ライフサイエンスコーパス: organic solvent

1 ace between an aqueous ionic solution and an organic solvent.

2 cetyltrimethylammonium chloride (CTMA) in an organic solvent.

3 in water and UV-initiated polymerisation in organic solvent.

4 are soluble solely in mixtures of water and organic solvent.

5 ed throughout the solution in the absence of organic solvent.

6 oiety with an amine-containing surfactant in organic solvent.

7 ves playing the dual role of acyl source and organic solvent.

8 into a spray with the use of excess volatile organic solvent.

9 ( S)-1 which are soluble in water as well as organic solvents.

10 ecule that binds anions in both water and in organic solvents.

11 , a goal difficult for electrolytes based on organic solvents.

12 additionally incorporating lithium salts and organic solvents.

13 lly perform label-free monitoring of various organic solvents.

14 h volatility and low surface tension of most organic solvents.

15 ical and thermal stability and solubility in organic solvents.

16 her yields than in pure water or many common organic solvents.

17 roplets but not in microdroplets composed of organic solvents.

18 bicity increases with decreasing polarity of organic solvents.

19 ars, most of this work has been conducted in organic solvents.

20 s (HBAs) and neutral H-bond donors (HBDs) in organic solvents.

21 onic hydrogel insoluble in either aqueous or organic solvents.

22 es are comparable to those observed in polar organic solvents.

23 .5Te3 or n-type Bi2Te2.7Se0.3), binders, and organic solvents.

24 d, which exhibited good solubility in common organic solvents.

25 omplex in high yield in several common polar organic solvents.

26 formational differences of MK-2 in different organic solvents.

27 talyst reusability, and precludes the use of organic solvents.

28 non-chlorinated solvent and small amounts of organic solvents.

29 e are the high efficiency and the absence of organic solvents.

30 conditions, without the need for voltage or organic solvents.

31 nown about their supramolecular chemistry in organic solvents.

32 poly(N-isopropylacrylamide) (poly(NIPAM)) in organic solvents.

33 or high reactivity while limiting the use of organic solvents.

34 of ferromagnetic nanoparticles in aqueous or organic solvents.

35 e is generally carried out using chlorinated organic solvents.

36 is similar to that of analogous compounds in organic solvents.

37 le to corrosive aqueous solutions and common organic solvents.

38 ic nanostructures that are highly dynamic in organic solvents.

39 nm, while retaining their high permeances to organic solvents.

40 n and increase solubility of the products in organic solvents.

41 (1M) and H(+)/H(*) (C(G)) couples in several organic solvents.

42 fluence the response of soil microbes to the organic solvents.

43 cal manipulations employing large volumes of organic solvents.

44 side of the molecules, even in highly polar organic solvents.

45 at promise as enzyme mimics that function in organic solvents.

46 en limited to studies conducted in hazardous organic solvents.

47 borate syntheses, tedious purifications, and organic solvents.

48 dienophiles requiring mixtures of water and organic solvents.

49 phobic species from water without the use of organic solvents.

50 mising for discrimination of closely related organic solvents.

51 ry is usually carried out in either water or organic solvents.

52 ubstrates in water without the use of any co-organic solvents.

53 fficiency have typically been synthesized in organic solvents.

54 4% range in water and in the 42-84% range in organic solvents.

55 es to extract anions from aqueous media into organic solvents.

56 ducts are purified by recrystallization from organic solvents.

57 isrupts the isotropic motion of molecules in organic solvents.

58 Yet it is completely soluble in common organic solvents.

59 enerally involve multi-step procedures using organic solvents.

60 widely studied as a homogeneous catalyst in organic solvents.

61 ed to leverage the large potential window of organic solvents.

62 eeded nanowire building blocks in a range of organic solvents.

63 ely aqueous solution, without involvement of organic solvents.

64 lling ratio of the PDMS in the corresponding organic solvents.

65 acidic, heterogeneous) in protic and aprotic organic solvents.

66 e-variable-at-a-time methodology as follows: organic solvent: 1-octanol+2.5% (V/V) di-(2-ethylhexyl)

67 r extraction time (1.83-2.09 times) and less organic solvent (3.39-173.25 times) to operate at a lowe

68 itectures was achieved without the use of an organic solvent, a secondary emulsifier, or high-energy

69 s because GO membranes appear impermeable to organic solvents, a phenomenon not yet fully understood.

70 torical use as an industrial producer of the organic solvents acetone, butanol, and ethanol.

71 species that ferments sugar to a mixture of organic solvents (acetone, butanol and ethanol).

72 Organic solvents alone had a higher yield of PHNQs than

73 NaCl solution of large volume to extract the organic solvent and harden the embryonic microspheres.

74 igher-order structures were obtained in both organic solvent and in water.

75 s efficiently under mild basic conditions in organic solvent and may therefore also enjoy synthetic u

76 cule shows high solubility in various common organic solvents and achieves a high reversible capacity

77 o be achieved in water that usually requires organic solvents and also facilitates the enrichment of

78 ines at elevated temperature in a mixture of organic solvents and aqueous CH3CO2H, which catalyzes im

79 compounds are effective gelators for several organic solvents and aqueous solutions.

80 d fluorescence properties were determined in organic solvents and aqueous surfactants.

81 les reported in the literature take place in organic solvents and are driven by the reagents' interac

82 NP is soluble in various organic solvents and can be fully characterized by commo

83 d on-skin devices are dissolvable in several organic solvents and can be recycled to reduce electroni

84 Stability of CsPbBr(3) in organic solvents and ease-of-tuning their bandedges garn

85 hod that is fast and avoids the use of toxic organic solvents and extensive drying times.

86 Effect of water, organic solvents and five different aqueous surfactant f

87 ] (1) in the presence of water in a range of organic solvents and is also slowly converted in the sol

88 Gamma-oryzanol was extracted with organic solvents and its extracts were characterized by

89 evated temperature, ion strength, buffer pH, organic solvents and keeping time.

90 rate detection and identification of similar organic solvents and mixtures of such solvents.

91 dified proteins that can be transferred into organic solvents and represent the structural material o

92 rsion reaction has been performed in several organic solvents and room-temperature ionic liquids (RTI

93 tivity was enhanced after pre-treatment with organic solvents and SDS.

94 ructures that allow for facile permeation of organic solvents and selection between similarly-sized g

95 l strategy is rapid and minimizes the use of organic solvents and strong acids during synthesis, allo

96 pproximately 1000 times higher than those in organic solvents and strongly enthalpically favored at 2

97 (-1) in aqueous solutions without the use of organic solvents and time-consuming multiple centrifugat

98 tion included the addition of trace water to organic solvents and trace organic liquids to water.

99 The formulation protocol did not involve organic solvents and was rapid and efficient as confirme

100 cessful approach to solubility prediction in organic solvents and water using a combination of machin

101 As anticipated, this peptide forms gels in organic solvents and water via hydrogen-bonded beta-shee

102 ed" clays, in as-received and "contaminated" organic solvents and water, at 60 degrees C and atmosphe

103 in the membrane reactor can be performed in organic solvents and without contamination by electrolyt

104 e the reactions in brine, without the use of organic solvent, and by employing an almost stoichiometr

105 reaction as a function of reaction time, pH, organic solvent, and chaotropic reagents (urea, guanidin

106 device reproducibility, toxic and hazardous organic solvent, and incompatibility with scalable fabri

107 o the hydrophilic beads upon the addition of organic solvent, and various solutions of volatile salts

108 lize Pickering emulsions formed by water and organic solvents, and also, gas-filled g-C3N4 frameworks

109 fects of the use of surfactants and volatile organic solvents, and deepens our understanding of inter

110 ility, resist denaturation by chaotropes and organic solvents, and have applicability as scaffolds fo

111 It possesses a long-lived singlet state in organic solvents, and it shortens upon the addition of w

112 olvatochromism of each dye was studied in 28 organic solvents, and it was found that all compounds ex

113 mpatibility, excellent resistance to various organic solvents, and its ability to withstand relativel

114 CdS nanocrystals requires Cu(I) precursors, organic solvents, and neutral atmosphere, but these cond

115 stability against temperature, dehydration, organic solvents, and or aggressive pH, and (iii) enabli

116 stprocessing, e.g. via reactive gas plasmas, organic solvents, and photolithography.

117 elevated temperature and in the presence of organic solvents, and provides a simple platform for int

118 aphene oxide (S-rGO) membranes are stable in organic solvents, and strong acidic, alkaline, or oxidat

119 of these examples have been realized only in organic solvents, and systems operating in water are rel

120 drogen-containing molecules persist in polar organic solvents, and the spectral evolution of the DF p

121 The macrocycles are freely soluble in common organic solvents, and their identities were confirmed by

122 skite films are soluble in most of the polar organic solvents, and thus until now, they were not cons

123 LTCC technology, such as high-temperature or organic solvents applications, while using a simple fabr

124 t for Fischer glycosidations in low-polarity organic solvents are described.

125 arge carrier mobility and high solubility in organic solvents are overviewed.

126 litate the chemical synthesis of peptides in organic solvent as well as the enzymatic synthesis of gl

127 To overcome this impediment, we tested organic solvents as denaturants during on-line pepsin di

128 ns of CDs was similar to that obtained using organic solvents as ethanol.

129 t TPGS-750-M, thereby eliminating the use of organic solvents as the reaction medium.

130 nt emissive responses are seen for different organic solvents as their respective vapours or when the

131 to detect one analyte with the volume of the organic solvent at ~50 muL.

132 hemical oxidation of the Ir(IV,V) complex in organic solvents at 1.9 V vs NHE.

133 -H6](2-) (1), reacts with carbon monoxide in organic solvents at 40 degrees C to cleanly form an enca

134 consistent with lasso peptide unthreading in organic solvents at room temperature.

135 The progressive replacement of organic solvent-based coatings by waterborne latex polym

136 n the POT film was in direct contact with an organic solvent-based electrolyte.

137 ow for great printability of both water- and organic solvent-based inks thus facilitating the full-in

138 (pH = 2-14, hydrothermal conditions, heated organic solvents, biological media, SO(2) and H(2)S), at

139 ethyl formamide (DMF) is an extensively used organic solvent but is also a potent pollutant.

140 emonstrate high efficiencies in deoxygenated organic solvents but do not function in air-saturated aq

141 s were successfully generated in a number of organic solvents by the reaction between shelf-stable re

142 t endo:exo ratios, when compared to those in organic solvents, can be used to distinguish between the

143 lyst system, previously described for use in organic solvents, can hydrogenate CO2 to formate in wate

144 ies, a dramatic enhancement of solubility in organic solvents (CH2Cl2, CHCl3) is observed for n >/= 8

145 e performed under inert atmospheres in toxic organic solvents, chemoselective addition of organolithi

146 The alkoxy-terminated SiQDs are soluble in organic solvents, colloidally stable, and show bright an

147 Transfer to organic solvents commonly used in polymer and peptide sy

148 ormed in the chemical industry take place in organic solvents, compounds that are generally derived f

149 t phenolics are usually associated with high organic solvent consumption and long extraction times.

150 f small amounts of water, thereby decreasing organic solvent consumption by a considerable amount.

151 Due to the low organic solvent consumption, FPSE meets all green analyt

152 UHPLC method allowed reduction of the organic solvents consumption (8 times lower) and decreas

153 nge of 2-13, ionic strength of 10-100 mM and organic solvent content from 0% to 40%.

154 (tri-, tetra-, and pentasaccharides) at low organic solvent content hampers their detection.

155 ension column succeeded in overcoming pH and organic solvent content mismatch.

156 Preserving DNA hybridization in organic solvents could someday serve to significantly ex

157 However, poor solubility in organic solvents coupled with limited strategies to cont

158 he solutions of obtained target complexes in organic solvents demonstrate high fluorescence quantum y

159 even after exposure to high temperatures and organic solvents, demonstrating their potential for bioc

160 ally ordered polydisperse LCOs and isotropic organic solvent (dichloromethane) phase-separate at the

161 Fullerene C60, co-introduced via an organic solvent, did not influence the response of soil

162 corporation of a chelating agent in a common organic solvent, dimethyl sulfoxide (DMSO).

163 hosphorene flakes are thinner than anhydrous organic solvent dispersions, thus allowing the observati

164 or the model compound fluorescein, where the organic solvent DMSO is exchanged against an aqueous buf

165 ipid bicontinuous cubic single crystals: (i) organic solvent drying speed, (ii) membrane charge densi

166 exfoliated MoS2 sheets in high boiling point organic solvents enabled by surface functionalization an

167 ovalbumin >90% reduction of OVA present) and organic solvent (ethanol >95% reduction) in less than 4

168 ration) and consuming only 0.85mL of a green organic solvent (ethanol).

169 SDS)), elevation of temperature, addition of organic solvents (ethanol (EtOH), isopropanol (IPA), ter

170 s of ripe pistachios were extracted with two organic solvents (ethanol and methanol) and characterize

171 ing devices as a mediator, e.g. fullerene in organic solvents exhibits five stages of reversible oxid

172 ive couplings-processes that usually require organic solvents, expensive and often dangerous coupling

173 acroporous resins as an alternative to using organic solvent extraction alone.

174 ed for recovery of essential oil (EO), while organic solvent extraction using Soxhlet apparatus, micr

175 to develop a novel and simple method without organic solvent extractions for the detection of bovine

176 OHE) system that uses draw solutions with an organic solvent for enhanced thermal separation efficien

177 se of dimethyl sulfoxide (DMSO) acting as an organic solvent for simultaneous sample analyte solubili

178 hydrophobic nature, requiring use of harmful organic solvents for administration, and poor selectivit

179 stable in a nitrogen atmosphere or in select organic solvents for at least one month.

180 cessible using established methods), unusual organic solvents for metabolite isolation and microbial

181 -IL-DLLME using low-density ionic liquid and organic solvents for preconcentration of Sb and Sn.

182 prepared without using cholesterol and toxic organic solvents for the first time.

183 No isomerization was detected in other organic solvents, for example, acetonitrile, N,N-dimethy

184 new procedure is simple, convenient, almost organic solvent free, and causes far less damage to the

185 SOM compounds by a combination of different organic solvents from soils with a wide range of C conte

186 st the extensive literature on GO systems in organic solvents-furnish quantitative explanations for t

187 external complicated treatments, e.g., UV or organic solvent have to be applied, which in turn impair

188 f-emulsification process without the need of organic solvents, heat or high shear forces.

189 ging with dosing restrictions and the use of organic solvents impacting on both the bioactivity and t

190 The use of organic solvents improves digestion, generating more pep

191 sequences of tube radial distribution of the organic solvent in an aqueous-organic system within the

192 hese techniques have thus far used anhydrous organic solvents in an effort to minimize exposure to kn

193 h-value chemicals pretreats the biomass with organic solvents in aqueous solution.

194 e dispersed and exfoliated both in water and organic solvents in the presence of two different PDI de

195 These nanodroplets are stable in organic solvents, in water or in polymer matrices up to

196 ed electrochemically with protons but in any organic solvent. In this article, we outline a series of

197 th nanoparticles prior to ultrafiltration or organic-solvent-induced protein precipitation for optima

198 been proposed, including ultrafiltration and organic-solvent-induced protein precipitation, there is

199 pull out the upconversion nanoparticles from organic solvent into an aqueous phase.

200 processing industry involves large losses of organic solvent into the atmosphere and long extraction

201 ity of covalent organic frameworks (COFs) in organic solvents is one of the major obstacles for the p

202 reservation without the need for any (toxic) organic solvents is reported.

203 with beta-cyclodextrins, without the use of organic solvents, is described.

204 more, water, rather than traditional aprotic organic solvents, is used to dissolve the precursors.

205 crobial activity of WGO and PGO delivered in organic solvent (isopropanol) showed dose-dependent anti

206 nd their photophysical properties in various organic solvents, laser performances, and photostabiliti

207 fabricated using a single emulsion and mixed organic solvent method.

208 ectively in PCR screening as DNA purified by organic solvent methods, are stable for up to 1 year at

209 y of synthesis procedure, low consumption of organic solvent, mild working temperature during the syn

210 New immunosensors working in organic solvent mixtures (OPIEs) for the analysis of tra

211 y-antigen pairs by the use of water-miscible organic solvent mixtures, and its application in the dir

212 bling nanostructures in select polar aprotic organic solvent mixtures.

213 mer conjugates in good yields (up to 40%) in organic solvents (N,N-dimethylformamide, N,N-dimethylace

214 The potential of ultrathin GO laminates for organic solvent nanofiltration is demonstrated by showin

215 lene glycol (PEG) continuous phase (using an organic solvent not penetrating into dextran matrix).

216 e of NaClO2/TEMPO/NaClO in either aqueous or organic solvent, not only allows the Calpha-H oxidation

217 e with temperature increase, addition of the organic solvent, octanol and in the stationary growth ph

218 between the surface energies of aqueous and organic solvents on a Teflon substrate, a fully automate

219 aggregates of different particle size or via organic solvents on soils with different organic matter

220 The effect of pH and organic solvents on the extraction efficiency was invest

221 of surfactant type, concentration and common organic solvents on the extraction of TPC and AA (%) was

222 stewater was performed without the use of an organic solvent or sample preparation steps, with only t

223 be amorphous or crystalline, and soluble in organic solvents or aqueous media.

224 mpound libraries using parallel synthesis in organic solvents or aqueous media.

225 1) template DNA without requiring the use of organic solvents or centrifugation steps.

226 Addition of polar organic solvents or common anions to the ensembles leads

227 required final purification step, the use of organic solvents or concentrated hydrochloric acid (HCl)

228 olid state machine is induced by exposure to organic solvents or grinding and gives rise to different

229 is issue since they rely on extractions with organic solvents or on in vitro digestion without a subs

230 PEG-b-PCL are less toxic than commonly used organic solvents or solubilizers for injection, such as

231 hus, their synthesis suffers from the use of organic solvents or surfactants, which raise environment

232 traction method (mechanical pressing, MP and organic solvent, OS) and the specie (Cucurbita argyrospe

233 tial and linear dependence, respectively, on organic-solvent percentage and salt percentage.

234 We attribute organic solvent permeation and sieving properties to ran

235 With increasing membrane thickness, organic solvent permeation rates decay exponentially but

236 10 nm, which translates into fast water and organic solvent permeation.

237 elop high-performance sensors for monitoring organic solvents, primarily due to the environmental imp

238 he system can also handle common buffers and organic solvents, promising a simple and reliable microf

239 gainst extreme external stressors, including organic solvents, proteases, and ethylene oxide gas ster

240 city of C-Cl bond cleavage was reduced in an organic solvent (reaction with arene radical anions in g

241 This simple, economical, fast, and green (no organic solvent required) sample preparation scheme was

242 reactions and purification procedures use no organic solvents, resulting in an eco-friendly method to

243 used on the evaluation of quantitation using organic solvents revealed a surprisingly poor performanc

244 ended to hollow fiber membranes operating in organic solvent reverse osmosis mode, highlighting the p

245 tive with currently used materials, removing organic solvent, solving the inherent incompatibility be

246 e quantum dots were prepared in a variety of organic solvents stabilized with a quaternary ammonium h

247 itions such as heat resistance, contact with organic solvents, sterilization, storage and immobilizat

248 Postcolumn addition of organic solvents strongly enhanced the electrospray effi

249 nterions and that is soluble in low polarity organic solvents such as bromobenzene.

250 tection of trace amounts of water in various organic solvents such as CH3OH, THF, CH3CN, and acetone

251 ysaccharide fractions of plant cell walls in organic solvents such as chloroform or acetonitrile, whi

252 emonstrated that by tuning the ratio between organic solvents such as N-methyl-2-pyrrolidinone or ort

253 At high concentrations, the presence of organic solvents, such as those present in AFFF formulat

254 ntermediate points of transitions induced by organic solvents, such as trifluoroethanol (TFE) and met

255 imaging of FFA in its native environment, an organic solvent, suggests that in this system a Pre-Nucl

256 Unlike organic solvent swelling effects, this chemical process

257 eveloped in our group, where a mixed aqueous-organic solvent system containing N,N-dimethylacetamide

258 reported thus far are largely restricted to organic solvent systems, and it is likely that the move

259 standard potential of O2 reduction to H2O in organic solvents, taking into account the presence of an

260 onstant water repellency after corrosion and organic solvents tests, strong resistance under UV light

261 gates are weak and dissociate when placed in organic solvents (tetrahydrofuran, methyl tert-butyl eth

262 f these cellular bodies behaves more like an organic solvent than like water.

263 e tether, exhibits an affinity toward C60 in organic solvents that is dramatically higher than the or

264 technique, in which the bilayers contain an organic solvent, the Montal-Mueller or solvent-free tech

265 Moreover, due to the very low solubility in organic solvents, the developed nonsupported catalyst co

266 ion of 5,6-dihydropyrimidin-5-yl radicals in organic solvent through the synthesis of new lipophilic

267 er, adhesive droplets are prepared by adding organic solvent to an aqueous polymer solution at elevat

268 trogenase cofactors can be extracted into an organic solvent to catalyze the reduction of cyanide (CN

269 f extracted compounds via the use of limited organic solvent to desorb analytes and perform electrosp

270 11 s, and it reduces the required amount of organic solvent to do the sample preparation.

271 p flow (PCMF) that supplies an ion-promoting organic solvent to separated glycans prior to their dete

272 weight fractions of </=0.25; and varying the organic solvent to water ratio used in their preparation

273 iscipline that remains highly dependent upon organic solvents to one that will be sustainable, based

274 Hydrogen gas was used instead of organic solvents to release trapped atoms.

275 modern membrane filtration processes and no organic solvents to yield on average 23 mL of 10(11) pla

276 trasonicated in a micellar solution, free of organic solvent, to extract the analytes, and the supern

277 be used to clean up different types of oil, organic solvents, toxic and corrosive contaminants.

278 oic acid (BA) over Ru nanoparticles (NPs) in organic solvent under mild conditions, which cannot be a

279 catalyst selectively converts CO(2) to CO in organic solvents under UV/Vis light (AM 1.5G, 100 mW cm(

280 avoidance of any additive/catalyst and toxic organic solvents, use of water as reaction medium, clean

281 n the COF membranes is incompatible with the organic solvents used for the COF IP process.

282 il paintings, ambient moisture and water and organic solvents used in conservation treatments are kno

283 Imprinted polymers produced in organic solvent using acrylamide as a functional monomer

284 quantum dots (GOQDs) by simply changing the organic solvents utilized in the PLE processing.

285 Briefly, BAs are extracted into an organic solvent via the use of an ion pairing agent, fol

286 e size-dependence of aromatic stacking in an organic solvent was examined.

287 a triazabutadiene that is soluble in aprotic organic solvents, we noted a similar light-induced chang

288 tions of the constituents in the BGE and the organic solvent were simplified to a 1-dimensional probl

289 rsors) partially soluble in both aqueous and organic solvents were produced employing a relatively fa

290 Different aqueous/organic solvents were tested to isolate proteins, an ace

291 d redox potentials of MK-2 differed in three organic solvents, where MK-2 was most easily reduced in

292 arboxylate while also allowing solubility in organic solvents whereas phosphorus functionalization is

293 i(hydroperoxy)propane adducts are soluble in organic solvents which enables oxidation reactions in on

294 gy and can be de-plasticized easily using an organic solvent, which enables immuno-staining of serial

295 stered to patients, without determination of organic solvents, which reduces the overall synthesis-to

296 , hydrophilic molecules to solubilize DNA in organic solvents, which reduces the shielding around the

297 uctor nanocrystals/colloidal quantum dots in organic solvents with special emphasis on earth-abundant

298 lications in solution were so far limited to organic solvents, with a current maximum of the excited-

299 s show outstanding separation performance in organic solvents, with up to two orders of magnitude hig

300 ion of lactose with lauric acid in different organic solvents without using lipase or other enzymes.