ライフサイエンスコーパス: CO

1 CO and longer-lived VOCs, largely overlooked in previous

2 CO protein is stable only in the afternoon of long days,

3 CO release is chaperoned by turn-on fluorescence and can

4 CO was observed as the main product at high catalyst loa

5 CO+OHE and HOSO+OHE decreased the formation of polar com

6 CO-applied as the CO-releasing molecule, CORM-2-prolonge

7 nto the surface of gold nanoparticles ((10Os)CO-Au NPs) greatly enhanced the CO stretching vibration

8 ent thiocholine-induced aggregation of (10Os)CO-Au NPs can be monitored by the change in color of the

9 Here, we show that 14 CO-like (COL) proteins bind CONSTITUTIVELY PHOTOMORPHOGE

10 There are 16 CO-like proteins whose functions are only partly underst

11 for the complex, {fac-Mn(I)([(MeO)2Ph]2bpy)(CO)3(CH3CN)}(OTf), containing four pendant methoxy group

12 The cothermolysis of As4 and [Cp''2Zr(CO)2] (Cp'' = eta(5)-C5H3tBu2) results in the formation

13 erate a product characterized as [(C5Me5)3Th(CO)][BPh4], 5, the first example of a molecular thorium

14 dies and 5850 patients (1157 MV-PCI and 4693 CO-PCI).

15 r pollution and the consistency of the PM2.5-CO relationship across different study settings and cond

16 A CO-delivery device has been assembled to deliver CO to a

17 er in the presence of alkaline cations for a CO dimer compared to a CO monomer.

18 her reaction with CO leads to formation of a CO analogue, which can be independently prepared using N

19 lkaline cations for a CO dimer compared to a CO monomer.

20 e(CO)5}2(mu-Ag)][B{3,5-(CF3)2C6H3}4] with a (CO)5Fe-Ag-Fe(CO)5 core, respectively, illustrating that

21 Additionally, CO starts to be observed at an ultralow overpotential of

22 d subsurface hydrogen reacting with adsorbed CO.

23 than a fraction of a percent of adventitious CO and CO2 .

24 The treatment of [B{3,5-(CF3)2C6H3}4]AgFe(CO)5 with 4,4'-dimethyl-2,2'-bipyridine (Me2Bipy) and Fe

25 5 afforded a heterobimetallic [(Me2Bipy)AgFe(CO)5][B{3,5-(CF3)2C6H3}4] species with a Ag-Fe(CO)5 bond

26 Pt favour the adsorption of O2, alleviating CO poisoning and promoting the catalysis.

27 5% CI 1.06-1.08), NO2 (1.09, 1.08-1.10), and CO (1.09, 1.08-1.10).

28 1.08, 1.07-1.09), NO2 (1.12, 1.10-1.13), and CO (1.09, 1.08-1.10).

29 PM2.5 and CO exposures were moderate [geometric means (GSD) were 4

30 ds ratio (aOR) = 5.5; 95% CI: 1.1, 26.8] and CO measurements (aOR = 2.5; 95% CI: 1.0, 6.4) in adjuste

31 tion between the C-site in the carbanion and CO resulted in the superior CO absorption capacities.

32 rbonyls governs the selectivities to CH4 and CO.

33 environments, and we show that H2, CH4, and CO feature prominently in many of their predicted metabo

34 CONSTANS (CO) and CO-LIKE (COL) genes regulate photoperiodicity in Arabido

35 irect correlation with the amount of CO2 and CO evolved and has a relationship with O2 evolved from t

36 pure Pt system forms highly stable COH* and CO* intermediates, leading to catalyst deactivation.

37 s plant development through CO-dependent and CO-independent mechanisms.

38 d CO2 reduction products such as formate and CO.

39 les are positive for AChE, NADPH-d, GAD, and CO throughout the rostrocaudal LCIC.

40 d by studies of the reduction of glyoxal and CO, key intermediates along the reaction pathway to fina

41 m also describe the dependence of the H2 and CO current densities on cathode voltage that are in stri

42 Difficulties associated with handling H2 and CO in metal-catalyzed processes have led to the developm

43 , producing 99.34% high-purity Sn and H2 and CO.

44 OHE showed an antioxidant effect on HOSO and CO under the studied conditions.

45 transmission electron microscopy imaging and CO probe molecule infrared spectroscopy.

46 Under NO and CO oxidation conditions, similar features are observed.

47 luate the association between PM10, NO2, and CO concentrations and risk of incident estimated glomeru

48 ncreasing association between PM10, NO2, and CO concentrations and risk of kidney outcomes.

49 e to higher concentrations of PM10, NO2, and CO is associated with increased risk of incident chronic

50 m occurs by a cooperative rotation of the Ar-CO and Ar-Ar' bonds depending on substituent location is

51 These phenotypes are CO independent.

52 [(CAAC)B(CO)Ar] is a source of the dicoordinate [(CAAC)ArB:] bory

53 served SC-independent strategy for balancing CO:NCO ratios.

54 ting the strong specific interaction between CO and the iron porphyrin provides a highly selective an

55 pressure on a Ngb mutant (V140W) that binds CO with a similar rate and affinity to the wild-type, de

56 cits do not necessarily correlate with blood CO levels but likely result from the pleiotropic effects

57 ied electrodes show 2-fold increases in both CO and H2 production.

58 Group 6 metal carbonyl complexes ([M(bpy)(CO)4], M = Cr, Mo, W) are potentially promising CO2 redu

59 of the catalytically active species [Mo(bpy)(CO)3](2-) via a second pathway at more positive potentia

60 measurements of the electrocatalyst [Mo(bpy)(CO)4] at platinum and gold electrodes.

61 ding the need for the generation of [Mo(bpy)(CO)4](2-).

62 /Pt surface proximity disfavors poisoning by CO or oxidized species.

63 sequential C-N bond formation followed by C(CO)-C(alkyl) bond cleavage.

64 acylation of amidines via oxidative C(CO)-C(CO) bond cleavage of 1,2-diketones to afford N,N'-diaroy

65 y dual acylation of amidines via oxidative C(CO)-C(CO) bond cleavage of 1,2-diketones to afford N,N'-

66 rmore, the subsequent conversion of captured CO into valuable chemicals with good reactivity was also

67 y hydroxyl (OH) > nitrate (ONO2) > carbonyl (CO) approximately ester (COO) > methylene (CH2).

68 In HEK293 cells, CO inhibited wild-type, but not C723S mutant, Kv11.1 K(+

69 The kinetic response of ChCooA-CO is nonexponential at all temperatures, including 298

70 etching mode in the IR spectrum of [B12 Cl11 CO](-) and theoretically by investigation of its electro

71 dy covariance flux measurements of NOx, CO2, CO and non methane volatile organic compound tracers in

72 easy-to-generate chemicals like N2, O2, CO2, CO, H2, or methane gas to value-added products is a live

73 the interconversions of H(+)/H2, O2/H2O, CO2/CO, and N2/NH3, is an ongoing challenge.

74 Te8(PEt3)6 and high electron affinity Co6Te8(CO)6 have closed electronic shells marked by high HOMO-L

75 CONSTANS (CO) and CO-LIKE (COL) genes regulate photoperiodicity in

76 ates the major flowering regulator CONSTANS (CO) and positively modulates FLOWERING LOCUS C (FLC).

77 In Arabidopsis thaliana, CONSTANS (CO) plays an essential role in the regulation of photope

78 t interaction between FKF1 and COP1 controls CO stability to regulate flowering time.

79 vides a new way of separating and converting CO.

80 s, resulting in the reduction of coordinated CO to a siloxymethyl (LnFe-CH2OSiMe3) group.

81 Bifunctional Mo complexes, [CpMo(CO)(kappa(3)-P2N2)](+) (P2N2 = 1,5-diaza-3,7-diphosphacy

82 taposition, with implications for crossover (CO) patterning/interference.

83 stock accumulate large numbers of crossover (CO) events between founder haplotypes, and thus present

84 nteractions and the completion of crossover (CO) formation between homologs during meiosis I.

85 e segregation in meiosis requires crossover (CO) recombination, which is regulated to ensure at least

86 elivery device has been assembled to deliver CO to a suspension of human colorectal adenocarcinoma ce

87 electronic structures of unligated (deoxy), CO-inhibited (carboxy), and O2-bound (oxy) hemes in myog

88 Pd particles along with single atoms during CO oxidation experiments.

89 Highly efficient CO absorption by carbanion-functionalized ILs provides a

90 in combination with in situ electrochemical CO stripping/FTIR data revealed subtle, but important, d

91 rption energies from in situ electrochemical CO/FTIR investigations suggested that balanced annealing

92 nd sensitive ex vivo detection of endogenous CO in a realistic model with facile, inexpensive synthes

93 ms, the permeability of gasses (for example, CO) through them is significantly affected, making these

94 e number of sites and select four exhibiting CO binding stronger than the (211) step surface.

95 re embedded in electrospun nonwoven fabrics, CO was liberated upon irradiation with low-intensity red

96 eoretical studies show that energetics favor CO oxidation on single Pd atoms supported on theta-alumi

97 )5][B{3,5-(CF3)2C6H3}4] species with a Ag-Fe(CO)5 bond and a heterotrimetallic [{Fe(CO)5}2(mu-Ag)][B{

98 The nu(CO) bands of the molecules with Ag-Fe(CO)5 bonds show a notable blue shift relative to those o

99 g)][B{3,5-(CF3)2C6H3}4] with a (CO)5Fe-Ag-Fe(CO)5 core, respectively, illustrating that it is possibl

100 4'-dimethyl-2,2'-bipyridine (Me2Bipy) and Fe(CO)5 afforded a heterobimetallic [(Me2Bipy)AgFe(CO)5][B{

101 shift relative to those observed for free Fe(CO)5, indicating a significant reduction in Fe-->CO back

102 Ag-Fe(CO)5 bond and a heterotrimetallic [{Fe(CO)5}2(mu-Ag)][B{3,5-(CF3)2C6H3}4] with a (CO)5Fe-Ag-Fe(

103 genation of the Diels-Alder adducts with Fe2(CO)9 followed by oxidative aromatization with 2,3-dichlo

104 signatures of CO bound to each site and find CO adsorption energy is ordered: Ptiso << Ptmetal < Ptox

105 he antioxidant potential and the ability for CO to inhibit CBS activity to alter redox homeostasis in

106 pproximately 80,000-fold higher affinity for CO than O2, causing it to rapidly take up and retain car

107 t, a relatively high absorption capacity for CO (up to 0.046 mol mol(-1) ) was achieved under ambient

108 te is also included as an active channel for CO binding.

109 ited a 2-fold greater turnover frequency for CO oxidation than 1 nm Ptmetal clusters but share an ide

110 The Arrhenius prefactor for CO binding to ChCooA and protoheme ( approximately 10(11

111 evelops in which the high affinity of Pt for CO helps to decrease the overpotential for the reduction

112 redox mechanism with carbon deposits forming CO, whereby the reduced Fe restores the original Ni-Fe a

113 talytic reactivity, CO turnover frequencies, CO faradaic efficiencies and demonstrate that Fe-N-C and

114 the reversible synthesis of acetyl-CoA from CO and a methyl group through a series of nickel-based o

115 Furthermore, CO sensitized breast cancer cells to doxorubicin.

116 istant to poisoning by small reactive gases (CO and H2S) that may interact with embedded metallic sit

117 with the Stratis device (Pharmajet, Golden, CO, USA) in each deltoid.

118 , indicating a significant reduction in Fe-->CO back-bonding upon its coordination to silver(I).

119 ealed by DFT computation was CO2 -->*COOH-->*CO-->*COCO-->*COCH2 OH-->*CH2 OCH2 OH-->CH3 CH2 OH.

120 crystallographic data of the chiral [Ru(I)H(CO)((S,S)-f-binaphane)(PPh3)] complex, which we identifi

121 omplexes bearing protonated amines, [CpMo(H)(CO)(P2N2H)](+), were characterized by spectroscopic stud

122 nder atmospheric pressure conditions and H2 /CO=2.

123 ecedented, uncatalyzed reactivity toward H2, CO, and ethylene.

124 el reaction conditions for DME synthesis (H2:CO:CO2 ratio of 16:8:1, up to 250 degrees C).

125 for deoxygenative reduction of CO2 with high CO generation rate (825 mumol h(-1) g(-1)) and outstandi

126 Characterization of the Ni(I)-CO species through spectroscopic and computational techn

127 oxidase (CO) stripes in area V2: neurons in CO blob columns project to thin stripes while neurons ou

128 Negative order in CO and positive orders in alkene and H2 were found and t

129 This 3-cluster solution was replicated in CO-MED and was similar for the HAM-D scale.

130 l voltage at 10 mA cm(-2), reducing CO2 into CO and oxidizing H2O to O2 with a 64% electricity-to-che

131 rth abundant materials to transform CO2 into CO at significantly milder conditions.

132 ition is caused by the reduction of CO2 into CO, whose high affinity with platinum triggers the forma

133 Therefore, we investigated CO reduction on Cu(100), Cu(111), and Cu(polycrystalline

134 ddition of triflic acid to ((tBu)4)(POCOP)Ir(CO) species show an Ir-H (1)H NMR chemical shift depende

135 of H2 to five-coordinate [((tBu)4)(POCOP)Ir(CO)(H)]OTf [((tBu)4)(POCOP) = kappa(3)-C6H3-2,6-(OP((t)B

136 ng step to methane and ethylene formation is CO hydrogenation, which is considerably easier in the pr

137 d CO pressure, these materials exhibit large CO separation capacities with only small changes in temp

138 ulfonyl azides and substituted amides at low CO pressure is reported.

139 The medial portion had lower CO activity and fewer ITD-sensitive neurons.

140 ,2'-bipyridine ligand in [fac-Mn(I)(mes2bpy)(CO)3(CH3CN)](OTf), which prevents Mn(0)-Mn(0) dimerizati

141 er limitation influencing energy metabolism (CO/H2 oxidation for cofactor generations) more prominent

142 see text] DO mice, and localized 2.2 million CO events to intervals with a median size of 28 kb.

143 e abstraction from an alkyl iodide by (.) Mn(CO)5 .

144 hain reaction mechanism propagated by (.) Mn(CO)5 .

145 metal catalyst, decacarbonyldimanganese Mn2 (CO)10 , to generate alkyl radicals from alkyl iodides ha

146 ed in solid-state materials: when PS and Mn2(CO)10 were embedded in electrospun nonwoven fabrics, CO

147 (3)PS* to a photolabile triplet state of Mn2(CO)10, which, like under near-UV irradiation, led to com

148 nstrated to activate classical photoCORM Mn2(CO)10 using red light (635 nm).

149 mental studies of reactions of C1 molecules (CO, CO2, CH3OH, etc.), the reactions of water will also

150 Syngas, a mixture of carbon monoxide (CO) and hydrogen (H2), is an important chemical precurso

151 nitrogen dioxide (NO2), and carbon monoxide (CO) and risk of incident chronic kidney disease, chronic

152 ique diiron site with three carbon monoxide (CO) and two cyanide (CN(-)) ligands (e.g., in the oxidiz

153 dioxide (CO2) reduction to carbon monoxide (CO) but not for the competing hydrogen (H2) evolution re

154 Carbon monoxide (CO) outcompetes oxygen when binding to the iron center o

155 Genes for aerobic carbon monoxide (CO) oxidation, polysulfide metabolism and hydrogen utili

156 Carbon monoxide (CO) poisoning affects 50,000 people a year in the United

157 Carbon monoxide (CO) reduced GSH/GSSG in three breast cancer cell lines b

158 .e., nitrogen oxides (NOx), carbon monoxide (CO), and volatile organic compounds (VOCs)) from East As

159 s (EFs) were calculated for carbon monoxide (CO), carbon dioxide (CO2), and particulate matter (PM).

160 erates the gaseous molecule carbon monoxide (CO), exhibit sleep apnea characterized by high apnea and

161 , carbon dioxide (CO2), and carbon monoxide (CO), or with H2 and CO2.

162 catalytic hydrogenation of carbon monoxide (CO), produces long chain hydrocarbons and offers an alte

163 ticulate matter (PM2.5) and carbon monoxide (CO), respectively.

164 of bovine CcO (bCcO) in the carbon monoxide (CO)-bound state at a resolution of 2.3 A, obtained by se

165 tion of several small gases (H2, D2, Ne, N2, CO, CH4, C2H6, Ar, Kr, and Xe) on the metal-organic fram

166 involved in CCAAT recognition, abolishes NF-CO binding to DNA.

167 We term this complex NF-CO.

168 fic membrane antigen (PSMA) inhibitor Glu-NH-CO-NH-Lys(Ahx) using the (68)Ga chelator HBED-CC (PSMA(H

169 ut in a reducing atmosphere containing NH3 + CO.

170 predict that PtZn systems go through a "non-CO" pathway for MOR because of the stabilization of the

171 ced via an ER process of H* with nonadsorbed CO (a unique result).

172 The nu(CO) bands of the molecules with Ag-Fe(CO)5 bonds show a

173 Thus, the observed CO oxidation has contributions from both single Pd atoms

174 In the absence of CO (under N2 atmosphere), the reaction did not proceed,

175 (1H)-benzo-1,2,3-triazoles in the absence of CO through a common intermediate was proposed.

176 (CO2RR) in which selectivity and activity of CO and C2 products are both enhanced at the borders of o

177 likely that COL12 represses the activity of CO rather than CO levels.

178 HCl3 is a convenient and safe alternation of CO gas, provides milder reaction conditions with high fu

179 ever, in the presence of catalytic amount of CO or in the presence of Ph3P in catalytic amounts as ad

180 o trackability and spatiotemporal control of CO release.

181 from siloxide precursors: no coordination of CO and oligomer formation during the polymerization of e

182 e-activated sensitivity for the detection of CO comprising iron porphyrin and functionalized single-w

183 d find use in delivering controlled doses of CO to cellular targets such as malignant tissues in remo

184 ikely result from the pleiotropic effects of CO on cellular mitochondrial respiration, cellular energ

185 manent neurological and affective effects of CO poisoning, a portion of survivors still have substant

186 stream inflammatory and oxidative effects of CO poisoning.

187 method can be applied for the enrichment of CO with capsinoids, thus giving it additional health pro

188 e control of visible light and the extent of CO-induced apoptotic death of the cancer cells has been

189 ischer-Tropsch conversions and extraction of CO from industrial waste feeds, which currently underuti

190 ture range and compared with the kinetics of CO binding in other heme systems such as myoglobin (Mb)

191 The ultrafast kinetics of CO rebinding to carbon monoxide oxidation activator prot

192 rmation decreases, mainly due to the loss of CO surface sites, which are replaced by H*.

193 time periods using satellite measurements of CO and CH4, nearly twice the decrease expected from prio

194 n summary, a unifying molecular mechanism of CO function relates it to the NF-YA paradigm, as part of

195 st other noninvasive and invasive methods of CO quantification in a cohort of patients with heart fai

196 Pd atoms are exposed to a gaseous mixture of CO + O2.

197 l reactions in the preferential oxidation of CO in excess H2.

198 materials, for example for the oxidation of CO.

199 a larger volatile inventory, particularly of CO or CO2 ices, or contained amorphous ice, which could

200 culations to develop a systematic picture of CO* binding on Cu-enriched Au surface model systems.

201 -1,2,3-triazin-4(3H)-ones in the presence of CO and1-aryl-(1H)-benzo-1,2,3-triazoles in the absence o

202 ropose that bicarbonate enhances the rate of CO production on Au by increasing the effective concentr

203 er and methanol, as well as the reactions of CO and CO2 over TMC surfaces.

204 demonstrating net four-electron reduction of CO to CH3OSiMe3 at a single Fe site.

205 plexity of the electrocatalytic reduction of CO to CH4 and C2H4 on copper electrodes prevents a strai

206 identify unique spectroscopic signatures of CO bound to each site and find CO adsorption energy is o

207 mbined theoretical and experimental study of CO hydrogenation on a Ni(110) surface, including studies

208 However, as many as [Formula: see text] of CO intervals do not overlap any putative hotspots, sugge

209 nd CC bond-breaking reactions that split off CO.

210 ctively) on thermal stability of canola oil (CO) and high oleic sunflower oil (HOSO) during French po

211 oil (EVOO), peanut oil (PO) and canola oil (CO), and compared for diverse chemical components and se

212 ets supplemented (2.8% wt:wt) with corn oil (CO; n-6) or fish oil (FO; n-3) for 28 d.

213 T This phenotype is genetically dependent on CO.

214 n, which is regulated to ensure at least one CO per homolog pair.

215 roduction of CO2 (unlike steam reforming) or CO (by complete methanol dehydrogenation).

216 aid putative recombination hotspots onto our CO intervals.

217 Medications to Enhance Depression Outcomes (CO-MED) trial (n = 640).

218 Cardiac output (CO) is a key indicator of cardiac function in patients w

219 s are widely used to measure cardiac output (CO).

220 , these cells consistently projected outside CO blob columns in all layers.

221 -OH DENs strongly favor formation of H2 over CO.

222 projections to distinct cytochrome oxidase (CO) stripes in area V2: neurons in CO blob columns proje

223 cid decarboxylase (GAD), cytochrome oxidase (CO), and calretinin (CR).

224 idine-2-carboxamide) and the S = 0 [Fe(PaPy3)CO](+) reference compound.

225 ion (MV-PCI) versus culprit vessel-only PCI (CO-PCI) in patients with multivessel disease, ST-segment

226 This photoactive CO-releasing polymer could find use in delivering contro

227 hat can be liberated by selective photolytic CO extrusion and that, although highly reactive, is suff

228 he material can be triggered to photorelease CO remotely by low-power broadband visible light (<1mWcm

229 Applicability of phototherapeutic CO-releasing molecules (photoCORMs) is limited because t

230 V1-to-V2 connections of L4B neurons preserve CO-stream segregation, suggesting that across-stream int

231 with platinum triggers the formation of a Pt-CO film that prevents the reaction process.

232 (I) complexes of the general formula fac-[Re(CO)3(NN)(OH2)](+) where NN = 2,2'-bipyridine (8), 4,4'-d

233 udies have been centered on a few reactions: CO oxidation, the hydrogenation of CO2, and the producti

234 tigate their intrinsic catalytic reactivity, CO turnover frequencies, CO faradaic efficiencies and de

235 evolution, oxygen evolution, CO2 reduction, CO oxidation reactions, etc.

236 t via detection of thiols and then releasing CO when triggered with visible light and O2.

237 wever, the mechanism by which CDF1 represses CO and FT transcription remained elusive.

238 en BC concentrations and satellite-retrieved CO, tropospheric NO2, and aerosol optical depth (AOD) (R

239 pled from a contaminated aquifer near Rifle, CO.

240 Milstein's complex, (PNN)RuHCl(CO), catalyzes the efficient reduction of aryl and alkyl

241 t selective reconstruction due to saturation CO coverage, where {100} facets roughen into vicinal ste

242 Crucially, such "triplet-sensitized CO-release" occurred in solid-state materials: when PS a

243 n and the variation in intensity of the SERS CO signal.

244 he carbanion and CO resulted in the superior CO absorption capacities.

245 A significant number of patients who survive CO poisoning suffer from long-term neurological and affe

246 ls), but their direct synthesis from syngas (CO + H2) would comprise a more environmentally-friendly,

247 socyanide analogue of the highly unstable Ta(CO)6 and represents the only well-defined zerovalent tan

248 L12 represses the activity of CO rather than CO levels.

249 We found that CO intervals are enriched in hotspots compared to the ge

250 Our data suggest that CO induces arrhythmias in guinea pig cardiac myocytes vi

251 The CO photorelease rates of photoCORP-1 (determined by spec

252 The CO stretch vibrations are very sensitive to the redox ch

253 CO-applied as the CO-releasing molecule, CORM-2-prolonged the APs and indu

254 icles ((10Os)CO-Au NPs) greatly enhanced the CO stretching vibration signal at 2100cm(-1), which is

255 CO2, is the primary source of carbon in the CO formed at the Au electrode by a combination of in sit

256 r clusters as heterogeneous catalysts in the CO-->CO2 reaction (COox) is presented.

257 efficiency at pH 7, we need to increase the CO concentration by changing the solvent or alloying the

258 ite-selective isotope editing to monitor the CO/CN(-) stretching vibrations in [FeFe]-hydrogenase HYD

259 Examination of the O2 requirements of the CO release step revealed that the SL-photoCORM is suitab

260 ly by the observation of a blue shift of the CO stretching mode in the IR spectrum of [B12 Cl11 CO](-

261 identify active sites, we first predict the CO binding at a large number of sites and select four ex

262 In the SFX structure, the CO is coordinated to the heme a3 iron atom, with a bent

263 This indicates that the CO binding reaction is adiabatic, in contrast to the com

264 atomic coordination sphere composed of three CO and two CN(-) ligands affecting its redox properties

265 go a spin-state transition above a threshold CO pressure, these materials exhibit large CO separation

266 that COL12 affects plant development through CO-dependent and CO-independent mechanisms.

267 rdered AuCu NPs selectively converted CO2 to CO at faradaic efficiency reaching 80%.

268 nt and selective electrocatalysts for CO2 to CO conversion.

269 in the understanding of trends in the CO2 to CO electrocatalysis of metal- and nitrogen-doped porous

270 electrocatalysts for the reduction of CO2 to CO in organic media.

271 tion of molecular catalysts to reduce CO2 to CO is a sustainable route to storable solar fuels.

272 Electrocatalytic reduction of CO2 to CO is reported for the complex, {fac-Mn(I)([(MeO)2Ph]2bp

273 ases the activity of CO2 electroreduction to CO.

274 was to evaluate the validity of exposure to CO as a surrogate of exposure to PM2.5 in studies of hou

275 Exposure to CO causes early afterdepolarization arrhythmias.

276 Our results suggest that exposure to CO is not a consistently valid surrogate measure of expo

277 loading was shown to preferentially lead to CO formation, whereas at lower surface loading the elect

278 selectively electrocatalyze CO2 reduction to CO in tetrahydrofuran at -0.48 V vs NHE, the least negat

279 erblob columns, as projecting selectively to CO blobs in L2/3, suggesting convergence of blob/interbl

280 hydroformylation of styrene is sensitive to CO concentration, and drastically different kinetic regi

281 nism for photocatalytic reduction of CO2 -to-CO over ZrPP-1-Co is also proposed.

282 of Tri-Ag-NPs as a catalyst for CO2RR toward CO formation.

283 a significant increase in sensitivity toward CO when negative gate voltage is applied.

284 s to the support and binds and activates two CO molecules, while Ag binds and activates O2 , and Ag/P

285 etermining step (RDS) is C-C coupling of two CO, with DeltaG(double dagger) = 0.69 eV.

286 The rapid agglomeration of Pd atoms under CO oxidation conditions even at 6 degrees C leads to the

287 In this sense, it qualitatively resembles V(CO)6 , the only paramagnetic homoleptic metal carbonyl i

288 esting functional specialization of V1-to-V2 CO streams.

289 The objective of this study was to validate CO measurement using the inert gas rebreathing (IGR) met

290 e in short-term mortality with MV-PCI versus CO-PCI (odds ratio [OR], 1.08; 95% confidence interval [

291 f CO2, CH4, N2O, PM2.5, PM10, NOx, SO2, VOC, CO, NH3, Hg, Pb, Cd, Cr (VI), Ni, As, and dioxins.

292 s detailed, highlighting the roles of water, CO, and amine in the generation of a more complete catal

293 h as 1 can react with N2 reversibly and with CO irreversibly under photochemical conditions.

294 reduced Arrhenius prefactors associated with CO binding in Mb and Hb.

295 eved under ambient conditions, compared with CO solubility in a commonly used IL [Bmim][Tf2 N] (2x10(

296 nefit with single-stage MV-PCI compared with CO-PCI.

297 5.63; P=0.57) with MV-PCI when compared with CO-PCI.

298 ) methoxy groups that can further react with CO to dimethyl carbonate.

299 Further reaction with CO leads to formation of a CO analogue, which can be ind

300 [(C5Me5)3Th][BPh4], 2, reacts with CO to generate a product characterized as [(C5Me5)3Th(CO

301 It was trapped with CO to give an O-[Zr] bonded borata-beta-lactone.