallium(iii) complexes of the form [Ga(S2COR)3], where R = Me (1), Et (2), iPr (3), nPr (4), nBu (5), sBu (6) and iBu (7), have been synthesized and fully characterised. The crystal structures for 1 and 3-7 have been solved and examined to elucidate if these structures are related to their decomposition. Thermogravimetric analysis was used to gain insight into the decomposition temperatures for each complex. Unlike previously explored metal xanthate complexes which break down at low temperatures (2S3 was the sole product formed. In the case of R = Me, Chugaev elimination did not occur and amorphous GaxSy products were formed. We conclude therefore that the low-temperature synthesis route offered by the thermal decomposition of metal xanthate precursors, which has been reported for many metal sulfide systems prior to this, may not be appropriate in the case of gallium sulfides.
Synthesis of nanostructured powders and thin films of iron sulfide from molecular precursors
Almanqur, Laila,Vitorica-Yrezabal, Inigo,Whitehead, George,Lewis, David J.,O'Brien, Paul
, p. 29096 - 29103 (2018/08/29)
Iron(iii) xanthate single-source precursors [Fe(S2COR)3] (R = methyl, ethyl, isopropyl and 1-propyl) were used to deposit iron sulfide thin films and nanostructures by two simple, efficient and low-cost methods (spin coating and solid state deposition). The single-crystal X-ray structures of the iron(iii) n-propyl xanthate and iron(iii) iso-propyl xanthate have been determined. Thermogravimetric analysis (TGA) studies of the complexes shows that decomposition of the complexes produces iron sulfide, pyrite or trolite. The crystallinity of iron sulfide thin films and powder samples was studied using X-ray diffraction (XRD), and their morphology was studied by scanning electron microscopy (SEM).
