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1 in the electron microscope when stained with osmium.
2 ion protocols which use toxic metals such as osmium.
3 n spherules, aciniform carbon, platinum, and osmium.
4 aining precious metals such as ruthenium and osmium.
5 and impacted the global geochemical cycle of osmium.
9 zed to NAD by a thermostable redox mediator, osmium (1,10-phenanthroline-5,6-dione)2-poly(4-vinylpyri
10 he best catalyst, platinum(44)/ruthenium(41)/osmium(10)/iridium(5) (numbers in parentheses are atomic
11 ic lavas from Hawaii show enrichments in the osmium-186/osmium-188 ratio (186Os/188Os) of 0.008 to 0.
13 om Hawaii show enrichments in the osmium-186/osmium-188 ratio (186Os/188Os) of 0.008 to 0.018%, relat
16 s-linked FcepsilonRI and GM1 also accumulate osmium, a stain for unsaturated lipids, and are sites fo
18 lation technique to analyse large numbers of osmium alloy grains to quantify the distribution of depl
19 In particular, peridotites with unradiogenic osmium and ancient rhenium-depletion ages (to 1.36 x 10(
22 sm remains a probable source of unradiogenic osmium and light carbon and a causative mechanism of OAE
23 in the marine isotopic ratios of strontium, osmium and lithium suggest that extensive uplift of moun
24 anomalous scattering from the LIII edges of osmium and lutetium to obtain the necessary phasing sign
27 uence of two well-defined and iso-structural osmium and ruthenium polypyridyl complexes results in in
28 cessive deposition of redox-active layers of osmium and ruthenium polypyridyl complexes, leads to sel
30 lts place new constraints on the behavior of osmium (and possibly other platinum group elements) duri
31 tween the PFET reagent, tris(2,2'-bipyridine)osmium, and standards ((ferrocenylmethyl)trimethylammoni
33 ymium, or europium; M is iron, ruthenium, or osmium; and X is phosphorus, arsenic, or antimony) and r
34 mical proton-coupled electron transfer of an osmium aquo complex attached to a self-assembled monolay
36 in a Pt(PBu(t)3) group that is bonded to the osmium atom and a bridging alkenyl ligand that is pi-bon
40 doped graphitic support on which individual osmium atoms hop and migrate to form 3D-nanocrystals, as
41 Horseradish peroxidase cross-linked in an osmium based redox polymer hydrogel (HRP-Os) was physica
42 anodic and cathodic bioelectrocatalysts with osmium based redox polymers and home-made enzymes we cou
44 f a new nonvolatile, stable, and recoverable osmium-based reagent devised for the stoichiometric cis
45 a number of attempts to harness alternative osmium-based reagents, including microencapsulation and
46 ccase of Trametes versicolor and a series of osmium-based redox polymer mediators covering a range of
48 The choice of metal catalyst (cobalt- or osmium-based) allowed for the formation of THF rings wit
51 s derived from the divalent attachment of an osmium bis-bipyrdine complex to histidine residues withi
52 7-trithiacyclononane (Co(TTCN)2(3+/2+)), and osmium bis-dimethyl bipyridine bis-imidazole (Os(Me2bpy)
53 nd theoretical analyses of the nature of the osmium-bound, "elongated" dihydrogen ligands in [Cp*OsH(
58 rd (E)-alpha,beta-unsaturated ester 16, then osmium-catalyzed asymmetric dihydroxylation for the intr
60 y steps in the syntheses are as follows: (i) osmium-catalyzed asymmetric dihydroxylation of 4-O-prote
61 Key steps in the synthesis of 1 include the osmium-catalyzed asymmetric dihydroxylation of olefin 13
62 The key transformation was the sequential osmium-catalyzed bis-dihydroxylation reaction of substit
63 omplishing the synthesis of heterocycles via osmium-catalyzed oxidative cyclization onto an alkene is
64 ormed nitrogen sources in the intermolecular osmium-catalyzed oxyamination reaction of a variety of m
65 nearly identical to those of (mes)3Ir=O, the osmium complex (ArN)3Os=O transfers its oxygen atom 12 o
69 etal are found to be larger for the ethylene-osmium complex than for the analogous ethylene-iron comp
73 sphere chloride ligand of the polymer-bound osmium-complex: Cross-linking and electrodeposition of t
74 and (NHC)PH with the dinuclear ruthenium and osmium complexes [(eta(6)-p-cymene)MCl(2)](2) (M = Ru, O
75 tuted of polyallylamine bearing redox-active osmium complexes and glycosidic residues (lactose) is us
76 ult when inner-sphere chloride anions of the osmium complexes are exchanged by imidazole functions of
77 ven at 1 atm, whereas excited states of both osmium complexes are quenched in the presence of oxygen.
80 is thus applicable for such measurements in osmium complexes of other oxidation states, including th
87 t to platinum drugs, exposure to this organo-osmium compound does not cause significant apoptosis wit
88 To the best of our knowledge, 4 is the first osmium compound to induce ER stress in cancer cells.
89 as we revealed that at least three different osmium-containing complexes can be found depending on th
94 al tool to investigate stratified copper and osmium distribution in LbL thin films relevant to biosen
97 Time-series RNA sequencing suggested that osmium-exposed A2780 cells undergo a metabolic shunt fro
99 of the sarcoplasmic reticulum (visualized by osmium ferricyanide staining of thin tissue sections), w
100 , as demonstrated by electron micrographs of osmium ferrocyanide-stained SR in the two smooth muscles
103 core, formed through the fast dealloying of osmium from an Ir25Os75 alloy, exhibits an exceptional b
107 h's surface anthropogenic fluxes of iridium, osmium, helium, gold, ruthenium, antimony, platinum, pal
108 ine)(2+) bis-hexafluorophosphate (Ru-PZn-A); osmium(II) [5-(4'-ethynyl-(2,2';6',2' '-terpyridinyl))-1
109 idine)(2+) bis-hexafluorophosphate (Ru-PZn); osmium(II) [5-(4'-ethynyl-(2,2';6',2''-terpyridinyl))-10
112 n the A2780 ovarian carcinoma cells for four osmium(II) arene complexes [(eta(6)-arene)Os(4-methyl-pi
113 (2,2':6',2' '-terpyridine)ruthenium(II) and -osmium(II) centers connected via a geometrically constra
116 ipyridine)chloro(4,4'-trimethylenedipyridine)osmium(II) in fast-scan voltammetric measurements (scan
117 ves Dexter energy transfer from photoexcited osmium(II) photocatalysts to the diazo, thus revealing a
120 of a dilute (submillimolar) solution of the osmium(II) polypyridyl complex [Os(bpy)2dcbpy](PF6)2 (dc
121 ) [5-(4'-ethynyl-(2,2';6',2' '-terpyridinyl))osmium(II)-15-(4'-ethynyl-(2,2';6',2''-terpyridinyl))-10
122 microscopy (TEM) samples, our technique uses osmium impregnation (OTO) to make the samples conductive
124 We show that the measured accumulation of osmium in fixed tissue obeys empirically a quadratic dep
125 ng scenario and suggests that the radiogenic osmium in ocean-island basalts can better be explained b
129 y of magmatic sulphides (the main carrier of osmium) in abyssal peridotites and show that the 187Os/1
130 ite, a lithology known to carry unradiogenic osmium inherited from prior convection and melt depletio
131 ntaining five elements (platinum, ruthenium, osmium, iridium, and rhodium), 80 binary, 280 ternary, a
134 rites from the conglomerates yield a rhenium-osmium isochron age of 3.03 +/- 0.02 gigayears and an in
135 this study, we report PGE concentrations and osmium isotope ((187)Os/(188)Os) ratios of airborne part
142 We infer that the gaussian shape of the osmium isotope distribution is the signature of a random
146 produce observable excursions in the marine osmium isotope record, suggesting that previously unreco
149 ges extend to 2.5 Gyr, and we infer that the osmium isotope signature is unlikely to be derived from
150 /Si and Al/Si ratios, oxygen-isotope ratios, osmium-isotope ratios and D/H, Ar/H2O and Kr/Xe ratios s
157 ates and in the Japan arc have neodymium and osmium isotopic compositions that are consistent with ad
158 k between DT volcanism as recorded in marine osmium isotopic data and global climate change documente
161 restimated and consequently there is no true osmium isotopic gap between MORBs and abyssal peridotite
163 e measured rotational constants for the main osmium isotopomer ((192)Os) are A = 929.3256(6), B = 755
164 idging hydrogen atom interacts directly with osmium; it exchanges rapidly with the other two methyl C
167 with a catalytic amount of Lewis acid in the osmium mediated oxidative cyclization results in higher
170 tly less stable than the previously reported osmium-methane complex [eta(5)-CpOs(CO)(2)(CH(4))][Al(OC
172 (OCP) transfers a P atom to an electrophilic osmium nitride complex to form a metal-bound P=N ligand.
177 pose of this work was to develop an accurate osmium (Os) solution standard that is traceable to the I
178 s difference between the iridium-iridium and osmium-osmium exchange rates can be rationalized by an a
179 ct cholesterol and osmium-thiocarbohydrazide-osmium (OTO) to detect neutral lipids in Bruch's membran
180 phile elements (HSEs; namely, gold, iridium, osmium, palladium, platinum, rhenium, rhodium and ruthen
181 Using deep-red or near-infrared light and an osmium photocatalyst, we demonstrate an enhanced scope o
182 lectrodes (SPCEs) modified with a conductive osmium polymer (Os-PVP) complex were employed to quantif
183 The device comprises a lactate oxidase and osmium-polymer -based anode connected to a coplanar 3 x
184 irect wiring of the FDH in a highly original osmium-polymer hydrogel was found to offer a better enzy
185 , rope-like fibres; K, fibril-like clumps of osmium positivity; L, cellular debris along and within n
186 at subduction zones will retain high Re/Os (osmium) ratios and become enriched in radiogenic 187Os.
190 yranose dehydrogenase as an enzyme catalyst, osmium redox polymers [Os(4,4'-dimethoxy-2,2'-bipyridine
191 d" to graphite electrodes with two different osmium redox polymers: [Os(4,4'-dimethyl-2,2'-bipyridine
192 ectioning of large samples but is limited to osmium-resistant probes, and is technically difficult.
194 s into half-sandwich complexes of ruthenium, osmium, rhodium and iridium might lead to the developmen
195 osmium isotope compositions of more than 700 osmium-rich platinum-group element alloys derived from t
196 f SO(2) and CO(2) during the observed marine osmium shifts with diverse effects on the global climate
197 nvolved in oxidation-reduction cycles of the osmium sites, the ellipsometric enzyme film thickness, a
199 or osmium tetroxide, clears the tissue after osmium staining and that the tissue expands in osmium te
201 design criteria for a class of ruthenium and osmium sulfoxide complexes that undergo phototriggered i
203 g technology, probes are tagged with a bulky Osmium tag (Osmium tetroxide 2,2'-bipyridine), in a way
205 identified by the potassium pyroantimoniate-osmium technique and as the electron-dense vacuoles obse
207 tivity of meso-substituted porphyrins in the osmium tetraoxide reaction nor the general substituent m
209 ituents upon the reaction of porphyrins with osmium tetraoxide, and the pinacol-pinacolone rearrangem
210 lled carbon nanotubes have been reacted with osmium tetroxide (OsO(4)) in solution in the presence of
211 e transition states) of ethylene addition to osmium tetroxide (OsO(4), and amine ligated), rhenate (R
213 , probes are tagged with a bulky Osmium tag (Osmium tetroxide 2,2'-bipyridine), in a way that preserv
214 obtained from tissue biopsy samples fixed in osmium tetroxide and analyzed by Beckman Coulter Multisi
217 We present here a comparison of CCM with osmium tetroxide and with potassium permanganate, tested
219 oride insensitive and tolerates aldehyde and osmium tetroxide fixation better than common fluorescent
220 er (HPA-S, Anton Paar), sparging of volatile osmium tetroxide from the sample solution, and measureme
224 ul, we did develop a sensitive test for free osmium tetroxide leached from the reagent in situ: this
228 xylation of these didehydro derivatives with osmium tetroxide or with AD-mix alpha gave a mixture of
231 mium staining and that the tissue expands in osmium tetroxide solution, but shrinks in potassium ferr
232 talyzed oxidations, for example, acting with osmium tetroxide to catalyze the aerobic dihydroxylation
233 m ferrocyanide, a classic reducing agent for osmium tetroxide, clears the tissue after osmium stainin
234 3% glutaraldehyde, postfixed in 1% buffered osmium tetroxide, dehydrated, and embeded in araldite.
235 tructure, demonstrated by hyperreactivity to osmium tetroxide, hydroxylamine, and diethyl pyrocarbona
236 utaraldehyde alone, and those postfixed with osmium tetroxide, were imaged under ethanol according to
237 1w cells were not distinctively stained with osmium tetroxide, which interacts specifically with UFA
238 light-microscopic cross-sectional images of osmium tetroxide-stained rat nerves including various ax
244 essing, for the enhancement of contrast with osmium tetroxide/potassium ferricyanide, for BSE imaging
245 ectron microscopy (EM) or for ruthenium-, or osmium-tetroxide vapor fixation, followed by immediate e
246 ained with filipin to detect cholesterol and osmium-thiocarbohydrazide-osmium (OTO) to detect neutral
249 ey were labeled with an electrochemical tag (osmium(VI) complex), which binds only to glycans, increa
250 y, pyramidalization of the planar tris(imido)osmium(VI) fragment requires placing a pair of electrons
253 ellular response evoked by antiproliferating osmium(VI) nitrido compounds of general formula OsN(N^N)
254 e interactions and Os-specific vibrations in osmium(VI) species and is thus applicable for such measu