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1 ol (80 times faster than the slowest case in methanol).
2 6 +/- 0.07/0.86 +/- 0.06 eV (dichloromethane/methanol).
3 and 710 +/- 20/680 +/- 20 K (dichloromethane/methanol).
4 the blockage of unwanted pathways by adding methanol.
5 a polyurethane to produce diol, diamine, and methanol.
6 erated from renewables with CO(2) to produce methanol.
7 s subsequently used as a reactant to produce methanol.
8 erted by the addition of 4-methoxyindol-3-yl methanol.
9 tant of (4.1 +/- 0.6) x 10(6) M(-1) s(-1) in methanol.
10 milk and fresh milk is feasible with acidic methanol.
11 at the substrate and eluting the sample with methanol.
12 ydrogenation of in situ formed formamides to methanol.
13 90 bar H(2)/20 bar CO(2)) in the presence of methanol.
14 -C couplings of dienes or CF(3)-allenes with methanol.
15 enters are involved in converting methane to methanol.
16 oduction from hydrogen-stored liquid carrier-methanol.
17 C, 50 bar) carbon monoxide hydrogenation to methanol.
18 ldehyde, and not formate, during growth with methanol.
19 2) (CZZ) catalyst for CO(2) hydrogenation to methanol.
20 rogen/deuterium (H/D) exchange in deuterated methanol.
21 llent performance for CO(2) hydrogenation to methanol.
22 bited hydroalkoxylation-like reactivity with methanol.
23 en demonstrated by tuning isotopic water and methanol.
24 catechin carbocation and the methyl group of methanol.
25 orms the challenging oxidation of methane to methanol.
26 CO(2) hydrogenation and producing high-grade methanol.
27 nvestigation on the sensing mechanism toward methanol.
28 s for the selective conversion of methane to methanol.
31 ed the highest membrane integrity (V2; 1.5 M methanol + 5.5 M Me(2)SO + 0.5 M sucrose + 10% egg yolk
34 ased on reversed-phase chromatography with a methanol-acetone gradient and coupling to the ICP-sfMS v
36 est that the AA formation mechanism involves methanol activation on ReO(4), followed by CO insertion
40 from polymers like pectin and xylan, forming methanol and acetate, the availability of which could ex
43 modified by core and bridge substituents, in methanol and aqueous solutions are reported in this work
45 tually new approach, high selectivity toward methanol and catalyst turnover numbers (up to 3170) was
46 imized extraction solvents consisting of 10% methanol and chloroform were evaluated under dynamic and
47 ents at atmospheric pressure with 30 mbar of methanol and CO (1:1 molar ratio) showed that bulk Re(2)
48 used to increase the reaction selectivity to methanol and encourages further detailed investigations
49 of methanol, favourably oxidising water over methanol and enhancing the selective CO(2) reduction to
52 er and CO(2) with nearly 100% selectivity to methanol and internal quantum efficiency of 2.1% in the
53 0) precatalysts, and protic solvents such as methanol and isopropanol were identified as optimal.
54 The corresponding ciders presented higher methanol and lower 2-phenylethanol contents than those o
55 drated or prehydrated Zr-nodes showed higher methanol and methane formation rates over the dehydrated
57 ion kinetics are retarded in the presence of methanol and natural organic matter as sulfate radical s
59 nt-secreted metabolites, 4-methoxyindol-3-yl-methanol and S-(4-methoxy-indol-3-yl-methyl) cysteine we
63 homogeneous (cyclohexane, acetonitrile, and methanol) and micellar (SDS) solution was investigated b
64 n of an outer-sphere redox couple (ferrocene methanol) and two inner-sphere redox couples (potassium
65 of different solvents, including 2-propanol, methanol, and acetonitrile, pure or as mixture with dime
66 O(2) to fuels and chemicals such as methane, methanol, and C(2+) hydrocarbons or syngas are still far
68 Efficient electro-oxidation of formic acid, methanol, and ethanol is challenging owing to the multip
70 different hydroxyl compounds, such as water, methanol, and ethanol, and the concentrations of their m
72 urface towards electro-oxidation of ethanol, methanol, and formic acid, with mass activities of 1.55
73 n, these results highlight the importance of methanol, and solvents in general, in biomembrane and pr
74 ane), refrigerant R-125 (pentafluoroethane), methanol, and water] and a range of model potentials (ha
76 hosphane probe (2-(diphenylphosphanyl)phenyl)methanol as a C-terminus activator has been demonstrated
77 indicate that ethanol can be used to replace methanol as an activation, extraction/elution solvent.
85 oxy or ethoxy groups on a benzene or benzene-methanol backbone were clustered into one group with sim
88 ogenous lanthanum increases growth rate with methanol by 9-12% but does not correlate with changes to
94 is not favorable for CO(2) hydrogenation to methanol, causing low activity and poor methanol selecti
96 m can provide quantitative information about methanol concentration in the liquid phase of microbial
97 included analytes extraction with acidified methanol, concentration by evaporation and filtration of
100 ith natural methylotrophs in a wide range of methanol concentrations, this synthetic methylotrophic s
105 elementary steps of the catalytic cycle for methanol coupling, using scaling methods augmented by de
108 group has shown a 40-fold higher activity of methanol decomposition over single-site Pt(1)/CeO(2) cat
109 ns AM1, the periplasmic lanthanide-dependent methanol dehydrogenase XoxF1 produces formaldehyde, whic
110 oloquinoline quinone (PQQ) in bacterial XoxF methanol dehydrogenases (MDHs) and ExaF ethanol dehydrog
113 e alternative, calcium-dependent, MxaFI-type methanol dehydrogenases, when Ln(3+) are available.
114 t, and as we show here, lanthanide-dependent methanol dehydrogenases, which are more prevalent in the
115 (BN) nanosheet (Ni/BN) catalysts with higher methanol dehydrogenation activity and selectivity, and g
116 hough addition of water was found to promote methanol desorption, water does not change the methanol
118 the "differentiating effect" of the solvent methanol, deuterations of electron-rich aromatic systems
119 P) cycle used by methylotrophs to assimilate methanol differs from the typical sugar metabolism by on
125 and 10.5 ppm was obtained in exposure to the methanol, ethanol and propanol vapours, respectively, in
127 In alloxan-induced diabetic mice, the AFS methanol extract (AFSE) rich in caffeoylquinic acids and
129 content were found in ethyl acetate extract, methanol extract possessed the strongest DPPH and ABTS r
130 method involving sequential basic and acidic methanol extractions was developed and evaluated for rec
131 In the current work, the phenolic profile of methanol extracts obtained from the inflorescences and f
133 om CN and prevents the surface adsorption of methanol, favourably oxidising water over methanol and e
134 pair, such as ferrocenemethanol/ferrocenium methanol (FcMeOH/FcMeOH(+)), which acts as the cosubstra
137 anic frameworks (MOFs), key intermediates in methanol formation are adsorbed at open Zr-sites at the
138 functional theory (DFT) modeling, targeting methanol formation from CO(2)/H(2) feeds at 170 degrees
140 90% of Cu exhibits the highest mass-specific methanol formation rate of 524 g(MeOH)kg(cat)(-1)h(-1) a
142 d readily by first responders to distinguish methanol from ethanol poisoning and monitor in real time
143 CN stably produces stoichiometric oxygen and methanol from water and CO(2) with nearly 100% selectivi
144 grated in the electrical circuit of a direct methanol fuel cell (DMFC), working in passive mode and u
148 tyl hydroperoxide and KOH in dichloromethane/methanol gave a benzocarbachlorin and two related aldehy
155 xture significantly influenced the levels of methanol (higher in mono-varietal ciders), 2-phenylethan
158 alyzed by a manganese pincer complex, yields methanol in addition to amine and alcohol, which makes t
159 w fluorescence probe for direct detection of methanol in aqueous and ethanol medium based on the ZnS:
160 so catalyze the reaction from CO(2) or CO to methanol in aqueous electrolytes at ambient conditions o
161 rrent increase for the redox probe ferrocene-methanol in comparison with the same surface treated by
162 e calculations revealed weaker adsorption of methanol in defective or dehydrated nodes, in agreement
164 ostic capability for accurate measurement of methanol in spiked breath, promising for rapid screening
166 , the formamides are hydrogenated in situ to methanol in the presence of a commercially available rut
168 sound amplitude 47%, solvent composition 80% methanol in water at pH 4.25, and sample to solvent rati
169 10-70 degrees C), solvent composition (0-50% methanol in water), cycle (0.2-0.7 s(-1)), ultrasound am
178 erall, the study provides firm evidence that methanol is formed at the interface of Pt NPs and linker
180 sisted homogeneous hydrogenation of CO(2) to methanol is one of the most effective approaches to inte
181 d (ii) upon addition of 3% vol/vol methanol; methanol is thought to act as a substrate water analog.
182 efficiencies into chloroform (CHCl(3)) with methanol (MeOH) as cosolvent, consistent with MeOH compe
183 esence of amines to formate, formamides, and methanol (MeOH) is a promising approach to streamlining
184 solvents, such as trifluoroethanol (TFE) and methanol (MeOH), indicating a lower propensity of the ox
185 oligosaccharide mixtures were compared using methanol (MeOH)-, isopropanol (IPA)-, and acetonitrile (
187 methyl sulfoxide (DMSO), glycerol (GLY), and methanol (METH; listed in order from least to most toxic
188 factor; and (ii) upon addition of 3% vol/vol methanol; methanol is thought to act as a substrate wate
193 m formate and ammonium acetate in water-rich methanol modifier, the ammonium hydroxide in water addit
196 duction, water splitting, CO(2) reduction to methanol, nitrogen fixation, and water depollution.
199 MPa) reveal that the CO(2) hydrogenation to methanol on the CZZ catalysts follows the formate pathwa
203 L were extracted with hexane, diethyl ether, methanol, or butanol, but activity was observed with dim
204 duced in the partial oxidation of methane to methanol over Cu-SSZ-13 in a continuous-flow reactor.
205 re (NR-Ni(OH)(2)) is able to show remarkable methanol oxidation activity with an onset potential of 0
206 l and durable non-platinum group metal-based methanol oxidation catalyst is critical for a cost-effec
207 While Ni(OH)(2) has been widely studied as methanol oxidation catalyst, the initial process of oxid
208 hanced electrocatalytic performance for both methanol oxidation reaction (MOR) and ethanol oxidation
209 bine the catalytic activity of Pd toward the methanol oxidation reaction (MOR) and the visible-light
210 on is that XoxF enzymes produce formate from methanol oxidation, which could impact organisms that re
215 the main source of the oxygen present in the methanol produced in the partial oxidation of methane to
216 gh yield, selectivity, and TONs obtained for methanol production at low reaction temperature (145 deg
220 ic excitation that can cooperatively promote methanol-production at the copper-zinc oxide interfacial
221 a heterogeneous catalyst system for enhanced methanol productivity in methane oxidation by in situ ge
222 ient gas flow and shows the best competitive methanol productivity under industrially applicable cond
223 ol selectivity reached 92%, corresponding to methanol productivity up to 91.6 millimoles per gram of
227 hrough two leading hydrogenation mechanisms: methanol reaction and Fischer-Tropsch based carbon dioxi
231 dependent ethanol dehydrogenase ExaF reduces methanol sensitivity in the fae mutant strain when lanth
232 n of the singlet alpha-carbonyl carbene with methanol shows that the enol forms without a barrier and
233 exogenous application of 4-methoxyindol-3-yl methanol slightly elevated cytosolic Ca(2+) levels and e
234 identification of CM inhibitors (chloroform/methanol soluble proteins) as main contributors of tryps
236 cules, leads to significant ordering of bulk methanol solvent and the ionic liquid [EMIM][BF(4)].
237 ed from frozen sperm in 1:2 (v/v) chloroform-methanol solvent, fractionated into neutral and polar fr
238 ) P)(2) NH) has N(2) O reductase activity in methanol solvent, mediating 2 H(+) /2 e(-) reduction of
240 erformance of the detector is validated with methanol-spiked breath of 20 volunteers (105 breath samp
241 thanol desorption, water does not change the methanol steady state reaction rate, while it has a subs
243 tegy opens up the feasible avenue to develop methanol-storable solar H(2) fuel with facile chemical r
245 etallic composition, from which a convenient methanol synthesis based on flexible feedstock compositi
246 The Rh-In catalyst can effectively catalyze methanol synthesis but inhibit the reverse water-gas shi
247 d space time yield of Cu based heterogeneous methanol synthesis catalysts through CO(2) hydrogenation
249 bility to turn into a selective catalyst for methanol synthesis in CO(2) hydrogenation which exhibits
250 The proposed general catalytic cycle for methanol synthesis is supported by model studies and det
251 hances CO dissociation and also stabilizes a methanol synthesis pathway not present in the unpromoted
252 model nanocrystalline In(2)O(3) catalyst for methanol synthesis via CO(2) hydrogenation (300 degrees
254 , that more readily undergo hydrogenation to methanol than the C-O dissociation associated with hydro
255 vents (water, ethanol, and a small amount of methanol that could be reused), the developed method pro
256 n polar NOM fractions (which elute with <50% methanol) the TIC intensity and number of assigned molec
257 copper sites are able to convert methane to methanol, the copper oxyl sites with much lower free ene
261 ion pathway for H-SSZ-13: dehydrogenation of methanol to CO is followed by CO-methylation leading to
262 formate and acetate ligands by reaction with methanol to form esters, interior active sites in UiO-66
263 ed with silver(I) acetate in dichloromethane-methanol to give stable nonaromatic structures with two
266 was applied after extraction with acidified methanol, to determine 12 bioactive phenolic compounds i
271 ing silk layering, water vapor annealing and methanol treatment to stabilize the protein cargo and im
272 t from carbon monoxide and carbon dioxide to methanol under a reaction environment with methane, oxyg
273 quiv of [2,2'-bithiophene]-5,5'-diylbis(aryl)methanol under mild acid-catalyzed conditions in CH(2)Cl
275 catalyze the partial oxidation of methane to methanol using only oxygen and water at low temperatures
276 -Robinson buffer (pH 4) containing 10% (v/v) methanol using square-wave voltammetry when five differe
277 pai-extended 3-hydroxyflavone photoCORM, in methanol using steady-state and transient absorption spe
281 dition reaction of S,S-dioxobenzothiophene-2-methanol was explored in microcrystalline powders and it
282 l (Ac) were synthesized, and KHSO(5)/AcCl in methanol was identified as an easy, mild, selective, and
284 microsome-based assays, 4-methoxyindol-3-yl-methanol was transported in a PEN3-dependent manner, sug
286 raction was accomplished using acetonitrile, methanol, water, ammonia, 50:40:9:1 (v/v/v/v) as the sol
287 cm(-1) for cyclohexane, DMSO, acetonitrile, methanol, water, benzene, and toluene using broadband SR
288 lvents; p-toluenesulfonic acid (PTSA) in 1:1 methanol-water gave a >20:1 stereoselectivity favoring t
289 ium hydroxide in water; C, ethyl acetate; D, methanol: water (1:1, v/v); and E, acetonitrile: water (
292 are then reacted to form the energy carrier methanol, which is conveniently shipped to the end consu
293 e, and it directly converted this species to methanol, while oxygen reoxidized the reduced surface.
294 is and extraction method was developed using methanol with 2 M sulfuric acid with incubation at 65 de
295 cule-based electrocatalyst converts CO(2) to methanol with considerable activity and selectivity and
296 trated by the simultaneous quantification of methanol with H(3)O(+), acetone with NO(+), and dimethyl
297 onate and formate salts were hydrogenated to methanol with high yields in a solution of ethylene glyc
299 ase in carbon dioxide (CO(2)) conversion and methanol yield in CO(2) hydrogenation for methanol produ