ライフサイエンスコーパス: redox couple

1 NADH and NAD(+) are a ubiquitous cellular redox couple.

2 Ag/AgCl corresponding to heme Fe(III)/Fe(II) redox couple.

3 a stepwise manner in the title 2e(-) + 2H(+) redox couple.

4 ric reduction signal of the [Fe(CN)6](4-/3-) redox couple.

5 /-5mV versus Ag/AgCl due to the Cu(II)/Cu(I) redox couple.

6 the equilibrium potential for the substrate redox couple.

7 o the resultant potential of the NADH/NAD(+) redox couple.

8 phenol (4-HATP)/4-nitrosothiophenol (4-NSTP) redox couple.

9 ons of the oxidized and reduced forms of the redox couple.

10 of -264 +/- 1.77 mV is approximated for the redox couple.

11 t on the potassium ferrocyanide/ferricyanide redox couple.

12 sane and return the mediator to the original redox couple.

13 irrespective of the formal potential of the redox couple.

14 tial, E(H), of the interfacial Fe(3+)/Fe(2+) redox couple.

15 play a key role in modulating the accessible redox couple.

16 on rigorously controlling the Ce(III)/Ce(IV) redox couple.

17 s characterized using the ferri/ferrocyanide redox couple.

18 ration of the [Fe(4)S(4)](2+)/[Fe(4)S(4)](0) redox couple.

19 fer and the formal potential for the protein redox couple.

20 bserved by EIS and CV in the presence of the redox couple.

21 I2 molecules, suggesting a 2I(-)-->I2+2e(-) redox couple.

22 ductive dissolution by the 2,6-DMBQ/2,6-DMHQ redox couple.

23 des in a process involving the Nb(V)/Nb(III) redox couple.

24 d 769 +/- 2 mV for the aqueous Fe2+-hematite redox couple.

25 ch is assigned to a [4Fe-4S](2+)/[4Fe-4S](+) redox couple.

26 . Ag/AgCl attributing to heme Fe(III)/Fe(II) redox couple.

27 eaction impedance for the ferro-ferricyanide redox couple.

28 lution contains other PCR components and the redox couple.

29 ng S(4)(* -)/S(4)(2-) and S(3)(* -)/S(3)(2-) redox couples.

30 ry for both solution-phase and surface-bound redox couples.

31 n a solution that contains some irreversible redox couples.

32 ss I behavior as indicated by closely spaced redox couples.

33 nism that is independent of changes in other redox couples.

34 ies or, in marked contrast, reduced cellular redox couples.

35 by serial quantification of GSH, NADPH, NADH redox couples.

36 midpoint reduction potentials of the flavin redox couples.

37 for this series of one-electron outer-sphere redox couples.

38 relatively minor variations in the different redox couples.

39 ss common due to less-accessible metal-based redox couples.

40 xide lowering EH values of aqueous Fe3+/Fe2+ redox couples.

41 and Fe(II)2Fe(III)2/Fe(II)Fe(III)3 (0.018 V) redox couples.

42 hane-producing community cooperating through redox-coupling.

43 -centered redox potential for Mn(III)/Mn(II) redox couple: +228 mV for Mn(III)TE-2-PyP(5+) and +219 m

44 Using the highly soluble iodide/triiodide redox couple, a discharge energy density of 167 Wh l(-1)

45 ll-known feature of the heme [Fe(3+)/Fe(2+)] redox couple: a surface-controlled electrochemical proce

46 ration of the ascorbate/semidehydroascorbate redox couple across the membranes of secretory vesicles.

47 ed well defined and reversible Fe(+)/ Fe(3+) redox couple activity, with NO detection by oxidation at

48 o be of importance for the enzyme-catalyzed, redox-coupled acyl transfer to phosphate, which requires

49 state voltammetry of the ferri/ferrocyanide redox couple allows quantitation of the amount of mediat

50 Measurements of these redox couples along with the pH in rain yields pe(-) bet

51 f 768 +/- 1 mV for the aqueous Fe2+-goethite redox couple and 769 +/- 2 mV for the aqueous Fe2+-hemat

52 ide attributed to the (Co(III/II)TCPP)CoPIZA redox couple and a quasi-reversible peak at -1.45 V vs f

53 OCP moves toward the formal potential of the redox couple and eventually becomes poised at this value

54 Molar volume changes for the I3(-)/I- redox couple and for the alkali cation migration contrib

55 wered midpoint potential of the Q(A)/Q(A)(-) redox couple and increased thermosensitivity of photosys

56 red Jahn-Teller effect of the Mn(4+) /Mn(3+) redox couple and multiple biphasic structural transition

57 independent of presence of iodide/triiodide redox couple and of the pH of the peptization step used

58 acter that dramatically affects the Mo(IV/V) redox couple and points to a potentially noninnocent rol

59 n the N that is part of the phenylenediamine redox couple and R indicates the substituent on the othe

60 f reactions catalyzed within the P(III)/P(V) redox couple and suggest additional opportunities for or

61 P2 is a superior probe for the trypanothione redox couple and that the mitochondrial matrix harbors a

62 t is independent of both the identity of the redox couple and the nature of the linkage of the couple

63 transfer mechanism in the Pdr-putidaredoxin redox couple and their mammalian counterparts, adrenodox

64 nment to show a clean, reversible Rh(III/IV) redox couple and to have a stable Rh(IV) form, which we

65 S(4)](1+) and [Fe(4)S(4)](2+)/[Fe(4)S(4)](0) redox couples and both were inactive.

66 e deduce standard rate constants for the two redox couples and demonstrate that HET based solely on c

67 ves rise to the observed overlap in Mn and O redox couples and reveals that the onset potential of ox

68 d exhibits six clear one-electron reversible redox couples and two, closely spaced one-electron quasi

69 ffect dye regeneration (with I(-)/I(3)(-) as redox couple) and hole transport in NiO-based p-DSCs.

70 e, calculations of the Fermi level using the redox couple, and a proposed model encompassing these ef

71 ous devices applying the [Co(bpy)(3)](2+/3+) redox couple, and an open circuit voltage (V(oc)) of alm

72 netics of the Ni(III)/(IV) bis(dicarbollide) redox couple, and electron interception is found to be a

73 t various potentials above that of the H+/H2 redox couple, and H2 oxidation activities are thus limit

74 o-electron charge transfer via Mn(2+)/Mn(4+) redox couple, and provides facile pathway for Na-ion tra

75 oncentrations, two reversible proton-coupled redox couples appear over the capacitive response with 0

76 ge, positive shifts in the E1/2 of the PQ0/- redox couple are observed in the presence of these ureas

77 at slow scan rates if low concentrations of redox couple are used.

78 under physiological conditions assuming the redox couples are in equilibrium.

79 pies (XAS), which together indicate that all redox couples are ligand-localized.

80 e domain, but in P450BM3 the ox/sq and sq/hq redox couples are reversed, so it is the sq that transfe

81 The Cn(*)/Cn(-) and (Py)Cn(*)/(Py)Cn(-) redox couples are reversible, and the reaction of Cn(*)

82 potential (EH) of the Fe(III) oxide/Fe(II)aq redox couple as a function of dissolved Fe(II) where EH

83 d ratio of oxidized and reduced species of a redox couple as redox buffer and used them to make SC-IS

84 atteries, based on the ferrocene/ferrocenium redox couple as the active catholyte material.

85 with carbon dioxide and reductants and uses redox couples as the energy source.

86 use of the ferrocenium/ferrocene (Fc + /Fc) redox couple, as well as the values used for the absolut

87 The redox couple associated with the low potential heme coul

88 This complex has a Ni(II/I) redox couple at -0.83 V and a Ni(I/0) redox couple at -1

89 (II/I) redox couple at -0.83 V and a Ni(I/0) redox couple at -1.03 V versus Fc(+/0).

90 f a KCl aqueous solution of [Fe(CN)6](3-/4-) redox couple at a Pt electrode.

91 Then, increasing amounts of a redox couple at equimolar amounts of oxidized and reduce

92 the reaction kinetics of ferro-ferricyanide redox couple at the electrode upon hybridization by mean

93 ween the oxidation and reduction of the same redox couple at the same tip position, which is ascribed

94 and the ability of solids to access the same redox couple at two very different potential windows dep

95 ograms of 1 and 2 displayed quasi-reversible redox couples at +16 and +108 mV vs ferrocene/ferroceniu

96 materials that exhibit up to two reversible redox couples at low potentials in the presence of Li-io

97 cal electron transfer usually occurs between redox couples at standard redox potentials ranging from

98 tting reaction with one-electron, reversible redox couples at the electrodes and demonstrates the abi

99 ysts on Cu-modified CeO(2) supports based on redox-coupled atomic layer deposition.

100 substrate gold electrodes and the ferrocene redox couple attached to the electrode surface by variab

101 er ferrocene or pentaaminepyridine ruthenium redox couples attached to the electrode surface by vario

102 NAD redox status and demonstrated metabolic redox coupling between cell compartments in leaves.

103 This study demonstrates the distinct redox coupling between the two parts of the H-cluster an

104 ation of the [Fe(4)S(4)](2+)/[Fe(4)S(4)](1+) redox couple, but with Ti(III) as reductant the [Fe(4)S(

105 n decreases the potential of the bulk oxygen redox couple by > 1 V, leading to a reordering in the an

106 ry the potential of the nitroxyl/oxoammonium redox couple by 0.95 V.

107 udied in the presence of K3Fe(CN)6/K4Fe(CN)6 redox couple by AC impedance measurements.

108 ransfer dynamics of the MP-11 Fe(III)/Fe(II) redox couple by cyclic voltammetry and cyclic voltabsorp

109 electrodes for oxidation-state speciation of redox couples by cyclic voltammetry has been explored.

110 he potentials for the IP(1-/0) and IP(2-/1-) redox couples by up to 0.9 V.

111 complexes exhibit U(V)/U(IV) and U(VI)/U(V) redox couples by voltammetry, with the potential separat

112 the voltammetric response of an outer sphere redox couple can be used to track changes in the structu

113 electrochemical systems, such as reversible redox couples, carbon nanotubes, and conducting polymers

114 The potency of the method to unravel complex redox coupled chemical reactions was also demonstrated w

115 new opportunities for characterizing complex redox-coupled chemical reactions not only with redox pro

116 the volatile and corrosive iodide/triiodide redox couple commonly used as an electron-transfer media

117 formal potential of a ferrocenium/ferrocene redox couple confined within thin layers of the two orga

118 core of FeMo-co cycles through only a single redox couple connecting two formal redox levels: those a

119 e flavin reductase domain and the FeIII/FeII redox couple contained in the heme domain, with formal p

120 NADH/NAD(+) is the main redox couple controlling mitochondrial energy production

121 The 0.34 V spacing between redox couples corresponds to a conproportionation consta

122 Speciation of both forms of a redox couple could be achieved voltammetrically at the m

123 Herein, we report an unprecedented Cross Redox Coupling (CRC) reaction catalyzed by Cu(OAc)2.H2O.

124 charge transfer entropy for the cytochrome c redox couple [(cytc)ox/(cytc)red] in Tris-HCl (pH 8) buf

125 For the Phe82His variant mixed redox couple, DeltaS0'Rxn = -80 J/mol.K compared to Delt

126 ytes in the TiO2 film, which accelerated the redox couple diffusion in the electrolyte solution and i

127 ion peak signal of ferrocyanide/ferricyanide redox couple due to the removal of the negatively charge

128 te electrode at pH 7.5, two quasi-reversible redox couples emerge at -0.170 and +0.032 V, respectivel

129 he reduction potential of the Fe(III)-Fe(II) redox couple, facilitating more-rapid oxidation of Fe(II

130 ation was analyzed through monitoring of the redox couple Fe(2+)/Fe(3+) by electrochemical impedance

131 The voltammetric response of redox couples Fe(CN)(6)(3-/4-) and IrCl(6)(3-/2-) are co

132 and KNO(3)) for thermodiffusion effect and a redox couple [Fe(CN)(6) (4-)/Fe(CN)(6) (3-)] for thermog

133 n transfer process of the negatively charged redox couple [Fe(CN)(6)](3-)/[Fe(CN)(6)](4-) at the elec

134 terms of core oxidation states, exhibit the redox couples [Fe(4)S(4)](3+/2+) and [Fe(4)S(4)](2+/1+).

135 , XRD, FTIR, XPS, TGA, BET, and CV using the redox couples [Fe(CN)6](-3/-4) and [Ru(NH3)6](+3/+2) res

136 ve investigations of two of the most studied redox couples, Fe(CN)(6)(4-/3-) and Ru(NH(3))(6)(3+/2+).

137 and the mobile charge carrier Q/Q(-) is the redox couple FeEDTA(-)(/2)(-) or Ru(NH(3))(6)(3+/2+).

138 ein A (SpA) in the presence of electroactive redox couple ferri/ferro cyanide (K(3)/K(4)[Fe(CN)(6)]).

139 ctrodes for the oxidation of an outer-sphere redox couple (ferrocene methanol) and two inner-sphere r

140 The midpoint potential of the PN/P2+ redox couple for the apo-MoFe protein was shown to be sh

141 shifted by -63 mV when compared to the same redox couple for the intact MoFe protein.

142 a practical evaluating rule associated with redox couples for air-stable Na(x)TmO(2) cathodes.

143 Analytical measurements of both halves of redox couples for dissolved iron, mercury, and the nitra

144 ethyl-2,2'-bipyridine), are presented as new redox couples for DSCs.

145 improves electron transfer, and offers extra redox couples for NRR.

146 SG (-250 mV) and thioredoxin (Trx1, -280 mV) redox couples for the cysteine/cystine couple to functio

147 e (CySS) are the predominant thiol/disulfide redox couple found in human plasma.

148 The glutathione redox couple, GSH/GSSG, oscillated in parallel with Delt

149 f-exchange rate constants indicated that the redox couples had reorganization energies of 0.64-0.69 e

150 The mechanism of the Pdr.Pdx redox couple has been investigated by a variety of techn

151 method for obtaining absolute potentials of redox couples has the advantage that no explicit solvati

152 izing power of surface nitroxide/oxoammonium redox couple, hence showing the practical importance of

153 0 mAh/g, without accessing the Ni(3+)/Ni(4+) redox couple, implying that more than two-thirds of the

154 exchange between the oxygen electrochemical redox couple in an adsorbed water film and electronic st

155 nsfer between diamond and an electrochemical redox couple in an adsorbed water film has recently been

156 is used as a fast, one-electron outer sphere redox couple in dye-sensitized solar cells.

157 try, incorporating the elusive Au(I)/Au(III) redox couple in gold-catalyzed transformations.

158 The major thiol/disulfide redox couple in human plasma is cysteine (Cys) and its d

159 odulation of the midpoint potential for each redox couple in the flavodoxin.

160 rovide absolute reduction energies for these redox couples in bulk aqueous solution.

161 eriments highlighting the contribution of Fe redox couples in controlling Pu desorption at low H2O2 c

162 ng the potential importance of minerals with redox couples in increasing the rate of Pu(V) removal fr

163 s in contact with a series of viologen-based redox couples in methanol through analyses of the behavi

164 with a series of outer-sphere, one-electron redox couples in nonaqueous electrolytes.

165 lytic cycle along the relaxation pathway for redox couples in nonequilibrium reducing environments, w

166 f-discharge is low, due to adsorption of the redox couples in the charged state to the activated carb

167 First, the major redox couples in the mitochondrial matrix (NAD, NADP, th

168 fic species but exchanges electrons with all redox couples in the solution.

169 emistry of Ti(IV)/Ti(III) and Ti(III)/Ti(II) redox couples in these sodium superionic conductor (NASI

170 al the presence of two separate two-electron redox couples in Yap1-RD, with redox midpoint potentials

171 with photoelectrochemical cells with several redox couples, including I3(-)/I(-), Fc/Fc(+), DMFc/DMFc

172 ctron-transfer resistance of Fe (CN)6(3-/4-) redox couple increased considerably on the aptasensor su

173 t properly equilibrates with the glutathione redox couple: Inhibition of endogenous glutaredoxin 1 (G

174 blished that these two enzymes allow for the redox-coupled interconversion of L-idonate and D-glucona

175 redox potentials for the [Fe(4)S(4)](2+/3+) redox couple involved in these complexes were measured b

176 in couple is metal-based, and the ferredoxin redox couple involves extensive electronic relaxation.

177 s 50% ligand character, and hence, the HiPIP redox couple involves limited electronic relaxation.

178 IM carbon-based reference electrodes without redox couple is as low as 1.7 muV/h over 110 h, making t

179 The presence of sulfide/polysulfide redox couple is crucial in achieving stability of metal

180 The formal potential of the Y32-O(*)/Y32-OH redox couple is determined to 918 +/- 2 mV versus the no

181 mino reaction, in which a chromium-manganese redox couple is employed both to catalytically reduce an

182 ial for the [Fe(4)S(4)(SCH(3))(4)](1)(-)(/0) redox couple is in good agreement with that estimated fo

183 When a redox couple is introduced as an internal reference spec

184 reduction steps, we predict that the PyH2/Py redox couple is kinetically and thermodynamically compet

185 It has been proposed previously that a redox couple is operative.

186 under conditions where only one form of the redox couple is present in appreciable concentrations.

187 lytic cycle that relies on a cobalt(I)-(III) redox couple is proposed.

188 mediator based on the iodine(I)/iodine(III) redox couple is reported.

189 studies, which show that its Fe(III)-Fe(II) redox couple is set at an unusual potential (-89 +/- 11

190 the FAD couples [midpoint potential for FAD redox couples is -340 mV, cf-320 mV for NAD(P)H].

191 of ATP utilization depends on which of these redox couples is dominant.

192 As examples, redox couples K3Fe(CN)6/K4Fe(CN)6 and K2IrCl6/K3IrCl6 ar

193 y hydrophilic ionic liquid and a hydrophobic redox couple, leading to well-defined constant potential

194 in order to reveal systematic trends in the redox couples M(III/II) and M(V/IV) (M = Cr, Mo, W), Mn(

195 results suggest that two distinct Fe protein redox couples may be functional during nitrogenase catal

196 imbalances by directly targeting circulating redox-coupled metabolites.

197 g the midpoint potential of the P680(+)/P680 redox couple more negative.

198 ent consensus, we exclude the possibility of redox-coupled Na(+) transport by B. taurus complex I.

199 The ME-R model incorporates four main redox couples (NADH/NAD(+), NADPH/NADP(+), GSH/GSSG, Trx

200 ron-transport chain using the Fe(II)-Fe(III) redox couple of a covalently attached heme prosthetic gr

201 ported by computational modeling, based on a redox couple of Au(I)-Au(III) species.

202 ed GR and CMF modified SPCEs, a well-defined redox couple of Cu(I)/Cu(II) for laccase was observed at

203 fference FT-IR spectra of the Fe(II)/Fe(III) redox couple of myoglobin in reduction and oxidation NPS

204 face, and the apparent rate constant for the redox couple of O(2)/O(2)(*-) is determined to be about

205 The Em value for the 2+/1+ redox couple of the cluster was -0.394 V.

206 of the energetically accessible one-electron redox couple of the first row metal ion in generating we

207 he present work, it is demonstrated that one redox couple of the P-cluster (P2+/1+) undergoes coupled

208 in the midpoint reduction potentials of the redox couples of both flavin cofactors, in contrast to a

209 n transfer between catalytically significant redox couples of FMN and heme in a nNOS holoenzyme.

210 ng cathode is presented that operates on the redox couples of I(2) /[ZnI(x) (OH(2) )(4-x) ](2-x) in a

211 Two reversible redox couples of the immobilized Fld are observed electr

212 The midpoint potentials for both redox couples of the noncovalently bound flavin mononucl

213 avodoxin protein is able to separate the two redox couples of the noncovalently bound flavin mononucl

214 chemically active transition metals with the redox couples of Ti(4+) /Ti(3+) and Mn(3+) /Mn(2+) worki

215 Although anion redox coupling of S(2-) and (S(2))(2-) through dimerizat

216 cal microscopy approach curves for all three redox couples over a conductive substrate fit theoretica

217 indicate that the reduction potential of the redox couple P(+)/P can be appreciably modulated both po

218 om DEMS analysis further suggest that the Ni redox couples play a profound role in the evolution of C

219 the environment, and the clay-Fe(II)/Fe(III) redox couple plays important roles in abiotic reduction

220 system consisting of gold electrodes and the redox couple potassium ferrocyanide/potassium ferricyani

221 le (ferrocene methanol) and two inner-sphere redox couples (potassium ferrocyanide and dopamine).

222 o explore the fundamental mechanisms of such redox-coupled proton pumps, we develop kinetic models at

223 nificant redox tuning via its influence over redox-coupled proton transfer and the energy associated

224 es during the catalysis by facilitating both redox-coupled proton transfer processes leading to the r

225 lectrostatics, altered H-bonding and altered redox-coupled proton transfer.

226 Redox-coupled proton translocation in the membrane domai

227 Several redox-coupled proton translocation mechanisms have been

228 ve to the wild-type protein, suggesting that redox-coupled protonation of H99 is required for high re

229 Equilibration with the C(60)/C(60)(-) redox couple provides a means to determine the apparent

230 half-cell reduction potentials of different redox couples provides confirmation of the veracity of t

231 s, we first confirmed that the reaction is a redox-coupling reaction between retinals and retinols.

232 c studies of this reaction (aldehyde-alcohol redox-coupling reaction), we found that formation of a t

233 (IV)/Ce(III) with one electron complementary redox coupling reactions, the ceria promotion to Au cata

234 med poorly due to cross-diffusion of soluble redox couples, reduced cycle life, and low operating vol

235 hus depends on the standard potential of the redox couple relative to those of the ND surface states.

236 The redox couple resazurin-resorufin exhibits electrofluoroc

237 of the reducible and oxidizable species of a redox couple, respectively.

238 .67 V, assigned to the [3](-)/3 and 3/[3](+) redox couples, respectively.

239 emical response for the (Co(II/I)TCPP)CoPIZA redox couple revealed non-Nernstian reduction with a non

240 tial (E degrees ', n = 2) of the FAD/FADH(2) redox couple revealed that the potentials of the Y93A an

241 rn the redox potentials of the Cu(+2)/Cu(+1) redox couples, ROS generation ability, and intracellular

242 , while its impact on the positively charged redox couple [Ru(NH(3))(6)](2+)/[Ru(NH(3))(6)](3+) is mi

243 The Fc(+/0) redox couple's voltammetry is used to detect the adsorpt

244 rptivity of the freely diffusing form of the redox couple, so that the surface redox conversion can b

245 Ag film served as the counter electrode, the redox couple species were regenerated inside the interna

246 Charge equilibration with redox couple such as C60/C60*- shows the ability of thes

247 and environments for tuning the Ni(II)/(III) redox couple such as strongly donating thiolates in Ni s

248 SOD by analogy) by optimizing the NiII/NiIII redox couple such that it is close to the midpoint of th

249 queous solution, voltammetric waves of other redox couples, such as Ru(NH(3))(6)(3+/2+), could also b

250 However, the role of cytosolic redox couples, such as the NADH/NAD(+) redox system, for

251 e permits the measurement of an intermediate redox couple that is a function of the equilibrium that

252 ly, low-cost ferrocene/ferrocenium molecular redox couple that shows about 95% energy efficiency and

253 cellular processes involving two interacting redox couples that are physically separated by a phospho

254 The redox couples that interrelate 2, 2(+), and 2(2+) are st

255 er, Ox + e = Red, between an electrode and a redox couple, the Butler-Volmer formalism predicts that

256 Using the equilibrium of Ag/AgCl redox couple, the free chloride activities were measured

257 In dilute solutions of the redox couple, the OCP deviates from the redox potential

258 ing fast electron transfer) for outer sphere redox couples, the following factors must be considered.

259 the formal potential of the Y32-O(*)/Y32-OH redox couple to 1,070 +/- 1 mV versus the normal hydroge

260 studied NTO reduction by the hematite-Fe(2+) redox couple to assess the importance of this process fo

261 idation and reduction of the NADH/ubiquinone redox couple to proton translocation, the interaction of

262 rs the access of a ferrocyanide/ferricyanide redox couple to the aptasensor surface.

263 first time to fine-tune the potential of the redox couple to the requirements of the dye through coor

264 e in the electron transfer resistance of the redox couple using Faradaic electrochemical impedance sp

265 ertaken to exploit the hydroxylamine/nitroso redox couple using LC-DED detection for the measurement

266 The I(-)/I(3)(-) redox couple was employed as a mediator and allowed sens

267 The benzoquinone and hydroquinone redox couple was examined as a representative two-electr

268 The FMN semiquinone/hydroquinone redox couple was found to be similar in both constructs.

269 reductant the [Fe(4)S(4)](2+)/[Fe(4)S(4)](0) redox couple was functional and MoFe inhibition was not

270 A Cu(I)(L)/Cu(II)(L) redox couple was identified that showed dramatically dif

271 A plot of Em2 versus the pH for this redox couple was linear and revealed a change of -53 mV/

272 Reversible voltammetry for the Ru(II/III) redox couple was observed, the current for which increas

273 erraquinone-ferrahydroquinone organometallic redox couple was prepared and characterized.

274 An Fe(2+)/Fe(3+) redox couple was used to help elucidate details of the b

275 voltammetry (CV) of the quinone/hydroquinone redox couple was used to monitor the nucleophilic additi

276 rameters using outer-sphere and inner-sphere redox couples, we measured pH by reducing the surface-bo

277 d monolayers (SAMs) bearing a ferrocene (Fc) redox couple were chemically assembled on H-terminated s

278 hotoelectrodes in contact with the H(+)/H(2) redox couple were very close to the bulk recombination/d

279 Two oxidation and 2-3 reduction redox couples were observed, and the UV-visible spectra

280 The kinetics of these redox couples were studied using cyclic voltammetry, cyc

281 Quinone/hydroquinone PCET redox couples were used to produce a photovoltage along

282 suggest that, in contrast to the Pdx-P450cam redox couple where complex formation is predominantly el

283 proceeds via the flavin semiquinone/quinone redox couple, where ground-state flavin semiquinone prov

284 rmining charge transfer entropies of protein redox couples which cannot be studied by direct electroc

285 ft in electrolyte systems containing the HCF redox couple, which can mask the accuracy of the analysi

286 lectrolytes containing the iodide/tri-iodide redox couple, which causes serious problems such as elec

287 A surface redox couple, which is associated with the adsorption/de

288 hanism is involved in stabilizing the oxygen redox couple, which we observe spectroscopically to pers

289 ation of the [Fe(4)S(4)](2+)/[Fe(4)S(4)](1+) redox couple while ATP/2e values of 2.0 could arise from

290 rs evolved to use oxygen as a high-potential redox couple while concomitantly mitigating its toxicity

291 cled widely across the formal potential of a redox couple while the reactant or product of a substrat

292 heory values for each type of redox site and redox couple, while the environmental contribution is ca

293 These fundamental studies on redox coupling will help to guide the design of efficien

294 ration of the [Fe(4)S(4)](2+)/[Fe(4)S(4)](0) redox couple with hydrolysis of only 2 ATPs per pair of

295 thermodynamic shift in E(0) for the Ag/Ag(+) redox couple with size.

296 ter using the [Fe(4)S(4)](2+)/[Fe(4)S(4)](0) redox couple with Ti(III) as reductant.

297 of nonadsorbing, one-electron, outer-sphere redox couples with formal reduction potentials that span

298 les accurate thermochemical measurements for redox couples with irreversible or distorted electrochem

299 Up to eight redox couples within the accessible potential window of

300 inone/hydroquinone couple with the Br2/Br(-) redox couple, yields a peak galvanic power density excee