ライフサイエンスコーパス: oxidation reaction

1 n intriguing type of catalysts for the water oxidation reaction.

2 ty and durability towards efficient methanol oxidation reaction.

3 ancement of catalytic activity for the water oxidation reaction.

4 e dosed simultaneously, i.e., running the CO oxidation reaction.

5 ffective peroxidase mimic to catalyze the co-oxidation reaction.

6 poisons the Pt NP, deactivating the N(2)H(4) oxidation reaction.

7 ed electrocatalytic activity in the methanol oxidation reaction.

8 on nitrogen in their ability to promote the oxidation reaction.

9 f the TiO(2)(110)-(1 x 1) support for the CO oxidation reaction.

10 yze the synthetically useful Baeyer-Villiger oxidation reaction.

11 cytochrome c- and H(2)O(2)-driven enzymatic oxidation reaction.

12 re stable and efficient cycling of the water oxidation reaction.

13 in cones and improves the efficiency of the oxidation reaction.

14 mogeneous Co-catalyzed electrochemical water oxidation reaction.

15 191 of CaV3.2 in a localized metal-catalysed oxidation reaction.

16 are incorporated into the alcohol during the oxidation reaction.

17 NH group of Trp, the initial step of the Trp oxidation reaction.

18 om this phospholipid was determined for each oxidation reaction.

19 was insufficient to activate the thermal CH4 oxidation reaction.

20 improved electrocatalysis toward the ethanol oxidation reaction.

21 p, which is an intermediate in the PEC water-oxidation reaction.

22 idual nanoelectrodes catalyzing the hydrogen-oxidation reaction.

23 ticle level during electrocatalytic hydrogen-oxidation reaction.

24 pha-oxo MIA was likely formed via a two-step oxidation reaction.

25 e in-situ obtained by finely controlling the oxidation reaction.

26 d as co-catalytic redox mediators in aerobic oxidation reactions.

27 e, Fe(II)- and alpha-ketoglutarate-dependent oxidation reactions.

28 ocesses in which microbes catalyse reduction-oxidation reactions.

29 on without promoting potentially deleterious oxidation reactions.

30 PR) to transfer electrons when they catalyze oxidation reactions.

31 ated in both catalytic oxygenation and water oxidation reactions.

32 onger than 15 days, due to isomerisation and oxidation reactions.

33 t has not been previously observed in olefin oxidation reactions.

34 key intermediates in various cobalt-mediated oxidation reactions.

35 e detected for the first time as a result of oxidation reactions.

36 efficient catalytic systems for challenging oxidation reactions.

37 trol of automobile emissions, and industrial oxidation reactions.

38 e, Fe(II)- and alpha-ketoglutarate-dependent oxidation reactions.

39 esign of catalysts with greater activity for oxidation reactions.

40 ovel catalytic systems for these challenging oxidation reactions.

41 prior to the emergence of dechlorination and oxidation reactions.

42 dation for understanding Cu(II)-mediated C-H oxidation reactions.

43 is an intermediate often involved in natural oxidation reactions.

44 phase and undergo a new round of SOA forming oxidation reactions.

45 protection, and RuO4-catalyzed aromatic over-oxidation reactions.

46 rocatalysts for carbon monoxide and methanol oxidation reactions.

47 e arylamine N-hydroxylation and hydroquinone oxidation reactions.

48 from petroleum feedstock require a series of oxidation reactions.

49 dify proteins by non-enzymatic glycation and oxidation reactions.

50 inal iron reductase, we used metal-catalyzed oxidation reactions.

51 c acid decomposition and formic acid electro-oxidation reactions.

52 ions for numerous other Cu-catalyzed aerobic oxidation reactions.

53 trophic metabolism downstream of the primary oxidation reactions.

54 en, which is a crucial issue in Au catalyzed oxidation reactions.

55 porting the involvement of V(III) in aerobic oxidation reactions.

56 n nature where they catalyze a vast array of oxidation reactions.

57 range of reactions in nature including many oxidation reactions.

58 expansion of the scope of accessible aerobic oxidation reactions.

59 s, which is capable of catalyzing subsequent oxidation reactions.

60 dine reagents for a broad array of substrate oxidation reactions.

61 capable of effecting hydride abstraction and oxidation reactions.

62 uired to permit chemoselective reduction and oxidation reactions.

63 rophotometry and the heat flux dissipated by oxidation reactions.

64 n similar time scales as analogous gas-phase oxidation reactions.

65 lications for other Pd-catalyzed aerobic C-H oxidation reactions.

66 ater is the only by-product in H2O2 involved oxidation reactions.

67 ormance for the oxygen reduction and alcohol oxidation reactions.

68 tro-oxidation of CO2 and a poison in partial oxidation reactions.

69 redox-active organic cocatalysts in aerobic oxidation reactions.

70 a promising route for enhancing the rates of oxidation reactions.

71 is exposed to free chlorine in water due to oxidation reactions.

72 e utility of DAF as a ligand in Pd-catalyzed oxidation reactions.

73 degrees C and shown to be active in various oxidation reactions.

74 (water electrolysis) and reverse (H2 electro-oxidation) reactions.

75 rates showed excellent activities for the NO oxidation reaction, a critical step that demands heavy u

76 This oxidation reaction affords the corresponding trichlorost

77 ies in two prototypical Pd-catalyzed aerobic oxidation reactions: allylic C-H acetoxylation of termin

78 In addition to fatty acid oxidation reactions, an oxidation of endogenous N-arachi

79 hibit enhanced catalytic activity in both an oxidation reaction and a reduction reaction, in comparis

80 forms of Hg-thiols are produced by the Hg(0) oxidation reaction and that the local coordination envir

81 Elucidating the dynamics of this oxidation reaction and the lifetime of hmC in DNA is fun

82 hod was shown to provide fast photocatalytic oxidation reactions and analysis with throughput of abou

83 owed that the REM was active for both direct oxidation reactions and formation of hydroxyl radicals (

84 unctional enzyme that catalyzes a cascade of oxidation reactions and is the major linalool metabolizi

85 rophotometry and the heat flux dissipated by oxidation reactions and measured directly in water-in-oi

86 hey can effectively inhibit or slow negative oxidation reactions and scavenge free radicals and react

87 Progenitors solely undergo single-oxidation reactions and terminate in the hydroxylamine o

88 ed with the ability of flavonoids to prevent oxidation reactions and the presence of vicinal hydroxyl

89 We compared oxidation reactions and the turnover of oxidation interm

90 freeze-quench to stop the arginine and NOHA oxidation reactions and trap reaction intermediates.

91 used to support palladium-catalyzed aerobic oxidation reactions and, where possible, describes mecha

92 Mechanisms were proposed for the oxidation reactions, and observed stereo- and regio-chem

93 e important for controlling overall rates of oxidation reactions, and the intrinsic reactivities of C

94 er salts find widespread use in Pd-catalyzed oxidation reactions, and they are typically used as oxid

95 oxygen reduction reaction (ORR) and alcohol oxidation reaction (AOR), respectively.

96 ther advantages of this new C-C coupling and oxidation reaction are its operational simplicity and th

97 ve and durable electrocatalysts for methanol oxidation reaction are of critical importance to the com

98 Several representative oxidation reactions are also presented to demonstrate th

99 ture-dependent functions for the first-order oxidation reactions are as follows: log k = 13.2-15.2/2.

100 cts as tools to implement selectivity in C-H oxidation reactions are briefly discussed.

101 ons avoid the (001) surface, indicating that oxidation reactions are favoured on this surface.

102 Such oxidation reactions are limited by steric saturation at

103 Oxidation reactions are rarely encountered in frustrated

104 synthetic intermediates resulting from these oxidation reactions are readily transformed into a range

105 These oxidation reactions are relevant to green chemistry in t

106 Furthermore, the anodic oxidation reactions are very clean, producing only H(2)

107 Oxidation reactions are vital parts of metabolism and si

108 n order to facilitate an otherwise difficult oxidation reaction, as well as biomineralization.

109 ndergoes both electrophilic and nucleophilic oxidation reactions, as well as O2-transfer between meta

110 During charging, the oxidation reaction at significantly reduced charge poten

111 The initial step of photocatalytic water oxidation reaction at the metal oxide/aqueous interface

112 s evolved after four sequential light-driven oxidation reactions at the Mn4CaO5 oxygen-evolving compl

113 The reduction-oxidation reaction between aqueous selenite (SeO(3)(2-))

114 severely deficient in catalyzing the normal oxidation reaction, but that D2HG production efficiency

115 amin B2, is essential for cellular reduction-oxidation reactions, but is not readily synthesized by m

116 effective ligand in a number of Pd-catalyzed oxidation reactions, but the mechanistic basis for its u

117 cocatalysts in Cu-catalyzed aerobic alcohol oxidation reactions, but the nature of the cooperativity

118 Monitoring the [Ir(Cp*)(phpy)(NCAr(F))](+) oxidation reaction by low-temperature NMR techniques rev

119 dying titanium dioxide (TiO2) photocatalytic oxidation reactions by performing reactions on a TiO2-co

120 n pH and concentration of the substrate, the oxidation reaction can be directed toward selective prod

121 role in governing these interactions, as the oxidation reactions carried out by the first community m

122 cal coenzyme for enzymes that fuel reduction-oxidation reactions, carrying electrons from one reactio

123 l cell is hindered by the lack of a hydrogen oxidation reaction catalyst at the anode.

124 convert them into red ketocarotenoids via an oxidation reaction catalyzed by a previously unknown ket

125 chloride followed by a 5-exo-dig cyclization/oxidation reaction catalyzed by copper(II) chloride.

126 compound is a key intermediate of the water oxidation reaction catalyzed by the peroxido-bridged com

127 luminates a multinuclear pathway for aerobic oxidation reactions catalyzed by Pd complexes.

128 There is a distinct regiospecifity of the oxidation reaction caused by intermolecular interactions

129 ated temperature (40 degrees C) enhanced the oxidation reactions causing higher viscosity drop.

130 es exhibit surprising catalytic activity for oxidation reactions compared to noble bulk gold which is

131 Can classical and modern chemical C-H oxidation reactions complement biotransformation in the

132 obilizes and activates these complexes under oxidation reaction conditions.

133 very well and therefore the progress of the oxidation reaction could be predicted.

134 biosynthesis, which requires three separate oxidation reactions, culminating in an enigmatic aromati

135 iques showed BHT to be efficient in limiting oxidation reactions during digestion, almost inhibiting

136 n bifurcation mechanism for the two-electron oxidation reaction, during which one electron ends up on

137 The coupling between the oxidation reaction, e.g., dopamine oxidation, on the car

138 mechanism to directly couple a conventional oxidation reaction, e.g., the oxidation of ferrocene, to

139 lights relevant applications of chemical C-H oxidation reactions, electrochemistry and microfluidic t

140 oundation for broader development of aerobic oxidation reactions employing quinone-based catalysts.

141 strategy features an enantioselective alpha-oxidation reaction enabled by a chiral amine in conjunct

142 tion involves decarboxylation followed by an oxidation reaction enabled just by using DMSO as the sol

143 much enhanced stability for ORR and ethanol-oxidation reaction (EOR) than those of disordered PdCuM

144 are active electrocatalysts for the ethanol oxidation reaction (EOR), but inactive for splitting the

145 ercial Pt/C catalysts applied to the ethanol oxidation reaction (EOR).

146 olution, oxygen evolution, CO2 reduction, CO oxidation reactions, etc.

147 Palladium(II)-catalyzed oxidation reactions exhibit broad utility in organic syn

148 oquinone (BQ) reduction, and the formic acid oxidation reaction (FAOR) at a Pt microelectrode substra

149 structure, and further promotes formic acid oxidation reaction (FAOR).

150 We report a novel, efficient oxidation reaction for As(III) conversion to As(V) using

151 yzed radical methylation/sp(3) C-H amination/oxidation reaction for the facile synthesis of quinazoli

152 ulfoxide/Bronsted acid catalyzed allylic C-H oxidation reaction for the synthesis of oxazolidinones f

153 suggesting new opportunities in light-driven oxidation reactions for energy conversion and photocatal

154 ydrogenase (HDH, EC 1.1.1.23), catalyses two oxidation reactions: from L-histidinol (HOL) to L-histid

155 ed in the system, indicated that the Cr(III) oxidation reaction had ceased between 30 min and 1 h und

156 The oxidation reaction has also been investigated by XPS and

157 Unusual oxidation reactions have also been discovered, commonly

158 A range of oxoammonium salt-based oxidation reactions have been explored computationally u

159 Aerobic oxidation reactions have been the focus of considerable

160 Palladium-catalyzed aerobic oxidation reactions have been the focus of industrial ap

161 The slow kinetics of hydrogen evolution and oxidation reaction (HER/HOR) in alkaline media limits ma

162 ell nanocatalysts for hydrogen evolution and oxidation reactions (HER-HOR) using hanging strips of ga

163 well as unambiguous evidence of a reduction-oxidation reaction history between Al-Cu-Fe alloys and s

164 Pt/CuNWs are studied as a hydrogen oxidation reaction (HOR) catalyst in base along with Cu

165 ever, to date, the slow rate of the hydrogen oxidation reaction (HOR) in alkaline environments has hi

166 action with the Pt-electrocatalyzed hydrogen-oxidation reaction (HOR), we combine single-molecule flu

167 Preliminary studies of Fe(III)-NaBH(4)/air oxidation reaction illustrate a generalizable trisubstit

168 both oxygen reduction reaction and methanol oxidation reaction in 0.1 M HClO4 solution.

169 odium bicarbonate, and the sodium persulfate oxidation reaction in acidic media is employed to achiev

170 odel, coupling O2 transfer and ascorbic acid oxidation reaction in the bottled juice, confirmed that

171 re of a Cu(111) model catalyst during the CO oxidation reaction in the CO+O2 pressure range of 10-300

172 on release, in stark contrast to the As(III) oxidation reaction in the presence of dissolved oxygen.

173 ly robust and undergoes a clean two-electron oxidation reaction in the presence of PhICl(2) to afford

174 However, due to oxidation reaction in vivo, no significant difference be

175 he discovery of a bacterial catalyzed indole oxidation reaction in which complete conversion of (13)C

176 perfamily (P450s) catalyze a huge variety of oxidation reactions in microbes and higher organisms.

177 re soluble in organic solvents which enables oxidation reactions in one phase.

178 SCE), which allows to drive demanding photo-oxidation reactions in photoelectrochemical cells (PECs)

179 YP71AV1) enzyme, responsible for a series of oxidation reactions in the artemisinin biosynthetic path

180 ic drug that undergoes similar H2 O2 induced oxidation reactions in the blood as other Cr supplements

181 tion metal complexes can be used to catalyze oxidation reactions, in some cases with high turnover nu

182 Stereoselective oxidation reactions, including dihydroxylation, aminohyd

183 We then followed the oxidation reactions initiated by this process with the f

184 Thus, the overall oxidation reaction involves cooperative electron loss fr

185 veloped with Oxone (2KHSO5.KHSO4.K2SO4); the oxidation reaction involves the stirring of methoxy/hydr

186 e of p-OR-DTBP substrates via a two-electron oxidation reaction involving hydrolysis steps which libe

187 potentials, suggesting a possible origin via oxidation reactions involving electron loss and subseque

188 O(2) is the most critical step in catalytic oxidation reactions involving gold and remains poorly un

189 Predicting site selectivity in C-H bond oxidation reactions involving heteroatom transfer is cha

190 benchmark our reactor using an aqueous-phase oxidation reaction: iron-catalyzed hydroxyl radical prod

191 This single step of the water oxidation reaction is assigned to the first hole transfe

192 lective catalytic system for aerobic alcohol oxidation reaction is built in PCN-700 through linker in

193 irst time that the electronically excited CO oxidation reaction is caused by an electron-mediated pro

194 ryptic peptide fragments generated after the oxidation reaction is quenched.

195 gen-reduction reaction (ORR) and liquid fuel oxidation reaction is very important for the commerciali

196 However, the impact of such oxidation reactions is affected by the reactions of Crie

197 te ligands in electrophilic and nucleophilic oxidation reactions is reported, and can be correlated t

198 ind)) and first-order rate constants for the oxidation reactions (k(ox)).

199 arge carrier density and accelerated surface oxidation reaction kinetics become the key points for im

200 face region but also accelerated the surface oxidation reaction kinetics, synergistically contributin

201 induced electron rearrangement (RIER), where oxidation reactions lead to the reduction of carbon unit

202 ecies can provide a lower energy barrier for oxidation reactions, leading to the conclusion that this

203 y of these compounds undergo metal-catalysed oxidation reactions, leading to the generation of hydrog

204 hiol groups on RyR2, further indicating that oxidation reactions may be involved in the actions of th

205 There is much interest in the nitration and oxidation reaction mechanisms initiated by superoxide ra

206 is a key step in selective catalytic aerobic oxidation reactions mediated by transition metals.

207 Catalysts for methanol oxidation reaction (MOR) are at the heart of key green-e

208 cidic and basic solution toward the methanol oxidation reaction (MOR) compared to larger PtZn iNPs sy

209 roscopy (ATR-SEIRAS) studies of the methanol oxidation reaction (MOR) on Ru/Pt thin film and commerci

210 bility to withstand CO poisoning in methanol oxidation reaction (MOR) than do binary NCs (FePt and J-

211 g of electrocatalyst arrays for the methanol oxidation reaction (MOR), with the optimization of an ef

212 ition to its role as a cofactor in reduction-oxidation reactions, NAD(+) is required for certain post

213 rface electrons into a conduction band in an oxidation reaction, O(delta(-)) + CO --> CO(2)(delta-) -

214 cs and decrease in the overpotential for the oxidation reaction of A and G.

215 was a one-pot cascade oxidation-cyclization-oxidation reaction of a Boc-protected amino alcohol, pre

216 with moderate light intensity, a significant oxidation reaction of ACHT1 arises and counterbalances i

217 cs and decrease in the overpotential for the oxidation reaction of adenine.

218 cationic bisguanidinium-catalyzed asymmetric oxidation reaction of alkenes with potassium permanganat

219 The second one-electron oxidation reaction of ascorbic acid leading to the disap

220 her highlighted by the subsequent sequential oxidation reaction of cyclized 7-iodo-12-phenylindeno[2,

221 ic current is resulted from an HRP-catalyzed oxidation reaction of H(2)O(2) (to O(2)).

222 kinetic mechanism for the first two-electron oxidation reaction of MauG-dependent TTQ biosynthesis, i

223 effect of silver nanoparticle (AgNPs) on the oxidation reaction of tartrazine by potassium iodate in

224 An efficient oxidation reaction of various electron-poor quinoxaline-

225 sis provides a fast and easy method to study oxidation reactions of biomolecules, such as peptides.

226 Electrochemical studies of the reduction and oxidation reactions of five different organic nitroxyls

227 cations (e.g. oxygen reduction reaction, and oxidation reactions of formic acid, methanol and carbon

228 e low intrinsic reactivity of N2O, selective oxidation reactions of highly reactive compounds are pos

229 nd radical pathway latent in metal-catalyzed oxidation reactions of methane at low temperatures.

230 ional photosystem capable of single-electron oxidation reactions of Mn.

231 The outcome of diol oxidation reactions of some N-oxide diolchlorins varies

232 ARD and ARD', catalyze completely different oxidation reactions of the same substrate, 1,2-dihydroxy

233 ciency and regioselectivity in catalytic C-H oxidation reactions of these structurally rich complexes

234 ind this antagonism was investigated through oxidation reactions of Trolox via mass spectrometry anal

235 Here we investigate the water-oxidation reaction on haematite using infrared spectrosc

236 s are used to probe the carbon monoxide (CO) oxidation reaction on ruthenium (Ru) initiated by an opt

237 tional theory + U calculations for the water oxidation reaction on the fully hydroxylated hematite (0

238 We study the effects of the CO oxidation reaction on the size distributions and atomic

239 h2P)C6H4)2SbCl)AuCl (1-Cl) undergoes a clean oxidation reaction on treatment with PhICl2.

240 Catalyst loadings as low as 0.12 mol % in oxidation reactions on a 10 g scale can be used.

241 od type pathways that have been proposed for oxidation reactions on single supported atom.

242 d interfaces, that the near-equilibrium H(2) oxidation reaction pathway is dominated by electrocataly

243 an unprecedented ability to sustain the full oxidation reaction pathway on an extended time scale of

244 50 enzymes primarily catalyze mixed-function oxidation reactions, plus some reductions and rearrangem

245 inant, more stable intermediate of the water oxidation reaction, possibly a surface bound oxo, may re

246 The simple one-step oxidation reaction proceeded selectively in aqueous medi

247 Moreover, this oxidation reaction proceeds at room temperature without

248 The allylic C-H oxidation reaction proceeds with the broadest scope and

249 Computational analysis of the oxidation reaction proposes two plausible flattened tetr

250 icant inhibition by a factor of 22 in the CO oxidation reaction rate is observed at 120 K when the Au

251 ion in the presence of free chlorine and the oxidation reaction rates increase with free chlorine con

252 able structure insensitivity observed for CO oxidation reactions reflects average CO binding properti

253 anol to dimethyl ether and the total methane oxidation reactions, respectively.

254 lecular oxygen to the system and modeled the oxidation reaction resulting in the mature protein-bound

255 Site-selective aliphatic C(sp(3))-H bond oxidation reactions serve as the cornerstone of this wor

256 of important chemical and enzymatic aerobic oxidation reactions, such as alcohol oxidation mediated

257 On the other hand some important oxidation reactions, such as the aerobic oxidation of al

258 f resazurin has enabled the study of analyte oxidation reactions, such as the oxidation of dopamine a

259 lenging chemical reactions involve selective oxidation reactions, such as the selective oxidation of

260 nsity) and thermal energy to drive catalytic oxidation reactions--such as ethylene epoxidation, CO ox

261 Characterization of the photo-oxidation reaction suggests H2O2 or *OH production with

262 tives to TEMPO-based catalysts for selective oxidation reactions (TEMPO = 2,2,6,6-tetramethyl-1-piper

263 A mechanism is proposed for the NO. oxidation reaction that involves formation of both Fe(II

264 ex photosystem II (PSII) catalyzes the water oxidation reaction that takes place in oxygenic photosyn

265 min A retention was related to the extent of oxidation reactions that occurred in flours during stora

266 rate by promoting, through diverse pathways, oxidation reactions that perturb the electron orbitals o

267 However, for many triterpenoid oxidation reactions, the corresponding enzyme remains un

268 Nature often utilizes molecular oxygen for oxidation reactions through monoxygenases and dioxygenas

269 2-oxoglutarate) as a co-substrate in so many oxidation reactions throughout much of nature is notable

270 and CeO2 were synthesized and utilized in CO oxidation reactions to compare the catalytic activities

271 ment, followed by a subsequent hydroboration oxidation reaction, to afford substituted amino alcohol

272 The success of the current permanganate oxidation reaction together with mechanistic insights sh

273 K) temperature, which is relevant for the CO oxidation reaction under cold-start conditions in the ca

274 erential accumulation of 5fC in the in vitro oxidation reactions under both neutral and acidic condit

275 C-H bond oxidation reactions underscore the existing paradigm whe

276 uffer from the sluggish kinetics of the urea oxidation reaction (UOR) owing to a 6 e(-) transfer proc

277 have been developed to catalyze hydrocarbon oxidation reactions using H2O2 in the presence of added

278 catalyst and solar O(2) evolution are photo-oxidation reactions using the photogenerated holes.

279 manganese in metallic particles are prone to oxidation reactions via gas/particle conversion mechanis

280 Rutin oxidation reaction was followed by recording of spectral

281 A possible mechanism of the oxidation reaction was proposed and the reaction product

282 preferentially oxidized amino acid, but the oxidation reaction was significantly inhibited by its ph

283 r complexation and an Arrhenius plot for the oxidation reaction were constructed.

284 fferences between first formal reduction and oxidation reactions were correlated to HOMO-LUMO energy

285 The nitrite oxidation reactions were incorporated into a widely acce

286 ffective extraction of phosphorus through an oxidation reaction, which promotes the outward diffusion

287 review is devoted to dealing with selective oxidation reactions, which are important from the viewpo

288 t the unsaturated fatty acids easily undergo oxidation reactions, which lead to the reduction of shel

289 y catalytically competent for the subsequent oxidation reaction, while the overall turnover is at lea

290 propagators to trigger the onset of the auto-oxidation reaction with an apparent turnover frequency o

291 Contrary to the classical heme peroxidase oxidation reaction with hydrogen peroxide that produces

292 oxidized to isoquinolinediones by a tunable oxidation reaction with N-haloimides.

293 ione and sodium azide) indicating a possible oxidation reaction with the CFTR polypeptide.

294 s acted as oxidase substrates and induced co-oxidation reactions with anthocyanins.

295 he former catalyst was used in batch aerobic oxidation reactions with different primary alcohols and

296 s-phase benzyl alcohol oxidation and toluene oxidation reactions with remarkable oxidative activity p

297 Amine deprotonation triggers the oxidation reaction, with cleavage of the substrate NH an

298 t, metal-free electrocatalysts for hydrazine oxidation reaction, with low overpotential and high curr

299 oked in catalytic Cu/aminoxyl-driven alcohol oxidation reactions, with similar findings.

300 ailed kinetic studies of Ce(4+)-driven water oxidation reactions (WORs) catalyzed by the MOFs using U