ライフサイエンスコーパス: hydroxide

1 of water protons donating a hydrogen bond to hydroxide.

2 on steps using phosphoric acid and potassium hydroxide.

3 ance when the Ag is provided as OVA-aluminum hydroxide.

4 eins in the absence and presence of aluminum hydroxide.

5 ene in the presence of 10 equiv of potassium hydroxide.

6 ecific antibodies in the absence of aluminum hydroxide.

7 oxo dimer and a unique monomeric arylbismuth hydroxide.

8 on platinum-group metals in the presence of hydroxide.

9 ulate to be Ser-491 and the iron-bound water/hydroxide.

10 a potentially exchangeable water molecule or hydroxide.

11 s3 N-terminus protein (rAls3p-N) in aluminum hydroxide.

12 m R* coupling to a halogen ligand cis to the hydroxide.

13 s), 1-alkyl-4-(pyrrolidin-1-yl)pyridin-1-ium hydroxide.

14 structural differences between the iron (oxy)hydroxides.

15 oupling between ruthenium and layered double hydroxides.

16 H for the first time using Co and Co-V layer hydroxides.

17 t metallic configuration of transition-metal hydroxides.

18 gth of 1 mm, we were able to suppress 100 mM hydroxide @ 100 nL/min (10 neq/min).

19 urolite A530E (104 mg/g), and layered double hydroxides (28 mg/g).

20 chloride (5.0g.L(-1)), citrate (6.5g.L(-1)), hydroxide (4.0g.L(-1)), hypochlorite (0.2g.L(-1)), starc

21 ed of chloroform:methanol:water:25% ammonium hydroxide (70:30:4:2 v/v/v/v), derivatization with Carr-

22 of chloroform:methanol:acetone:25% ammonium hydroxide (75:15:10:1.6 v/v/v/v), derivatization with Dr

23 with a second nucleophile (HNuc(2)), such as hydroxide, a phenol (4-methylumbelliferone), an amine (p

24 -like components bind on freshly formed iron hydroxides, a process that affects both DOC stability in

25 DFT results indicate that both hydrogen and hydroxide achieve optimal binding energies at the Ni/NiO

26 is, the growth of a self-assembled metal oxy(hydroxide) active layer.

27 , double-blind trials of ZPIV with aluminium hydroxide adjuvant.

28 tibody responses and efficacy of an aluminum hydroxide adjuvanted purified inactivated Zika vaccine (

29 20 mug dose [of each serotype] of aluminium hydroxide-adjuvanted investigational vaccine) or placebo

30 of orthophosphate to WEOM-adsorbed iron (oxy)hydroxide AFM tips suggesting that the molecular mass of

31 Aluminum hydroxide (AH) salts are the most widely used adjuvants

32 ed in products marketed in Europe: aluminium hydroxide (Al(OH)(3) ) is the most frequently used adjuv

33 se reduction through adsorption to aluminium hydroxide (Al) is a promising option, and establishing i

34 nge accompanied by precipitation of aluminum hydroxide allows progress of the cation exchange reactio

35 Aluminum hydroxide (alum) is the most commonly used vaccine adjuv

36 2P in combination with CpG 1018 and aluminum hydroxide (alum) was found to be the most potent immunog

37 erichia coli or subcutaneously with aluminum hydroxide (Alum)-adsorbed rBet v 1.

38 6&CG7V) gD-gp120 proteins formulated in alum hydroxide (ALVAC/Env) or DNA encoding SIVenv/SIVGag/rhes

39 Aqueous miscible organic layered double hydroxides (AMO-LDHs) can act as organophilic inorganic

40 nto the germ structure to 2.1 w/w of calcium hydroxide and 9h steeping time.

41 ts which indicated a first order reaction in hydroxide and a full negative charge in the rate-determi

42 Finally, when adjuvanted with aluminum hydroxide and administered to BDD-naive calves using a p

43 atalyst resting states: an arylpalladium(II) hydroxide and arylpalladium(II) chloride.

44 ) is used that can recognize and extract the hydroxide and carbonate anions as their cesium salts, as

45 The rampant generation of lithium hydroxide and carbonate impurities, commonly known as re

46 Hydroxide and fluoride terminations are identified, foun

47 , to produce chalcones, is the final loss of hydroxide and formation of the C horizontal lineC bond.

48 The anomalously high mobility of hydroxide and hydronium ions in aqueous solutions is rel

49 with the in situ generated nickel-iron oxide/hydroxide and iron oxyhydroxide catalysts at the surface

50 is hydrogen-bonded to the Zn(II)-bound water/hydroxide and likely functions as the general acid-base.

51 of the growth rate on the concentrations of hydroxide and metal ions is approximately linear and qua

52 s an accelerated digestion step using sodium hydroxide and nitric acid in combination to digest all o

53 Its component ions-hydroxide and protons-diffuse much faster than other ion

54 gradient elution of aqueous solvents sodium hydroxide and sodium acetate, in contrast to conventiona

55 hat the main Cr-bearing product is a Cr(III)-hydroxide and that Fe remains in the clay structure afte

56 small set of adsorption reactions for uranyl hydroxide and uranyl carbonate complexes to surface site

57 employed to fabricate well-defined iron oxy-hydroxides and transitional metal doped iron oxy-hydroxi

58 ly verify the presence of the hydroperoxide, hydroxide, and ketone oxidation products of linoleic and

59 formaldehyde-, hydrogen peroxide-, citrate-, hydroxide- and starch-adulterated samples was implemente

60 The hydroxide anion exchange polymer is a key component of a

61 , sterically protected poly(arylimidazolium) hydroxide anion exchange polymers that possess a combina

62 s between the H-donors of the ligand and the hydroxide anion when the ligand is in its trianionic for

63 decade, thanks to the recent developments in hydroxide-anion conductive membranes.

64 22 adjuvanted with either CAF01 or aluminium hydroxide appears to be safe and well tolerated.

65 ADO) with hydrogen atom donors yields ferric hydroxide ((Ar) L)Fe(OH)(AZAD).

66 (kappa(1) -TEMPO) reacts to give a diferrous hydroxide [((Ar) L)Fe]2 (mu-OH)2 , the reaction of four-

67 tions, and lithium hydroperoxide and lithium hydroxide are identified as predominant discharge produc

68 , metal-containing anions and layered double hydroxides are employed to control the components and mo

69 the abundance of precipitated iron(III) (oxy)hydroxides, are hot spots for the removal and redissolut

70 guanidine, NaOEt, or benzyltrimethylammonium hydroxide as a base.

71 licate (TCS)-based materials produce calcium hydroxide as a byproduct of their hydration reaction.

72 ), His(257), Asp(116), Asn(216), and a water/hydroxide as ligands.

73 kel foils, GaIn eutectic, and layered double hydroxides as model materials.

74 a family of thin-film transition metal (oxy)hydroxides as OER catalysts.

75 was present in the soil as Zn-layered double hydroxide, as tetrahedral and octahedral sorbed Zn speci

76 The performance of transition metal hydroxides, as cocatalysts for CO(2) photoreduction, is

77 itial deprotonation and nitrite elimination, hydroxide attachment accompanied by cycle cleavage, and

78 cts caused by a series of C-N bond ruptures, hydroxide attachments, and proton transfers.

79 Hydroxide base regeneration at low temperatures was obse

80 irect switching occurs with triflic acid and hydroxide base.

81 mical dehydrogenation reactions on oxide and hydroxide-based catalytic electrodes.

82 The first example of an alkali hydroxide-based system for CO(2) capture and conversion

83 ng efficient earth-abundant transition metal hydroxides-based cocatalysts on graphene and other two-d

84 the high capture efficiency and stability of hydroxide bases make them superior to existing amine-bas

85 from TEMPO-H (2,2,6,6-tetramethylpiperdine-N-hydroxide, BDFE = 66.5 kcal/mol in THF), forming the hyd

86 the study of silicate clays, layered double hydroxides, believed to be common on the early Earth, ha

87 Common descriptors such as the substrate-hydroxide binding energy and the interactions in the dou

88 equires an activation step, likely forming a hydroxide bridge at a dinuclear Mn(II) site.

89 ow that of type 1 Cu(II/I) by formation of a hydroxide-bridged binuclear complex, Mn(II)(mu-OH)Mn(II)

90 uranyl peroxide POMs studied, clusters with hydroxide bridges have lower DeltaH(f,(aq)) and are more

91 eover, we found selective removal of Fe (oxy)hydroxides by aggregation at increasing salinity, while

92 duction of tolerance to proteins in aluminum hydroxide can be achieved in Foxp3-deficient mice using

93 ncentrations of key chemical species such as hydroxide, carbonate and bicarbonate ions.

94 Copper inorganic complexes (hydroxides, carbonates) played a role in metal bioavaila

95 Potassium hydroxide caused a total reduction of aflatoxins, while

96 oxide, that have a Pt(II) bond to an As(III) hydroxide center.

97 th human and mouse DPCs treated with calcium hydroxide (CH) or mineral trioxide aggregate (MTA) showe

98 vel sorbent, lithium aluminum layered double hydroxide chloride (LDH), is synthesized and characteriz

99 (IV) and Mo(VI), are anchored as metal-oxide,hydroxide clusters to NU-1000 followed by Co(II) ion dep

100 Specifically, the Co-doped iron oxy-hydroxides (Co0.54Fe0.46OOH) show the excellent electroc

101 s study, a magnesium-aluminum layered double hydroxide coated on graphene oxide nanosheets was synthe

102 mobile phase mixture consisting of ammonium hydroxide combined with high water concentration in the

103 igated the stability of Cr(III)-Fe(III)-(oxy)hydroxides, common Cr(VI) remediation products, with a r

104 the challenge in preparing a suitable metal-hydroxide complex at the correct oxidation level.

105 The hydroxide complex was found to be a competent electrocat

106 The selectivity of the hydroxide complex with hydrazine to form aryl over diary

107 Reduction of a dicopper(II) bis(hydroxide) complex with silanes in the presence of exter

108 he rates of HAT by the corresponding Cu(III)-hydroxide complexes from substrates with C-H bonds of va

109 ed for an electron transfer series of copper hydroxide complexes supported by a tridentate redox-acti

110 rn oil deterioration were 2.1 w/w of calcium hydroxide concentration and 9h of steeping time.

111 an appropriate moisture content and calcium hydroxide concentration and milled using HEM.

112 However, durable hydroxide-conducting polymer electrolytes in highly caus

113 andom copolymer demonstrated a high level of hydroxide conductivity (134 mS/cm at 80 degrees C).

114 However, low hydroxide conductivity and poor long-term alkaline stabi

115 , the polymers provide AEMs with exceptional hydroxide conductivity at relatively low ion-exchange ca

116 zed corn flours as a function of the calcium hydroxide content (from 0 to 2.1 w/w) and steeping time

117 h soil clay, and iron and aluminum oxide and hydroxide content.

118 1) to receive HPV 16/18 vaccine or aluminium hydroxide control, with an internet-based system.

119 ults in uncoordinated hydroxamate ligands or hydroxide-coordinated Fe centers.

120 Terminal hydroxide coordination to CuIV in the CuZ degrees interm

121 Here we examine the role that layered hydroxides could have played in prebiotic peptide format

122 522:CAF01), CTH522 adjuvanted with aluminium hydroxide (CTH522:AH), or placebo (saline).

123 tempts to recycle spent Cu/Fe layered double hydroxide (Cu/Fe-LDH) which is generated from the adsorp

124 give the S-nitrosothiol RSNO and copper(II) hydroxide [Cu(II)]-OH.

125 Ps of silver (Ag), copper (Cu), copper oxide/hydroxide (CuO, Cu(OH)(2)), zinc oxide (ZnO), manganese

126 Metallic copper (Cu), cupric oxide/hydroxide (Cuox), and copper sulfide (CuxS) NPs were inv

127 thus detected against a low diethylammonium hydroxide (DEAOH) background (5-31 muS/cm) as negative p

128 rrelated to the number of oxygen vacancy and hydroxide defects present in the system.

129 as postulated at pH values where neither the hydroxide-dependent nor the general-acid-catalyzed mecha

130 omoting amino acid formation: Purely ferrous hydroxides did not drive reductive amination but instead

131 ed pyruvate reduction to lactate, and ferric hydroxides did not result in any reaction.

132 We use fluoride- and hydroxide-doping to generate high concentrations of tita

133 tion were discovered for mixed nickel/cobalt hydroxide electrocatalysts, which were derived in one-st

134 form consists of cadmium sulphide and nickel hydroxide electrodeposited on fluorine-doped tin oxide c

135 electroreduction on copper in 7 M potassium hydroxide electrolyte (pH ~ 15) with an ethylene partial

136 olycrystalline) electrodes in 0.1 M alkaline hydroxide electrolytes (LiOH, NaOH, KOH, RbOH, CsOH) bet

137 though CO2 introduction is possible prior to hydroxide eluent generation, this configuration causes c

138 thin a factor of 2-3 of best case suppressed hydroxide eluent operation.

139 tion of soil indium was associated with iron hydroxides, even in acidic soils.

140 owever, an alternative technology to PEMELs, hydroxide exchange membrane electrolyzers (HEMELs), has

141 , high-performance platinum-group-metal-free hydroxide exchange membrane fuel cell is hindered by the

142 The hydroxide exchange membrane fuel cell with Ru(7)Ni(3)/C

143 ecently, however, an alternative technology, hydroxide exchange membrane fuel cells (HEMFCs), has gai

144 The development of cost-effective hydroxide exchange membrane fuel cells is limited by the

145 /C, making it highly promising in economical hydroxide exchange membrane fuel cells.

146 layer with those efficient near the alkaline hydroxide-exchange layer, we demonstrate a BPM driving W

147 itions has hindered the commercialization of hydroxide-exchange membrane hydrogen fuel cells.

148 rformance in comparison to the pure iron oxy-hydroxide (FeOOH) catalysts, originate from the branch s

149 ata set for chromate adsorption on iron (oxy)hydroxides (ferrihydrite and goethite).

150 on resulted in a decreased long-term calcium hydroxide formation which was associated with neutralise

151 pH increase owing to the leaching of calcium hydroxide from concrete, Aspergillus nidulans (MAD1445),

152 nanotubes, and a polyvinyl alcohol-potassium hydroxide gel as the anode, cathode, and solid-state ele

153 ponification reaction of 23c using anhydrous hydroxide generated in situ to obtain 2.

154 Layered Fe(II)-Fe(III) hydroxides (green rusts, GRs) are promising reactants fo

155 mics of water's constituent ions, proton and hydroxide, has been a subject of numerous experimental a

156 n water-rich methanol modifier, the ammonium hydroxide in water additive showed better chromatographi

157 luding: A, formic acid in water; B, ammonium hydroxide in water; C, ethyl acetate; D, methanol: water

158 N-O bond homolysis to ferrous or ferric iron hydroxides in the presence of 1,4-cyclohexadiene.

159 ide rate constant (k(1)('), rho = 0.87), the hydroxide-independent rate (k(1), rho = 0.65), and the p

160 Aluminium hydroxide initially boosts Th2 responses, while the othe

161 for the growth of peptides at layered double hydroxide interfaces in an early Earth environment.

162 OER intermediates at NiO/NiFe layered double hydroxide intersection, by which the adsorption energy o

163 Herein, we propose a hydroxide ion (OH(-) )-initiated degradation mechanism f

164 hydronium ion is produced, the corresponding hydroxide ion adds to MV(2+) to form a covalently bound

165 The enzyme operates by hydroxide ion attack, which is intrinsically associated

166 It was found to be related to the hydroxide ion concentration, which must be 11 times grea

167 mote the nucleophilic attack of a zinc-bound hydroxide ion onto the ceramide amide carbonyl.

168 c amide, regenerating SP after eliminating a hydroxide ion.

169 enzimidazoles (HMT-PMBI), charge balanced by hydroxide ions (IEC from 2.1 to 2.5 mequiv/g), and comme

170 a high concentration of partially desolvated hydroxide ions around the bound guest arising from ion-p

171 fully prevent recombination of hydronium and hydroxide ions at 3-coordinate bridgehead sites.

172 This method relies on in situ formation of hydroxide ions by electro mediated water reduction at a

173 on is used to generate high concentration of hydroxide ions in proximity to a metal electrode.

174 low populated species such as hydronium and hydroxide ions in water.

175 ing water dissociation (WD) into protons and hydroxide ions is important both for fabricating bipolar

176 azole in the cavity and (2) polar binding of hydroxide ions to sites on the cage surface, both of whi

177 synergistic participation of the Ba(2+) and hydroxide ions, as well as the blockage of unwanted path

178 Imidazolium cations were deprotonated by hydroxide ions, leading to carbenes formation that self-

179 ates aldehyde disproportionation promoted by hydroxide ions, which leads to the formation of the corr

180 tahedral Fe(III) ions connected by oxide and hydroxide ions.

181 rbed monomer dissociates and forms a pair of hydroxide ions.

182 tion of the tris(pyrazolyl)borate copper(II) hydroxide [(iPr2) TpCu]2 (mu-OH)2 with triphenylsilane u

183 nds on the amount of P-PONb present); and c) hydroxide is far less active against the above simulants

184 A bridging hydroxide is in optimal position for nucleophilic attack

185 The hydroxide is involved in both H(2) production and in sit

186 a redox-active Fe(II)-Fe(III) layered double hydroxide, is a potential environmentally relevant miner

187 ynergetic effect of nickel, colloidal nickel hydroxide islands, and the enhanced surface area of the

188 reatment confirmatory testing with potassium hydroxide (KOH) stain followed by periodic acid-Schiff (

189 Potassium exists mainly as potassium hydroxide (KOH), potassium chloride (KCl), and atomic po

190 igner, non-toxic, degradable, layered double hydroxide (LDH) clay nanosheets.

191 urring green rust, that is, a layered double hydroxide (LDH) containing iron (Fe).

192 igh aspect ratio 2D non-toxic layered double hydroxide (LDH) nanosheet dispersions using a non-toxic

193 y demonstrates that ultrathin layered-double-hydroxide (LDH) photocatalysts, in particular CuCr-LDH n

194 Layered double hydroxide (LDH)-based nanomaterials are considered as pr

195 was immobilized in Mg2Al-NO3 Layered Double Hydroxides (LDH) and the electrochemical detection was a

196 NiFe and CoFe (MFe) layered double hydroxides (LDHs) are among the most active electrocatal

197 Iron-doped nickel layered double hydroxides (LDHs) are among the most active heterogeneou

198 orks (ZIFs) on the surface of layered double hydroxides (LDHs) for preparation of porous nanocomposit

199 Layered double hydroxides (LDHs) have been considered as effective phas

200 ic dyes from wastewater using layered double hydroxides (LDHs) through their formation is presented.

201 Layered double hydroxides (LDHs) with similar compositions to the miner

202 Layered double hydroxides (LDHs) with their highly flexible and tunable

203 In recent years layered hydroxides (LHs) have been studied for a range of electr

204 eatures show that CuZ degrees has a terminal hydroxide ligand coordinated to CuIV, stabilized by a hy

205 u-oxo diamond core structure with a terminal hydroxide ligand to the Mn(IV).

206 ted electrochemical decomposition of lithium hydroxide (LiOH) likely occurs through a different mecha

207 The hydroxide-mediated cleavage of ketones into alkanes and

208 ry measurements of the growth of a manganese hydroxide membrane in a microfluidic channel, and this e

209 for two extraction methods [methanol/sodium hydroxide (MeOH/NaOH) and methanol/ammonium hydroxide (M

210 hydroxide (MeOH/NaOH) and methanol/ammonium hydroxide (MeOH/NH4OH)].

211 ic matter (WEOM) for adsorption to iron (oxy)hydroxide mineral surfaces is an important factor in det

212 Layered (oxy) hydroxide minerals often possess out-of-plane hydrogen a

213 biotic chemistry driven by redox-active iron hydroxide minerals on the early Earth would therefore be

214 sorbed by iron (Fe) and aluminium (Al) (oxy) hydroxide minerals.

215 Impedance measurements demonstrate that hydroxide mobility is attenuated by lithium relative to

216 ith NS1 combined with aluminum and magnesium hydroxide, monophosphoryl lipid A + AddaVax, or Sigma ad

217 e processing with N-acetyl-l-cysteine-sodium hydroxide (NALC-NaOH), chemicals that compromise M. tube

218 N-Acetyl-l-cysteine-sodium hydroxide (NALC-NaOH)-decontaminated specimens were inoc

219 oxides and transitional metal doped iron oxy-hydroxides nanomaterials, which show good catalytic perf

220 of amino acid (L-Cysteine) capped lanthanum hydroxide nanoparticles [Cys-La(OH)3 NPs] towards the fa

221 dically arranged four-six-coordinated nickel hydroxide nanoribbon structure (NR-Ni(OH)(2)) is able to

222 alysts, synthesized from NiFe layered double hydroxide nanosheet arrays on three-dimensional Ni foams

223 The membranes were also treated with sodium hydroxide (NaOH) to increase membrane selectivity, and t

224 sulfonic acid (CHES) and 5 mmol L(-1) sodium hydroxide (NaOH).

225 ical component of record-activity Ni/Fe (oxy)hydroxide (Ni(Fe)OxHy) oxygen evolution reaction (OER) c

226 consisting of ultrathin Ni-Fe layered-double-hydroxide (Ni-Fe LDH) nanosheets or porous Ni-Fe oxides

227 cted ultrafine amorphous NiFe-layered double hydroxide (NiFe-LDH) (<5 nm) and nanocarbon using the mo

228 allic iron-magnesium centre that positions a hydroxide nucleophile in-line with the P(alpha)-O(5') bo

229 monia coexist with their ionic counterparts, hydroxide (OH(-)) and ammonium [Formula: see text] ions.

230 l performance of nickel and copper oxide and hydroxide on a conductive template leads to fabrication

231 proposal is the nucleophilic attack by water hydroxide on a pendant Mn horizontal lineO moiety, thoug

232 ission takes place by nucleophilic attack of hydroxide on the ketone followed by fragmentation of the

233 electrochemical deposition of nickel-cobalt hydroxide on the nickel foam substrate at ambient temper

234 nal assembly of a series of transition metal hydroxides on graphene to act as a cocatalyst ensemble f

235 Titration of indole with sodium hydroxide or ammonium hydroxide yields an increasing vis

236 cals; waste could be transformed into sodium hydroxide or caustic soda (NaOH) and hydrochloric acid (

237 ginates from chloride ligand displacement by hydroxide or H(2)O at the Ru center, which reversibly ge

238 y (ILIT) with MAT-Feld1 adsorbed to aluminum hydroxide or just aluminum hydroxide (placebo) in a doub

239 on, Bet v 1 COPs (50 and 100 mug in aluminum hydroxide) or placebo (saline and aluminum hydroxide) we

240 n of materials as diverse as metal hydrides, hydroxides, or carbonates for thermochemical storage is

241 BiVO(4), Si) paired with various metal-(oxy)hydroxide overlayers (e.g., Ni(Fe)O (x)H (y) and CoO (x)

242 erformance when coated with metal-oxide/(oxy)hydroxide overlayers that are catalytic for the water-ox

243 (d)) is estimated by the limiting current of hydroxide oxidation in accordance with the electrocataly

244 synthesis of well-dispersed amorphous cobalt hydroxide/oxide-modified graphene oxide (CoOxH-GO) posse

245 the interactions in the double layer between hydroxide-oxides and H---OH are found to control individ

246 Dental materials to date including calcium hydroxide paste, mineral trioxide aggregate, and glass i

247 This work explores the proton/hydroxide permeability (PH+/OH-) of membranes that were

248 orbed to aluminum hydroxide or just aluminum hydroxide (placebo) in a double-blind setting.

249 is is likely due to the formation of a Np(V) hydroxide precipitate preventing incorporation into the

250 ille) from solution, consistent with Fe(III) hydroxide precipitation from Fe(II)-bearing solution.

251 (H), rho = -1.17), the apparent second-order hydroxide rate constant (k(1)('), rho = 0.87), the hydro

252 e functionalized MMSNs were uranyl or uranyl hydroxide, rather than uranyl carbonates as expected.

253 lkene intermediate which, upon activation by hydroxide, reacts with a second aldehyde to the unsymmet

254 Layered-double hydroxides remained stable during extractions and repres

255 Nickel hydroxide represents a technologically important materia

256 , 3a, and 7a with aqueous tetrabutylammonium hydroxide results in ring opening to linear triphosphate

257 e than one U(VI) species (UO2(2+) and uranyl hydroxide(s) and/or carbonate(s)) and calculated the res

258 Moreover, unlike resins and layered double hydroxides, SBN is fully reusable and displays 96% regen

259 an oxygen vacancy and a Lewis basic surface hydroxide site in In2O3-x(OH)y become more acidic and ba

260 l ligands on the dissolution of Cr(III)-(oxy)hydroxide solids and associated Cr isotope fractionation

261 a derivatization with an ethanolic potassium hydroxide solution resulted in fluorescent coumarin zone

262 Results showed that 60% potassium hydroxide solution with acetone in the ratio of 0.1 (ml/

263 ocking of a phosphate anion, while in alkali hydroxide solutions (MOH, M = Na, K, Cs), OH* intermedia

264 he impact of alkali metal counter cations on hydroxide solvation and mobility.

265 ric addition of a one-electron oxidant and a hydroxide source.

266 Multiple oxide and hydroxide species exist on all Cu surfaces at negative p

267 ntermediate is best described as an iron(IV) hydroxide species.

268 anically complexed Fe, and colloidal Fe (oxy)hydroxides, stabilized by surface interactions with OM.

269 determined that HPC-II exists in an iron(IV) hydroxide state up to pH 11.

270 by thermal transformation of aluminium (oxy)hydroxides, structural differences between them arise fr

271 is of arbitrary guests (e.g. metals, oxides, hydroxides, sulfides).

272 inner-sphere surface complex on the aluminum hydroxide surface.

273 prepare phenols with benzaldehyde oxime as a hydroxide surrogate.

274 these intermediates with tetrabutylammonium hydroxide ([TBA][OH]) yields adenosine and uridine tetra

275 F, scale-up, ratio of 2-MeTHF/MeOH, utilized hydroxide, temperature, and reaction time.

276 ligand) with 2,2,6,6-tetramethylpiperdine- N-hydroxide (TEMPOH) and the para-substituted phenols (X)A

277 a rational synthesis of X-ray amorphous IrOx hydroxides that contain a favorable arrangement of struc

278 ssisted extraction using tetramethylammonium hydroxide (TMAH) and ethylenediaminetetraacetic acid (ED

279 ish fillet samples with tetramethyl ammonium hydroxide (TMAH) for the determination of Ca, Fe, Zn and

280 by ultrasound energy in tetramethylammonium hydroxide (TMAH) media and determination by flame atomic

281 ce powder into 5% (v/v) tetramethyl ammonium hydroxide (TMAH) solution in an ultrasonic bath.

282 um pyrophosphate (TSPP), tetramethylammonium hydroxide (TMAH)), soil-to-reagent ratio, homogenization

283 ne, which was further treated with potassium hydroxide to get stable colored complex.

284 hase transformation from amorphous iron (oxy)hydroxide to goethite, resulting in pyrite surface passi

285 arge amounts of carboxylic acids or ammonium hydroxide to LC eluents postcolumn can improve MS sensit

286 Hydroxide transport, with approximately 2-fold-lower bul

287 Optimization of the hydroxide-treatment process was found to reduce the impe

288 maize samples were incubated with potassium hydroxide, trifluoromethanesulfonic acid and several enz

289 nsitively detected after anion conversion to hydroxide using a standard suppressor, permitting 3-17 p

290 ple (previously alkalinized with 0.5% sodium hydroxide) using 5mL acetonitrile.

291 ormation, while precipitation of the lithium hydroxide was not observed.

292 s, epoxides and aldehydes); the formation of hydroxides was clearly favoured over that of hydroperoxi

293 basic pH cis-12-OH-TBOH decayed quickly via hydroxide/water addition, behavior that theory attribute

294 m hydroxide) or placebo (saline and aluminum hydroxide) were administered as 5 subcutaneous injection

295 o-located with aluminium and iron oxides and hydroxides, which are known to strongly adsorb P.

296 lenides and surface in situ generated oxides/hydroxides, which play a critical role in synergisticall

297 on the surface of cobalt iron layered double hydroxides, which possesses a strong electronic coupling

298 (+)) or tetrabutylphosphonium ([P(4444)](+)) hydroxide with adenine (HAd) and thymine (HThy) led to h

299 nalization (SUCNs-SF) converted from layered hydroxides with inheritance of included anion groups (OH

300 of indole with sodium hydroxide or ammonium hydroxide yields an increasing visible fluorescence as w