ライフサイエンスコーパス: sulfonate

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

2 H species with the methyl group trans to the sulfonate.

3 ate or rectal application of trinitrobenzene sulfonate.

4 , and mutagenized it with 50 mm ethylmethane sulfonate.

5 luorooctane sulfonamide, and perfluorooctane sulfonate.

6 e exposed surface with sodium dodecylbenzene sulfonate.

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

8 thyl sulfonate, triflate, and perfluorobutyl sulfonate.

9 ionic synthetic polymers such as polystyrene sulfonate.

10 f the title compounds involved tetramic acid sulfonates.

11 d by binding/efficacy studies of synthesized sulfonates.

12 fluoroalkyl carboxylates and perfluoroalkane sulfonates.

13 converted to perfluorinated carboxylates and sulfonates.

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

15 xylic acid ethers, and novel polyfluoroalkyl sulfonates.

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

17 0:2-FTSAS) and fluorotelomer sulfoxide amido sulfonate (10:2-FTSAS-sulfoxide) were also occasionally

18 , [Polyethyleneimine](+) (PEI), [Polystyrene sulfonate](2-) (PSS) and neutral polymer Polychlorotrifl

19 1:3-FTB and 9:1:2 FTB) and 6:2 fluorotelomer sulfonate (6:2-FTSA) were ubiquitously identified in the

20 genic substrates for glycosidases based on a sulfonated 7-hydroxycoumarin scaffold.

21 gularly in peat samples with perfluorooctane sulfonate (85-655 ng kg(-1)), perfluorooctanoate (150-39

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

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

24 with 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) and self-decay of ferrate(VI) in phosp

25 Cluster II includes sulfonated acrylamide/acrylate copolymers and surfactant

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

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

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

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

30 ntified and confirmed as 1,3-benzothiazole-2-sulfonate, an oxidation product of a vulcanization accel

31 ally labile tyrosine sulfates with isosteric sulfonate analogues.

32 y infiltrating sulfonated sodium polystyrene sulfonate and (2) micro-fabricated paper chambers by pat

33 ence interval: 1.0, 2.8) for perfluorooctane sulfonate and 2.1 (95% confidence interval: 1.2, 3.6) fo

34 A mixture of 3-(10'-phenothiazinyl)propane-1-sulfonate and 4-morpholinopyridine was used as potent en

35 mental data to include pyridine-3-yl benzene sulfonate and its N-oxide and N-methylpyridinium derivat

36 ation ratios (+/-SE) between perfluorooctane sulfonate and its precursor perfluorooctane sulfonamide

37 uartile of maternal level of perfluorooctane sulfonate and perfluorooctanoic acid (P for trend < 0.01

38 Perfluorooctane sulfonate and perfluorooctanoic acid are perfluorinated

39 Perfluorooctane sulfonate and perfluorooctanoic acid were each associate

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

41 the concentrations of plasma perfluoroalkyl sulfonates and perfluoroalkyl carboxylates in Svalbard b

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

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

44 d for catalytic reduction of 1 degrees alkyl sulfonates, and 1 degrees and 2 degrees iodides in the p

45 perfluoroalkyl carboxylates, perfluoroalkyl sulfonates, and fluorotelomer sulfonates) per and polyfl

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

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

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

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

50 cations, which are stabilized by the pendant sulfonate anions.

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

52 rsors to the perfluorinated carboxylates and sulfonates are present in aqueous film-forming foams (AF

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

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

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

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

57 n of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) at the heme channel similar to those of the e

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

59 catalysts stabilized by imidazolium propane sulfonate based zwitterionic surfactants, allowing the s

60 mples in the presence of imidazolium propane sulfonate-based zwitterionic surfactants obtained using

61 in the lowest quartiles: for perfluorooctane sulfonate, beta = -0.18 (95% confidence interval: -0.41,

62 under anaerobic conditions and then further sulfonated by the SULTs in the presence of 3'-[(35)S]pho

63 y cytokine and further cysteine oxidation to sulfonates by reactive oxygen species abrogates both act

64 ution of C(4), C(6), and C(8) perfluoroalkyl sulfonates, C(6)-C(14) perfluoroalkyl carboxylates, and

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

66 Polyfluoroalkyl sulfonates (C2nH2F4nSO3) were detected in all collected

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

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

69 ers of hydroxyethyl methacrylate and styrene sulfonate complex with isolated gliadin (the toxic fract

70 lphosphino)ferrocene; OTf = trifluoromethane-sulfonate) complexes.

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

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

73 e coumarin from droplets, no exchange of the sulfonated coumarins being detected over 24 h at 30 degr

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

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

76 Para-chloromercuribenzene sulfonate covalently modifies beta2M286C side-chain sulf

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

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

79 Its sulfonated derivative yields ordered carbon when pyrolyz

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

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

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

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

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

85 Sulfonate ester hydrolysis has been the subject of recen

86 itrile, ketal, trifluoromethyl, sulfonamide, sulfonate ester), both aryl and vinyl halides, and five-

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

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

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

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

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

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

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

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

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

96 , 6:2, and 8:2 fluorotelomer thioether amido sulfonate (FtTAoS) were characterized by determining the

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

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

99 ) (PEG) hydrogels with aminooxy- and styrene sulfonate-functional groups were fabricated.

100 Similar to previous observations from CAD of sulfonated glycosaminoglycan anions, higher charge state

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

102 ty is observed for the 2-trimethylsilylethyl sulfonate group (SES), which is easier to remove.

103 one featuring the methyl ligand trans to the sulfonate group and another with the methyl trans to the

104 )S]phosphoadenosine 5'-phosphosulfate as the sulfonate group donor.

105 We found that the presence of the sulfonate group effectively prevents leakage of the coum

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

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

108 ormer isomer with the CH3 group trans to the sulfonate group is 2-9 kcal/mol lower.

109 owering the electron density of the adjacent sulfonate group, thereby weakening its hydration.

110 nes with the strongly N-activating p-toluene sulfonate group.

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

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

113 also operates in negative ion mode in which sulfonate groups are less labile than in positive ion mo

114 Molecular modeling predicted that sulfonate groups on C2-phenylethynyl substituents would

115 bind guanidinium cations (blue) between the sulfonate groups on its periphery, as well as accommodat

116 igands as binding sites, is demonstrated for sulfonate groups resulting in an enhancement of the memb

117 a higher probability of deprotonation at the sulfonate groups thus yielding charge-localized fragment

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

119 tion technique that can effectively preserve sulfonate groups while providing extensive backbone frag

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

121 -localized fragmentation without loss of the sulfonate groups.

122 cile proton-driven loss of the highly labile sulfonate groups.

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

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

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

126 nce, IR: cyanophenyl ether), leaving groups (sulfonate, halide, NHS, bromoacetate), and other reactiv

127 in an analogous molecule without the charged sulfonate headgroup are investigated by observing spectr

128 which is analogous to AOT but has no charged sulfonate headgroup, were also studied.

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

130 ecursors and perfluorinated carboxylates and sulfonates) in groundwater and solids samples, respectiv

131 logy models successfully predicted sites for sulfonate incorporation, for delineating adenosine's CNS

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

133 pol beta-deficient cells from methylmethane sulfonate-induced cytotoxicity.

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

135 ied by the formation of equimolar amounts of sulfonate ion and phthalimide which serve to buffer the

136 ydroxyl (HO(*)) radicals with perfluorinated sulfonated ionomer membrane, Nafion 211, is described.

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

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

139 Analogues 17 and 24, containing the benzyl sulfonate leaving group and a neutral DNA minor groove-b

140 ol-1-yl)methyl sulfonate prodrugs containing sulfonate leaving groups and 7-substituted electron-with

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

142 The use of sulfonated materials in the FO process opens up a fronti

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

144 scripts involved in sulfate assimilation and sulfonate metabolism were dramatically decreased in met3

145 nalysis of cells treated with methyl methane sulfonate (MMS), hydroxyurea (HU) or camptothecin (CPT),

146 idation (H2O2) and alkylation (methylmethane sulfonate, MMS) stresses induced nearly identical patter

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

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

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

150 Sulfonated molecules exhibit high water solubility, a pr

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

152 ial EPS does not affect the transport of the sulfonated nanoparticle, but the LB coating leads to dec

153 protecting group improved the synthesis of a sulfonated near-IR fluorophore and the mild deprotection

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

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

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

157 ubstrate is switched from a nonsulfonated to sulfonated one.

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

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

160 of poly(hydroxyethyl methacrylate-co-styrene sulfonate (P(HEMA-co-SS)).

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

162 poly(3,4-ethylenedioxythiophene)/polystyrene sulfonate (PEDOT/PSS) which was synthesized by electrode

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

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

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

166 on, while the latter one is a self-assembled sulfonated pentablock copolymer (Nexar copolymer) layer.

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

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

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

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

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

172 perfluoroalkyl sulfonates, and fluorotelomer sulfonates) per and polyfluorinated alkyl substances (PF

173 pril, when concentrations of perfluorooctane sulfonate, perfluorooctanoate, and numerous PFAA-precurs

174 sulfonic acids measured were perfluorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS), and

175 ne sulfonate (PFOS, 8.4%/y), perfluorodecane sulfonate (PFDS, 10%/y), and perfluorooctanoate (PFOA, 3

176 PFPIA), as well as perfluoroethylcyclohexane sulfonate (PFECHS) in indoor dust.

177 rfluorononanoate (PFNA), and perfluorohexane sulfonate (PFHxS) and age at natural menopause among wom

178 orononanoic acid (PFNA), and perfluorohexane sulfonate (PFHxS) and calculated eGFR in 9,660 children

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

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

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

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

183 uorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS), and perfluorooctane sulfonate (PFOS).

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

185 orononanoic acid (PFNA), and perfluorohexane sulfonate (PFHxS).

186 s either remained unchanged (perfluorooctane sulfonate (PFOS) and perfluorocarboxylates) or declined

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

188 Perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) are norma

189 kyl chemicals (PFCs) such as perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) have been

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

191 ults of a study on levels of perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), anal

192 erfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS) are persistent, synthetic industrial ch

193 environmental occurrence of perfluorooctane sulfonate (PFOS) can arise from its direct use as well a

194 1) ww, respectively, whereas perfluorooctane sulfonate (PFOS) concentrations did not change significa

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

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

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

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

199 Great variability exists in perfluorooctane sulfonate (PFOS) isomer patterns in human and wildlife s

200 uorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) levels have been shown to be positively

201 Exposure to perfluorooctane sulfonate (PFOS) may arise directly, from emission and e

202 uorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) may be associated with adverse pregnanc

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

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

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

206 Perfluorooctane sulfonate (PFOS) was the compound found in the highest n

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

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

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

210 pentachlorophenol (PCP), and perfluorooctane sulfonate (PFOS), compete with thyroxin (T4) for binding

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

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

213 rfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), perfluorononanoic acid (PFNA), and per

214 ured serum creatinine, PFOA, perfluorooctane sulfonate (PFOS), perfluorononanoic acid (PFNA), and per

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

216 biodegradation potential of perfluorooctane sulfonate (PFOS)-precursor candidates have focused on lo

217 exane sulfonate (PFHxS), and perfluorooctane sulfonate (PFOS).

218 erfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS).

219 ersistent organic pollutant, perfluorooctane sulfonate (PFOS).

220 tly, levels of FOSA (22%/y), perfluorooctane sulfonate (PFOS, 8.4%/y), perfluorodecane sulfonate (PFD

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

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

223 Perfluorinated sulfonates (PFSAs) and perfluorinated carboxylates (PFCA

224 9-14% yearly decline of C6-8 perfluoroalkyl sulfonates (PFSAs) following the cease in C6-8 PFSA prec

225 perfluorinated alkylcarboxylates (PFCAs) and sulfonates (PFSAs) in water.

226 in duplicate for 25 PFASs (5 perfluororalkyl sulfonates (PFSAs), 13 perfluoroalkyl carboxylates (PFCA

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

228 (26-29 kcal/mol) agreed with experiment for sulfonated polyethylene (~31 kcal/mol).

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

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

231 centration of perfluorinated carboxylate and sulfonate precursors in archived AFFF formulations and A

232 tro-2,3-dihydro-1H-benzo[e]indol-1-yl)methyl sulfonate prodrugs containing sulfonate leaving groups a

233 t species, a SiF disulfide product and a SiF sulfonate product.

234 Here we report a sulfonate protecting group that is resistant to nucleoph

235 d the interaction appears to involve heparan-sulfonated proteoglycans.

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

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

238 apsules were fabricated by using polystyrene sulfonate (PSS) to encapsulate gold nanoparticles (AuNPs

239 A single dose of purified polystyrene sulfonate (PSS)-coated gold nanorods was added to a seri

240 Sequential adsorption of poly(styrene sulfonate) (PSS) and proteases in porous nylon yields en

241 anostatic method using sodium poly(styrene-4-sulfonate) (PSS) as electrolyte and surfactant.

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

243 PAA, with the strong polyanion poly(styrene sulfonate), PSS, to layer alternately with the polycatio

244 mmonium chloride), PDADMAC, and poly(styrene sulfonate), PSS.

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

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

247 erage sequence coverage of 82% with complete sulfonate retention from singly- and doubly-deprotonated

248 Sulfonate retention has also been reported following neg

249 CAD, EDD, and negative ETD (NETD) result in sulfonate retention mainly at higher charge states with

250 ing between the guanidinium (G) ions and the sulfonate (S) groups of TSPB.

251 ce of 100 mg L(-1) of sodium dodecyl benzene sulfonate (SDBS), and Suwannee River Humic Acid (SRHA) a

252 that deletion of TPA1 causes methyl methane sulfonate sensitivity in S. cerevisiae.

253 function, as evidenced by our methylmethane sulfonate sensitivity studies.

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

255 A sulfonate-silica hybrid strong cation exchange monolith

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

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

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

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

260 f O-sulfopeptides precludes determination of sulfonated sites due to facile proton-driven loss of the

261 anslating to sequence information, including sulfonated sites) with little to no noninformative small

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

263 , carboxylate (-COOH), phosphate (-PO3H2) or sulfonate (-SO3H) groups affects adsorption and orientat

264 sed proton exchange membrane by infiltrating sulfonated sodium polystyrene sulfonate and (2) micro-fa

265 t with oxygen to form a sulfinate and then a sulfonate species, as demonstrated by mass spectrometry.

266 mixture of 3-(10'-phenothiazinyl)-propane-1-sulfonate (SPTZ) and 4-morpholinopyridine (MORPH) was us

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

268 on, and N- to O-sulfonyl migration, giving 2-sulfonate-substituted pyridines which are readily deriva

269 derivatives were probed for sites of charged sulfonate substitution, which precludes diffusion across

270 olytic cleavage of a carbon-sulfur bond from sulfonated substrates.

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

272 ated with hydroxyurea but not methyl-methane-sulfonate, suggesting a regulation of the complex as a f

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

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

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

276 The sulfonated surfactant diglycol ether sulfate was identif

277 omer of the parent NiBDP was obtained with a sulfonate tagged ligand, H(2)BDP_SO(3)H.

278 tridodecylmethylammonium-dinonylnaphthaline sulfonate (TDMA-DNNS).

279 tridodecylmethylammonium-dinonylnaphthalene sulfonate (TDMA/DNNS) ion-exchanger salt.

280 of dextran sodium sulfate or trinitrobenzene sulfonate than mice with lower mucosal levels of ATP.

281 uran-2-yl)undecyloxy)carbonylamino)propane-1-sulfonate, the challenges of in-gel protein digestion ar

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

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

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

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 g polymer, a copolymer consisting of styrene sulfonate units and methyl methacrylate units bearing po

289 ontrol conjugate system in which the styrene sulfonate units were omitted from the polymer structure.

290 f additional perfluorinated carboxylates and sulfonates upon remediation of contaminated groundwater

291 tem and (ii) repressors of genes for toluene sulfonate uptake (TSUP) family transporters.

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

293 onsisting of perfluorinated carboxylates and sulfonates was greater in groundwater and solid samples

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 perfluorocarboxylic acids and perfluoroalkyl sulfonates were five and seven times higher, respectivel

297 oly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) were controlled electrically by varying the g

298 zed S (inorganic sulfate, ester sulfate, and sulfonate)-were identified in PPL sediments.

299 m-catalyzed cascade reaction of 2-chloroaryl sulfonates with arylamine and amide nucleophiles provide

300 on of unactivated primary alkyl bromides and sulfonates with CO2 at atmospheric pressure is described