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1 accurate and sensitive analytical method for cobalt.
2 n complex with hepcidin and the iron mimetic cobalt.
3 acids using readily prepared bis(phosphine) cobalt(0) 1,5-cyclooctadiene precatalysts is described.
4 ctional groups was observed with the reduced cobalt(0) precatalysts, and protic solvents such as meth
5 e were exposed to a lethal dose (9.75 Gy) of Cobalt-60 gamma radiation and euthanized at four time po
6 ispersion LA setup is based on the tube-type COBALT ablation cell in combination with the aerosol rap
8 ultrafast) ablation cell geometry within the Cobalt ablation chamber, integrated into a nanosecond la
9 Whereas rapid beta-hydrogen elimination from cobalt alkyls occurred under an N(2) atmosphere, alkylat
10 terials (titanium and its alloys, aluminium, cobalt-alloys, stainless steel, poly-ethylene, polyureth
11 we reveal aluminum dopants in lithium nickel cobalt aluminum oxide are partially dissolved in the bul
12 this regard, for a new CO(2)-to-CO reduction cobalt aminopyridine catalyst, a detailed experimental a
15 tively, continuously, and efficiently remove cobalt and cesium from a feed of dissolved lithium, coba
17 key phases in the natural biogeochemistry of cobalt and in relevant remediation and resource recovery
18 produce oxygen from water after loading with cobalt and in the presence of an electron scavenger are
19 ral to the crystallization buffer (extrinsic cobalt and intrinsic potassium ions), (iii) extrinsic br
21 entify signatures resulting from exposure to cobalt and vinylidene chloride and link distinct human s
22 MI, and levels of organochlorine pollutants, cobalt, and molybdenum were associated with lower BMI.
24 d in complex multi-step reactions, including cobalt- and rhodium-catalyzed hydroformylation and an Ir
25 e an interface catalyst consisting of atomic cobalt array covalently bound to distorted 1T MoS(2) nan
26 atinum (Pt), palladium, rhodium, nickel, and cobalt, as well as a library of bimetallic compositions,
27 pite the absence of an auxiliary ligand, the cobalt assay is applicable to aromatic and aliphatic com
28 various configurations, the triangular-shape cobalt atom cluster with a central sulfur vacancy (3Co(M
29 hous boron nitride prevents the diffusion of cobalt atoms into silicon under very harsh conditions, i
30 MIT9215 can sustain growth with less than 50 cobalt atoms per cell, ~100-fold lower than minimum iron
32 C-N) bond formation, while a photoredox- and cobalt-based catalytic system progressively desaturates
34 lished new hybrid molecular photoanodes with cobalt-based molecular cubane cocatalysts on hematite as
37 1.5G, 100 mW cm(-2) , lambda>300 nm) with a cobalt-based turnover number of 90 for CO after 60 h.
38 netic machinery for the synthesis and use of cobalt-bearing cofactors (cobalamins) in their genomes.
39 rt on the host-guest complexation of several cobalt bis(1,2-dicarbollide) anions (COSANs) with cyclod
40 Here, we present nine derivatives of the cobalt bis(dicarbollide)(1-) anion substituted at the bo
41 e based 2D conjugated MOF with square-planar cobalt bis(dihydroxy) complexes (Co-O(4) ) as linkages (
42 fined as cobalt complexes featuring a carbon-cobalt bond, are largely used to produce carbon-centered
45 ents, notably iron, will be exhausted before cobalt can be fully depleted, helping to explain the per
47 he absence of MCM, ATR induces a sacrificial cobalt-carbon bond homolysis reaction in an unusual reve
48 utational studies provided evidence that the cobalt-carbon bonds of the relevant intermediates in ((i
50 rity-reversal strategy based on light-driven cobalt catalysis, which enables the generation of nucleo
52 ore-shell nanofibre system that integrates a cobalt catalyst and a photosensitizer in close proximity
53 during the reaction, and both light and the cobalt catalyst are important for the dehydrogenation st
55 he catalytic amount of manganese, the active cobalt catalyst can be regenerated, which provides a pos
57 developed by merging a photocatalyst with a cobalt catalyst for the synthesis of isoindolone spirosu
59 is the use of a commercially available cheap cobalt catalyst to produce a wide variety of 2-substitut
68 ccess quaternary centers bearing nitriles by cobalt-catalyzed C-H bond activation and sequential addi
75 ed strategy for identifying and optimizing a cobalt-catalyzed oxidizing system for the bioinspired di
76 After having identified the most promising cobalt-catalyzed oxidizing system, the automated screeni
78 ctivity of gem-difluoroalkenes, we present a cobalt-catalyzed regioselective unsymmetrical dioxygenat
83 by introducing a material with site-isolated cobalt centers embedded in the stable matrix of Mo(2)CT(
84 s out the intersheet coupling between active cobalt centers, as this scenario would impair electrolyt
85 e delaminated nanosheets, with quite distant cobalt centers, precludes the direct coupling between th
88 of HIF-1alpha in MeHg-induced neurotoxicity, cobalt chloride (CoCl2), 2-methoxyestradiol (2-MeOE2), s
89 ble factor (HIF), including desferrioxamine, cobalt chloride, and dimethyloxalylglycine, raised NCOA4
91 luding aluminum, antimony, arsenic, cadmium, cobalt, chromium, copper, iron, lead, manganese, nickel,
92 undergo either PCI with fluoropolymer-based cobalt-chromium everolimus-eluting stents (PCI group, 94
93 modern ultrathin strut biodegradable polymer cobalt-chromium sirolimus-eluting Orsiro stent in an all
94 etic acid (NTA)-coated FO probes chelated by cobalt (Co(III)) and exposed to anti-ADAMTS13 autoantibo
95 node connectivity of Fermi arcs, whereas on cobalt (Co) termination, the connectivity is across adja
96 ramework-74 containing mixed combinations of cobalt (Co), cadmium (Cd), lead (Pb), and manganese (Mn)
98 With these expected increases in demand, cobalt (Co)-dependent technologies face the risk of sign
99 ovel planar and conjugated N(4) -macrocyclic cobalt complex (Co(II)CPY) derived from phenanthroline s
101 le and catalytic amount of manganese, active cobalt complex can be generated in situ and can catalyze
105 obalt(III) complexes (R-Co(III)), defined as cobalt complexes featuring a carbon-cobalt bond, are lar
108 lore the structure-function relationships of cobalt complexes in the catalytic hydrogen evolution rea
110 lexes and have allowed the identification of cobalt complexes that show promise for the development o
111 tic developments based on the use of iron or cobalt complexes to promote radical reactivity which hav
112 talyzed by bis(phosphino)pyridine ((iPr)PNP) cobalt complexes was studied to understand the origins o
113 ed long sought-after cationic bis(phosphine) cobalt complexes, [(R,R)-((iPr) DuPhos)Co(eta(2) ,eta(2)
116 onic structures and VT behavior for the four cobalt complexes; one-step one-electron partial VT, two-
118 introduce us to the world of cobamides-those cobalt-containing compounds, like B(12), that appear to
120 vary concentrations of 5 essential minerals (cobalt, copper, manganese, molybdenum, and zinc), 4 meta
122 amin (Znbl), the Zn-analogues of the natural cobalt-corrins cobyric acid and vitamin B(12) , respecti
123 We now show that water oxidation with the cobalt-corrole CoBr(8) as electrocatalyst affords H(2)O(
124 es with the unpaired electron located on the cobalt d(z2) orbital, which is well positioned for subst
125 leted, helping to explain the persistence of cobalt-dependent metabolism in marine cyanobacteria.
126 Recovery results for cobalt in cobalamin and cobalt detected by the HPLC-ICP-OES system were calculat
127 le liquid-liquid microextraction (SLLME) for cobalt determination by flame atomic absorption spectrom
128 cobalt limitation are used to interpret the cobalt distribution in the equatorial Pacific Ocean, whe
130 catalyst synthesized through electrospinning cobalt-doped zeolitic imidazolate frameworks into select
132 data explain the previously reported extreme cobalt exposures in children and support the need to man
136 have as viable candidates in next-generation cobalt-free lithium-ion batteries is highlighted here.
138 To address these challenges, a new class of cobalt-free materials with general formula of LiNi(x) Fe
139 thod was used to separate and preconcentrate cobalt from sage tea and vitamin B12 samples after compl
142 derivatives using first-row transition-metal cobalt has been demonstrated wherein the pivaloyl group
143 st-row transition metals, including iron and cobalt, has gained considerable recent attention as a po
144 tion suggests that alkene insertion into the cobalt hydride occurred in the presence of free carboxyl
145 H(2) produced the corresponding aldehyde and cobalt hydride, demonstrating the feasibility of element
146 inary study of the mechanism suggests that a cobalt-hydride pathway is involved in the reaction.
147 ne solution were discovered for mixed nickel/cobalt hydroxide electrocatalysts, which were derived in
148 ated by electrochemical deposition of nickel-cobalt hydroxide on the nickel foam substrate at ambient
149 triazacyclononane) such as a highly reactive cobalt(I) (1((I))) and a cobalt(I) carbonyl (1((I))-CO)
152 are far more active than traditional neutral cobalt(I) catalysts and approach rhodium catalysts in ac
154 catalyst tetrakis(4-methoxyphenyl)porphyrin cobalt(II) (TMPPCo) on the side chains of an ionomer (po
155 rtex-assisted solid-phase microextraction of cobalt(II) and nickel(II) from canned foodstuffs prior t
156 -band EPR experiments revealed bis(phosphine)cobalt(II) bis(carboxylate)s were generated in catalytic
160 ned nickel(II) bromide, nickel(II) chloride, cobalt(II) chloride and iron(II) chloride sheets through
161 nopyridyl)-2,2'-bipyridine) is a polypyridyl cobalt(II) complex bearing both a redox-active bipyridin
163 l azides can be effectively activated by the cobalt(II) complexes of D(2)-symmetric chiral amidoporph
164 s, including trihexyl(tetradecyl)phosphonium cobalt(II) hexafluoroacetylacetonate ([P(66614)(+)][Co(h
168 reactive catalysts can be generated from the cobalt(II)-complexes using trimethylaluminum, methyl alu
170 st described as an intermediate spin (S = 1) cobalt(III) center that is antiferromagnetically coupled
171 The polymers are prepared using the salen cobalt(III) complex catalyzed copolymerization of CO(2)
172 oromethane from [(18)F]fluoride ion and then cobalt(III) fluoride mediated gas phase fluorination.
177 erate-strength hydrogen bonding stabilizes a cobalt(III)-superoxo species formed upon O(2) adsorption
180 presence of pyridine with a four-coordinate cobalt imido ((Ar)L)Co(NAd)(py) ( K(a) = 8.04 M(-1)), as
181 a synergistic effect between the ligand and cobalt in Co(II)CPY plays a critical role in boosting it
184 method was applied for the determination of cobalt in egg yolk and Vitamin B12 and the recovery resu
185 ) has been proposed for the determination of cobalt in egg yolk and Vitamin B12 at trace levels.
186 eparation and determination of cobalamin and cobalt in kefir samples by high performance liquid chrom
187 uccessfully applied for the determination of cobalt in linden tea samples and the recovery results ob
189 tep favors the formation of ortho-fluoroaryl cobalt intermediates due to the ortho fluorine effect, a
190 ecific role in predisposing the incarcerated cobalt ion for organometallic catalysis has remained obs
192 ts and as a cytotoxic agent due to the known cobalt ion toxicity, allowing the achievement of both he
193 of a Co(1)O(x) single molecule with only one cobalt ion, the minimum unit of the cobalt-based oxygen-
195 oxides such as Cobalt oxide, Iron oxide, and Cobalt Iron oxide, at three different concentrations.
197 le of Co(2+)/Co(3+) in Co-Black TNT prevents cobalt leaching and enhances catalyst stability over a w
199 Quantitative descriptions of Prochlorococcus cobalt limitation are used to interpret the cobalt distr
202 cobalt oxide (LiCoO(2) ) and lithium nickel cobalt manganese oxide (LiNi(0.8) Co(0.1) Mn(0.1) O(2) ,
204 ssly combine two canonical radical reactions-cobalt-mediated hydrogen-atom transfer and copper-promot
208 iveness of this UBU strategy is shown with a cobalt MOF (denoted SNNU-45) in which octahedral cages w
209 describes the development of easy-to-prepare cobalt nanoparticles (NPs) in solution as promising alte
211 the first example of an isolable, bimetallic cobalt nitride complex, and it has been fully characteri
212 nyl) (3a) in THF cleanly forms the binuclear cobalt nitride Na(THF)(4){[((ket)guan)Co(N(3))](2)(mu-N)
214 ing UV irradiation to further activate these cobalt NPs not only to enhance their catalytic performan
217 recycling via the upcycling of spent lithium cobalt oxide (LCO) as a new promising solid lubricant ad
218 um-ion battery cathode nanomaterial, lithium cobalt oxide (LCO), on the growth, development, hemoglob
219 nthic species Chironomus riparius to lithium cobalt oxide (Li (x)Co(1- x)O(2), LCO) and lithium nicke
220 1- x)O(2), LCO) and lithium nickel manganese cobalt oxide (Li (x)Ni (y)Mn (z)Co(1- y- z)O(2), NMC) at
222 tructured electrocatalysts, platinum/lithium cobalt oxide (Pt/LiCoO(2) ) composites with Pt nanoparti
223 -metal anode can be coupled with a potassium cobalt oxide cathode to achieve dendrite healing in a pr
224 ich, coupled with a lithium nickel-manganese-cobalt oxide cathode with a high nickel content, can lea
225 e report the discovery of subnanometer sized cobalt oxide clusters for oxidative dehydrogenation of c
226 rodeposition protocol for preparing isolated cobalt oxide single molecules (Co(1)O(x)) and clusters (
227 in mass activity at 0.85 V, when compared to cobalt oxide, Co(3)O(4)/C, and a negligible degradation
228 functionalized with metallic oxides such as Cobalt oxide, Iron oxide, and Cobalt Iron oxide, at thre
231 strategy for stabilization of the molecular cobalt-oxo cubane core (Co(4)O(4)) by immobilizing it as
233 ectroscopy, to study the mechanism of OER on cobalt oxyhydroxide (CoOOH), an archetypical unary OER c
234 pectroscopy study confirmed the formation of cobalt oxyhydroxide species and the iron stimulated the
235 Here, we report a platinum-trimer decorated cobalt-palladium core-shell nanocatalyst with a low plat
236 Newly developed combination of magnetic cobalt particles based dispersive solid-phase microextra
237 ides (up to the formation of nanocrystalline cobalt pentlandite, Co(9)S(8)) and lower crystallinity f
238 ranslation of a low-cost, non-precious metal cobalt phosphide (CoP) catalyst from 1 cm(2) lab-scale e
240 MOF-1992, is achieved by linking tetratopic cobalt phthalocyanin-2,3,9,10,16,17,23,24-octaol linkers
241 CO(2) reduction that consists of a polymeric cobalt phthalocyanine catalyst (CoPPc) coupled with meso
242 ned with a cathode consisting of a polymeric cobalt phthalocyanine on carbon nanotubes to construct a
243 Encapsulating molecular catalysts such as cobalt phthalocyanine within coordination polymers such
248 e formation of *COOH is lower than that with cobalt porphyrin, thus leading to enhanced CO production
249 form via admixing with liposomes containing cobalt-porphyrin-phospholipid (CoPoP) potently enhances
252 g an anodic bias to a commercially available cobalt precursor and Nafion binder mixture coated on a g
253 ent Li-ion batteries on the ever-fluctuating cobalt prices poses serious environmental and sustainabi
256 enzyme are consistent with a metal-centered cobalt radical ~6 angstroms away from the tertiary carbo
257 f decontaminated water and the percentage of cobalt removed, which offers flexibility in operating th
259 rns the extraction of poly-metallic nodules, cobalt-rich crusts and sulphide deposits from the ocean
260 for provenance discrimination were lithium, cobalt, rubidium, strontium, uranium and the rare earth
262 transformation, a cheap and easily available cobalt salt and P(CH(2)CH(2)PPh(2))(3) (PP(3)) ligand we
265 plexes of a metal centre (manganese, iron or cobalt) sandwiched between two bulky Cp(ttt) ligands (wh
269 k, we developed a facile route to synthesize cobalt single atoms/nitrogen-doped hollow porous carbon
271 formation of the electrocatalytically active cobalt species for the oxygen evolution reaction (OER).
274 cting as a support and ligand, to modify the cobalt species via Co-O-SiO(n) linkages, which favor the
275 te or ink solution effectively activated the cobalt species, and most of the first row transition met
277 urface terminations) that is obtained from a cobalt-substituted bulk molybdenum carbide (beta-Mo(2)C:
278 d O(2) reactivities of active-site models of cobalt-substituted ring-cleaving dioxygenases are presen
280 entrations of iridium, platinum, nickel, and cobalt suggest mixing of melted local sediment with smal
281 low, polar and catalytic bipyramid prisms of cobalt sulfide as efficient sulfur host for sodium sulfu
282 nce of the polar and catalytic properties of cobalt sulfide as hosts for soluble sodium polysulfides
283 The polar catalytic bipyramid prisms sulfur@cobalt sulfide composite exhibits a high capacity of 755
286 a high mass loading of 9.1 mg cm(-2), sulfur@cobalt sulfide shows high capacity of 545 mAh g(-1) at a
287 isotope exchange experiments, we discover a cobalt superoxide species as an active intermediate in t
288 with O(2) generates a rare thiolate-ligated cobalt-superoxo species Co(O(2))(Me(3)TACN)(S(2)SiMe(2))
289 e redox noninnocence of the TAML scaffold in cobalt-TAML (tetra-amido macrocyclic ligand) complexes h
291 rage stations, and a shortage of lithium and cobalt, the increasing cost gives impetus to exploit low
292 ned by different combinations of pH, initial cobalt to iron ratios ([Co](aq)/[Fe](aq)), with/without
293 ong with the mild hyperthermia and intrinsic cobalt toxicity, leads to complete tumor regression and
295 , iron, manganese, zinc, phosphorous, boron, cobalt, Vitamins A, D, B6, thiamine, riboflavin, niacin
300 ere, we report an investigation of supported cobalt, which is known for its hydrocarbon production an