sulfonyl


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Related to sulfonyl: sulfinyl

sul·fo·nyl

(sŭl′fə-nĭl′)
n.
The bivalent radical SO2. Also called sulfuryl.
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In the aromatic region of the 1H-NMR spectrum signals appeared at I' 7.30 (d, J = 2.0 Hz, 1H, H-5), 7.21 (dd, J = 8.4, 2.4 Hz, 1H, H-7) and 6.85 (d, J = 8.4 Hz, 1H, H-8) were assigned to the phenyl ring attached to sulfonyl group; whereas three aromatic signals at I' 6.71 (s, 2H, H-2' and H-6'), 6.66 (s, 1H, H-4') were assigned to the benzene ring of 3,5-dimethylphenyl group.
Moreover, the presence of nitrogen atoms and rigid sulfonyl groups in PBz-tepa restricts the thermal degradation of the polymer at lower temperatures.
1-Ethyl-3-methyl-imidazolium acetate ([Emim][OAc]), 1ethyl-3-methyl-imidazolium bromide ([Emim][Br]), 1-ethyl3-methyl-imidazolium iodide ([Emim][I]), 1-ethylpyridinium iodide ([Epyr][I]), and di-ethyl-methylsulphonium bis(trifluoromethyl sulfonyl)imide ([EMS][BFSI]) were purchased from Iolitech (Germany).
250%, Glucosamine HCL Powder 1500 mg., Methyl Sulfonyl (Methane MSM) 250 mg., and Aloe Vera (leaf).
Twenty-four further contributions then cover materials including vinyl monomers, cannabis indica fibers, jute fibers, hydroxypropyl methylcellulose, oxidized regenerated cellulose, polyacrylamide, cellulose nanowhisker, and sulfonyl terminals; techniques such as azide alkyne cycloaddition, gamma and electron beam irradiation, radical polymerization, UV grafting, self-assembly, and click chemistry; perspectives on the field in general including an assessment of progress in the field and characterization of copolymers; and applications such as toxin removal, antimicrobial activity, bleeding control, wound healing, intelligent response, and drug delivery.
Glyburide is a second generation sulfonyl urea oral hypoglycaemic agent (OHA).
Recently, we described the Pd-catalyzed intramolecular N-arylation of some 2-aminopyrroles containing a (2-chlorophenyl) sulfonyl group at the 3-position to give a novel tricyclic ring system.
This distortion leads to trans-geometry of n-butyryl fragment around one nitrogen atom and the sulfonyl moiety of the other nitrogen atom.
It shows that the carboxyl group or the group of sulfonyl hydroxide can form a H-bond with key residue Arg316 in the docking pose.
The method is comprised of attaching a reactive group X--Y to a surface of a pigment; and subsequently displacing Y with an organic substrate N--S--ZM to form a surface-modified pigment having attached X--N--S--ZM; wherein X is a sulfonyl, phosphoryl, or 1,3,5-triazine group; Y is fluorine, chlorine, bromine or iodine; N is an amine, an imine, a pyridine, or a thiol group; S is substituted or unsubstituted alkyls, aryls, or polymer chains having a molecular weight range from approximately 300-8000; Z is a carboxyl, sulfonyl, phenolic, phosphoryl, ammonium, trimethylammonium, or tri-butylammonium group; and M is a halide, a negatively charged ion, a proton n salt form, or a cation in salt form.
Furthermore, the intermediate 3 was reacted with various sulfonyl chlorides (R-S[O.sub.2]-Cl) in DCM to obtain piperazine derivatives such as S1, S3, S4, and S7 (Figure 1).