monosulfide


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mon·o·sul·fide

 (mŏn′ō-sŭl′fīd′)
n.
A sulfide with each molecule containing one sulfur atom.
References in periodicals archive ?
For pentachlorobenzene and tetramethylthiuram monosulfide, the specific mechanism of acute toxicity was not found.
Luther, "Kinetics of pyrite formation by the [H.sub.2]S oxidation of iron(II) monosulfide in aqueous solutions between 25 and 125[degrees]C: the mechanism," Geochimica et Cosmochimica Acta, vol.
After depositing the conjugates on a glassy carbon electrode (GCE) surface, single-stranded DNA (ssDNA) was attached to the conjugates by gold monosulfide bonding [98].
At elevated temperatures, some of the polysulfide and disulfide bonds in the rubber are converted to monosulfide bonds, which lead to the formation of uncured rubber [24].
Functional components in garlic of antimicrobial activities included allicin, thiosulfinates, diallyl monosulfide, diallyl disulfide, diallyl trisulfide, diallyl tetrasulfide, and ajoene; nevertheless, major functional components in onion of antimicrobial activities contained saponins and Ace-AMP1 (see Table 1).
The concentration of soluble S[O.sub.4.sup.2-] throughout the profile in all sites exceeded the trigger value (1.04 mmol [kg.sup.-1]) for potential formation of monosulfide (Bush et al.
These five peaks can be assigned to monosulfide ([S.sup.2-]), disulfide ([S.sub.2.sup.2-]), polysulfide ([S.sub.n.sup.2-]), sulfite (S[O.sub.3.sup.2-]), and sulfate (S[O.sub.4.sup.2-]), respectively [38].
Grieco, "An efficient approach for monosulfide bridge formation in solid-phase peptide synthesis," Tetrahedron Letters, vol.
In other laboratories, nickel subsulfide and green nickel oxide did not induce mutation to ouabain resistance in C3H/10T12 mouse embryo cells, nor did nickel subsulfide induce mutation to ouabain resistance or to 6-thioguanine resistance in cultured human diploid fibroblasts, although crystalline nickel monosulfide and green nickel oxide did induce amplification of the ect-2 protooncogene in C3H/1OT1/2 mouse embryo cells (Biedermann and Landolph 1987; Clemens et al.
The vulcanization accelerators used in this study were ethylenethiourea (ETU), 2-mercaptobenzothiazole (MBT), N-cyclohexyl-2-benzothiazylsulfenamide (CBS), tetramethylthiuram monosulfide (TMTM) and zinc dimethyldithiocarbamate (ZDMDC).
Analysis of the composition of compact and dispersed framboids shows mainly pyrite ([Fe.sub.2]S), with only a few having monosulfide (Fe[S.sub.2-x]) composition.