ライフサイエンスコーパス: palladium

1 ogen absorption capacity and HER activity of palladium.

2 g an aryl halide-containing substrate with a palladium(0) source.

3 side-chain, Boc-Arg(Nap)-OH, was prepared by palladium(0)-catalyzed coupling of Boc-Arg-OH with a 4-b

4 The palladium(0)-catalyzed intramolecular annulation of 12 1

5 We report the development of palladium(0)-catalyzed syn-selective 1,2-carboboration a

6 Herein, we present a mild and convenient palladium(0)-catalyzed synthesis of N-acylsulfonamides v

7 Palladium-103 plaque brachytherapy.

8 action (HER) is complicated by the fact that palladium absorbs hydrogen concurrently with HER.

9 ridone-assisted dissociation of the trimeric palladium acetate [Pd(3)(OAc)(6)] is found to be crucial

10 cludes a formal dehydrative step followed by palladium AcOH-induced CH(sp(3))-CH(sp(2)) oxidative cro

11 Ultrafine palladium active phases can be highly dispersed and ther

12 Judicious selection of the ligand on palladium allows selective access to either the trans is

13 nds whose elements have many isotopes (e.g., palladium alloys).

14 Mechanisms of palladium-aminooxyacetic acid and 2-pyridone-enabled coo

15 ution reaction catalyzed by a combination of palladium and a chiral phosphoric acid was investigated

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

17 athode through electrochemical deposition of palladium and chemical oxidation to carry out the sulfit

18 ylation of 1,1-disubstituted olefins by dual palladium and copper hydride catalysis as a convenient a

19 etal reagents or by transition metal (mainly palladium and copper) catalyzed alkynylations, carbon mo

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

21 The enallene is initially activated by palladium and reacts with the allenyne to give the cross

22 sition are prepared from the co-reduction of palladium and silver precursors in aqueous solution usin

23 ng reactions, particularly those mediated by palladium, are some of the most broadly used chemical tr

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

25 urface area (138.7 square metres per gram of palladium) as well as high atomic utilization, resulting

26 ds the ORR of 16.37 amperes per milligram of palladium at 0.9 volts versus the reversible hydrogen el

27 the population of weakly bound states on the palladium at high hydrogen atom coverages which are near

28 The structure contains a central palladium atom surrounded by three hydride and three mag

29 Here, the direct observation of palladium atoms from a nanoparticle passing through a de

30 trast, in the CrFeCoNiPd alloy, in which the palladium atoms have a markedly different atomic size an

31 try, electronic structure, and reactivity of palladium atoms, dimers, and trimers.

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

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

34 ed oxygen biosensor employs the quenching of palladium-benzoporphyrin by molecular oxygen to transduc

35 readily accessible starting materials using palladium binaphthyl nanoparticles (Pd-BNPs) has been de

36 combined with bulky monophospine ligands on palladium, can direct the arylation of tri- and tetrasub

37 report a new class of initiators, (pai-allyl)palladium carboxylate dimers, which polymerize ethyl dia

38 n principles proposed in this work extend to palladium-catalysed benzylic substitution, demonstrating

39 The key reaction is a palladium-catalysed polyenyne cycloisomerization that no

40 Here, we report a palladium-catalysed strategy that confers the formed pal

41 Palladium catalysis induced by visible light is an emerg

42 Treatment with an aryl iodide under palladium catalysis leads to rearomatizing gamma-selecti

43 Comparison with palladium catalysis showed that rhodium catalysis is mor

44 to be a versatile reactant when coupled with palladium catalysis.

45 sis of polysubstituted cyclopentenones using palladium catalysis.

46 monophosphine ligand, GPhos, that supports a palladium catalyst capable of promoting carbon-nitrogen

47 -) were investigated using CHMs with varying palladium catalyst densities, and mass transport of reac

48 quentially in the same flask, preventing the palladium catalyst from being inhibited by the high conc

49 n promoted by cooperative action of a copper/palladium catalyst system.

50 eaction mixture: generation of more reactive palladium catalyst versus deactivation of a substrate by

51 sily accessible and low-cost equipment and a palladium catalyst were successfully used for the synthe

52 tion in an electronically asymmetric neutral palladium catalyst.

53 ated with stoichiometric allyl acetate and a palladium catalyst.

54 o five-membered carbocycles with a different palladium catalyst.

55 that the rate of oxidative addition between palladium catalysts and alkyl/aryl electrophiles can be

56 unctionalization reactions, where the active palladium catalysts contain carboxylate ligands.

57 etathesis reactions (Nobel Prize in 2005) or palladium catalysts for C-C bond forming reactions such

58 to afford highly active and enantioselective palladium catalysts for the arylation of methylene C(sp(

59 The analogous palladium catalysts provide the means for a detailed mec

60 e reactivity was observed in the presence of palladium catalysts.

61 is study provided insightful information for palladium catalytic system design to generate heteroaryl

62 (p)) and (S(c),R(p)) Phosferrox (PPh(2)), to palladium catalyzed allylic alkylation of trans-1,3-diph

63 ferent dioxiranes, as well as chemodivergent palladium catalyzed cross-coupling reactions using boron

64 Efficient ligand-free palladium catalyzed Mizoroki-Heck reaction allowed the f

65 A photoinduced palladium-catalyzed 1,2-carbofunctionalization of conjug

66 talline lactone intermediate via a selective palladium-catalyzed 4-methylimidazole N(1)-arylation usi

67 Here, we report a palladium-catalyzed [3 + 2] reaction that utilizes twofo

68 The palladium-catalyzed [4 + 1] reaction generates a 1-aryli

69 The palladium-catalyzed addition of primary alcohols gave th

70 Likewise, a palladium-catalyzed alkyne alkoxycarbonylation reaction

71 de homologations, radical hydroindation, and palladium-catalyzed alkyne-1,2-bis-stannation.

72 n an arene and an arenophile, and subsequent palladium-catalyzed allylic substitution of the resultin

73 he long-standing challenge of conducting the palladium-catalyzed alpha-arylation of carboxylic aids a

74 ngs to a wide range of aromatic compounds by palladium-catalyzed alpha-arylation of cyclopropyl, cycl

75 Palladium-catalyzed amination reactions using soluble or

76 al-group compatibility is highlighted in the palladium-catalyzed aminocarbonylation, alkoxycarbonylat

77 A palladium-catalyzed and norbornene-mediated methodology

78 d that overcomes the limitations of previous palladium-catalyzed approaches.

79 This system is not only the first reported palladium-catalyzed arylation of NHC-bound homoenolates

80 cess these alkaloids by use of a challenging palladium-catalyzed asymmetric allylic alkylation of an

81 AMPP* ligands were studied in palladium-catalyzed asymmetric allylic alkylations, lead

82 The first palladium-catalyzed asymmetric allylic trifluoromethylat

83 yl-beta-amino acids has been developed via a palladium-catalyzed auxiliary-directed regioselective Cs

84 lhydrazones and bromophenols, proceeds via a palladium-catalyzed Barluenga-Valdes cross-coupling, fol

85 um ylides are efficient directing groups for palladium-catalyzed beta-arylation and alkylation of sp(

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

87 hypervalent iodine(III) aryl substrates in a palladium-catalyzed C-H activation/beta-arylation reacti

88 Palladium-catalyzed C-H bond arylation of imidazoles has

89 simple workflow for easier design of popular palladium-catalyzed C-H functionalization reactions, whe

90 A palladium-catalyzed C-H iodination of unactivated alkene

91 The palladium-catalyzed C-N bond formation proceeds in excel

92 We report a palladium-catalyzed C-N coupling using Et(3)N as a weak,

93 Palladium-catalyzed carbene insertion was utilized in a

94 We apply this strategy to a palladium-catalyzed carboetherification/hydrogenation se

95 The palladium-catalyzed carbonylation of 2-(propynylthio)ben

96 DA-boronate was also examined and applied in palladium-catalyzed carbonylation.

97 Development of a palladium-catalyzed carbonylative Suzuki-Miyaura couplin

98 e synthesis of functionalized isoxazoles via palladium-catalyzed cascade annulation/allylation of alk

99 nthetic strategy relied on an intramolecular palladium-catalyzed coupling reaction to complete the te

100 Subsequent palladium-catalyzed coupling reactions were utilized to

101 We report the evolution from classic palladium-catalyzed cross-coupling approaches to more mo

102 Herein, we report the palladium-catalyzed cross-coupling of aryl bromides and

103 A palladium-catalyzed cross-coupling of aryl chlorides/bro

104 f potassium acyltrifluoroborates (KATs) by a palladium-catalyzed cross-coupling of boronic acids and

105 agon encircled by 30 hexagons, by means of a palladium-catalyzed cross-coupling reaction.

106 Palladium-catalyzed cross-coupling reactions have transf

107 effective nucleophilic coupling partners in palladium-catalyzed cross-coupling reactions with (heter

108 zannulation of alkyne precursors prepared by palladium-catalyzed cross-coupling reactions.

109 through a sequence involving two consecutive palladium-catalyzed cross-coupling reactions.

110 Subsequent palladium-catalyzed cross-coupling with haloarenes furni

111 rmediate that participates in the subsequent palladium-catalyzed cross-coupling, which furnishes benz

112 The reported palladium-catalyzed cyanoboration of 1,3-enynes is site-

113 ynthesis of heteroaryl-containing cycles via palladium-catalyzed cyclization is reported.

114 xadienyl ketoesters which are subjected to a palladium-catalyzed DcA reaction, providing a variety of

115 A protocol for palladium-catalyzed dearomative functionalization of sim

116 A palladium-catalyzed dearomative syn-1,4-oxyamination pro

117 ation of the bridged diazadecalin core and a palladium-catalyzed decarboxylative allylation to instal

118 lectron-withdrawing groups in substrates for palladium-catalyzed decarboxylative allylation was explo

119 roxymethyl handle enhances the yields of the palladium-catalyzed decarboxylative cross-coupling react

120 This review focuses on the palladium-catalyzed dehydrogenative C-H/X-H (X = C, N, O

121 A palladium-catalyzed direct alpha-C(sp3) heteroarylation

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

123 A novel palladium-catalyzed Heck-type reaction of thiocarbamates

124 Thus, palladium-catalyzed homocoupling of arylboronates (Ar(F)

125 mployed as the starting substrate to undergo palladium-catalyzed intramolecular C-H/C-Br bond cross-c

126 es a dihydrobenzothienooxepine formation via palladium-catalyzed intramolecular direct C-H arylation

127 ienooxepines in good to excellent yields via palladium-catalyzed intramolecular direct C-H arylation,

128 ormed into dibenzoazaspiro compounds after a palladium-catalyzed intramolecular N-arylation.

129 t herein synthetic and DFT investigations of palladium-catalyzed ligand-controlled regiodivergent hyd

130 thylcyclohexane-1,4-dicarboxylate (+)-1, via palladium-catalyzed methoxycarbonylation of an enol trif

131 ibes the development of a remarkably general palladium-catalyzed monoacylation of carbazoles using to

132 Palladium-catalyzed N-arylations of amino acid tert-buty

133 The palladium-catalyzed O-allylation of alpha-hydroxyphospho

134 Palladium-catalyzed oxidation of isopropyl N-acetyl-alph

135 We report a challenging palladium-catalyzed oxidation of primary C-H bonds beta

136 ral limitations of previously reported allyl-palladium-catalyzed oxidation, and is further leveraged

137 The key step was a palladium-catalyzed oxidative annulation of 3-alkylindol

138 An efficient palladium-catalyzed oxidative C-C bond forming cascade r

139 Such a regiodivergent palladium-catalyzed process is unique in ynamide chemist

140 This palladium-catalyzed process provides direct access to al

141 we propose to use iron-catalyzed instead of palladium-catalyzed reaction.

142 a bidentate diamidophosphite ligand class in palladium-catalyzed reactions that allow a challenging t

143 ganozinc reagents at room temperature during palladium-catalyzed reactions.

144 A novel palladium-catalyzed ring opening carbonylative lactoniza

145 An appropriate and efficient Q-tube-assisted palladium-catalyzed strategy for the synthesis of novel,

146 Later, the palladium-catalyzed sulfonamidation of aryl nonaflate 33

147 Palladium-catalyzed sulfur dioxide insertion using the s

148 ugh indole- and benzo[b]thiophene synthesis, palladium-catalyzed Suzuki coupling, oxidative cyclizati

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

150 The palladium-catalyzed Suzuki-Miyaura borylation is the mos

151 ron complex can be effectively modified by a palladium-catalyzed Suzuki-Miyaura cross-coupling reacti

152 ed by functionalization of bromine through a palladium-catalyzed Suzuki-Miyaura cross-coupling reacti

153 acid) as an in situ CO surrogate for various palladium-catalyzed transformations is described.

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

155 The palladium-catalyzed, alpha-selective hydroarylation of a

156 The key and ultimate step is a double palladium-catalyzed, carbon monoxide mediated reductive

157 show that a modular, practical, and general palladium-catalyzed, radical three-component coupling ca

158 We report a palladium-catalyzed, three-component carbosilylation rea

159 nation of the remote protecting group to the palladium center is determinant for the control of the r

160 om an optically pure Cu complex to a gold or palladium center reveals, for the first time, a full ste

161 tion of bromobenzene to a ligand-coordinated palladium center.

162 licity by switching the valence state of the palladium centre (Pd(0) and Pd(II), respectively).

163 scope to be prepared from either an isolated palladium-CF(3) complex, or from Pd(PPh(3))(4) and other

164 A water-soluble and charge-tagged palladium complex (PdMAI) was found to function inside b

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

166 of a fluorescent semiconducting polymer and palladium complex, for quantitative longitudinal imaging

167 ne) dipalladium (Tris DBA), a small-molecule palladium complex, has been shown to inhibit cell growth

168 relies on a neighbouring cationic pai-allyl palladium complex.

169 resentative subset of monomeric, monoligated palladium complexes allowed us to draw a unique parallel

170 s illustrate that the chain-walking of alkyl-palladium complexes can be controlled through the altera

171 ng to the formation of catalytically dormant palladium complexes that reactivate only upon heating.

172 The formation of alkyl-palladium complexes via the nucleopalladation of alkenes

173 33 was developed, promoted by electron-rich palladium complexes, including the novel phosphine ligan

174 Due to the electronic bias of the pai-alkene-palladium complexes, nucleopalladations with terminal al

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

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

177 ion of peptidomimetics employing cooperative palladium/copper catalysis in water is developed.

178 we report a platinum-trimer decorated cobalt-palladium core-shell nanocatalyst with a low platinum lo

179 The synthesis involved site-selective palladium cross-coupling reactions of chloropyrimidines

180 he amount of hydrogen that absorbed into the palladium decreased, and HER electrocatalytic activity i

181 ition between nucleophilic and electrophilic palladium difluorocarbene ([Pd]=CF(2)) is the key factor

182 m-catalysed strategy that confers the formed palladium difluorocarbene (Pd=CF(2)) species with both n

183 Palladium diimine-catalyzed polymerization of olefins us

184 , which slows the formation of the off-cycle palladium dimer.

185 Two-dimensional (2D) palladium diselenide (PdSe(2) ) has strong interlayer co

186 absorption and HER activity for a thin film palladium electrocatalyst.

187 to improve the electrocatalytic activity of palladium electrodes for reduction of carbon dioxide or

188 New neutral nickel and palladium ethylene polymerization catalysts have been pr

189 An efficient palladium-free Stille cross-coupling reaction of allylic

190 Here, we show that the chiral crystal palladium gallium (PdGa) displays multifold band crossin

191 Palladium-gold nanozyme shows excellent peroxidase mimet

192 ion-metal-catalyzed approaches championed by palladium have allowed the installation of a fluorine su

193 ase transition, crystals of (phenylazophenyl)palladium hexafluoroacetylacetonate of submillimeter to

194 observation of the formation and decay of a palladium(I) species during the reaction.

195 zi- and N-methyltropiporphyrins reacted with palladium(II) acetate to give stable palladium(II) compl

196 Under palladium(II) catalysis this [3 + 2] heteroannulation pr

197 eta sites, with arylboronic acids via tandem palladium(II) catalysis.

198 Specifically, an aryl palladium(II) complex interacts with a sigma-bond of a s

199 hylcarbaporphyrin-2-carbaldehyde also gave a palladium(II) complex, but this gradually rearranged at

200 , anionic trifluoromethyl and difluorobenzyl palladium(II) complexes undergo fluoride abstraction fol

201 ed with palladium(II) acetate to give stable palladium(II) complexes, demonstrating that N-alkylation

202 onate complex to enable addition of the aryl palladium(II) species and an organoboronic ester substit

203 nd 2,6-diformylpyridine subcomponents around palladium(II) templates.

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

205 ce transferred onto a protein substrate, the palladium(II)-aryl group facilitates conjugation by unde

206 t occurs without modification of a preformed palladium(II)-aryl group.

207 oxylations are among the most widely studied palladium(II)-catalyzed C-H oxidation reactions.

208 Palladium(II)-catalyzed carbon-hydrogen (C-H) oxidation

209 An efficient palladium(II)-catalyzed cascade reaction of ene-yne subs

210 A palladium(II)-catalyzed enantioselective alpha-alkylatio

211 Palladium(II)-catalyzed meta-selective C-H allylation of

212 Palladium(II)-catalyzed oxidation reactions represent an

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

214 The 16-palladium(II)-oxo cluster [Pd(16) O(24) (OH)(8) ((CH(3)

215 The 24-palladium(II)-oxo cluster [Pd(24) O(44) (OH)(8) ((CH(3)

216 ctures during reduction, resulting in silver-palladium intermixing.

217 ure of the molecular electronic junction for palladium ions complexed and reduced on 4-mercaptopyridi

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

219 Palladium is a promising material for electrochemical CO

220 tereospecific pathway of transmetallation to palladium is required to effect efficient chirality tran

221 ladium-silver interface length, with smaller palladium islands more efficiently supplying hydrogen at

222 e that, following dihydrogen dissociation on palladium islands, hydrogen atoms migrate from palladium

223 perties, and structural modifications to the palladium lattice of an industrial type interstitial bor

224 The palladium/Lewis acid cocatalyzed ring-opening reaction o

225 35 degrees C in less than 2 h with very low palladium loading (0.5 mol %).

226 edication Naproxen and Flurbiprofen with low palladium loading further highlights the practical value

227 re observed while using (+)-5 as a ligand in palladium-mediated asymmetric allylations.

228 A novel palladium-mediated carbonylogous 1,4-dipole was develope

229 ate was used to generate the highly reactive palladium-mediated dipoles for the first time, and a div

230 Subsequent, palladium-mediated double C-H oxidative coupling in a si

231 emendous efforts have focused on copper- and palladium-mediated/catalyzed trifluoromethylation of ary

232 experiments showing how hydrogenation in the palladium membrane reactor proceeds at faster reaction r

233 We report here the benefits of using a palladium membrane reactor to drive hydrogenation chemis

234 This technique uses a palladium membrane to physically separate the electroche

235 ide (2) is used for the stabilization of the palladium metal center.

236 Here we show that PdMo bimetallene-a palladium-molybdenum alloy in the form of a highly curve

237 A series of palladium N-heterocyclic carbene (NHC) complexes of type

238 ial engineering of orthogonal Lewis acid and palladium nanoparticle (NP) catalysts in a metal-organic

239 tigated 1,1,1-TCA and TCE co-reduction using palladium nanoparticle (PdNP) catalysts spontaneously de

240 an industrial type interstitial boron doped palladium nanoparticle catalyst system (Pd-(int)B/C NPs)

241 ules combined with catalytic bimetallic gold-palladium nanoparticles (Au-Pd NPs) in solution for an i

242 ctuation of graphene quantum dots (GQDs) and palladium nanoparticles (Pd NPs) for the rapid and label

243 The binaphthyl stabilized palladium nanoparticles (Pd-BNP) catalyzed single-step,

244 We show that gold-palladium nanoparticles supported on TiO(2) or carbon ha

245 Moreover, we discuss the use of palladium nanoparticles, in a polyol solvent, applied in

246 tachment of ~3-nanometer gold, platinum, and palladium nanoparticles.

247 nabled by a unique class of electrophiles in palladium-norbornene cooperative catalysis, which are su

248 on of common aryl and heteroaryl iodides via palladium-norbornene cooperative catalysis.

249 Palladium/norbornene (Pd/NBE) cooperative catalysis has

250 To show the synthetic utility of palladium/norbornene (Pd/NBE) cooperative catalysis, her

251 al difunctionalization of thiophenes via the palladium/norbornene (Pd/NBE) cooperative catalysis.

252 lation method is reported through a directed palladium/norbornene (Pd/NBE) cooperative catalysis.

253 zed via alkenyl halide- or triflate-mediated palladium/norbornene catalysis, which is enabled by a mo

254 ked methylation that is based on cooperative palladium/norbornene catalysis.

255 Palladium/norbornene cooperative catalysis has emerged a

256 When metalated with palladium, o-CF(2)H-functionalized 1,10-phenanthroline p

257 the field of the metal-based nanocatalysis, palladium occupies a privileged position mainly due to i

258 rogenolysis of tertiary benzylic alcohols on palladium on carbon (Pd/C) generally proceeds with inver

259 on mediated by para-toluenesulfonic acid and palladium on carbon, respectively.

260 d systematically explored for the capture of palladium, one of the most utilized PGEs.

261 Palladium oxidative addition complexes (OACs) are tradit

262 approach using stoichiometric quantities of palladium oxidative addition complexes (OACs) derived fr

263 of a silver surface oxide in the presence of palladium oxide compared to pure silver oxide resulting

264 ng from the transfer of atomic hydrogen from palladium oxide islands onto the surrounding surface for

265 ed/absorbed hydrogen and/or the premonolayer palladium oxide redox processes at Pd.

266 ation of the first three examples of neutral palladium-oxo clusters (POCs).

267 ) )(2) As)(8) ] (Pd(16) ) comprises a cyclic palladium-oxo unit capped by eight dimethylarsinate grou

268 a bicapped derivative of Pd(16) with a tetra-palladium-oxo unit grafted on either side.

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

270 istic interaction between partially oxidized palladium (Pd(delta+)) and oxygen-functionalized carbon

271 zed and quantified the following: (1) Pt and palladium (Pd) abundance, (2) geochemistry of 58 element

272 Among these, palladium (Pd) catalysts have played a prominent role in

273 en contain residual metal impurities such as palladium (Pd) clusters that are formed during the polym

274 exhibit poor catalyst performance with high palladium (Pd) loading (e.g., 10 mole %) and a need for

275 existing colloidal synthesis for corrugated palladium (Pd) nanoparticles to electrochemical growth o

276 The use of high-work-function palladium (Pd) or gold (Au) enables a high-quality p-typ

277 nulated donor and acceptor moieties based on palladium (Pd)-catalyzed [3+2] annulation reaction betwe

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

279 port commercially available carbon-supported-palladium (Pd/C)-catalyzed N-methylation of nitroarenes

280 ements (HSEs; namely, gold, iridium, osmium, palladium, platinum, rhenium, rhodium and ruthenium) in

281 Two types of functional linkers, a palladium-porphyrin photosensitizer and a bispyridine-de

282 Among the screened palladium precatalysts (3-5), the most active PEPPSI the

283 ed to the several reaction pathways that the palladium-propargyl intermediate can proceed by, and the

284 The method involves the synthesis of stable palladium-protein oxidative addition complexes (Pd-prote

285 uinoline as an N-ligand, and evidence of the palladium-quinoline interaction is provided by (1)H-(15)

286 A putative pai-allyl palladium radical-polar crossover path is proposed as a

287 ~500 nanometers) composed of platinum (Pt), palladium, rhodium, nickel, and cobalt, as well as a lib

288 d supported growth of ruthenium (bio-Ru) and palladium/ruthenium (bio-Pd@Ru) core@shell nanoparticles

289 nsity functional theory studies suggest that palladium's ligation state during oxidative addition is

290 rns of compression strengthening in gold and palladium samples down to the smallest grain sizes.

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

292 rrounding surface formed from oxidation of a palladium-silver alloy.

293 The palladium-silver interface also dynamically restructures

294 te of hydrogen atom migration depends on the palladium-silver interface length, with smaller palladiu

295 e results afforded with Pd(2)(dba)(3) as the palladium source.

296 These palladium-stabilized zwitterions participate in asymmetr

297 Palladium supported on cost-effective transition-metal c

298 We explored how palladium-tin alloys form mixed-composition phases with

299 lladium islands, hydrogen atoms migrate from palladium to silver, to which they are generally less st

300 indoles with boronic acids under sequential palladium/triflic acid catalysis is described.