ライフサイエンスコーパス: Co

1 Co-administration of a UV inactivated Ad4 vector with th

2 Co-administration of AZI with IDA did not show evidence

3 Co-altered RAS/RAF-TP53 remained independently associate

4 Co-circulation of LPAIVs with HPAIVs suggests their inte

5 Co-contamination of these two compounds has been detecte

6 Co-crystal structures of two IGHV3-53-neutralizing antib

7 Co-crystallization of the parental rabbit mAb in complex

8 Co-cultivation of limbal melanocytes with limbal epithel

9 Co-culture of isolated naive-like B cells from NSCLC pat

10 Co-culture of wild-type and mutant viruses in the presen

11 Co-cultures of human hepatoma and hepatic stellate (HSCs

12 Co-depletion of Mdm4 and Mdm2 further impaired DNA repli

13 Co-depletion of POT1B or BRD2 with TRF2 restores a canon

14 Co-depletion of TALP-3 and ANKR-26 specifically impairs

15 Co-detection of CHIKV with DENV were found in 22% of fat

16 Co-directionality of expression data provide new mechani

17 Co-enzyme Q(10) (CoQ(10)) an endogenous mitochondrial re

18 Co-evolution of gut commensal bacteria and humans has en

19 Co-existence of FD/IBS may contribute to this unsatisfac

20 Co-expressed genes ranked as the most stable genes in th

21 Co-expression analysis also revealed that the most downr

22 Co-expression and live imaging studies indicate that the

23 Co-expression networks identified region-specific altera

24 Co-expression of a therapeutic Arylsulfatase-A with RgE-

25 Co-expression of CERBERUS with LjVPY1 or LjVPY2 in N. be

26 Co-expression of TRAM and an antigen from adenoviruses i

27 Co-expression of Yin Yang 1 (YY1) is required for the fu

28 Co-housing of VDR(DeltaPC) and VDR(lox) mice made the VD

29 Co-housing rescued the defect of the mucus growth rate,

30 Co-immunoprecipitation confirmed that nuclear-targeted P

31 Co-immunoprecipitation data demonstrate that the maize C

32 Co-immunoprecipitation revealed an interaction between A

33 Co-immunoprecipitation studies showed interactions betwe

34 Co-incubation of HOPS, proteoliposomes bearing R-SNARE,

35 Co-incubation of linezolid significantly improved killin

36 Co-incubations between DMSP-producing microalgae and bac

37 Co-infection between Helicobacter pylori (Hp) and groups

38 Co-inoculation experiments with Wt and Deltaexlx-gh5 res

39 Co-localization of B- and T-lymphocytes was observed.

40 Co-localization of monomers, crosslinkers, and chain-tra

41 Co-located elevated concentrations of primary combustion

42 Co-occurrence networks of gene-microbe association were

43 Co-occurrence of aberrant hepatocyte growth factor (HGF)

44 Co-occurring fungal and bacterial communities persistent

45 Co-occurring genetic events have been shown to drive car

46 Co-occurring health issues, such as epilepsy and other n

47 Co-opting Cullin4 RING ubiquitin ligases (CRL4s) to indu

48 Co-parenting spouses who live together remain in close p

49 Co-primary endpoints were safety (assessed by incidence

50 Co-primary outcomes were mobility (performance-based Sho

51 Co-primary outcomes will include persistent bacterial co

52 Co-reactivity to more than one nut is frequent, and co-s

53 Co-relative analyses indicated that familial confounding

54 Co-staining of BrdU+ cells with NeuN or S100B permitted

55 Co-targeting the mTOR and EPH receptor pathways with the

56 Co-transfection assays (Col3a1 promoter-luciferase repor

57 Co-transfection of PCR cassettes with a Cas12a-encoding

58 pair of a neutral S= 1/2 and an anionic S=0 Co-H(2) adduct, both supported by a trisphosphine borane

59 We exemplify this on LiNi(0.8)Mn(0.1)Co(0.1)O(2) (NMC811)/graphite cells, which are typical h

60 ning behavior in a low SFE Fe(40)Mn(20)Cr(15)Co(20)Si(5) (at%) high entropy alloy, SFE ~ 6.31 mJ m(-2

61 hods revealed that 2 is a low-spin (S = 1/2) Co(IV) species with the unpaired electron located on the

62 Among these, Sm(2) Co(17) -based magnets are excellent candidates owing to

63 commercial cathode material LiNi(0.6)Mn(0.2)Co(0.2)O(2), full cells exhibit a gravimetric and volume

64 entrations of Zn(2+) but not Mg(2+), Cu(2+), Co(2+), or Mn(2+).

65 metal ions tested, including Mn(2+), Fe(2+), Co(2+), Ni(2+), and Cu(2+) We also demonstrate that mult

66 2+), Fe(2+), Al(3+), Ni(2+), Cu(2+), Zn(2+), Co(2+), Pb(2+) and Ru(3+)) and aqueous compatibility was

67 Electrochemical activation of a 2D-Co-MOF@Nafion-modified graphite electrode in aqueous sol

68 A new cobalt metal-organic framework (2D-Co-MOF) based on well-defined layered double cores that

69 ersible anionic redox reactions in LiNi(1/3) Co(1/3) Mn(1/3) O(2) .

70 Full cells with LiNi(1/3)Mn(1/3)Co(1/3)O(2) cathodes demonstrate >92% capacity retention

71 ng to the concerted catalysis, the ZnFe(0.4) Co(1.6) O(4) oxide demonstrates the highest nitrate prod

72 take double perovskite oxide PrBa(0.5)Sr(0.5)Co(1.5)Fe(0.5)O(5+delta) (PBSCF) as a model system to de

73 k, we investigate the Li(1.2)Ni(0.13)Mn(0.54)Co(0.13)O(2) particles morphologically, compositionally,

74 (55)Co is a promising isotope with high positron yield and a

75 a]Ga-DOTATATE, [(64)Cu]Cu-DOTATATE, and [(55)Co]Co-DOTATATE by PET/CT imaging in NOD-SCID mice bearin

76 Conclusion: [(55)Co]Co-DOTATATE demonstrated superior image contrast comp

77 ulations found that effective doses for [(55)Co]Co-DOTATATE were comparable to those for both [(64)Cu

78 Methods: (55)Co and (64)Cu were produced by the (54)Fe(d,n)(55)Co and

79 d (64)Cu were produced by the (54)Fe(d,n)(55)Co and (64)Ni(p,n)(64)Cu nuclear reactions, whereas (68)

80 anodes and commercially available LiNi(0.6) Co(0.2) Mn(0.2) O(2) (NCM(622) ) cathodes deliver ultrah

81 de (AlF(3) ) to create SPEs inside LiNi(0.6) Co(0.2) Mn(0.2) O(2) (NCM) || Li batteries that are able

82 C (6.6 mA cm(-2)), a 1.0 mAh cm(-2) LiNi(0.6)Co(0.2)Mn(0.2)O(2) electrode maintains a substantial 74%

83 2 months) in the male CD2F1 strain using (60)Co gamma irradiation (~0.6 Gy/min, 7.5-12.5 Gy).

84 Pairing with LiNi(0.8) Co(0.1) Mn(0.1) O(2) (NCM(811) ) further raises the ener

85 ium nickel cobalt manganese oxide (LiNi(0.8) Co(0.1) Mn(0.1) O(2) , NCM 811) cathodes exhibit 99.6-99

86 Focusing on Li(x)Ni(0.8)Co(0.15)Al(0.05)O(2) as a model compound, we use operand

87 Here, the perovskite oxide Bi(0.15) Sr(0.85) Co(0.8) Fe(0.2) O(3-) (delta) (BiSCF) is shown to exhibi

88 gh-nickel lithium layered oxide, Li(Ni(0.91) Co(0.06) Mn(0.03) )O(2) (NCM9163), with minimal side eff

89 The most active, a Co(III)/K(I) complex, shows a turnover frequency of 800

90 a high-valent nitrene intermediate such as a Co(III) iminyl ((Ar)L)CoBr((*)N(C(6)H(4)-p-(t)Bu)) or Co

91 ominating resting state of the catalyst as a Co(IV) species CoO(2).

92 h with a multigrain nanocrystal comprising a Co(3)O(4) nanocube core that carries a Mn(3)O(4) shell o

93 herefore, the deposit was close to that of a Co(1)O(x) single molecule with only one cobalt ion, the

94 we present the first crystal structure of a Co(III) iodosylbenzene complex and the unprecedented rea

95 Initially, tensile specimens of a Co-added stainless steel were heat treated by quenching

96 ng scanning tunneling microscopy images of a Co-doped iron arsenide superconductor and prove that the

97 Density functional theory supports a Co(III)=N=Co(III) canonical form with significant pai-bo

98 eycomb lattices compounds, A(4)B(2)O(9) (A = Co, Fe, Mn; B = Nb, Ta), have been explored owing to the

99 promotes the formation of the highly active Co(Fe)OOH phase, which enhances the OER electrocatalytic

100 In addition to this advantage, Co-Fe NCs have the unique ability to form growing chains

101 ent and that one-electron oxidation affords [Co(III)(TAML(sq))].

102 Incorporation of the amphiphilic [Co(L3)](2+) complex into the liposome bilayer produces a

103 Both Co-PB-1(6) and Co-rPB-1(6) cages produce 90-100 % H(2) O(2) from electr

104 types of reactions: Giese-type addition and Co/Ni-catalyzed cross-coupling.

105 sized ((Fc(2)PDI)MCl(2), M = Mg, Zn, Fe, and Co) and characterized crystallographically, spectroscopi

106 first-row transition metals (M = Mn, Fe, and Co) within a Keplerate cluster that was lined on the inn

107 s are observed between the N7 atoms of G and Co(II), an interaction that strongly preserves the centr

108 Cu-HAB and Co-HAB are determined to exhibit n-type conduction under

109 fully applied to determination of Ni(II) and Co(II) in canned foodstuffs prepared by microwave digest

110 optimization, the linearities for Ni(II) and Co(II) were 0.05-80 ng mL(-1) and 0.2-100 ng mL(-1), res

111 certain non-iron metals, such as Zn, Mn, and Co.

112 oxidation overpotential of bimetallic Ni and Co active sites (whereas Ni(2+) can be more easily activ

113 DEI between octahedrally coordinated Ni and Co resulted in the generation of superior OER active cen

114 mmonly used magnetic materials (e.g., Ni and Co) are not biocompatible, possess weak magnetic remanen

115 Enriched Fe, V, Ni and Co, together with petrographic context, suggests that th

116 , Zn, Hg, Se, As, Cu, Cd, Mn, Ni, Cr, Pb and Co) were determined in dorsal white and dark muscle of X

117 ] connecting ligand as a photosensitizer and Co(dmgH)(2) (PPA)Cl (PPA-Co, dmgH=dimethylglyoxime; PPA=

118 etween the surface Co[Formula: see text] and Co[Formula: see text] bonding quantified by exploiting t

119 triangular prism-assemble in concert around Co(II) template ions.

120 OES system were calculated as 0.07 mg/kg (as Co) and 0.06 mg/kg, respectively.

121 resource-sensitive transition metals such as Co and Ni.

122 Catalytic, asymmetric Co/Cr-mediated iodoallylation is adopted to incorporate

123 The reaction employs commercially available Co(II) catalyst in the presence of Mn(III) cooxidant and

124 thermally stable metalloradical, (P(3) (B) )Co(H(2) ), serves as a competent precursor for hydrogen

125 rprisingly large magnetic moment (0.5 mu(B) /Co) and Curie temperature (75 K), values larger than pre

126 o 8.0%, 1.6 to 6.6%, and 0.4 to 6.1% for Ba, Co, Fe and Ni, respectively.

127 cribes the simultaneous determination of Ba, Co, Fe, and Ni in nuts by high-resolution continuum sour

128 We develop an Individualized Network-based Co-Mutation (INCM) methodology by inspecting over 2.5 mi

129 tion and showed a consistent linkage between Co and Mn.

130 Both Co-PB-1(6) and Co-rPB-1(6) cages produce 90-100 % H(2) O

131 ished homolytic H(2) (or D(2)) activation by Co(0) and cis addition of H(2) (or D(2)) across alkene d

132 the distinct mechanism of O(2) reduction by Co-porphyrins.

133 kers to amines yields the more flexible cage Co-rPB-1(6).

134 in a ferromagnetic Weyl semimetal candidate, Co(2)MnAl, at room temperature.

135 nterconversions of the form {Co(III)-cat-cat-Co(III)} {Co(III)-cat-SQ-Co(II)} {Co(II)-SQ-SQ-Co(II)} (

136 analysis of 22 elements (As, Ba, Be, Bi, Cd, Co, Cr, Cu, K, Mn, Mo, Na, Ni, P, Pb, Th, Tl, Sb, U, V,

137 he generation of superior OER active centers Co((3-delta)+) and Ni(3+).

138 The Charlson Co-Morbidity Index was a fourth measure of frailty.

139 e single molecules (Co(1)O(x)) and clusters (Co (n) O(y)) on a carbon fiber nanoelectrode.

140 Cadmium (Cd), cobalt (Co), mercury (Hg), nickel (Ni), molybdenum (Mo), lead (P

141 these expected increases in demand, cobalt (Co)-dependent technologies face the risk of significant

142 immunoassay was then evaluated by comparing Co(III)- and nickel (Ni(II))-NTA stabilized surfaces, co

143 conjugated N(4) -macrocyclic cobalt complex (Co(II)CPY) derived from phenanthroline subunits is prepa

144 at the TAML backbone in the anionic complex [Co(III)(TAML(red))](-) is truly redox noninnocent and th

145 nonheme cobalt(III) iodosylbenzene complex, [Co(III) (TQA)(OIPh)(OH)](2+) (1), is synthesized and cha

146 The resulting single-component Co(-I) complex is proposed as the direct pre-catalyst.

147 Consequently, Co(4) N enables stable operation of high-rate (10 C, 16.

148 The Copenhagen Co-Morbidity in HIV Infection study included 453 partici

149 l condensation has been developed using a Cp*Co(CO)I(2) catalyst.

150 A Cp*Co(III)-catalyzed directing group-assisted C7 C-C coupli

151 mical performance of FLU and NF on the N-CQD@Co(3)O(4)/MWCNTs/GCE surface was examined using CV and d

152 eveloped for preconcentration of As, Cd, Cr, Co, Sb, Pb and Tl to inductively coupled plasma optical

153 ecipitates were composed of more crystalline Co sulfides and/or Co-rich mackinawite, the exact phase

154 chlores Y(1.8)M(0.2)Ru(2)O(7-delta) (M = Cu, Co, Ni, Fe, Y) controls the concentration of surface oxy

155 art of the U.S. Department of Energy's (DOE) Co-Optimization of Fuels and Engines (Co-Optima) initiat

156 bled the interception of (R,R)-((iPr) DuPhos)Co(CO)(2) C(O)CH(2) CH(2) Ph, which upon hydrogenolysis

157 tmosphere, alkylation of (R,R)-((iPr) DuPhos)Co(CO)(2) Cl in the presence of CO enabled the intercept

158 Under reduced pressure, (R,R)-((iPr) DuPhos)Co(CO)(2) Cl underwent CO dissociation to form (R,R)-((i

159 CO dissociation to form (R,R)-((iPr) DuPhos)Co(CO)Cl.

160 tes (Co, Cd, 85 degrees C), long duplicates (Co, Pb, 85 degrees C), and insertions (Co, Mn, 85 degree

161 m (Co, Cd, 120 degrees C), short duplicates (Co, Cd, 85 degrees C), long duplicates (Co, Pb, 85 degre

162 Here, a high-power and durable Co-N-C nanofiber catalyst synthesized through electrospi

163 terventions in the Organisation for Economic Co-operation and Development (OECD) countries during the

164 pril 2020 in eight Organisation for Economic Co-operation and Development countries (n = 21,649) to s

165 articles were from Organization for Economic Co-operation and Development countries.

166 nes defined by the Organization for Economic Co-operation and Development.

167 layer MoS(2) doped with the magnetic element Co is reported, and the magnitude of the valley splittin

168 (DOE) Co-Optimization of Fuels and Engines (Co-Optima) initiative.

169 nd Fe, 2D images revealed mutually exclusive Co and Fe mobilization.

170 tomically dispersed transition metal (M: Fe, Co, or/and Mn) and nitrogen co-doped carbon (M-N-C) cata

171 mplanted in N-doped carbon (M(1) -N-C; M=Fe, Co, Ni and Cu) has been developed starting from multivar

172 coordinated single metal sites (M-N-C, M=Fe, Co, Ni, Mn) are the popular platinum group-metal (PGM)-f

173 high-valent oxygenated complexes of Mn, Fe, Co, and Cu are increasingly well-known, high-valent oxyg

174 muL of serum and 12 elements (Mg, S, Mn, Fe, Co, Cu, Zn Se, Br, Rb, Mo, and Cs) in less than 250 000

175 20 elements (Mg, P, S, K, Ca, V, Cr, Mn, Fe, Co, Cu, Zn, Se, Br, Rb, Sr, Mo, I, Cs, and Ba) in 10 muL

176 its the production of crystals of MUV-101(Fe,Co,Ni,Zn) and MUV-102(Cu), heterometallic titanium MOFs

177 tic Al addition dilutes the ferromagnetic Fe/Co/Ni additions.

178 olated clusters obtained from the femtomolar Co(2+) solution through an atom-by-atom technique can re

179 cipitates displayed higher crystallinity for Co sulfides (up to the formation of nanocrystalline coba

180 dite, Co(9)S(8)) and lower crystallinity for Co-rich mackinawite, suggestive of mineral-specific bact

181 ed two-step VT interconversions of the form {Co(III)-cat-cat-Co(III)} {Co(III)-cat-SQ-Co(II)} {Co(II)

182 Forming Co(2)P/MP(x) core/shell NRs and subsequently converting

183 phere effects in the metal-organic framework Co(2)(OH)(2)(bbta) (H(2)bbta = 1H,5H-benzo(1,2-d:4,5-d')

184 etals, particularly those of the same group (Co and Rh).

185 tronic structure analyses revealed weak C-H->Co sigma-interactions, augmented by dispersive stabiliza

186 ((ket)guan)Co(mu-NH)](2) (6) and [((ket)guan)Co(mu-ND)](2) (6-D), respectively, as a result of dihydr

187 tion of the bis(imido) complexes [((ket)guan)Co(mu-NH)](2) (6) and [((ket)guan)Co(mu-ND)](2) (6-D), r

188 obaltate(II) complex [Na(THF)(x)][((ket)guan)Co(N(3))(2)] ((ket)guan = [(tBu(2)CN)C(NDipp)(2)](-), Di

189 uclear cobalt nitride Na(THF)(4){[((ket)guan)Co(N(3))](2)(mu-N)} (1).

190 w, a holey lamellar high entropy oxide (HEO) Co(0.2) Ni(0.2) Cu(0.2) Mg(0.2) Zn(0.2) O material with

191 s are reported that comprise heterodinuclear Co(III)/M(I) macrocyclic complexes (where M(I) = Group 1

192 The Co(II) /Co(II) products are reactive to oxidation and reduction.

193 Now, a Mg(II)Co(II) catalyst is reported that exhibits significantly

194 I)-cat-cat-Co(III)} {Co(III)-cat-SQ-Co(II)} {Co(II)-SQ-SQ-Co(II)} (cat(2-) = catecholate, SQ(*-) = se

195 ydrides of W(III), Mn(II), Fe(III), Ru(III), Co(II), and Ni(III).

196 sions of the form {Co(III)-cat-cat-Co(III)} {Co(III)-cat-SQ-Co(II)} {Co(II)-SQ-SQ-Co(II)} (cat(2-) =

197 the stable immobilization of the antigen in Co(III)-NTA-functionalized FO probes.

198 lations and emerges near the Fermi energy in Co(3)Sn(2)S(2).

199 e Coulomb-interaction strength (U ~ 4 eV) in Co(3)Sn(2)S(2).

200 first study that demonstrates that (*)OH in Co(2+)-activated PMS can play a significant role in cont

201 write and read operations simultaneously in Co(60)Fe(20)B(20)/Pb(Mg(1/3)Nb(2/3))(0.7)Ti(0.3)O(3) het

202 tion suggests that two types of inequivalent Co(2+) sublattices generate magnetic-field-dependent fer

203 ates (Co, Pb, 85 degrees C), and insertions (Co, Mn, 85 degrees C).

204 On the other hand, integrating Co, Mn, and Zn turns Li(2) S into a prelithiation agent,

205 ovel long noncoding RNA Noncoding Intergenic Co-Induced transcript (NICI) on chromosome 12p13.31 whic

206 increased stability towards the intermediate Co(I) species.

207 erate and boreal forests (ICP [International Co-operative Programme on Assessment and Monitoring of A

208 les that was suggestive of dysbiosis, and LV-Co increased the risk of association with this group.

209 Taken together, LV-Co resuscitation exacerbated the loss of bacterial diver

210 metal-organic frameworks M(3)(HITP)(2) (M = Co, Ni, Cu; HITP = 2,3,6,7,10,11-hexaiminotriphenylene).

211 t cofacial porphyrin prisms using MTPyP (M = Co(II) or Zn(II), TPyP = 4-tetrapyridylporphyrin) and fu

212 lar precursor [HNEt(3) ](2) [M(pdms)(2) ] (M=Co, Zn) allow for multiple charge transfers (CTs) betwee

213 e magnetic correlations in the kagome magnet Co(3)Sn(2)S(2).

214 The previously reported parent material, [Co(2) (S-mandelate)(2) (4,4'-bipyridine)(3) ](NO(3) )(2)

215 Merck & Co., Inc.

216 Sharp & Dohme Corp, a subsidiary of Merck & Co Inc, Kenilworth, NJ, USA.

217 Sharp & Dohme Corp, a subsidiary of Merck & Co, Inc.

218 n this study, heavy metals including Cr, Mn, Co, Ni, Cu, Zn, As, and Cd in 55 Thai local rice (4 vari

219 ivalent transition metal ions M(II) (M = Mn, Co, Ni, Cu, Zn, Pd, and Cd) under mild conditions.

220 ieve 80-99% leaching efficiencies of Ni, Mn, Co, and Li from the LIB "black mass".

221 etallic mixed-valent, mixed-ligand molecule [Co(II) (hfac)(3) -Na-Co(III) (acac)(3) ] (1).

222 ring isolated cobalt oxide single molecules (Co(1)O(x)) and clusters (Co (n) O(y)) on a carbon fiber

223 Co(13)C(2)(CO)(24)](4-), containing multiple Co-Co bonds to statistically enhance observed rates of P

224 nsity functional theory supports a Co(III)=N=Co(III) canonical form with significant pai-bonding betw

225 tic intermediates derived from complex [L(N4)Co(OTf)(2)] (1) (L(N4) = 1-[2-pyridylmethyl]-4,7-dimethy

226 mixed-ligand molecule [Co(II) (hfac)(3) -Na-Co(III) (acac)(3) ] (1).

227 s much better than most of the reported Ni-, Co-, and Fe-based bifunctional electrocatalysts.

228 A novel Co(II) -catalyzed polyene cyclization was developed that

229 ium to form an open core species X-Co(III)-O-Co(IV)-O (1-X).

230 Specifically, the assembly architecture of Co(2+) -bridged frameworks is shown to be dependent on t

231 this study allows for a better constraint of Co biogeochemistry in various natural and engineered env

232 An improved method for the deprotection of Co-complexes of cyclic enediynes using tetrabutylammoniu

233 ach sequence type, and the molar fraction of Co among all 12 samples was observed to vary from 0.4 to

234 (r (d)) which is approximately the length of Co-O bond in cobalt oxide.

235 rofiles showed apparent coincident maxima of Co, Mn, and Fe, 2D images revealed mutually exclusive Co

236 Herein, the mechanism of Co-catalyzed cross-dehydrogenative couplings of N-aryl g

237 precipitation and transformation pathways of Co (Fe) sulfides in this study allows for a better const

238 Studies of the stoichiometric reaction of Co(I) or Co(II) precursors with CyMgCl implicated cataly

239 group compatibility and site selectivity of Co(III) -catalyzed C(sp(2) )-H Dha amidation suggests th

240 Rapid uncaging of Co(2+) ions by patterned UV light activates Terminal deo

241 The activation energy of (Co(x)Ni(3-x))(HITP)(2) alloys scales inversely with an i

242 Electrochemical characterization of [Co(13)C(2)(CO)(24)](4-) in the presence and absence of p

243 Incorporation of [Co(L1)](2+) into the liposome aqueous core, followed by

244 to the delocalized electronic structure of [Co(13)C(2)(CO)(24)](4-).

245 n unquenched orbital moment of 0.42 mu(B) on Co, which is hybridized with neighboring Rh atoms with a

246 ovide insights into the key intermediates on Co and Ni single-atom configurations for the H(2) and CO

247 use of a catalytic amount of Cu(acac)(2) or Co(acac)(2) and Ag(2)CO(3) as an oxidant in alpha,alpha,

248 inant MtcB methylates either cob(I)alamin or Co(I)-MtqC in the presence of l-carnitine and, to a much

249 posed of more crystalline Co sulfides and/or Co-rich mackinawite, the exact phase being dependent on

250 minyl ((Ar)L)CoBr((*)N(C(6)H(4)-p-(t)Bu)) or Co(IV) imido ((Ar)L)CoBr(N(C(6)H(4)-p-(t)Bu)) complex.

251 s of the stoichiometric reaction of Co(I) or Co(II) precursors with CyMgCl implicated catalyst initia

252 egioselectivity with well-established Rh- or Co-catalysts has thus far proven elusive, thereby limiti

253 ation of nanocrystalline cobalt pentlandite, Co(9)S(8)) and lower crystallinity for Co-rich mackinawi

254 result in an unusual low-spin square planar Co(II) complex, which is unreactive towards external sub

255 with triflate as strong Lewis acids and PPA-Co as a hydrogen transfer catalyst.

256 photosensitizer and Co(dmgH)(2) (PPA)Cl (PPA-Co, dmgH=dimethylglyoxime; PPA=4-pyridinepropionic acid)

257 to SOT are identified, i.e., the lateral Pt-Co asymmetry as well as out-of-plane injected spin curre

258 ficantly up till the 2nd week (259,237.46 Pt/Co) of the experiment and started decreasing slowly ther

259 l and synthesis temperature used, as random (Co, Cd, 120 degrees C), short duplicates (Co, Cd, 85 deg

260 tylene, was performed using isolable reduced Co complexes.

261 y (DFT) calculations reveal the effect of Rh-Co bimetallic formation in facilitating the production o

262 tional metal-organic layer (MOL), Hf(12) -Ru-Co, composed of [Ru(DBB)(bpy)(2) ](2+) [DBB-Ru, DBB=4,4'

263 h three synergistic active sites, Hf(12) -Ru-Co-OTf competently catalyzed dehydrogenative tandem tran

264 extended this strategy to prepare Hf(12) -Ru-Co-OTf MOL with a [Ru(DBB)(bpy)(2) ](2+) photosensitizer

265 gy toward high-content SACs (such as Fe(SA), Co(SA), Ni(SA)).

266 e olefin isomerization catalyzed by the same Co(-I) active species appears to be responsible for the

267 e intrinsic activity and stability of single Co sites, along with unique catalyst architecture, provi

268 t-performing high-temperature magnets are Sm-Co-based alloys with a microstructure that comprises an

269 to reveal that the magnetization state in Sm-Co magnets results from curling instabilities and domain

270 In solution, ([Co(L1)](2+) ) forms two isomers as shown by (1) H NMR sp

271 rm {Co(III)-cat-cat-Co(III)} {Co(III)-cat-SQ-Co(II)} {Co(II)-SQ-SQ-Co(II)} (cat(2-) = catecholate, SQ

272 (III)} {Co(III)-cat-SQ-Co(II)} {Co(II)-SQ-SQ-Co(II)} (cat(2-) = catecholate, SQ(*-) = semiquinonate).

273 d on the *N site, while high oxidation state Co assists in stabilizing the absorbed OH(-) for the gen

274 vation (Fe) and concentrate supplementation (Co): FoCo fed high-quality Napier grass (Pennisetum purp

275 ticularly of chemical sintering of supported Co during Fischer-Tropsch synthesis.

276 tigate the relationships between the surface Co[Formula: see text] and Co[Formula: see text] bonding

277 n colocalization-dependent protein switches (Co-LOCKR) that perform AND, OR, and NOT Boolean logic op

278 his complex displays a high-spin tetrahedral Co(II) center, which is reactive towards external substr

279 eas Ni(2+) can be more easily activated than Co(2+) ) and induce the electronic interaction between t

280 Here, we show that [Co(13)C(2)(CO)(24)](4-), containing multiple Co-Co bonds

281 The Co NPs demonstrated high activity when used at 30 degree

282 The Co(II) /Co(II) products are reactive to oxidation and re

283 underlying stepwise radical pathway for the Co(II)-based C-H amination.

284 the spin density heavily delocalized in the Co(IV)-O unit.

285 verified that prior to the onset of OER, the Co/Fe spinel-like surface promotes the formation of the

286 retains a stable chemical environment of the Co/Fe ions, although its structure weakens after electro

287 ntical location TEM analyses reveal that the Co/Fe spinel-like surface retains a stable chemical envi

288 R catalysis in neutral pH water, whereas the Co-TPP monomer gives a 50 % mixture of H(2) O(2) and H(2

289 enzymatic activation as is the case with the Co-C5' bond of B(12).

290 The [Co(L2)](2+) complex has 1,8-pendants in a cis-configurat

291 ite, the exact phase being dependent on the [Co](aq)/[Fe](aq) value.

292 as an intradonor CT from the pdms ligand to Co ion upon electrocrystallisation.

293 and ligand, to modify the cobalt species via Co-O-SiO(n) linkages, which favor the reactivity of spec

294 A modified electrode was developed with Co-Ag bimetallic nanoparticles stabilized in poly(vinylp

295 High-nickel LiNi(1-) (x) (-) (y) Mn(x) Co(y) O(2) (NMC) and LiNi(1-) (x) (-) (y) Co(x) Al(y) O(

296 t equilibrium to form an open core species X-Co(III)-O-Co(IV)-O (1-X).

297 x) Co(y) O(2) (NMC) and LiNi(1-) (x) (-) (y) Co(x) Al(y) O(2) (NCA) are the cathode materials of choi

298 ider range of LTMOs including Li(x)(Ni,Fe)(y)Co(1-y)O(2) suggest that 5% substitution is sufficient t

299 taining cathode materials (e.g., LiNi(x)Mn(y)Co(z)O(2); NMCs), as they lose oxygen at lower operating

300 , Ca, Na, K, Mg) and micronutrients (Fe, Zn, Co, Mn, I) were sufficient to contribute to daily dietar