ライフサイエンスコーパス: palladium

1 t concentrate catalytically active levels of palladium.

2 th 2:1 and 1:1 stoichiometry with respect to palladium.

3 al catalysts including those of rhodium(II), palladium(0 and II), silver(I), mercury(II), copper(I an

4 , including promotion of direct oxidation of palladium(0) by O2, bypassing the typical requirement fo

5 s, derived from allylic ester carbonates and palladium(0) catalyst, were found to undergo the Friedel

6 ession of iris melanoma after treatment with palladium-103 ((103)Pd) plaque brachytherapy.

7 Iodine-125 and palladium-103 are each reasonable isotope options for pa

8 Palladium-103 plaque brachytherapy.

9 a highly efficient incorporation procedure, palladium-103, a brachytherapy radioisotope in clinical

10 Although levels of palladium accumulation in field-suitable species are bel

11 aminone precursors in the presence of either palladium acetate/cupric acetate catalytic system under

12 catalytic system under oxygen atmosphere or palladium acetate/silver carbonate in the presence of pi

13 ricidal activity was again platinum gold and palladium against all three bacteria.

14 lphosphino-2',6'-diisopropoxybiphenyl) based palladium amido complexes.

15 we report a 2-pyridone ligand that binds to palladium and accelerates non-directed C-H functionaliza

16 Overall, platinum, palladium and gold metal ion solutions in individual use

17 y inhomogeneous surfaces comprising of gold, palladium and nickel were generated on copper substrates

18 ations using ZoI assays, gold/platinum, gold/palladium and platinum/palladium were indicative of syne

19 tion catalyst that combines highly dispersed palladium and ultrafine molybdenum phosphate nanoparticl

20 ymethyl cellulose (CMC) coating, addition of palladium, and other iron species as metal surfaces on t

21 of rotation of three different (i.e., zinc, palladium, and platinum) metal dichloride complexes.

22 asily converted into polycyclic compounds by palladium- and gold-catalyzed reactions.

23 compared to halides, enabling chemoselective palladium- and nickel-catalyzed coupling sequences.

24 Platinum and palladium are frequently used as catalytic materials, fo

25 ture-grown Arabidopsis can take up and store palladium as nanoparticles.

26 regioselective alpha- and gamma-arylation of palladium azapentadienyl intermediates is presented.

27 single synthetic protocol to obtain uniform palladium-based bimetallic nanocrystals (PdM, M = V, Mn,

28 nced platinum alloys, core-shell structures, palladium-based catalysts, metal oxides and chalcogenide

29 isplays many advantages over the widely used palladium-based systems.

30 at by incorporating trace amounts of gold in palladium-based ternary (Pd6CoCu) nanocatalysts, the dur

31 r and stable aromatic backbone with multiple palladium binding sites to engineer the controlled synth

32 Devices fabricated with the palladium-binding deltarhodopsin enable light-activated

33 Through serendipitous discovery, a palladium bis(phosphine) complex was identified as a cat

34 ent, Cp*2Yb, with bipyrimidine (bipym) and a palladium bis-alkyl fragment, PdMe2, allows the rapid fo

35 ucleophilic addition of the generated carbon-palladium bond to a tethered cyano/aldehyde group.

36 A palladium-boronate/borane-system -catalyzed isomerizatio

37 ly in the latter case, where coordination of palladium by the pyridine is hindered, 3'-halogenation d

38 Here we show that palladium-capped hafnium thin films show a highly reprod

39 The products result from insertion of a palladium-carbene ligand into the N-H bond of the aromat

40 via an intermediate, possibly a zwitterionic palladium carbenoid species.

41 A de novo palladium carbon-catalyzed synthesis of trisubstituted n

42 rends between the charge distribution at the palladium-carbon interface and the metal's selectivity f

43 at conformation of the substrates to achieve palladium-catalysed amine-directed conversion of C-H bon

44 Here we report a straightforward method for palladium-catalysed arylation of aryl(heteroaryl)methane

45 Palladium-catalysed non-directed C-H activation could po

46 Here, we report an efficient Palladium-catalysed protocol for reactions of beta-subst

47 Although palladium catalysis has historically dominated the field

48 When an allenic sulfone is treated under palladium catalysis in the presence of a weak acid, isom

49 n and alkenyl nucleophiles that couple under palladium catalysis leading to sp-, sp(2) -, and sp(3) -

50 eact with alpha-aryl-alpha-diazoesters under palladium catalysis to form alpha-(N-indolyl)-alpha-aryl

51 acted with aromatic and vinyl halides, under palladium catalysis, to produce 4-substituted homopropar

52 sly, these were not readily accessible using palladium catalysis.

53 ss has been achieved in specific cases using palladium catalysis.

54 iolates is reported through the use of allyl-palladium catalysis.

55 amma positions proceeds in the presence of a palladium catalyst and a catalytic amount of amino acid.

56 d by C-C bond formation when the appropriate palladium catalyst and alpha-fluoro enolate precursor we

57 In addition, the same palladium catalyst can be employed in an initial Sonogas

58 kinetic analysis of CO2 hydrogenation over a palladium catalyst in order to address the factors gover

59 ed using a chiral pyridine oxazoline-ligated palladium catalyst under mild conditions.

60 n with aromatic halides in the presence of a palladium catalyst with exceptionally high levels of ste

61 ine complex represents a new class of chiral palladium catalyst.

62 Currently used palladium catalysts are reactive only with electron-rich

63 We show that the addition of tin to palladium catalysts coupled with an appropriate heat tre

64 onal effects of several transition metals on palladium catalysts for methane oxidation.

65 Palladium catalysts generally undergo substitution by a

66 Palladium catalysts have been widely adopted for organic

67 cial charge distribution in carbon-supported palladium catalysts with consequential changes in hydrog

68 nd allylic carbonates, engaging vanadium and palladium catalysts, is an exemplary case of a cooperati

69 e design and application of cancer-targeting palladium catalysts, with their specific uptake in brain

70 any important synthetic methods that utilize palladium catalysts.

71 ociated with the lack of sufficiently active palladium catalysts.

72 Synergistic gold-palladium catalytic processes have been intensively soug

73 f dibromoaromatic scaffolds using air-stable palladium catalytic systems was carried out.

74 lene acceptor groups can be synthesized by a palladium catalyzed copolymerization between 9,10-dibrom

75 hydrocarbon embedded ladder polymers using a palladium catalyzed cyclopentannulation polymerization f

76 acid acceptor were synthesized by utilizing palladium catalyzed direct (hetero)arylation reaction.

77 h a vinyl cyclohexenone and a regioselective palladium catalyzed hydrogenation.

78 The telescoping of allyl-palladium catalyzed ketone dehydrogenation with organocu

79 Although palladium catalyzed oxidative homocoupling of aryl boron

80 We describe a modular, palladium catalyzed synthesis of aryl(hetero)aryl benzop

81 C-gamma(sp(3))-H bonds have been oxidized by palladium-catalyzed acetoxylation reaction.

82 o generate the dihydrobenzodioxolone core by palladium-catalyzed aerobic dehydrogenation.

83 erent ligands that have been used to support palladium-catalyzed aerobic oxidation reactions and, whe

84 Palladium-catalyzed aerobic oxidation reactions have bee

85 of substituted gamma- and delta-lactams via palladium-catalyzed alkene carboamination reactions betw

86 his study describes the first para-selective palladium-catalyzed alkenylation of tertiary amines.

87 Herein we report a palladium-catalyzed alkoxycarbonylation of secondary alk

88 xploited, regioselective, and stereospecific palladium-catalyzed allyl-aryl coupling reaction.

89 isubstituted allylic N-arylamines based on a palladium-catalyzed allylic amination has been developed

90 y from 2-halobenzoates and ketones through a palladium-catalyzed alpha-arylation step followed by an

91 e tricyclic tetrahydrocarbazolone core via a palladium-catalyzed amination and oxidative indole forma

92 A three-component palladium-catalyzed aminocarbonylation of aryl and heter

93 orward synthesis of 2-amidoglycals through a palladium-catalyzed aminocarbonylation reaction between

94 Palladium-catalyzed aminocarbonylation reactions have be

95 inhibitors by a chemo- and diastereospecific palladium-catalyzed arylation reaction.

96 nt intramolecular C-N bond formation through palladium-catalyzed aza-Michael reaction.

97 noline-based ligand effectively promotes the palladium-catalyzed borylation of C(sp(3))-H bonds.

98 A continuous-flow synthesis of aziridines by palladium-catalyzed C(sp(3) )-H activation is described.

99 Key steps were a palladium-catalyzed C(sp3)X-C(sp3)ZnX Negishi cross-coup

100 Synthesis was achieved through efficient palladium-catalyzed C-H activated annulation between abu

101 compounds were synthesized through a rapid, palladium-catalyzed C-H activation route.

102 itroquinoxaline, are shown to undergo facile palladium-catalyzed C-H direct arylation with a variety

103 Many site-selective palladium-catalyzed C-H functionalization methods requir

104 nistic insight, a new ligand (EPhos) for the palladium-catalyzed C-N cross-coupling between primary a

105 opment of a general catalytic system for the palladium-catalyzed carbocyclization of unactivated alky

106 Palladium-catalyzed carboetherification-Heck reactions t

107 In particular, palladium-catalyzed carbonylation reactions have found b

108 nones is described applying a four-component palladium-catalyzed carbonylative coupling of aryl boron

109 aroylquinolin-4(1H)-ones, prepared through a palladium-catalyzed carbonylative cyclization of N-(2-io

110 A palladium-catalyzed cascade carbonylative spirolactoniza

111 Palladium-catalyzed conjunctive cross-coupling is used f

112 The development of a decarboxylative palladium-catalyzed coupling of 1,3-dicarbonyl compounds

113 y rhodium-catalyzed alkyne hydroboration and palladium-catalyzed coupling reactions of E-1,2-dichloro

114 A series of palladium-catalyzed cross-coupling and other reactions w

115 me, we report the use of bromo-carboranes in palladium-catalyzed cross-coupling for efficient B-N, B-

116 Pd at the crossroads: The palladium-catalyzed cross-coupling of nitroarenes has el

117 and validated for effective room-temperature palladium-catalyzed cross-coupling reactions (CCRs) of a

118 uted indene derivatives through conventional palladium-catalyzed cross-coupling reactions and iodine-

119 promise as reaction media for thermomorphic palladium-catalyzed cross-coupling reactions is demonstr

120 o-functionalized IF-TTF building block using palladium-catalyzed cross-coupling reactions, such as th

121 direct use of organolithium reagents in the palladium-catalyzed cross-coupling reactions.

122 Subsequent palladium-catalyzed cross-coupling with haloarenes furni

123 Palladium-catalyzed cyanation of an elaborated and isome

124 Conditions have been developed for the palladium-catalyzed cyanation of aryl bromides utilizing

125 ion of unsaturated secondary lactams via the palladium-catalyzed cyclization of O-phenyl hydroxamates

126 es has been achieved in 39-94% yield through palladium-catalyzed cyclocondensation of aryl/vinyl iodi

127 s of alpha-chloro ketones and pyrazoles, and palladium-catalyzed cyclopropanation reactions on labora

128 Palladium-catalyzed decarbonylative Heck reaction of ami

129 ihydroxylation step followed by a late-stage palladium-catalyzed decarboxylation-allylation procedure

130 amide enolates and of a (2) enantioselective palladium-catalyzed decarboxylative allylic alkylation r

131 origin of an enantiodivergent effect in the palladium-catalyzed decarboxylative asymmetric protonati

132 sted Liebeskind-Srogl C-C cross-coupling and palladium-catalyzed decarboxylative coupling reactions.

133 Breaking the mirror (plane): A palladium-catalyzed desymmetrization strategy via beta C

134 d at 6,7,13,14-positions are synthesized via palladium-catalyzed dialkylacetylene insertion/C-H aryla

135 An "on water" palladium-catalyzed direct (hetero)arylation of 2H-pyraz

136 nstruction of a C(aryl)-C(sp(3)) bond by the palladium-catalyzed direct allylation of arenes with all

137 Palladium-catalyzed direct arylation of 4-(2-bromophenyl

138 Herein, we report the palladium-catalyzed direct arylation of unactivated alip

139 The palladium-catalyzed directed C-H halogenation of bipyrid

140 he synthesis of alpha-ketoamide compounds by palladium-catalyzed double-carbonylative amination react

141 A method for the palladium-catalyzed fluorination of cyclic vinyl triflat

142 A palladium-catalyzed fluorosulfonylvinylation reaction of

143 Distinct from widely used palladium-catalyzed formylation processes, this reaction

144 have been prepared with each subjected to a palladium-catalyzed intramolecular Alder-ene (IMAE) reac

145 rther converted into phenanthrothiazoles via palladium-catalyzed intramolecular direct arylation.

146 a chiral BINOL derivative was followed by a palladium-catalyzed Mizoroki-Heck cyclization, resulting

147 A palladium-catalyzed monoselective C3 arylation of 2-oxin

148 A palladium-catalyzed multicomponent route to polycyclic p

149 A palladium-catalyzed one-pot stepwise coupling-annulation

150 Palladium-catalyzed ortho-arylation of anilides was achi

151 The palladium-catalyzed ortho-arylation of diethyl carbamate

152 cess of iridium-catalyzed C-H borylation and palladium-catalyzed ortho-C-H arylation directed to acce

153 We report an efficient palladium-catalyzed ortho-C-H arylation of acetophenone

154 Palladium-catalyzed oxidation can single out the seconda

155 of overall four C-C bonds and proceeds via a palladium-catalyzed oxidative transformation with insert

156 uoro-3-methylphenol in six steps featuring a palladium-catalyzed phenyl carboxylation in the last ste

157 This palladium-catalyzed process allows for the conversion of

158 This palladium-catalyzed process provides direct access to al

159 In addition, an efficient and versatile palladium-catalyzed reductive azo cleavage is disclosed

160 Palladium-catalyzed stereoselective beta-arylations of p

161 A soluble copolymer is obtained by a palladium-catalyzed Stille polymerization and demonstrat

162 sing arenophile cycloaddition and subsequent palladium-catalyzed substitution with nonstabilized lith

163 Recently, the first palladium-catalyzed Suzuki-Miyaura and Buchwald-Hartwig

164 INOL derivatives is accomplished through the palladium-catalyzed Suzuki-Miyaura coupling of the unpro

165 zation and tosylate formation, followed by a palladium-catalyzed Suzuki-Miyaura cross-coupling of the

166 A palladium-catalyzed tandem oxidative annulation of prima

167 A palladium-catalyzed thiocarbonylation of styrene derivat

168 The site-selective palladium-catalyzed three-component coupling of deactiva

169 Compounds such as 20 were prepared using a palladium-catalyzed Ullmann cross-coupling reaction betw

170 ituted cyclohexenone 12, generated through a palladium-catalyzed Ullmann cross-coupling reaction betw

171 ich is readily prepared through an efficient palladium-catalyzed Ullmann cross-coupling reaction, is

172 A palladium-catalyzed, ortho-selective C-H halogenation me

173 We have developed a method for palladium-catalyzed, pyrazole-directed sp(3) C-H bond ar

174 ne and vinyltrialkoxysilanes to the cationic palladium center have been determined.

175 ssembled by addition of a slight excess of a palladium chelator, and the interaction can be reversibl

176 n of nitrogen tethered alkenols catalyzed by palladium chloride leads to substituted morpholines in g

177 nd that the ground state structures of small palladium clusters are more sensitive to the charge stat

178 The photoelectron spectra (PES) of palladium clusters are simulated based on the time-depen

179 NHC-, P,S-, and O,P-catalysts, and rhodium, palladium, cobalt, and iron catalysts.

180 nnels of the ultrapure two-dimensional metal palladium cobaltate (PdCoO2) has a large viscous contrib

181 ,4-ethylenedioxythiophene (EDOT-BPI) and its palladium complex (EDOT-PdBPI) were synthesized and char

182 spensable to the enzyme immobilization, with palladium complex bearing monomer, which is mediate the

183 The palladium complex was reused up to four cycles in an ope

184 alpha-fluoro carbonyl compounds catalyzed by palladium complexes have been reported, but palladium fl

185 Two of the intermediate palladium complexes in the catalytic cycle have been pre

186 ates with alpha-fluoroindanones catalyzed by palladium complexes of a BINOL-derived monophosphine and

187 rphyrin and carbachlorin, and the nickel and palladium complexes, were characterized by X-ray crystal

188 reaction promotes the formation of dinuclear palladium complexes, wherein only a single metal center

189 utations of noble and base metals (platinum, palladium, copper, nickel, and cobalt) were synthesized

190 y oxidized to the corresponding aldehydes by palladium/copper/nitrite catalysis.

191 (II)Cl2(o-dppp)2] (o-dppp = o-(Ph2P)C6H4), a palladium dichloride complex featuring a Lewis acidic tr

192 suggest that acetophenone is formed from the palladium enolate intermediate by protonation from H2O2.

193 mpetitive processes, one of which involves a palladium enolate intermediate that has not been previou

194 l hydroperoxide and found that, although the palladium enolate intermediate was observed, it was not

195 palladium complexes have been reported, but palladium fluoroenolate intermediates relevant to such r

196 dicates that the use of plants to accumulate palladium for industrial applications has the potential

197 hese species were able to grow, and take up, palladium from both synthetic and mine-sourced tailings.

198 ic assays against biofilms demonstrated gold/palladium, gold/platinumand platinum/palladium resulted

199 elective label free colorimetric assay using palladium-gold nanorod as nanozyme is reported for malat

200 tudy demonstrated the catalytic potential of palladium-gold nanorods, which can be employed as nanozy

201 Palladium-gold nanozyme shows excellent peroxidase mimet

202 The palladium hydride was also found to be directly involved

203 A reaction mechanism involving a palladium hydride, generated from insertion of palladium

204 Pyreniporphyrin reacted with palladium(II) acetate to give excellent yields of a pall

205 both the Cl(-) and H(+) and is catalyzed by palladium(II) acetate, with loadings as low as 25 ppm.

206 Palladium(II) carboxylate salts have been shown to catal

207 he complex coordination chemistry of DAF and palladium(II) carboxylate salts.

208 um(II) acetate to give excellent yields of a palladium(II) complex that showed weakly diatropic prope

209 s the C-bound isomer of the ligand-supported palladium(II) complexes and leads to significantly impro

210 Here we show that water-soluble palladium(II) complexes are excellent reagents for the e

211 Ni(OAc)2 or Pd(OAc)2 afforded nickel(II) and palladium(II) complexes.

212 us hydrogen peroxide (H2O2) and the cationic palladium(II) compound, [(PBO)Pd(NCMe)2][OTf]2 (PBO = 2-

213 then encapsulating bis[tri(2-furyl)phosphine]palladium(II) dichloride in a biocompatible poly(lactic-

214 scopic studies and isotope effects support a palladium(II) hydride-mediated pathway and reveal crucia

215 Palladium(II) in combination with a monodentate phosphin

216 and on the exohedral faces of the peripheral palladium(II) ions.

217 ll-defined metal polypyridyl complexes and a palladium(II) salt to form electrochemically addressable

218 of a substituted pyrazole ring catalyzed by palladium(II) was straightforward and convenient for ary

219 er(III), silver(III), gold(III), nickel(II), palladium(II), platinum(II), rhodium(III), iridium(III),

220 nce of a preformed biarylphosphine-supported palladium(II)-aryl complex and a weak base, lysine amino

221 A palladium(II)-catalyzed 1,2-dicarbofunctionalization rea

222 methyl)arylmethylamines that consists of the palladium(II)-catalyzed addition of arylboroxines to imi

223 f isochroman motifs has been accomplished by palladium(II)-catalyzed allylic C-H oxidation from termi

224 A new enantioselective palladium(II)-catalyzed benzylic C-H arylation reaction

225 The palladium(II)-catalyzed beta- and gamma-alkynylation of

226 The first example of palladium(II)-catalyzed beta-C(sp(3))-H iodination of a

227 We herein report the palladium(II)-catalyzed bromination and iodination of a

228 The palladium(II)-catalyzed C(sp(3) )-H alkynylation of olig

229 d anilines also overcomes the limitations of palladium(II)-catalyzed C-H amination reactions.

230 Palladium(II)-catalyzed C-H carbonylation reactions of m

231 ays where electron-rich substrates undergo a palladium(II)-catalyzed decarboxylation and electron-def

232 the first example of kinetic resolution by a palladium(II)-catalyzed enantioselective C-H activation

233 Palladium(II)-catalyzed meta-C-H arylation and alkylatio

234 Palladium(II)-catalyzed oxidation reactions exhibit broa

235 strained cyclic dienes were accomplished via palladium(II)-catalyzed oxidative cyclizations of termin

236 trocyclization pathway was demonstrated by a palladium(II)-catalyzed oxidative homocoupling/8pi-elect

237 ienyne complexes were readily synthesized by palladium(II)-catalyzed oxidative macrocyclizations of b

238 lic C-H amination reaction is reported under palladium(II)/bis-sulfoxide/Bronsted base catalysis.

239 We demonstrate that the minimum level of palladium in Arabidopsis dried tissues for catalytic act

240 The current approach expands the use of palladium in protein chemistry and should significantly

241 transfer of the organic moiety from boron to palladium in the key transmetalation step.

242 onates and organolithium reagents, engage in palladium-induced metallate rearrangement wherein 1,2-mi

243 hyl quinoline ligands that enable asymmetric palladium insertion into prochiral C-H bonds on a single

244 ble desymmetrization of isopropyl groups via palladium insertion into the C(sp(3))-H bonds of one of

245 ligand, the reaction proceeds via an alkoxy palladium intermediate that increases the proton acidity

246 the chain ends, small molecule ligands, and palladium ions; polyMOCs are formed via metal-ligand coo

247 Moreover, palladium is also able to rapidly remove propargyloxycar

248 Here we show that nanoencapsulated palladium is an effective means to target and treat dise

249 So far, palladium is considered to be the most effective hydroge

250 The use of pyridine ligands has allowed the palladium loading to be reduced to 2.5 mol %.

251 DIME has enabled mild reaction conditions at palladium loads as low as 500 ppm.

252 dition, through experiments on gram scale in palladium, mechanistically important additional Pd- and

253 original methods including electrophilic or palladium-mediated cyclization of unsaturated hydroxylam

254 We describe palladium-mediated S-arylation that exploits natural met

255 the pathway was concluded to be initiated by palladium metal catalyzed partial hydrogenation of the p

256 nic replacement reaction was carried out for palladium modification on template electrodeposited copp

257 Here, the authors report a palladium-molybdenum mixed catalyst for the selective hy

258 ding skyrmions in an exchange-coupled cobalt/palladium multilayer at room temperature with Lorentz tr

259 cavitation process that can transform solid palladium nanocrystals into hollow palladium nanocrystal

260 orm solid palladium nanocrystals into hollow palladium nanocrystals through insertion and extraction

261 during the hydriding phase transformation of palladium nanocrystals.

262 Pd-Au bimetallic nanoparticles starting from palladium nanocube seeds.

263 tion-the hydrogenation of single-crystalline palladium nanocubes from 15 to 80 nm-to better understan

264 rings in the para-position were prepared by palladium nanoparticle-catalyzed Suzuki-Miyaura cross-co

265 Palladium nanoparticles (Pd-NPs) were created by screeni

266 led synthesis and stabilization of ultrafine palladium nanoparticles (PdNPs).

267 N-acetylcysteine- and l-cysteine-stabilized palladium nanoparticles are introduced, and carbon polar

268 was 160 nm, demonstrating that non-spherical palladium nanoparticles coupled with 2D MXene yield a br

269 n one-step hybridization of silver, gold and palladium nanoparticles from solution onto exfoliated tw

270 tion was investigated indicating that 1-5 nm palladium nanoparticles may serve as the active catalyst

271 We used colloidal gold-palladium nanoparticles, rather than the same nanopartic

272 The resulting thin palladium nanoshells exhibit enhanced catalytic activity

273 vity comparable to commercially available 3% palladium-on-carbon catalysts was achieved from dried pl

274 that required for commercially available 3% palladium-on-carbon catalysts, this study both sets the

275 horylation of a wide range of amides using a palladium or nickel catalyst giving aryl phosphonates in

276 on of hydrogenocarbonate ions on metals like palladium or platinum, a model is developed that allows

277 or selenium) or expensive catalysts (such as palladium or rhodium).

278 In the case of palladium, our calculated SPR wavelength for the planar

279 entity of three different species containing palladium-oxygen-boron linkages, a tricoordinate boronic

280 demonstrate the NHC being coordinated to the palladium particles and affecting their electronic prope

281 Doping the NZVI surface with palladium (Pd-NZVI) increases its reactivity to pollutan

282 is selective cathode with a carbon-supported palladium (Pd/C) anode to establish a membrane-free, roo

283 ying energetic minima of neutral and charged palladium Pdn(Q) (n = 2-20, Q = 0, + 1 and -1) clusters

284 phosphorus from the compound nanocrystals of palladium phosphide and consequently the inward diffusio

285 tionalization of cyclic 1,3-dienes where the palladium plays a remarkable dual role, catalyzing both

286 more sustainable alternative to traditional palladium precatalysts for the Suzuki-Miyaura coupling r

287 ts, and, most importantly, the nature of the palladium precursor and the choice of the phosphine liga

288 s cell membranes on its own, addition of the palladium reagent induces an efficient cell internalizat

289 ed gold/palladium, gold/platinumand platinum/palladium resulted in the greatest antimicrobial efficac

290 In contrast, reduction of palladium salts in the absence of the cages form structu

291 Platinum, gold and palladium showed the greatest antimicrobial efficacy in

292 In most of these reactions, the palladium species are proposed to exist exclusively in e

293 ed investigation of the catalytically active palladium species pointed toward a dual role of the NHC

294 Metallic palladium surfaces are highly selective in promoting the

295 lladium hydride, generated from insertion of palladium to O-H of an allyl alcohol, that is responsibl

296 ronmental impacts associated with extracting palladium using present-day mining processes.

297 , gold/platinum, gold/palladium and platinum/palladium were indicative of synergy.

298 olutions (silver, copper, platinum, gold and palladium) were determined individually and in combinati

299 ption resonances the spatial distribution of palladium (with average elemental concentration of 0.4

300 ical genosensor based on Zinc oxide/platinum-palladium (ZnO/Pt-Pd) modified fluorine doped tin oxide