ライフサイエンスコーパス: sulfonate

1 yl amine hydrochloride/poly(sodium 4-styrene sulfonate)).

2 e sulfonamide, and 6:2 and 8:2 fluorotelomer sulfonates).

3 such as hydrogen peroxide and methylmethane sulfonate.

4 ly(3,4-ethylene dioxy thiophene) polystyrene sulfonate.

5 thyl sulfonate, triflate, and perfluorobutyl sulfonate.

6 ionic synthetic polymers such as polystyrene sulfonate.

7 haldialdehyde and sulfite to form isoindol-1-sulfonate.

8 activation of hydroxy groups into halides or sulfonates.

9 th for C8-C14 PFCAs and C6-C8 perfluoroalkyl sulfonates.

10 xylic acid ethers, and novel polyfluoroalkyl sulfonates.

11 Fluorotelomer thioether amido sulfonate (10:2-FTSAS) and fluorotelomer sulfoxide amido

12 0:2-FTSAS) and fluorotelomer sulfoxide amido sulfonate (10:2-FTSAS-sulfoxide) were also occasionally

13 3-(6-bromo-1H-indole-3-carbonyl)-1H-indole-1-sulfonate (2).

14 ious literature, almost no 6:2 fluorotelomer sulfonate (6:2 FTS) was detected in teleost fish.

15 the reaction mechanism of 6:2 fluorotelomer sulfonate (6:2 FTS) with Co(2+)-activated PMS.

16 1:3-FTB and 9:1:2 FTB) and 6:2 fluorotelomer sulfonate (6:2-FTSA) were ubiquitously identified in the

17 Fluorotelomer sulfonates (6:2 FTS, 8:2 FTS, and 10:2 FTS) and FtB were

18 se 1A3 (SULT1A3)-the isoform responsible for sulfonating ~80% of the serotonin in the extracellular b

19 (with 2,2-azinobis-3-ethylbenzothiazoline-6-sulfonate (ABTS)).

20 with 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulfonate) (ABTS) and 17beta-estradiol (E2) as the probi

21 of putative sulfonate biosynthesis genes and sulfonate abundances in natural plankton communities ove

22 ) were obtained using sodium anthraquinone-2-sulfonate, adenosine-5'-monophosphate, dl-tryptophan, an

23 the development of phosphonate amidines and sulfonate amidines as isosteres of pArg and then use the

24 s reaction sequence enables the formation of sulfonated amino acids during embryo development in the

25 Use of sodium anthraquinone-2-sulfonate (AMS) as a cocatalyst enhances the product yie

26 in aqueous solution with sodium 1-naphthol-4-sulfonate, an aromatic alcohol, which, in the electronic

27 ally labile tyrosine sulfates with isosteric sulfonate analogues.

28 disulfur-containing DBPs, like bromosultone sulfonate and bromohydrin disulfonate, originated from o

29 ane anchor group based on negatively charged sulfonate and dodecyl chain.

30 Counterintuitively, the negatively charged sulfonate and nitronate functional groups of our analogs

31 Integrated peak area for putative sulfonated and glucuronidated E2 metabolites showed a si

32 Certain neurotransmitters are extensively sulfonated and inactivated by human sulfotransferase 1A3

33 rs to be similarly effective at sequestering sulfonates and carboxylate PFAS compounds and is less ef

34 (EST or SULT1E1), a conjugating enzyme that sulfonates and deactivates estrogens, in sepsis response

35 ystem can be applied to a wide range of aryl sulfonates and shows excellent C-3 regioselectivity of i

36 an important role in estrogen homeostasis by sulfonating and deactivating estrogens, but studies on t

37 poly(3,4-ethylenedioxythiophene):polystyrene sulfonate, and +10 to +15% for polymers such as poly(2-(

38 ocysteine, N-acetyl-cysteine, mercaptoethane-sulfonate, and glutathione) were detected with total con

39 tanoate, perfluorononanoate, perfluorohexane sulfonate, and perfluoroundecanoate in maternal blood.

40 fluoroalkyl, polyfluorochloroalkyl acids and sulfonates, and potential ether forms.

41 nce of three sulfonamides, two fluorotelomer sulfonates, and several polyfluoroalkyl phosphate dieste

42 midoalkyl betaine, 6:2 and 8:2 fluorotelomer sulfonates, and short chain perfluorocarboxylic acids.

43 gly ionized acids (carboxylates, phenolates, sulfonates, and sulfates), three types of strongly ioniz

44 es and indicate that, given the low pK(a) of sulfonated- and hydroxy-sulfonated-PCBs, they possess ne

45 on for an alkali metal cation connecting the sulfonate anion and a substrate's phosphate group to for

46 rmation of a redox mediator, anthraquinone-2-sulfonate (AQS), during microbial goethite reduction by

47 ydroxymethanesulfonate (HMS), C(2), and C(3) sulfonates are major products detected by electrospray i

48 n this study, we show that BODIPYs bearing a sulfonated aromatic group at the meso position provide a

49 lfonate surfactant mixture revealed dodecene sulfonate as a likely precursor for most detected DBPs;

50 poly(3,4-ethylenedioxythiophene) polystyrene sulfonate as a transparent and stretchable anode, a pero

51 onventional approaches with alkyl halides or sulfonates as alkylating agents, the use of unactivated

52 By using alkynyl sulfones or sulfonates as substrates, the oxidative gold catalysis i

53 ner diameter of 19-28 mum) were successfully sulfonated at room temperature using a cocktail of ClSO3

54 Adsorption of sulfonated azo dyes Tartrazine (E102), Sunset Yellow FCF

55 We report here on a sulfonate-based water-soluble photoswitch that, in contr

56 Expression of putative sulfonate biosynthesis genes and sulfonate abundances in

57 We outline the route to a suite of 5 new sulfonated BODIPYs with 2,6-disubstitution patterns span

58 To highlight the utility of these new, sulfonated BODIPYs, we further functionalize them to acc

59 (P)SOH) to the sulfinate (C(P)SO(2) (-)) and sulfonated (C(P)SO(3) (-)) forms, redirecting the C(P)SO

60 C5-C18), organosulfates (C2-C7, C12-C17) and sulfonates (C16-C22).

61 Polyfluoroalkyl sulfonates (C2nH2F4nSO3) were detected in all collected

62 , we devise a synthetic route to halogenated sulfonated carbofluoresceins from readily available, ine

63 The "sulfonated carbons" are a new class of metal-free solid

64 Contemporaneous expression of sulfonate catabolism genes in heterotrophic bacteria hig

65 orking electrode both bare and coated with a sulfonated charge selective polymer film, polystyrene-bl

66 dip appear before anions) only with lightly sulfonated columns.

67 promoted by a Cu-based complex with a chiral sulfonate-containing N-heterocyclic carbene, are broadly

68 Latex attachment on sulfonated COP surfaces are much stronger; several types

69 he order Ga < Fe < Al < Mn < Sb < Au for bis-sulfonated corroles; and, importantly, that they correla

70 llows the directional synthesis of desired 3-sulfonated coumarins in a one-pot, two-step process.

71 ABCO(SO2 )2 , and aryl propiolates affords 3-sulfonated coumarins in good to excellent yields.

72 Herein, we demonstrate a lithium sulfonated covalent organic framework (denoted as TpPa-S

73 nt, the DML was labeled with the far-red dye sulfonate cyanine 5 (sCy5), site-specifically conjugated

74 dies revealed that the probe incorporating a sulfonated cyanine-5 fluorophore was the most appropriat

75 ssor coupled to an AS18 latex-coated surface-sulfonated cyclo-olefin polymer (COP) capillary column w

76 s a C3-organosulfonate, 2,3-dihydroxypropane sulfonate (DHPS), is excreted.

77 ort and catabolism of 2,3-dihydroxypropane-1-sulfonate (DHPS).

78 he intermediary product 5,6-dihydrouridine-6-sulfonate (dhU6S) (generated by reaction of bisulfite wi

79 ly brominated species, including bromohydrin sulfonates, dihalo-bromosulfonates, and bromosultone sul

80 n spin resonance experiments on poly(styrene-sulfonate)-doped poly(3,4-ethylenedioxythiophene) ( PEDO

81 hieved by using a 0.1% poly(sodium 4-styrene-sulfonate) draw solution).

82 phenoxide solubility and the formation of a sulfonate ester impurity.

83 n employs fac-[Ir(ppy)3] together with Tz(o) sulfonate esters and sulfonamides to facilitate the site

84 readily transformed into sodium sulfonates, sulfonate esters, and sulfonamides, as well as styrenes

85 ve to the use of genotoxic alkyl halides and sulfonate esters.

86 l network based on organic sulfur compounds (sulfonates) exists among key lineages of eukaryotic phyt

87 Here we use the incorporation of sulfonated fluorescent dyes to gain new understanding of

88 g bacterial taxa, T. pseudonana may use this sulfonate for targeted feeding of beneficial associates.

89 C8/C7 and C6/C5 polyfluorinated sulfonates from br-PFOS and br-PFHxS, respectively, were

90 ectrometry revealed the formation of OSs and sulfonates from photo-oxidation in the presence of sulfa

91 and produced 4:2, 6:2, and 8:2 fluorotelomer sulfonate (FtS), 6:2 fluorotelomer unsaturated carboxyli

92 ates, perfluorosulfonates, and fluorotelomer sulfonates (FTS) in biotic and abiotic samples from six

93 tes (PFSAs); 4:2, 6:2, and 8:2 fluorotelomer sulfonates (FTS); three perfluorooctane sulfonamides (PF

94 nts of sites contaminated with fluorotelomer sulfonates (FTSs) and related compounds should not be li

95 uoroalkane sulfonates (PFSAs), fluorotelomer sulfonates (FTSs), nonionic perfluoroalkane sulfonamides

96 m AFFF, which contains anionic fluorotelomer sulfonates (FtSs), zwitterionic fluorotelomer sulfonamid

97 , 6:2, and 8:2 fluorotelomer thioether amido sulfonate (FtTAoS) were characterized by determining the

98 The presence of sulfonate functional group on GO was confirmed using ele

99 arboxylic functional group and an unexpected sulfonate functional group on GO were characterized as t

100 orted based on work with a water-soluble bis-sulfonated gallium corrole in both cellular and rodent-b

101 advantage of the physical affinities between sulfonated GO and Fe3O4 nanoparticles, which allows tuni

102 studies suggest that the unusual active-site sulfonate group acts a proton relay even in strong acid,

103 oped membrane-targeting moiety composed of a sulfonate group and an alkyl chain of varied lengths.

104 Furthermore, the avibactam hydroxylamine-O-sulfonate group conformation varied according to pH, and

105 e anionic bipyridine ligand bearing a remote sulfonate group enables selective iridium-catalyzed bory

106 ging (XFI) at the sulfur K-edge to image the sulfonate group in taurine in situ in ex vivo tissue sec

107 nctional bipyridine ligand bearing a pendant sulfonate group, which had previously been successful fo

108 ented polyethylene-like materials containing sulfonate groups (PES23) with Li(+), Na(+), Cs(+), or NB

109 e replaced by four negative charges borne by sulfonate groups also installed in the para positions of

110 peting hydrogen-bonding interactions between sulfonate groups and the side chains of basic residues.

111 nduce reversible activation of the amine and sulfonate groups in HEPES and that electron redistributi

112 number of capture sites and by immobilizing sulfonate groups to passivate the surface between probe

113 e and squaraine dyes with water-solubilizing sulfonate groups were targeted in this study due to stro

114 ch bears negative charge due to incorporated sulfonate groups, with polyethylenimine (PEI) improved r

115 to those composed of phosphate, sulfate, or sulfonate groups.

116 ons and hydrogen bonding between the suramin sulfonated groups and Arg/Lys residues play critical rol

117 hydrogen-bonded two-dimensional guanidinium-sulfonate (GS) networks is demonstrated by using a serie

118 r long-chain perfluoroalkyl carboxylates and sulfonates (>/=C8 and >/= C6, respectively).

119 redict cellular sensitivity to methylmethane sulfonate, H2O2, and 5-FU from DRC.

120 Aromatic organosulfates and sulfonates have recently been observed in ambient aeroso

121 Aromatic organosulfates and sulfonates [hereafter called aromatic organosulfur compo

122 ute abundance of numerous HMOs, including 16 sulfonated HMOs we identified here in humans for the fir

123 s in infant immune markers, in contrast with sulfonated HMOs, whose expression correlated with suppre

124 rophic bacteria highlights active cycling of sulfonates in situ.

125 tive ionization mode and linear alkylbenzene sulfonates in the negative mode, are the most discrimina

126 The percentage of branched perfluorooctane sulfonate increased with depth, consistent with differen

127 protection for the corresponding phenyl aryl sulfonates increases with decreasing electrochemical pot

128 A sulfonated indium (In) metal organic framework (MOF) is

129 initial characterization of an ethyl methyl sulfonate-induced mutant population for the C(4) model S

130 isothiocyanate (SPITC) provided evidence for sulfonate interference with charge-directed mechanisms t

131 BTS, 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate), is a common chromogenic substrate for peroxi

132 Here we demonstrate that oxime sulfonates-known photoacid generators-are also acid gene

133 etramethyl-3-pyrroline-3-(methyl)methanethio-sulfonate label.

134 th an alkene surfactant (8-methylnon-7-ene-1 sulfonate) leading to "ene" hydroperoxides that in the d

135 cal effects of BPs with and without titanium sulfonate ligand (TiL4 ) modification are investigated.

136 nduced mechanochemical scission of the oxime sulfonate mechanophore also generates a ketone functiona

137 nthetic proton channels fabrication based on sulfonated metal-organic frameworks (MOFs), UiO-66-X, X

138 late-co-oligo(ethylene glycol) propyl sodium sulfonate methacrylate)]-b-polystyrene (POEGMA-PS), achi

139 ing anionic side groups via carboxylate- and sulfonate-modifications of tyrosine side chains in the s

140 ed ferrocene units and tetraalkylphosphonium sulfonate moieties in the side groups.

141 trong electrostatic interactions between the sulfonate moieties of FBDSA and basic sites to facilitat

142 the catechin-binding site of SULT1A3, which sulfonates monoamine neurotransmitters, is modeled on th

143 A copper-based complex that contains a sulfonate N-heterocyclic carbene ligand was first report

144 When the base is heavily sulfonated, neutrals elute after the anions.

145 ior art at the time of the advance involving sulfonate NHC-Cu catalysts and/or subsequent key develop

146 tic analysis of the structural attributes of sulfonate NHC-Cu catalysts that are responsible for thei

147 cular assemblies of protein complexes with a sulfonated NIR-II organic dye (CH-4T) to produce a brill

148 ltured eukaryotic phytoplankton taxa produce sulfonates, often at millimolar internal concentrations.

149 Alder cycloaddition to produce well-defined, sulfonated oligophenylenes and pre-functionalized polyph

150 In this design, having 1 sulfonate on the indole moiety adjacent to EuK ((99m)Tc-

151 nalogs with the carboxylate represented by a sulfonate or nitro and the thioester retained or represe

152 ion or benzylation of nitroazoles using aryl sulfonates or benzyl acetates is described.

153 Emerging PFASs such as fluorotelomer sulfonates or polyfluoroalkyl phosphate diesters account

154 Sulfonated-PCB levels were approximately 0.4-0.8% of the

155 soils and about twice the levels of hydroxy-sulfonated-PCBs and hydroxy-PCBs.

156 entification of two classes of contaminants: sulfonated-PCBs and hydroxy-sulfonated-PCBs.

157 The identification of sulfonated-PCBs was confirmed by the chemical synthesis

158 ven the low pK(a) of sulfonated- and hydroxy-sulfonated-PCBs, they possess negligible volatility, sup

159 of contaminants: sulfonated-PCBs and hydroxy-sulfonated-PCBs.

160 )}(4)Li(2)Cl(2) (3) in which four (phosphine-sulfonate)PdMe(py') units are arranged around the periph

161 poly(3,4-ethylenedioxythiophene)-polystyrene sulfonate ( PEDOT: PSS) as a cation-selective membrane m

162 poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) for 3D printing of conducting poly

163 poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) nanomaterials within poly(2-hydrox

164 poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) thin films, whose optical absorpti

165 poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS), is characterized using multimodal

166 poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS).

167 oly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) ( PEDOT: PSS) sensors on a fully biodegradabl

168 oly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) has been used, but no study has b

169 nd poly(ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS), in which PEDOT is intrinsically

170 and especially its complex with poly(styrene sulfonate) (PEDOT:PSS), is perhaps the most well-known e

171 oly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS), provide a promising electrical i

172 poly(3,4-ethylenedioxythiophene) polystyrene sulfonate, PEDOT:PSS electrode.

173 ch allows identification and annotation of S-sulfonated peptides across complex mixtures while provid

174 frared multiphoton dissociation (IRMPD) of S-sulfonated peptides in the background of unmodified pept

175 or selective dissociation and discovery of S-sulfonated peptides.

176 associated with the incorporation of a novel sulfonated peptidyl-amido sugar moiety whose structure i

177 This is the first report of a novel O-linked sulfonated peptidylamido-glycan moiety decorating a flag

178 rfluorooctanoic acid (PFOA), perfluorohexane sulfonate, perfluorononanoic acid, and 6:2 diPAP were si

179 e measured concentrations of perfluorooctane sulfonate, perfluorooctanoate, perfluorononanoate, perfl

180 hat the sulfur atom of the head group of the sulfonated PFASs retained an oxidation state of +V after

181 ir and drinking water, while perfluorobutane sulfonate (PFBS) dominated dust.

182 xane sulfonate (PFHxS), and perfluoroheptane sulfonate (PFHpS) quartiles compared with the lower quar

183 rohexane sulfonate (PFHxS), perfluoroheptane sulfonate (PFHpS), perfluorononanoic acid (PFNA), and pe

184 rohexane sulfonate (PFHxS), perfluoroheptane sulfonate (PFHpS), perfluorononanoic acid (PFNA), perflu

185 ategories of PFOA, PFNA, and perfluorohexane sulfonate (PFHxS) compared to the lowest categories.

186 erfluorooctanoate (PFOA) and perfluorohexane sulfonate (PFHxS) concentrations during pregnancy were a

187 Perfluorohexane sulfonate (PFHxS) is a widespread environmental contamin

188 ooctane sulfonate (PFOS) and perfluorohexane sulfonate (PFHxS) were positively associated with IGT (1

189 , perfluorononanoate (PFNA), perfluorohexane sulfonate (PFHxS), and perfluorodecanoate (PFDeA)] in ma

190 rfluorooctanoic acid (PFOA), perfluorohexane sulfonate (PFHxS), and perfluoroheptane sulfonate (PFHpS

191 uorooctane sulfonate (PFOS), perfluorohexane sulfonate (PFHxS), and perfluorononanoate (PFNA) concent

192 , prenatal exposure to PFOS, perfluorohexane sulfonate (PFHxS), perfluoroheptane sulfonate (PFHpS), p

193 n types of PFAS [PFOS, PFOA, perfluorohexane sulfonate (PFHxS), perfluoroheptane sulfonate (PFHpS), p

194 r perfluorodecanoate (PFDA), perfluorohexane sulfonate (PFHxS), perfluorooctanoate (PFOA), perfluoroo

195 l substances (PFAS), such as perfluorohexane sulfonate (PFHxS), perfluorooctanoate (PFOA), perfluoroo

196 uorooctane sulfonate (PFOS), perfluorohexane sulfonate (PFHxS), PFBS, and perfluorononanoic acid (PFN

197 CI: 1.12, 1.64), 37% higher perfluorooctane sulfonate (PFOS) (GM ratio = 1.37; 95% CI: 1.22, 1.54),

198 Perfluorooctane sulfonate (PFOS) and perfluorohexane sulfonate (PFHxS) w

199 Perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) concentra

200 Perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) were

201 tween early life exposure to perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), and

202 of legacy compounds such as perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), but

203 evaluations on PFAS, such as perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), but

204 Of the 36 target PFASs, perfluorooctane sulfonate (PFOS) dominated in all but one Icelandic and

205 uorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) in 2016.

206 s in the earthworms were for perfluorooctane sulfonate (PFOS) in the AFFF-impacted Soil A (2160 ng/g)

207 Perfluorooctane sulfonate (PFOS) is an environmental contaminant that ha

208 Perfluorocarbon chain of perfluorooctane sulfonate (PFOS) is not only hydrophobic but also oleoph

209 use of water scavengers and perfluorooctane sulfonate (PFOS) ligands.

210 g/L and the concentration of perfluorooctane sulfonate (PFOS) plus perfluorooctanoic acid (PFOA) rang

211 uoroundecanoate (PFUnDA), and perfluorooctyl sulfonate (PFOS) through inhalation and biotransformatio

212 in simulated cord plasma for perfluorooctane sulfonate (PFOS) was 2.72 g (95% CI: -3.40, -2.04), and

213 Perfluorooctane sulfonate (PFOS) was not significantly associated with a

214 rooctane sulfonamide (FOSA), perfluorooctane sulfonate (PFOS), and perfluoroalkyl carboxylates (EPFCA

215 , perfluorooctanoate (PFOA), perfluorooctane sulfonate (PFOS), and perfluorononanoic acid (PFNA), may

216 ooctane sulfonamide (PFOSA), perfluorooctane sulfonate (PFOS), and perfluorooctanoic acid (PFOA)] wer

217 , perfluorooctanoate (PFOA), perfluorooctane sulfonate (PFOS), and perfluoroundecanoate (PFUnDA) in b

218 Legacy PFAS, including perfluorooctane sulfonate (PFOS), have been regularly detected in marine

219 e substituted C8 PFSAs [keto-perfluorooctane sulfonate (PFOS), hydrogen-PFOS, and unsaturated PFOS] a

220 a perfluorooctanoate (PFOA), perfluorooctane sulfonate (PFOS), perfluorohexane sulfonate (PFHxS), and

221 is the first report of PFOA, perfluorooctane sulfonate (PFOS), perfluorohexane sulfonate (PFHxS), PFB

222 [perfluorooctanoate (PFOA), perfluorooctane sulfonate (PFOS), perfluorononanoate (PFNA), perfluorohe

223 samples (18 taxa) collected, perfluorooctane sulfonate (PFOS), perfluorooctane sulfonamide (FOSA), an

224 ere higher among the highest perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), perfluo

225 ersistent organic pollutant, perfluorooctane sulfonate (PFOS).

226 0 ng/L (median 850 ng/L) for perfluorooctane sulfonate (PFOS).

227 but to a lesser extent than perfluorooctane sulfonate (PFOS: BSAF ~ 21-29).

228 pression of immune response (perfluorooctane sulfonate; PFOS).

229 of PFASs were significant for perfluoroalkyl sulfonates (PFSAs) and C7-14 perfluoroalkyl carboxylates

230 9-14% yearly decline of C6-8 perfluoroalkyl sulfonates (PFSAs) following the cease in C6-8 PFSA prec

231 he dosing solution, C6 and C7 perfluoroalkyl sulfonates (PFSAs) were enriched in dosed mouse serum, s

232 ocarboxylic acids (PFCAs) and perfluoroalkyl sulfonates (PFSAs)) in the 13 samples ranged between 2.7

233 rinated carboxylates (PFCAs), perfluorinated sulfonates (PFSAs), alkyl sulfates (C (x)SO(4)), and 1-a

234 oalkyl carboxylates (PFCAs), perfluoroalkane sulfonates (PFSAs), fluorotelomer sulfonates (FTSs), non

235 creasing chain length for the perfluoroalkyl sulfonates (PFSAs).

236 C(4) through C(10) and C(12) perfluorinated sulfonates (PFSAs); 4:2, 6:2, and 8:2 fluorotelomer sulf

237 Five perfluoroalkane sulfonates (PFSAs, C(4-12)), 10 perfluoroalkyl carboxyli

238 "toolkit" comprising of two closely related sulfonated phosphine ligands and five bases, each posses

239 ion reactions of alcohols, carboxylic acids, sulfonates, phosphonates, and amines.

240 y(3,4-ethylenedioxythiophene):poly(4-styrene sulfonate), polyaniline) in combination with passive fib

241 mer membrane consisting of lithium-exchanged sulfonated polyether ether ketone embedded with polyhedr

242 the determination of the metal content in a sulfonated polyether ether ketone in the form of an indi

243 ute to prepare novel, sterically encumbered, sulfonated polyphenylenes possessing unprecedented struc

244 A thin (~4 nm) sulfonated-polystyrene (SPS) pre-coating is essential fo

245 lankton communities over the diel cycle link sulfonate production to light availability.

246 species, present as side-products of olefin sulfonate production.

247 lamino]-9,10-dioxo-9,10-dihydroanthrace ne-2-sulfonate (PSB-16133, 61) exhibited an IC50 value of 233

248 4+) ) within a nonporous anionic polystyrene sulfonate (PSS) matrix leads to a surface area increase

249 port a new approach to construct polystyrene sulfonate (PSS) threaded HKUST-1 metal-organic framework

250 he soluble additives Mg(2+) and poly(styrene sulfonate) (PSS) on the early stages of growth of calcit

251 ding homochiral 1 R-( -) or 1 S-( +) camphor sulfonate ( R-CSA or S-CSA), guest-to-host chirality tra

252 terial transformation of this diatom-derived sulfonate represents a previously unidentified and likel

253 lamino]-9,10-dioxo-9,10-dihydroanthra cene-2-sulfonate) represents the most selective P2Y4 receptor a

254 ing of arylboronic acids with perfluoroalkyl sulfonate salts based on a Bi(III)/Bi(V) redox cycle.

255 hat when the concentration of sodium dodecyl sulfonate (SDS) were lower than critical micelle concent

256 Our study provides evidence that sulfonates serve as an ecologically important currency f

257 th pKa </= 2 (i.e., alkyl sulfates and alkyl sulfonates) showed strong nonlinear distribution to the

258 A sulfonate-silica hybrid strong cation exchange monolith

259 A detachable sulfonate-silica hybrid strong cation-exchange monolith

260 We developed a new, sulfonated silicon rhodamine fluorophore and integrated

261 pH range and the complexation of Eu(III) to sulfonate site are more significant than that of U(VI).

262 ir sorption to GO; their complexation to the sulfonate site occurred at the lower pH range and the co

263 ally reversible adducts, such as acetals and sulfonates, so that sample preparation steps can generat

264 situ encapsulation of photoactive molecules (sulfonated spiropyran, SSP), as the molecular valve, int

265 oly(ethylene-ran-butylene)-block-polystyrene-sulfonate (SSEBS).

266 The ultrahigh proton selectivity in the sulfonated sub-1-nm MOF channels is mainly attributed to

267 he abundant dietary and host-derived organic sulfonate substrate in the gut, taurine (2-aminoethanesu

268 ontaining leaving group is not a fluorinated sulfonate such as triflate.

269 the majority of bacterial growth, among them sulfonates, sugar derivatives and organic nitrogen compo

270 mides can be readily transformed into sodium sulfonates, sulfonate esters, and sulfonamides, as well

271 (FTBs), 6:2 fluorotelomer mercaptoalkylamido sulfonate sulfone (FTSAS-SO2), 6:2 fluorotelomerthiohydr

272 These same phytoplankton-derived sulfonates support growth requirements of an open-ocean

273 Disinfection of a commercial C(12)-olefin sulfonate surfactant mixture revealed dodecene sulfonate

274 confined in a reverse spherical micelle of a sulfonate surfactant, given that the water pool in the r

275 We report the first identification of olefin sulfonate surfactant-derived DBPs from laboratory-disinf

276 The sulfonated surfactant diglycol ether sulfate was identif

277 We developed a sulfonate tag that can easily be installed and enables h

278 y for perfluoroalkyl acids and fluorotelomer sulfonates, the extraction of newly identified surfactan

279 ough the organo-catalyzed halocyclization of sulfonate thioimidate salts is also described.

280 administration of immunogen trinitrobenzene sulfonate (TNBS) in 10-d-old mouse pups produces an acut

281 ntra-colonic instillation of Trinitrobenzene Sulfonate (TNBS).

282 using fluorescent 2-p-toluidinonaphthalene-6-sulfonate (TNS) and validated using a molecular docking

283 ation is initiated by electron transfer from sulfonate to iron.

284 its involvement in pathways that enables C2 sulfonates to be used as terminal electron acceptors for

285 be due to the inability of L-perfluoroalkyl sulfonates to complex with VB12 and not an activation en

286 ind the model substrate tetraphenylporphyrin-sulfonate, TPPS, with Ka=3.8 10(5)mol/L in aqueous phosp

287 exafluorophosphate, hydrogen sulfate, methyl sulfonate, triflate, and perfluorobutyl sulfonate.

288 opening access to various monofunctionalized sulfonated trityl radicals.

289 e been devoted to utilizing highly activated sulfonate types of phenol derivatives (e.g., OTf, OTs, e

290 quence: H(+) >> K(+) > Na(+)> Li(+), and the sulfonated UiO-66 derivative channels show proton select

291 hiol reactive reagent p-chloromercuribenzene sulfonate was performed on the transport domain (interfa

292 atographic retentivity of phosphonate versus sulfonate was shown to be completely switched on this po

293 A test suite of aromatic sulfonates was used to characterize the chromatographic

294 Here, the sulfonated, water-soluble ferryl porphyrin complexes tet

295 lkyl carboxylates, alkyl sulfates, and alkyl sulfonates were determined at pH 7 by equilibration of t

296 Instead, the C-O functionalizations of aryl sulfonates will not be covered extensively unless they a

297 followed by treating the resultant glycosyl sulfonate with an enolate results in the stereospecific

298 aryl bromides and aryl chlorides as well as sulfonates with a wide range of primary and secondary al

299 For a series of aryl sulfonates with electron-withdrawing substituents, the r

300 es, dihalo-bromosulfonates, and bromosultone sulfonates, with chlorinated/iodinated analogues formed