ライフサイエンスコーパス: sulfur

1 nce, nontoxicity, and high sustainability of sulfur.

2 ic nucleophile, and quenching with elemental sulfur.

3 ed form of cysteine, as a source of cellular sulfur.

4 nstrate it to be a major reservoir of marine sulfur.

5 development in the egg at no cost of reduced sulfur.

6 strobiologically important elements iron and sulfur.

7 t differs from the much better-known lithium-sulfur.

8 eine is a quantitatively-significant sulfane sulfur acceptor, revealing MPST's potential to generate

9 ates; by contrast, at the edge sites, liquid sulfur accumulates if the thickness of the two-dimension

10 e found that on the basal plane, only liquid sulfur accumulates; by contrast, at the edge sites, liqu

11 wever, the molecular mechanisms that support sulfur acquisition during infection have not been establ

12 in the liver and heart, indicating that this sulfur acquisition strategy supports proliferation of S.

13 tudy is the first to experimentally validate sulfur acquisition systems in S. aureus and establish th

14 n a mouse model of CKD, we found that a high sulfur amino acid-containing diet resulted in posttransl

15 functional polymers directly from elemental sulfur, an industrial by-product.

16 ions for stable isotope values of carbon and sulfur and additionally breeding status and age slightly

17 al and climate impacts from the injection of sulfur and halogen species into the stratosphere as a re

18 nservation pathways, including heterotrophy, sulfur and hydrogen metabolism, denitrification, and fer

19 ides are present amid the transition between sulfur and lithium sulfide, nitrogen-doped carbon dots b

20 w York, a historical hotspot for atmospheric sulfur and nitrogen deposition, features abundant lakes

21 midal metalloid (Pb(II)) that binds to these sulfurs and (3) an adjacent layer of reduced steric bulk

22 to a binucleating H(2) ema(2-) with bridging sulfurs and carboxamide oxygens within Mn-mu-S-CH(2) -C-

23 iocyanate conversion into cyanate, elemental sulfur, and two reducing equivalents without involvement

24 the basis for this high potency is a unique sulfur-aromatic interaction network formed by the thiour

25 Because sulfur-aromatic interactions provide additional stabiliz

26 downregulation of miR-210 targets ISCU (iron-sulfur assembly proteins)1/2 and COX10 (cytochrome c oxi

27 expression of several genes involved in the sulfur assimilation and cysteine biosynthetic pathways.

28 Finally, genes involved in sulfur assimilation, the glutathione-ascorbate cycle, an

29 ng inositide signaling, gluconeogenesis, and sulfur assimilation.

30 at manipulating the expression levels of key sulfur assimilatory enzymes could be exploited to improv

31 some of these unknown chemicals contained a sulfur atom attached to an arsenic atom.

32 Recent structures of human SQOR revealed a sulfur atom bridging the SQOR active site cysteines in a

33 The sulfur atom was introduced in a specific benzylic positi

34 tmosphere is related to the rearrangement of sulfur atoms, and the formation of protruding covalent S

35 The SOC is capped by six interstitial sulfur atoms, giving a unique anionic cluster [Ag(6) @{(

36 here water can hydrogen bond to the cysteine sulfur atoms.

37 in green plants, purple bacteria, and green sulfur bacteria.

38 y and favorable interface compatibility with sulfur-based cathodes.

39 MS experiments revealed potential iron- and sulfur-based intermediates that decay as the [2Fe-2S] cl

40 Sulfur-based ligands are versatile donors that play impo

41 Lithium sulfur batteries (LSBs) are promising next-generation re

42 ed electrochemical performances in potassium-sulfur batteries compared with bare potassium metal anod

43 ercapacitors, lithium-ion batteries, lithium-sulfur batteries, lithium-air batteries, zinc-air batter

44 cell concepts such as lithium-air or lithium-sulfur batteries, they can also increase the energy dens

45 ions for their applications in alkali metals-sulfur batteries.

46 de insights for the design of future lithium-sulfur batteries.

47 petitive severe volume change during lithium-sulfur battery cycling.

48 ies has impeded the wide adoption of lithium-sulfur battery, which is one of the most promising candi

49 Sulfur belongs among H(2)O, CO(2), and Cl as one of the

50 ells, indicating that the role of CL in iron-sulfur biogenesis is highly conserved.

51 frataxin, an essential component of the iron-sulfur biogenesis machinery, in mitochondria from TAZ-KO

52 r cycle in serpentinizing fluids and suggest sulfur biogeochemistry provides a key link between terre

53 rom lithotrophy, based on inorganic iron and sulfur biotransformations, to autotrophy, to chemohetero

54 o acid substitutions by formation of optimal sulfur bond and adaptation of cyclopropyl ring in the S2

55 nstrate the synthesis and assembly of 1.2 nm sulfur-bridged copper (SB-Cu) clusters with tertiary hie

56 Sulfur bridges provide efficient binding of As to organi

57 one carbon-carbon (C-C) bond and one carbon-sulfur (C-S) bond.

58 ich reflects the transport properties in the sulfur/carbon composite electrode, can be determined fro

59 The sulfur cathode delivers a high reversible capacity of 89

60 dual oxides, the electrochemical kinetics of sulfur cathode is significantly accelerated.

61 multiply affect electrochemical behaviors of sulfur cathodes in terms of liquid-species clustering, r

62 With sulfur-centered radicals, the carbanions are further fun

63 unraveling the complex reaction mechanism of sulfur chemistries and for exploring the rich material p

64 ospheric lifetime, and to not participate in sulfur chemistry.

65 sful synthesis of MXenes with oxygen, imido, sulfur, chlorine, selenium, bromine, and tellurium surfa

66 sed to deliver iron to mitochondria for iron-sulfur cluster (ISC) and heme biosynthesis.

67 Heme biosynthesis and iron-sulfur cluster (ISC) biogenesis are two major mammalian

68 to target proteins by the mitochondrial iron-sulfur cluster (ISC) maturation system is not well-under

69 ors, model analysis revealed the 3Fe-4S iron-sulfur cluster as the primary [Formula: see text] source

70 ss is catalyzed by the bacteria-derived iron-sulfur cluster assembly (ISC) machinery and has been dis

71 Two auxiliary iron-sulfur cluster binding sites, designated as AuxI and Aux

72 mutants of HydF show that the isolated iron-sulfur cluster domain retains the capacity for binding t

73 ochondrial iron import is essential for iron-sulfur cluster formation and heme biosynthesis.

74 rocesses such as amino acid biogenesis, iron-sulfur cluster formation, and redox homeostasis.

75 ogether, our studies have identified an iron-sulfur cluster within FBXL5, which promotes IRP2 polyubi

76 WhiB1 is a monomeric iron-sulfur cluster-containing transcription factor in the Wh

77 gate the electronic properties of these iron-sulfur clusters and compare the catalytic efficiency of

78 Alkyl-ligated iron-sulfur clusters in the [Fe(4)S(4)](3+) charge state have

79 omponent protein system and a series of iron-sulfur clusters to perform this reaction, culminating at

80 facilitate the transfer of nascent 2-iron, 2-sulfur clusters to recipient mitochondrial proteins.

81 nters in the complex, namely FAD, three iron-sulfur clusters, and a transiently bound semiquinone.

82 The structures revealed that the two iron-sulfur clusters, Fe(4)S(4) in FdsB and Fe(2)S(2) in FdsG

83 rmophilus encases 16 subunits with nine iron-sulfur clusters, reduced by electrons from NADH.

84 omplexes and of catalysis by biological iron-sulfur clusters.

85 ly, at a high mass loading of 9.1 mg cm(-2), sulfur@cobalt sulfide shows high capacity of 545 mAh g(-

86 is as reliable as the gold-standard (99m)Tc-sulfur colloid ((99m)Tc-SC) for gastric emptying scintig

87 Sulfur compound, methionine and cysteine biosynthetic pr

88 , generates hydrogen sulfide-related sulfane sulfur compounds (H(2)S(n)), that exert their biological

89 ieved by detecting the secretion of volatile sulfur compounds (VSCs) in oral cavities.

90 (APPI)(+)) to characterize the nitrogen and sulfur compounds contained in these samples.

91 ntinental ophiolite to elucidate the role of sulfur compounds in fuelling in situ microbial activitie

92 ubiquitous and appreciable volatile organic sulfur compounds such as dimethyl sulfide and (2-methylt

93 , we predict a novel microbial metabolism - sulfur comproportionation (3H(2) S + SO42- + 2H(+) 4S(0)

94 Herein, the concept of sulfur container additives is proposed for the direct mo

95 The sulfur container is a strategy to directly modify PSs, e

96 prototype di(tri)sulfide-polyethylene glycol sulfur container is highly efficient in the reversible P

97 ed the LBD preference for l-Glu but also for sulfur-containing amino acids.

98 The interactions of the iron-sulfur-containing catalytic site with the local protein

99 To acquire sulfur-containing compounds from the environment, bacter

100 ree distinct bacterial ABC import systems of sulfur-containing compounds have been identified, but th

101 Typical sulfur-containing compounds, such as alliin and N-gamma-

102 Over 300 sulfur-containing DBPs, with 43 unique molecular formula

103 Glucosinolates (GSLs) are sulfur-containing defense metabolites produced in the Br

104 These results demonstrate that the use of sulfur-containing groups on a graphene surface can be ex

105 ed redox signaling and altered metabolism of sulfur-containing metabolites and proteins.

106 One of the most abundant extracellular sulfur-containing metabolites within the host is cystein

107 ties and differences within the nitrogen and sulfur-containing molecular classes from samples produce

108 Sulfate, cysteine, and some sulfur-containing secondary metabolites accumulated in h

109 binding of silver nanoparticles (AgNPs) with sulfur-containing species.

110 Recent studies of the sulfur-containing sulvanite Cu(3)VS(4) highlight the pre

111 Elemental analysis results indicated that sulfur content (S %) was very low for sulfuric acid hydr

112 However, the relationships between sulfur content and speciation and the properties of SNZV

113 Changes in the geological sulfur cycle are inferred from the sulfur isotopic compo

114 ght the importance of the complete inorganic sulfur cycle in serpentinizing fluids and suggest sulfur

115 irs where they play an important role in the sulfur cycle.

116 sitive feedbacks, mediated by the oxygen and sulfur cycles, that led to permanent state change in bio

117 itive feedbacks within the internal iron and sulfur cycling of the ocean.

118 eviously active and long-inactive sediments, sulfur-cycling Deltaproteobacteria became more dominant

119 ffect microbial communities and methane- and sulfur-cycling gene abundances in Arctic marine sediment

120 Here we illustrate that key sulfur-cycling taxa, including Dethiobacter, Desulfitisp

121 ional possibilities to improve adaptation to sulfur-deficiency conditions.

122 ibute to the dissection of mechanisms of the sulfur-deficiency response and provide additional possib

123 lowed us to obtain a complete picture of the sulfur-deficiency response and quantify the contribution

124 ontribution of EIL1 to the regulation of the sulfur-deficiency response but also identified genes spe

125 tion on Li(1.2)Ni(0.2)Mn(0.6)O(2) shows that sulfur deposition enhances stability of the cathode with

126 arbazole, whereas the emission maxima of the sulfur derivatives is shifted from 375 to 410 nm.

127 The antioxidants sulfur dioxide (50 ppm) and ascorbic acid (100 ppm) were

128 seed) in comparison with ascorbic acid (AA), sulfur dioxide (SO(2)) and bentonite.

129 of particulate sulfate from the oxidation of sulfur dioxide (SO(2)) emitted by coal combustion.

130 d the known carcinogen benzo(a)pyrene (BaP), sulfur dioxide (SO(2)), and nitrogen dioxide (NO(2)) ove

131 ant chemistry of primary particulate matter, sulfur dioxide (SO(2)), nitrogen oxide (NO(x)), and ammo

132 Large point source emissions of sulfur dioxide accounted for 6.685 [95% confidence inter

133 as the product of aqueous reactions between sulfur dioxide and formaldehyde.

134 st in marine air, related to the presence of sulfur dioxide and/or organic precursors in ship emissio

135 sed covariates for meteorology, traffic, and sulfur dioxide concentrations (a marker of secondary par

136 onate is responsible for the removal of free sulfur dioxide from the reaction medium, and the potassi

137 nium(II) complexes catalyze the insertion of sulfur dioxide into (het)aryl and alkenyl boronic acids.

138 Moreover, the direct incorporation of sulfur dioxide into the sulfonylated products via organo

139 tallic reagent to the commercially available sulfur dioxide surrogate, DABSO, generates a metal sulfi

140 ygen species, reactive nitrogen species, and sulfur dioxide.

141 lated mortality, we found that reductions in sulfur-dioxide emissions from large point sources and ni

142 Sulfane sulfur directly reacted with MexR, forming di- and trisu

143 The sulfur-displaced sites are distinct in the ability of pr

144 Parkin E3 ligase activity toward CDGSH iron sulfur domain 1 (CISD1) were increased.

145 ectroscopy identified Cys-261 on CblD as the sulfur donor.

146 ich shed light on the applications of liquid sulfur droplets in devices such as microlenses, and pote

147 We observe electrowetting and merging of sulfur droplets under different potentiostatic condition

148 regolith of asteroid 25143 Itokawa have lost sulfur during long-term space exposure.

149 cysteine and cystine as sources of nutrient sulfur during systemic infection.

150 critical discussion regarding the potassium-sulfur electrochemistry and on how it differs from the m

151 are significantly limited by the use of thin sulfur electrodes, flooded electrolytes and Li metal deg

152 To date, activation of the sulfur electrophile for protein modification has been as

153 trophilic thiolation of organostannanes with sulfur electrophiles.

154 cially available Lawesson's reagent produced sulfur-enriched-reduced GO (S-rGO).

155 sed by primary defects in mitochondrial iron-sulfur (Fe-S) cluster biogenesis.

156 NFU1, a late-acting iron-sulfur (Fe-S) cluster carrier protein, has a key role in

157 Iron-sulfur (Fe-S) clusters are inorganic cofactors that are

158 Iron-sulfur (Fe-S) clusters play an essential role in plants

159 mutant CSPalpha via ectopic binding of iron-sulfur (Fe-S) clusters.

160 Proteins incorporating iron-sulfur (Fe-S) co-factors are required for a plethora of

161 Numerous iron-sulfur (Fe-S) proteins with diverse functions are presen

162 junction of HoxE and HoxF, adjacent to iron-sulfur (FeS) clusters in both subunits.

163 d a significant source of organic carbon and sulfur for marine microbial ecosystems with the potentia

164 Most sulfur has negative delta(34)S and is subducted into the

165 compounds containing chlorine, bromine, and sulfur heteroatoms are easily determined.

166 n a photochemically transformed carbonaceous sulfur hydride system, starting from elemental precursor

167 with a passive air sampler (PAS) that uses a sulfur-impregnated carbon sorbent and a diffusive barrie

168 izes cysteine from O-acetyl serine (OAS) and sulfur in bacteria and plants.

169 he molecular universe and, in particular, of sulfur in our Galaxy.

170 VI) is affected by the amount and species of sulfur in the materials.

171 s is an important determinant of the fate of sulfur in the ocean.

172 compounds with E = silicon, phosphorus, and sulfur in the past few decades and highlights opportunit

173 Controlling the amount and speciation of sulfur in the SNZVI made it highly reactive (up to 0.41

174 ort that P. aeruginosa PAO1 produced sulfane sulfur, including glutathione persulfide and inorganic p

175 Sulfur incorporation extended the nano-Fe(0) BCC lattice

176 and the thioamide synthetase that catalyzes sulfur incorporation were recently discovered, the logic

177 and possibly introducing nicks to facilitate sulfur incorporation.

178 g microbes, which convert dietary sources of sulfur into genotoxic hydrogen sulfide (H(2)S), have bee

179 icrobial food web, whereas cleavage releases sulfur into the atmosphere.

180 Insertion of sulfur into the B-H bond of the BH borenium salt [IMes(C

181 he Dnd system, which uses DndABCDE to insert sulfur into the DNA backbone as a double-stranded phosph

182 hemical implications: demethylation channels sulfur into the microbial food web, whereas cleavage rel

183 g oxygen in the phosphodiester backbone with sulfur introduce chirality into the backbone such that a

184 exture of olivine is unambiguous evidence of sulfur-involved metasomatism in the interior of Vesta.

185 Indeed, correlated movements of iron and sulfur ions were observed in XFEL-irradiated ferredoxin

186 Quasi-solid-state LSBs, where sulfur is encapsulated in the micropores of carbon matri

187 Sulfur is essential for biological processes such as ami

188 6.4% (up to 20% maximum) of total subducted sulfur is released between 30-230 km depth, and the pred

189 Cellular selenocysteines, where sulfur is replaced with selenium, exhibit enhanced react

190 our model, with the two largest steps in the sulfur isotope record coinciding with the emplacement of

191 eological sulfur cycle are inferred from the sulfur isotopic composition of marine barite.

192 Herein, we report a sulfur (IV) mediated cross-coupling amendable for the ef

193 This is the first review on potassium-sulfur (K-S) batteries (KSBs), which are emerging metal

194 ree distinct characteristics: (1) a cysteine sulfur layer for metal coordination, (2) a thiophilic, t

195 for aprotic electrochemistry such as lithium-sulfur (Li-S) batteries are the cornerstone to enhance i

196 Lithium-sulfur (Li-S) batteries, despite having high theoretical

197 ct and lithium dendrite formation of lithium-sulfur (Li-S) batteries.

198 ic characteristic, a highly flexible lithium-sulfur (Li-S) full cell with rGO-guided planar Li layers

199 Here, we report that CblD provides a sulfur ligand to cob(II)alamin bound to CblC, forming an

200 The sulfur-ligated complex shows a temperature dependence on

201 tional level, this response is controlled by SULFUR LIMITATION1 (SLIM1), a member of the ETHYLENE-INS

202 ay remain relatively high regardless of fuel sulfur limits, mostly due to the nanosized particle emis

203 ces in a pouch cell configuration under high sulfur loading and lean electrolyte operation.

204 acropores enhance ionic transport under high sulfur loading by forming sufficient triple-phase bounda

205 under lean electrolyte conditions, but a low sulfur loading in carbon matrix (<40 wt %) and low sulfu

206 between 30-230 km depth, and the predominant sulfur loss takes place at 70-100 km with a net delta(34

207 Thus, self-produced H(2) S and sulfane sulfur may facilitate antibiotic resistance via inducing

208 ehavior include the lifecycle progression of sulfur metabolism and the diurnal flow of water througho

209 Investigation of sulfur metabolism elucidates frequent cross-compartment

210 PS), plays a significant role in controlling sulfur metabolism in plants.

211 mniotes, we identify in silico a pathway for sulfur metabolism present in chick embryos but not in ma

212 hways range from photosynthesis through iron sulfur metabolism to carbohydrate metabolism.

213 ciated with 43 bacterial species involved in sulfur metabolism.

214 oxidative stress, antibiotic resistance, and sulfur metabolism.

215 herence to a dietary pattern associated with sulfur-metabolizing bacteria in stool was associated wit

216 Sulfur-metabolizing microbes, which convert dietary sour

217 Increased sulfur microbial diet scores were associated with risk o

218 ed a novel turn-on fluorescence detection of sulfur mustard (SM) at "room temperature".

219 the TBPCExBox(4+) , for the elimination of a sulfur mustard simulant, has proved to be significantly

220 ositive response for degradation products of sulfur mustard, thereby indicating suitability of the SM

221 dimensional material is small, whereas solid sulfur nucleates if the thickness is large (tens of nano

222 the first examination of the alpha effect in sulfur nucleophiles, and sheds light on the chemical bas

223 Here, the effects of sulfur on the crystalline structure, hydrophobicity, sul

224 cities, as well as controlling the growth of sulfur on two-dimensional materials, could provide insig

225 t commercially available nitrogen-, oxygen-, sulfur-, or carbon-based nucleophiles and unactivated al

226 olites in the presence of various nitrogen-, sulfur-, or oxygen-containing nucleophiles (e.g., azide,

227 Here we demonstrate that the sulfur outgassing associated with emplacement of large i

228 equent oxidation of S(0) was achieved by the sulfur oxidation enzyme complex (SOX).

229 thways were specific to some MAGs, including sulfur oxidation, nitrate reduction, and flagellar assem

230 sediment was driven by chemolithoautotrophic sulfur oxidation.

231 pected to reduce WTW particulate matters and sulfur oxide emissions for further improvement of the en

232 It is possible that the sulfur oxidising bacteria also supported the persistence

233 hat the microbial community was dominated by sulfur oxidising bacteria, suggesting that primary produ

234 that was purified from the haloalkaliphilic sulfur-oxidizing bacterium of the genus Thioalkalivibrio

235 Sulfur-oxidizing Sulfurimonas spp. are widespread in sed

236 ubiquinol-cytochrome c reductase Rieske iron-sulfur polypeptide 1 (UQCRFS1), the Rieske FeS protein i

237 )-specific RyR2 knockout (KO) or Rieske iron-sulfur protein (RISP) knockdown inhibits the altered Ca(

238 Many iron-sulfur proteins involved in cluster trafficking form [2F

239 The bulk Earth's carbon/sulfur ratio is best explained by the delivery of most o

240 udges from full-scale anaerobic reactors for sulfur-reducing activity at pH 2.0-3.5 and 70 or 80 degr

241 philic anaerobic sludges as the inoculum for sulfur-reducing bioreactors operated at high temperature

242 Stable isotope values of carbon and sulfur reflect dietary source (e.g., marine vs terrestri

243 an, accounts for a large fraction of natural sulfur released to the marine atmosphere.

244 if heavy fuel oil is mainly replaced by low sulfur residual fuels.

245 We show that redox interfaces in sulfur-rich, alkaline aquifers may release concerning le

246 We investigated hyperalkaline, sulfur-rich, brackish groundwater in a serpentinizing co

247 of elemental silicon, phosphorus (P(4)), and sulfur (S(8)) from naturally occurring minerals (e.g., s

248 Reduced sulfur (S) has a contrasting role in the fate of arsenic

249 Our results suggest that iron (Fe) and sulfur (S) increase notably in the direct vicinity of th

250 nd colocalization of Pb, phosphorus (P), and sulfur (S), which are present at the micrometric scale r

251 symmetric displacements of the cofactor belt sulfurs (S2B or S3A and S5A) with distinct dinitrogen sp

252 ucts of SAM-dependent enzymes for carbon and sulfur salvage, contributing to cell growth.

253 xidant-free photoinduced strategy for thioxo sulfur-selective trifluoromethylation of beta-ketodithio

254 ovide evidence for participation of all belt-sulfur sites in this process.

255 the auxiliary [4Fe-4S] cluster is the direct sulfur source during catalysis.

256 obtained from a cheap and readily available sulfur source in moderate to good yields, with good func

257 , cysteine, or N-acetyl cysteine as the sole sulfur source.

258 (n=5,6; m=15,16; x=0,-2) with electrophilic sulfur sources (S(2) Cl(2) , S(8) ) results in the forma

259 n the crystalline structure, hydrophobicity, sulfur speciation, corrosion potential, and electron tra

260 Impacts of the main sulfur species (FeS and FeS(2) ) on hydrophobicity (wate

261 nic and geometric structures of all possible sulfur species and construct an electronic energy diagra

262 The sluggish electrochemical kinetics of sulfur species has impeded the wide adoption of lithium-

263 idence indicates the predominance of reduced sulfur species in slab fluids; those derived from metase

264 ease a persulfide (RSSH), a type of reactive sulfur species related to the gasotransmitter hydrogen s

265 ogen sulfide are mediated in part by sulfane sulfur species, including persulfides and polysulfides.

266 Reactive sulfur species, such as hydrogen sulfide, persulfides, a

267 By reversible storage and release of the sulfur species, the container molecule converts small PS

268 d in saline surface waters that were rich in sulfur species.

269 In a bare soil deposited by an extinct iron-sulfur spring, we found that WPS-2 comprised up to 24% o

270 Correlating the sulfur states with their respective areal capacities, as

271 otential role of the sulfated salicinoids in sulfur storage and homeostasis is discussed.

272 Furthermore, the electrophilic sulfur strategy has been extended to provide the first e

273 are discussed next, focusing on the role of sulfur structure, carbon host chemistry and porosity, an

274 reduced succinate dehydrogenase complex iron-sulfur subunit b (SDHB) expression and decreased content

275 or mediating defense at both low and normal sulfur supply).

276 radical SAM reaction to complete the oxygen-sulfur swapping.

277 c and (hetero)aromatic carboxylic acids with sulfur tetrafluoride.

278 duced sulfide reacts rapidly to form organic sulfur that is resistant to acid hydrolysis.

279 single atom changes such as an exchange of a sulfur to an oxygen, scission of a single bond in P2'-cy

280 arc mantle and cannot deliver (34)S-enriched sulfur to produce the positive delta(34)S signature in a

281 nt cysteine desulfurase enzyme IscS provides sulfur to the scaffold protein IscU, which templates the

282 Persulfides (RSSH/RSS(-)) participate in sulfur trafficking and metabolic processes, and are prop

283 centrations predicted that the proportion of sulfur transfer to thioredoxin increases ~3.5-fold as it

284 We conclude that modest slab-to-wedge sulfur transport occurs, but that slab-derived fluids pr

285 We recently introduced sulfur-triazole exchange (SuTEx) chemistry to demonstrat

286 loading in carbon matrix (<40 wt %) and low sulfur unitization (<70%) still limit the energy density

287 nanosheets with precisely tunable strain and sulfur vacancies (S-vacancies) along with rich edge site

288 improving local HER activities by producing sulfur vacancies using electrochemical reaction at the s

289 form around undercoordinated sites, such as sulfur vacancies.

290 nanoparticles and MoS(2) , rather than only sulfur vacancies.

291 lar-shape cobalt atom cluster with a central sulfur vacancy (3Co(Mo)-V(S)) renders the distinct elect

292 nimum of each host, attributed to the native sulfur vacancy.

293 is a general approach to O-sulfation by the sulfur(VI) fluoride exchange (SuFEx) reaction between ar

294 , a class of weak electrophiles that undergo sulfur(VI) fluoride exchange chemistry.

295 bose conformation and are transmitted to the sulfur via the S-C5' bond, but during catalysis thermall

296 When elemental sulfur was included with the grapes at crushing, extra i

297 To control the physical state of sulfur, we studied its growth on two-dimensional layered

298 g the rich material properties of the liquid sulfur, which shed light on the applications of liquid s

299 l AR inhibitor cemtirestat by replacement of sulfur with oxygen.

300 -protected enoldiazoacetates with alpha-acyl sulfur ylides, has been developed.