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1 ure to hydrogen gas in the presence of Raney cobalt.
2 are example of a side-on dioxygen complex of cobalt.
3 ment for water oxidation is 10 +/- 1 ions of cobalt, 13 +/- 4 ions of iridium, and 11 +/- 3 ions of n
4 ependent charge transport properties of a 2D cobalt 2,3,6,7,10,11-triphenylenehexathiolate framework.
5 m relaxes to the lowest manifold of divalent cobalt ((4) T 1) in 150-200 fs.
6 an interfacial layer of elemental nickel and cobalt, a few nanometres in thickness, whose moments are
7 EO800-PESn[Co2(CO)6]x ABA triblock copolymer/cobalt adducts (10-67 wt % PEO) were subsequently prepar
8                  Additionally, tandem nickel-cobalt affinity chromatography was used to prepare highl
9  16 using dihydogen in the presence of Raney cobalt afforded compound 17 (60%) that could be elaborat
10                          Open-shell iron and cobalt alkyl complexes have been synthesized that serve
11 odetermining with no evidence for erosion of cobalt alkyl stereochemistry by competing beta-hydrogen
12 g., iron, cobalt, nickel, copper, and nickel-cobalt alloy), accomplished by a facile low-temperature
13           The safety and efficacy of a novel cobalt alloy-based coronary stent with a durable elastom
14  surged among patients with a malfunctioning cobalt-alloy hip prosthesis.
15                             More than 25 new cobalt-(aminomethyl)pyridine complexes were developed as
16 the wire changes with the transition between cobalt and cobalt oxide controlled by a voltage applied
17                                         Both cobalt and cysteine coupling resulted in a high-density
18 ur and ZntR, only respond to Zn(II), RcnR to cobalt and FrmR to formaldehyde.
19 ecies with conjugated dienes using a unified cobalt and iridium catalytic system in order to access a
20                        Differences found for cobalt and iron showed that the results obtained by size
21 ighly crystalline, electrochemically active, cobalt and naphthalene diimide-based MOF that is an effi
22                           Excess supplies of cobalt and nickel altered root traits in a different way
23                             A combination of cobalt and nickel catalytic cycles enables a highly bran
24  report self-assembled growth of c-BN NDs on cobalt and nickel substrates by plasma-assisted molecula
25 phase-pure cobalt-doped SnO2 (Co/SnO2) and a cobalt and nitrogen co-doped SnO2 (Co-N/SnO2) nanocrysta
26 t-catalyzed [2+2+2] cycloaddition via a dual cobalt and photoredox catalyst manifold.
27 he essential but high-cost alloying elements cobalt and titanium with inexpensive and lightweight alu
28      Thus, despite the known cytotoxicity of cobalt and zinc ions, these results suggest that iron ox
29 ators includes metal sensors that respond to cobalt and/or nickel (RcnR, InrS) or copper (CsoR) plus
30 , and O,P-catalysts, and rhodium, palladium, cobalt, and iron catalysts.
31 quency of reaction to methylisothiazolinone, cobalt, and potassium dichromate.
32  report the development of second-generation cobalt- and maleimide-based liposomes that have improved
33  materials with atomically dispersed iron or cobalt are promising for catalytic use.
34  substrates containing inert C-H bonds using cobalt as catalyst is currently a topic attracting signi
35 ertically aligned two-dimensional layers and cobalt atoms doping demonstrated a high hydrogen evoluti
36 proach we deliberately place single iron and cobalt atoms in either of two different coordination env
37 nism, where spin is delocalized onto the two cobalt atoms.
38 imultaneous installation of multiple diverse cobalt-based active sites, including FeCo alloys and Co4
39                          Novel heterogeneous cobalt-based catalysts have been prepared by pyrolysis o
40 talytic performances ranks this new class of cobalt-based complexes among the most promising CO2-to-f
41 to create a new highly efficient and durable cobalt-based electrocatalyst for the oxygen evolution re
42                                           In cobalt-based Fischer-Tropsch synthesis (FTS), the size o
43                   We synthesized a series of cobalt-based hybrid molecules (HYCOs) that combine an Nr
44 and O2-adsorption strength, we conclude that cobalt-based moieties bind O2 too weakly for efficient O
45                                  We designed cobalt-based multilayered thin fi lms in which the cobal
46 ahertz (THz) magneto-plasmonic response of a cobalt-based periodic aperture array.
47 n under inert and aerobic conditions, with a cobalt-based turnover number (TON(Co)) of up to 420.
48                                              Cobalt-based WOCs are especially promising for knowledge
49 quantify HSA-bound LCFAs such as the albumin-cobalt binding assay.
50 esign of highly robust, active, and reusable cobalt-bipyridine- and cobalt-phenanthroline-based metal
51 on of an alkynylboronate to a Co-B bond of a cobalt boryl complex to form a vinylcobalt intermediate.
52 enzyme is active in the presence of zinc and cobalt but not with other divalent metals.
53  evaluation and experimental validation on a cobalt-C3N4 catalyst with a desired molecular configurat
54 l volume using the 'thinness ratio' and the 'cobalt-calcein' technique.
55          We herein report that manganese and cobalt can bind to the same nonheme site and confer HCO
56                                              Cobalt can cause a distinctive, rapidly progressive and
57 the solution-phase reaction of manganese and cobalt carbonyl complexes with trioctylphosphine.
58                    The clinical emergence of cobalt cardiomyopathy seems to require the coexistence o
59 e to the intermediacy of Co(IV)-O species in cobalt-catalysed oxidation of organic substrates as well
60  pressure and mild conditions using a simple cobalt catalyst and extends to diverse tosylate and dien
61 ality with a C1-symmetric bis(imino)pyridine cobalt catalyst is described and has been applied to the
62 ation of the 4-position of the pincer in the cobalt catalyst was faster than arene borylation.
63        The iridium congener of the optimized cobalt catalyst, 6-(H)2BPin, was prepared and crystallog
64 eme for the hydrogen evolution reaction by a cobalt catalyst, revealing unique information for the de
65 of the achiral aryl imine substituent on the cobalt catalyst.
66                            As such, iron and cobalt catalysts have garnered interest as replacements
67 ho-to-fluorine selectivity observed with the cobalt catalysts was maintained in the presence of a ben
68 red the next generation of 4-substituted PNP cobalt catalysts with electron donating and sterically b
69                                              Cobalt catalysts with electronically enhanced site selec
70 otoredox catalysis in tandem with low-valent cobalt catalysts, new methods by which functionalities m
71 bstitution patterns were synthesized using a cobalt-catalyzed [2 + 2 + 2] cycloaddition and subsequen
72 ir efficient construction was the photo- and cobalt-catalyzed [2 + 2 + 2] cycloaddition reaction betw
73 ein, we disclose the first light-controlled, cobalt-catalyzed [2+2+2] cycloaddition via a dual cobalt
74                                              Cobalt-catalyzed anti-Markovnikov reactions that involve
75                                  We report a cobalt-catalyzed asymmetric hydroboration/cyclization of
76 he mechanism of bis(phosphino)pyridine (PNP) cobalt-catalyzed C-H borylation of 2,6-lutidine using B2
77                              Electrochemical cobalt-catalyzed C-H functionalizations were achieved in
78                          The electrochemical cobalt-catalyzed C-H oxygenation proved viable on arenes
79 1,1-triborylalkanes was accomplished through cobalt-catalyzed hydroboration of 1,1-diborylalkenes wit
80                                            A cobalt-catalyzed method for the 1,1-diboration of termin
81                                            A cobalt-catalyzed proton-coupled electron transfer (PCET)
82                                  An original cobalt-catalyzed ynamide carbozincation leading mainly t
83 veals that O2 binds end-on to each framework cobalt center in a 1:1 ratio with a Co-O2 bond distance
84 ntial radiological dispersal devices (RDDs), cobalt, cesium, and strontium, were studied by DMS to de
85 p of urine metals including barium, cadmium, cobalt, cesium, molybdenum, lead, antimony, thallium, tu
86 omprising a redox-active, atomically precise cobalt chalcogenide cluster wired between two nanoscopic
87 exciting a low-spin Co(3+) ion by an iron-to-cobalt charge transfer.
88 e deletions sensitive to both low oxygen and cobalt chloride, a hypoxia mimetic.
89                         Balloon, expandable, cobalt-chrome covered stent (Jotec, E-ventus BX((R))) wa
90 nary artery disease randomized to BVS versus cobalt-chromium everolimus-eluting stents (EES).
91  intervention (PCI) with fluoropolymer-based cobalt-chromium everolimus-eluting stents (PCI group, 94
92  polymer drug-eluting stents: the thin-strut cobalt-chromium sirolimus-eluting Orsiro stent and the s
93  = 697) or everolimus-eluting (EES, n = 694) cobalt-chromium stents.
94 etal is lost from the taper junction between Cobalt-Chromium-Molybdenum (CoCrMo) and Titanium (Ti) co
95                      HPLC-ICPMS analysis for cobalt (Co) and Cbl gave detection limits of 0.18 ng/g a
96              The observed size dependence of cobalt (Co) catalysts for the Fischer-Tropsch reaction w
97 rowth of h-BN films on mechanically polished cobalt (Co) foils using plasma-assisted molecular beam e
98 r in controlling Se as well as vanadium (V), cobalt (Co), nickel (Ni), zinc (Zn), and aluminum (Al) c
99 and the other D35 dye with a tris(bipyridine)cobalt ([Co(bpy)3](3+/2+)) based mediator.
100 thesis and characterization of a hexanuclear cobalt complex 1 involving a nonheme ligand system, L1,
101 With this information, we identify a soluble cobalt complex that mimics the structure and reactivity
102 proceed in the presence of 0.25 mol % of the cobalt complex with 0.75 mol % of the alkylating agent t
103 tion catalyzed by a tetradentate macrocyclic cobalt complex with the formula [LCo(III)Cl2](+) (L = ma
104                                The molecular cobalt complex, Co(salophen), and para-hydroquinone (H2Q
105 g(TOF) vs E1/2(Co(III/II)) for the different cobalt complexes (TOF = turnover frequency).
106                 A large variety of molecular cobalt complexes are used as electrocatalysts for H2 pro
107                                      Several cobalt complexes based on the azacalix[4](2,6)pyridine f
108    A series of mononuclear pseudomacrocyclic cobalt complexes have been investigated as catalysts for
109 fluence of bound cations on the reduction of cobalt complexes of redox active ligands and explored th
110  porosity and stabilization effect of nickel-cobalt complexes on 1T phase MoS2.
111 id nanostructures combining amorphous nickel-cobalt complexes with 1T phase molybdenum disulfide (MoS
112 catalysts have been prepared by pyrolysis of cobalt complexes with nitrogen ligands on different inor
113 d been alleviated, the addition of cobalt or cobalt-containing vitamin B12 could further enhance chlo
114  stable for high iron concentration or for a cobalt content up to about 0.3 atom per formula unit.
115  after thermal activation under O2 to open a cobalt coordination site and to oxidize Co(II) to Co(III
116 d with systematically varied low loadings of cobalt (CoOx), manganese (MnOx), and nickel oxides (NiOx
117                  Accordingly, we tested both cobalt coupling and covalent linkage of the trimers to t
118                                              Cobalt dialkyl and bis(carboxylate) complexes bearing al
119 Aryl-substituted bis(imino)pyridine iron and cobalt dihalide compounds, when activated with alkyl alu
120                           The synthesis of a cobalt dihydrogen Co(I)-(H2) complex prepared from a Co(
121                             A triad of d(10) cobalt dihydrogen complexes was synthesized by utilizing
122          Reduced bis(imino)pyridine iron and cobalt dinitrogen compounds have also been discovered th
123  (T c = 23 to 25 K) by precipitating-out the cobalt dopants and giving larger overall a-lattice param
124 conducting-ordering temperature in optimally cobalt-doped BaFe2As2 crystal (T c = 23 to 25 K) by prec
125 ability of bacterially synthesized zinc- and cobalt-doped magnetite nanoparticles for biomedical appl
126 rved in cells containing the high-anisotropy cobalt-doped particles.
127           In this contribution, a phase-pure cobalt-doped SnO2 (Co/SnO2) and a cobalt and nitrogen co
128 cate that molybdenum disulfide with moderate cobalt doping content possesses the optimal activity.
129  phase (Bi3NdTi2CoO12-delta) with increasing cobalt doping level from 0 to 1.
130 from water dissociation at under coordinated cobalt edge sites of cobalt oxide nanoislands.
131                A series of nanocomposites of cobalt embedded in N-doped nanoporous carbons, carbon na
132  effusion, or goiter should be evaluated for cobalt exposure.
133 pared to normal compacted (NC) unsubstituted cobalt ferrite ( 0.8 x 10(-9) A(-1)m).
134 ved for magnetically compacted (MC) Zr doped cobalt ferrite (x = 0.2) ( 4.3 x 10(-9) A(-1)m) compared
135                    In contrast, conventional cobalt ferrite magnetic nanoparticles (MNPs) did not sho
136 s is dictated by magnetic characteristics of cobalt ferrite nanocrystal carriers.
137  Magnetic solid phase extraction (MSPE) with cobalt ferrite nanoparticles coated with oleic acid is d
138 cate these structures out of a ferrofluid of cobalt ferrite nanoparticles.
139 9) A(-1)m) compared to that of unsubstituted cobalt-ferrite ( 1.24 x 10(-9) A(-1)m), while a fivefold
140 lambda/dH was observed in Zr-doped (x = 0.2) cobalt-ferrite ( 4.3 x 10(-9) A(-1)m) compared to that o
141                               In this study, cobalt ferrites (C) decorated onto 2D material (porous g
142 n (MC) has been employed to process Zr-doped cobalt ferrites, Co1+xZrxFe2-2xO4 (0 </= x </= 0.4), to
143                We find that graphene-covered cobalt films have surprising magnetic properties.
144              However, this dense nonmagnetic cobalt has not yet been observed.
145                      As the medicinal use of cobalt has waned and measures to reduce industrial expos
146 ic atmospheres of RbCl, SrCl2, and CoHexCl3 (cobalt hexamine chloride) around a B-form DNA molecule.
147                Through the study of a stable cobalt hydride complex, we demonstrate the influence of
148 ctrocatalysts for H2 production, but the key cobalt hydride intermediates are frequently difficult to
149 solation of and open environments around the cobalt-hydride catalytic species at Zr8-SBUs are respons
150   Despite having very different ligands, the cobalt hydrides of both catalysts possess nearly identic
151 e-step synthesis of well-dispersed amorphous cobalt hydroxide/oxide-modified graphene oxide (CoOxH-GO
152 ng C-H activation from a fully characterized cobalt(I) boryl intermediate.
153 , the reaction of the diketiminate-supported cobalt(I) complex L(tBu) Co with O2 gives a rare example
154  structure of one-dimensional single-crystal cobalt (II) oxide (CoO) nanorods by creating oxygen vaca
155 mple and efficient assembly of permanganate, cobalt(II) acetate, and pyridine to form the cubane oxo
156 -((iPr)PNP)Co(H)2BPin (1) and the air-stable cobalt(II) bis(pivalate) 4-Me-((iPr)PNP)Co(O2C(t)Bu)2 (2
157 enerates coordinatively unsaturated low-spin cobalt(II) centers that exhibit a strong preference for
158 es from DNA damage and cell death induced by cobalt(II) chloride hexahydrate (CoCl2.6H2O) and the ant
159                                          The cobalt(II) complex of D2-symmetric chiral porphyrin [Co(
160 rain engineering of the outermost surface of cobalt(II) oxide nanorods can turn them into efficient e
161 structure properties and the activity of the cobalt(II) oxide surface, which results in the creation
162                 The compounds of choice were cobalt(II) porphyrin and cobalt(III) corrole-both charac
163              Thus, carbon nanotubes with the cobalt(II) porphyrin/cobalt(III) corrole system are prom
164 verify a clocklike transition for the hosted cobalt(II) spins in the framework [(TCPP)Co0.07Zn0.93]3[
165  and electrochemical techniques on monomeric cobalt(II) tetra(meso-4-pyridyl)porphyrinate (CoTPyP) an
166 y the addition of 5 mg L(-1) nickel(II), and cobalt(II), and their mixture in day(s).
167                                              Cobalt(II)-based metalloradical catalysis (MRC) has been
168                                              Cobalt(II)-based metalloradical catalysis has been succe
169 n of acylazirines combined with a subsequent cobalt(II)-catalyzed ring expansion with 1,3-diketones.
170 O2 adducts in Co-BTTri are best described as cobalt(II)-dioxygen species with partial electron transf
171 ylperoxide (DBPO) confirm the involvement of cobalt(III) carbene radical intermediates.
172 rbon nanotubes with the cobalt(II) porphyrin/cobalt(III) corrole system are promising alternatives fo
173 unds of choice were cobalt(II) porphyrin and cobalt(III) corrole-both characterized by a high stabili
174                       Both the air-sensitive cobalt(III) dihydride boryl 4-Me-((iPr)PNP)Co(H)2BPin (1
175 TEMPOH) to form a structurally characterized cobalt(III)-hydroperoxo complex, Co(III)(BDPP)(OOH) (4)
176  Co(III)-O(*) species and stabilization of a cobalt(III)-oxyl/propane transition state as the Lewis a
177 are most consistent with its assignment as a cobalt(III)-peroxo complex.
178 the stronger binding sites in Co-BDTriP form cobalt(III)-superoxo moieties.
179                       Our findings show that cobalt(III)-superoxo species are capable of performing h
180  question, we considered the substitution of cobalt in AdoCbl with rhodium to generate the rhodium an
181  the copper oxide superconductors containing cobalt in place of copper.
182 gistic interplay between tungsten, iron, and cobalt in producing a favorable local coordination envir
183 no evidence of redox cycling of manganese or cobalt in the enzymatic reactions and suggest that struc
184 osure can be confirmed by the measurement of cobalt in the serum, but serum levels of the ion are not
185  muPADs for instrument-free determination of cobalt in waters using distance-based readout, with exce
186 e volume variation from 10 to 110 cm(3)/g by cobalt insertion in the MoS2 crystallographic lattice, w
187 thesized as a stable salt and transferred to cobalt introduces potential new routes to magnetic mater
188 i BL21-Gold (DE3) and purified the enzyme by cobalt ion affinity chromatography.
189  a dissipative quantum-mechanical model of a cobalt ion coupled to a breathing mode.
190 ore, in our case Calcein Blue, quenched by a cobalt ion is add to the first one (4-MUP), and, in pres
191 theoretically demonstrated that the divalent cobalt ion reaches 90% of the [Formula: see text] value
192 icant intramolecular interaction between the cobalt ions across the 1,1'-bis(boratabenzene) unit.
193 aterial only comprising atomically dispersed cobalt ions and identify with X-ray absorption spectrosc
194 locations of the promoter ions and catalytic cobalt ions are determined.
195  the MOF c-axis, whereas the location of the cobalt ions varies with the promoter ions.
196 ochemical detection of femtomolar amounts of cobalt, iridium, nickel, and iron ions in solution by el
197                                              Cobalt-iron Prussian blue-type thin films, formed by che
198 helatases, CbiK(P) and CbiK(C) , that insert cobalt/iron into the tetrapyrrole macrocycle but are tho
199                                     Terminal cobalt(IV)-oxo (Co(IV)-O) species have been implicated a
200 -edge structure spectra were obtained on the cobalt K edge and Re L3 edge of the working catalyst.
201 -based multilayered thin fi lms in which the cobalt layer is sandwiched between two heavy metals and
202 xistence of ultrathin superdense nonmagnetic cobalt layers in a polycrystalline cobalt thin film.
203  excitations in KCoF3 single crystals at the cobalt M2,3-edge at FERMI FEL (Elettra-Sincrotrone Tries
204 his work, we report the synthesis of ternary cobalt manganese phosphide nanoparticles from the soluti
205  Perhydroquinoline 4, the product of a Raney-cobalt mediated reductive cyclization reaction, was read
206 n implicated as key intermediates in various cobalt-mediated oxidation reactions.
207                                 We show that cobalt moieties are unmodified from 0.0 to 1.0 V versus
208                  Here, the authors show that cobalt moieties have a higher redox potential, bind oxyg
209 -plane direction by less than 10 degrees per cobalt monolayer.
210 gate the internal distribution of engineered cobalt nanoparticles (Co NPs) in exposed individuals of
211 ive core-shell formation process in platinum-cobalt nanoparticles at elevated temperature under oxyge
212 onitoring of the electrodeposition of single cobalt nanoparticles down to a radius of 65 nm.
213 ped carbon by using chloride, while metallic cobalt nanoparticles encased in protective graphite laye
214 etric nanoporous carbons containing magnetic cobalt nanoparticles.
215      Among the as-synthesized materials, the cobalt/nanoporous N-doped carbon composites have demonst
216  the growth of hierarchical supercrystals of cobalt nanorods have been studied by in situ tandem X-ra
217 The specific/mass activities of the platinum-cobalt nanowires for oxygen reduction reaction are 39.6/
218 ategy for synthesizing hierarchical platinum-cobalt nanowires with high-index, platinum-rich facets a
219 se of earth-abundant metals, including iron, cobalt, nickel and manganese, and represents a generic p
220 libration curves at the femtomolar level for cobalt, nickel, and lead ions on carbon ultramicroelectr
221 hese results, the limits of quantitation for cobalt, nickel, and lead ions were reported at 10 s of f
222 g trace metals, including arsenic, chromium, cobalt, nickel, and lead, likely due to the microbial pr
223 on of diverse transition metals (e.g., iron, cobalt, nickel, copper, and nickel-cobalt alloy), accomp
224                  It is found that the active cobalt-nitrogen sites tend to be selectively constructed
225 been obtained on the catalyst dominated with cobalt-nitrogen sites, confirmed by the advanced spectro
226 ectronic ground state of the pentacoordinate cobalt nitrosyl complexes, [CoX2 (NO)(PMePh2 )2 ] (X=Cl,
227                     No correlations of total cobalt nor Cbl with fetal weight or weeks of gestation w
228                   Nanorod formation involves cobalt nucleation, a fast atom-by-atom anisotropic growt
229 egrees C) and pressures (1-6 bar) using a 5% cobalt on TiO2 catalyst and under UV irradiation.
230 itation had been alleviated, the addition of cobalt or cobalt-containing vitamin B12 could further en
231  at concentrations only slightly higher, and cobalt or Zn(II) shock triggers mal-responses that match
232 tinum (Pt) catalysts (where M can be nickel, cobalt, or iron).
233 y chain (HC) transfer), HA-oligosaccharides, cobalt, or Si bikunin prevented TSG-6 activity, preventi
234                The choice of metal catalyst (cobalt- or osmium-based) allowed for the formation of TH
235              Cyclic voltammetry of phosphate cobalt oxide (CoPi) films catalyzing O2-evolution from w
236 study the active surfaces of layered lithium cobalt oxide (LCO) for the oxygen evolution reaction (OE
237  is coupled with a water oxidation phosphate cobalt oxide anode in a home-made electrolyzer by means
238 er with good cyclability of a 4-volt lithium cobalt oxide cathode and operation as low as -60 degrees
239                              Low-dimensional cobalt oxide codoped manganese oxide nanoparticles (CMO
240 anges with the transition between cobalt and cobalt oxide controlled by a voltage applied to the top
241 mical properties for a manganese center in a cobalt oxide environment, and provides a molecular model
242 el the oxygen evolution reaction activity of cobalt oxide nanoislands and show that the nanoparticle
243 on at under coordinated cobalt edge sites of cobalt oxide nanoislands.
244 cathode layers based on graphite and lithium cobalt oxide, respectively, on thin flexible current col
245  segregation of a thin platinum, rather than cobalt oxide, surface layer occurs concurrently with ord
246                                     Few-atom cobalt-oxide clusters, when dispersed on a Zr-based meta
247  and provides a molecular model for Mn-doped cobalt oxides.
248  a representative structural model of oxidic cobalt oxygen-evolving catalysts (Co-OECs).
249 brid catalyst consisting of sulfur-deficient cobalt oxysulfide single crystals and nitrogen-doped gra
250  both oxygen-vacancy-rich, nonstoichiometric cobalt oxysulfides and edge-nitrogen-rich graphene nanom
251 s including skyrmions in an exchange-coupled cobalt/palladium multilayer at room temperature with Lor
252  active, and reusable cobalt-bipyridine- and cobalt-phenanthroline-based metal-organic framework (MOF
253 these two processes, as demonstrated for the cobalt phosphate (CoPi) water-splitting catalyst.
254  atoms around the vacancies in the resulting cobalt phosphoselenide favorably change the electronic s
255 es a novel ternary electrocatalyst of porous cobalt phosphoselenide nanosheets prepared by a combined
256 catalyst material based on pyrite-structured cobalt phosphosulfide nanoparticles grown on carbon nano
257    Nanocomposite molecular material based on cobalt phthalocyanine (CoPc) and multiwalled carbon nano
258                            On the nanoscale, cobalt phthalocyanine (CoPc) molecules are uniformly anc
259 fying a screen-printed carbon electrode with cobalt phthalocyanine, graphene and an ionic liquid (CoP
260                             Here we report a cobalt-phthalocyanine-based high-performance carbon diox
261                             Readily accessed cobalt pre-catalysts with N-heterocyclic carbene ligands
262 riles to primary amines using a bench-stable cobalt precatalyst under 4 atm of H2 is reported herein.
263 nd induction of heme oxygenase-1 (HO-1) with cobalt protoporphyrin (CoPP) markedly attenuated the dev
264                             The HO-1 inducer cobalt protoporphyrin IX diminished proinflammatory cyto
265                             The HO-1 inducer cobalt protoporphyrin IX more efficiently attenuated PGE
266 ection, HO-1 induction with metalloporphyrin cobalt protoporphyrin IX significantly reduces the loss
267 eudomallei Pharmacological administration of cobalt protoporphyrin IX to mice resulted in an enhanced
268                          Concomitantly, upon cobalt protoporphyrin IX treatment, there is a significa
269 pharmacologic induction of HMOX-1 in vivo by cobalt protoporphyrin-IX treatment eradicated intestinal
270 admium (Ptrend = 0.35), 1.21 (0.85-1.72) for cobalt (Ptrend = 0.59), 1.31 (0.90-1.91) for cesium (Ptr
271                                              CoBalT recruited patients aged 18-75 years who had adher
272 attachment process that continues well after cobalt reduction is complete.
273 ial exposure have been implemented, subacute cobalt-related cardiomyopathy had become rare.
274                                The course of cobalt-related cardiomyopathy may be progressive and fat
275 ecially, exhibit complex behavior because of cobalt's ability to adopt various valence and spin state
276 ng the illness and exhibit other evidence of cobalt's effects on the body (eg, polycythemia and goite
277 ic biosensor based on an ionic liquid tagged cobalt-salophen metal complex (Co-salophen-IL) immobiliz
278      The process uses commercially available cobalt salts and chiral ligands.
279         The mean lateral size of c-BN NDs on cobalt scales from 175 nm to 77 nm with the growth time.
280 favorably change the electronic structure of cobalt selenide, assuring a rapid charge transfer and op
281 ymium, neodymium, promethium, and samarium), cobalt, silver, tungsten, heavy rare earth elements (ytt
282 oordinates water and more open access to the cobalt site has higher electrocatalytic activity than CT
283           The obtained catalysts demonstrate cobalt-sites-dependent activity for oxygen reduction rea
284                              However, why is cobalt so fit for its role in B12 -dependent enzymes?
285 minary mechanistic studies indicate that the cobalt species is reduced to Co(0) during the reaction.
286 ve graphite layers are the dominant forms of cobalt species with nitrate ions.
287 lysis showed that the amount of redox-active cobalt-species in the film is small, less than 10% of to
288 igible participants were randomised into the CoBalT study.
289                                     The bare cobalt surface allows for low loss propagation of surfac
290 eport a catalyst derived from earth-abundant cobalt that enables preparation of cyclobutanones, with
291 nmagnetic cobalt layers in a polycrystalline cobalt thin film.
292  spin-dependent reflectivity measurements on cobalt thin films intercalated at the graphene/Ir(111) i
293              In a long-term follow-up of the CoBalT trial, we examined the clinical and cost-effectiv
294  mitogenic factor deoxyribonucleases, nickel/cobalt uptake and cobalamin biosynthesis.
295                                              CoBalT was a randomised controlled trial done across 73
296 nthetically useful selectivity observed with cobalt was applied to an efficient synthesis of the anti
297                             Tungsten carbide cobalt (WC-Co) matrix nanocomposites reinforced with var
298 ls (platinum, palladium, copper, nickel, and cobalt) were synthesized with average particle sizes fro
299 predicts a dense face-centred-cubic phase of cobalt, which would be nonmagnetic.
300                  The switch is composed of a cobalt wire placed under a GdOx layer and a Au top elect
301 ese substrate and similar divalents iron and cobalt, with several small amino acid replacements still

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