ライフサイエンスコーパス: Au

1 Au nanoparticles were deposited on TiO2 nanoparticles to

2 Au nanostars with uniform and sharp tips were immobilize

3 Au NB film was fabricated on carbon electrodes working a

4 Au-modified ITO electrodes show a faster and reproducibl

5 Au/CdSe nanocrystal clusters (NCs) are successfully fabr

6 Au/Fc-PAMAM(G2)/FA and Au/Fc-PAMAM(G2)/BA based cytosens

7 cobalt wire placed under a GdOx layer and a Au top electrode.

8 noparticles (NPs) undergoing collisions at a Au ultramicroelectrode (UME) (5 mum radius) using electr

9 under ultrahigh vacuum conditions between a Au-coated probe featuring embedded nanoscale thermocoupl

10 nable low-temperature water-gas shift over a Au/CeZrO4 catalyst.

11 e been conjugated to near-infrared-absorbing Au nanoshells (SiO2 core, Au shell), each forming a ligh

12 to probe the thermoelectric transport across Au/h-BN/graphene heterostructures.

13 cle geometry, we have synthesized MRI-active Au nanomatryoshkas.

14 {Si(TMS)3}2)(t)Bu2P]M(NHC(Dipp)) (M: Cu, Ag, Au) (4-6), in which compound 3 acts as a phosphine ligan

15 of compound 3 with NHC(Dipp)MCl (M: Cu, Ag, Au) yield the charge neutral zwitterionic compounds [(Ge

16 ide compounds [Au4M4(mu3-E)4(IPr)4] (M = Ag, Au; E = S, Se, Te) has been synthesized from the combina

17 tation of plasmonic metal nanoparticles (Ag, Au and Cu) can induce direct photochemical reactions.

18 The ORR rates of Ag, Au, Cu, Ni, Pd, Rh and Pt measured at 600 degrees C form

19 land to quantify the stocks and flows of Ag, Au, Pd, Ru, Dy, La, Nd, and Co in automotive embedded EE

20 sintering of nanoparticle assemblies for Ag/Au, CdSe/PbS nanocrystals (NCs).

21 The orientation change of Ag@Au NPLs is impelled by the deformation of polymer matrix

22 anoparticles and in-plane dipolar peak of Ag@Au NPLs relies on the intensity and duration of pressure

23 mer composite film was developed based on Ag@Au composite nanoplates (NPLs) and polyvinylpyrrolidone

24 ermodynamically less favorable core-shell Ag@Au nanostructure is kinetically stabilized by the interm

25 tic vesicle assembled from Janus amphiphilic Au-Fe3 O4 NPs grafted with polymer brushes of different

26 bond distance of 0.203-0.213 nm, forming an Au-O-Au-O-Au structure.

27 ate or collected at SECM substrate (e.g., an Au UME).

28 cle, the resonance-scattering spectrum of an Au nanobump exhibites two resonance peaks.

29 c electropolymerization as a thin film on an Au film electrode in an electrochemical miniaturized mic

30 oating graphene oxide/ssDNA (GO-ssDNA) on an Au-electrode for VEGF detection, and incorporated with p

31 ethyl-4-mercaptopyridine (1-m-4-MP) using an Au-S bond.

32 atomic force microscopy (CP-AFM) in which an Au-coated tip contacts a self-assembled monolayer (SAM)

33 aromatic carboxylic acids on the Ag(111) and Au(111) surfaces to give the corresponding terminal alky

34 the liquid metal alloy galinstan with Ag and Au.

35 ts created via sonication to produce Ag- and Au-based galinstan nanorice particles.

36 ithiol-Au, Au-terphenyl-4,4''-dithiol-Au and Au-4,4'-bipyridine-Au) and revealed the relationship bet

37 dney 293 cells (HEK 293) as normal cells and Au/Fc-PAMAM(G2)/FA electrode showed two times better sel

38 the 3DOM Co3O4-supported Au-Pd, Pd-CoO, and Au-Pd-xCoO nanocatalysts resulting from water vapor addi

39 d addition, nanoparticles are decomposed and Au signal is registered by means of ICP-MS.

40 Au/Fc-PAMAM(G2)/FA and Au/Fc-PAMAM(G2)/BA based cytosensors showed extremely go

41 s study, the sorption of Hg(II), Cd(II), and Au(III) onto Bacillus subtilis biomass with an elevated

42 ivity for the removal of Hg(II), Cd(II), and Au(III), especially in systems with dilute metal concent

43 nt spin glass (RSG) transitions in Ni-Mn and Au-Fe have been reassessed by acoustic measurements of t

44 inopropyltriethoxysilane (SBA-15-pr-NH2) and Au nanoparticles (AuNPs) modified graphite screen printe

45 we utilize the combination of PEO-b-P2VP and Au, Ag, and Cu salts as a model three-component system t

46 surfaces of Al, Cu, Ru, Rh, Pd, Ag, Pt, and Au.

47 athodic electrochemical deposition on Ti and Au electrode using a multimodal approach by examining th

48 their ability to inhibit TRAP activity and [Au(4,4'-dimethoxy-2,2'-bipyridine)Cl2][PF6] (AubipyOMe)

49 sult in faster reductive elimination from Ar-Au(X)-Ar and lead to the pi-complexation of the arene by

50 pact of the conformational flexibility of Ar-Au-Ar intermediates, via systematic modulation of the le

51 idal noble metal nanoparticles (NPs, such as Au NPs) on solids is a promising strategy for preparing

52 imensional helical chains, characterized as {Au(I)(mu-6-TG)} n , extending many mum in length that ar

53 positively charged coordination complexes at Au/MAPbI3 interface, whereas iodine anions (I(-)) can re

54 on of single Ag nanoparticles is observed at Au microelectrodes using stochastic single-nanoparticle

55 ical molecules (Au-biphenyl-4,4'-dithiol-Au, Au-terphenyl-4,4''-dithiol-Au and Au-4,4'-bipyridine-Au)

56 onto the gold atomic clusters makes Apt/AuAC/Au an excellent platform for the LPS detection.

57 The Apt/AuAC/Au sensor offers an ultrasensitive and selective detecti

58 ensitive electrochemical biosensor (Apt/AuAC/Au) for LPS detection without any additional signal ampl

59 proximity, light-matter interaction between Au NBs and QDs produces a local electric signal enhancem

60 enyl-4,4''-dithiol-Au and Au-4,4'-bipyridine-Au) and revealed the relationship between heating or coo

61 Both Au NBs and GQDs were conjugated with target FAdVs specif

62 uch higher photocatalytic activity than both Au and Pt nanoparticle-decorated CZTS (Au/CZTS and Pt/CZ

63 chloride silica hybrid (Fe3O4@SiO2/DABCO) by Au-S bond.

64 orption fine structure study of gold/carbon (Au/C) catalysts under acetylene hydrochlorination reacti

65 d a vesicular transport pathway that carried Au-labeled silicacomes from the blood vessel lumen to a

66 ce of catalytic amounts of the Au(I) cation [Au(PPh3)](+), a large variety of (Z)-beta-iodoenol ester

67 henyl propargyl ethers catalyzed by cationic Au(I) complexes, which forms a mixture of 5- and 7-subst

68 tive catalysts comprise single-site cationic Au entities whose activity correlates with the ratio of

69 s bearing many other elements (e.g., Ni, Co, Au, Se, and platinum group elements) are significantly l

70 thiocholine-induced aggregation of (10Os)CO-Au NPs can be monitored by the change in color of the NP

71 the surface of gold nanoparticles ((10Os)CO-Au NPs) greatly enhanced the CO stretching vibration sig

72 function of Au and Ir spacer layers in Pt/Co/Au,Ir/Pt.

73 ct angle measurements over PEDOT(PSS)-coated Au, GC, and Pt electrode surfaces.

74 on imaging and temporal evolution of colloid Au nanoparticles are recorded.

75 NA assay for ultralow target concentrations, Au nanoprobes on a lipid micropattern were monitored and

76 lated antibodies and streptavidin-conjugated Au nanoparticles.

77 ion-based self-assembly approach, containing Au nanoparticles (NPs) of size 2.8, 4.6, 7.2, or 9.0 nm

78 infrared-absorbing Au nanoshells (SiO2 core, Au shell), each forming a light-responsive drug delivery

79 Using the example of a Cu-Au solid solution, we demonstrate that compositional var

80 and trace element dataset from the paired Cu-Au (copper) and Sn-W (tin) magmatic belts in Myanmar.

81 both Au and Pt nanoparticle-decorated CZTS (Au/CZTS and Pt/CZTS) photocatalysts, indicating the MoS2

82 itu electrochemical conversion of the dative Au<--N bond into a new type of Au-N contact.

83 Here we report the discovery of well-defined Au(III) complexes that participate in rapid migratory in

84 e comparing with coarse-grained, fully dense Au.

85 ve peptides were used as additive to deposit Au nanostructures and it is compared with the structure

86 otential for aggregated 4 and 15 nm diameter Au NPs shifts positive by a maximum of 230 and 180 mV, r

87 V (vs Ag/AgCl) for 4, 15, and 50 nm diameter Au NPs, respectively, in line with their size-dependent

88 t shift at all for aggregated 50 nm diameter Au NPs.

89 anoantennas containing monomeric and dimeric Au nanostars.

90 -4,4'-dithiol-Au, Au-terphenyl-4,4''-dithiol-Au and Au-4,4'-bipyridine-Au) and revealed the relations

91 otypical molecules (Au-biphenyl-4,4'-dithiol-Au, Au-terphenyl-4,4''-dithiol-Au and Au-4,4'-bipyridine

92 rfaces for dissociation of N2 on an Fe-doped Au(111) surface.

93 es (HNC-SLs) self-assembled from quantum-dot-Au (QD-Au) satellite-type HNCs.

94 glass substrate-supported single and double Au nanoparticles ( 100-200nm), arranged in a periodic m

95 Ligand exchange drives Au nanocrystal fusion and forms a porous network, impart

96 be a graphite-based nanocomposite electrode (Au-rGO/MWCNT/graphite) that uses a simple electro-co-dep

97 plexes containing three-center, two-electron Au-H-Cu bonds have been prepared from addition of a pare

98 ed an electrochemical immunosensor employing Au sheet as working electrode, Fe3O4 magnetic nanopartic

99 ematic picture of CO* binding on Cu-enriched Au surface model systems.

100 ated Spiro-OMeTAD and a thermally evaporated Au back contact, under full 1 sun illumination, at 60 de

101 e revealing the additional role of COPT2 for Au mobilization in yeast and Arabidopsis.

102 314 for Al thermal conductivity and LEOS for Au/Al release equation-of-state show good agreement with

103 role in shaping the dendritic morphology for Au.

104 ved for single-component particle formation (Au > Ag > Cu).

105 rmal C(sp(3))-CF3 reductive elimination from Au(III) that accesses these compounds by a distinct mech

106 G-Au modified GCE exhibited an enhanced electrocatalytic r

107 oride occurs to produce highly crystalline G-Au nanocomposite.

108 the sensing performance of the fabricated G-Au modified electrode with stable and reproducible respo

109 Furthermore, this enzyme-free G-Au/GCE exhibited an excellent selectivity towards NO in

110 ised for the development of graphene-gold (G-Au) nanocomposite.

111 The G-Au nanocomposite was characterised by UV-vis, XRD, FTIR,

112 This G-Au nanocomposite introduces a new electrode material in

113 This G-Au nanocomposite was used to modify glassy carbon electr

114 nt fluxes ranged from <10 mug day(-1) (e.g., Au, In, and Lu) to >1 mg day(-1) (e.g., Zn, Sc, Y, Nb, a

115 Gold (Au) on ceria-zirconia is one of the most active catalyst

116 We synthesized layered gold (Au) clusters on a molybdenum carbide (alpha-MoC) substra

117 aterial in the fabrication of modified gold (Au) working electrode for electrochemical MG biosensor.

118 cortisol antibody (anti-CAB) on top of gold (Au) microelectrodes using 3,3'-dithiodipropionic acid di

119 Plasmonic gold (Au) nanotriangular arrays, functionalized with a near in

120 In in-vitro studies using gold (Au) nanoparticle-coated nanoelectrodes, we show that thi

121 urface modification of ITO anodes with gold (Au) is demonstrated, to enhance direct microbial biofilm

122 mbly is used to organize polystyrene-grafted Au nanocrystals at a fluid interface to form ordered sol

123 systems, where nucleation sites have greater Au content than the other metals.

124 As a consequence, unusual heterobimetallic Au(I)/Pt(II) complexes containing hydride (-H), acetylid

125 aped Hg/Pt ultramicroelectrode (UME) or a Hg/Au film UME, which were utilized as the SECM tips.

126 to dope single atoms of Ag or Cu into hollow Au nanoclusters, creating precise alloy nanoparticles at

127 supported analogs of single-site homogeneous Au catalysts and propose a mechanism, supported by compu

128 nd characterization of hitherto hypothetical Au(III) pi-alkyne complexes is reported.

129 l modeling, based on a redox couple of Au(I)-Au(III) species.

130 es are found to sensitize ground-state Cu(I)-Au(I) covalent bonds and near-unity phosphorescence quan

131 r-covalent bond with ligand-unassisted Cu(I)-Au(I) distances of 2.8750(8) A each-the shortest such an

132 activity correlates with the ratio of Au(I):Au(III) present.

133 opropargyl)-5-methoxyisoxazoles under Fe(II)/Au(I) relay catalysis was developed.

134 rts pointed to the probable role of COPT2 in Au transport based on the transcript accumulation of COP

135 age-controlled magnetic anisotropy (VCMA) in Au/[DEME](+) [TFSI](-) /Co field-effect transistor heter

136 yl- or carbonyl-stabilized diazoalkanes into Au-C bonds at temperatures >/= -40 degrees C.

137 M-MS technique was used to separate isomeric Au(I) metallopeptide ions that were formed by Zn(II) dis

138 performance and the reversibility of the ITO/Au electrodes.

139 An integrated platform for the ITO/Au transparent electrode with light-emitting diodes was

140 was used with different electrode materials (Au, Pd, Pt, and Ag) to assess the effect of the electrod

141 ld nanoparticles coated magnetic microbeads (Au NPs-MBs), which were prepared through a novel and sim

142 n deposited on the surface of a miniaturized Au electrode (7mm(2)) to prepare a miniaturized enzyme a

143 catalytic nature of V2O5 nanoplates modified Au electrode in the detection of MG.

144 Non-enzymatic V2O5 modified Au electrode showed a sensitivity of 4.519microAmicroM(-

145 f-assembled monolayer principle by modifying Au electrode with cysteamine (Cys) and immobilization of

146 gold junctions with prototypical molecules (Au-biphenyl-4,4'-dithiol-Au, Au-terphenyl-4,4''-dithiol-

147 chemical calculations, we describe the mono Au(I)-catalyzed dimerization of two alkyne units as well

148 (I)-catalyzed reactions of alkynes, the mono Au(I)-catalyzed pendant to the radical dimerization of n

149 an atomically well-defined Pd(sub-monolayer)/Au(111) bimetallic model catalyst at 3 nm resolution in

150 The MoS2/Au NPs/GOx bioelectrode exhibits a linear response to gl

151 , we report an artificial gold nanoparticle (Au NP)-discrete pi-conjugated molecule hybrid system tha

152 eguide was combined with gold nanoparticles (Au NPs) to amplify the mass loading effect of the acoust

153 effectively quenched by gold nanoparticles (Au NPs) via fluorescence resonance energy transfer (FRET

154 CW) laser excitation and gold nanoparticles (Au-NPs) to induce known thermal decomposition reactions

155 roscope at room temperature, that nanoporous Au indeed has significantly improved radiation tolerance

156 se of Ag(+) ions from a Janus polystyrene/Ni/Au/Ag activator motor to the activated Janus SiO2 /Pt na

157 100 nm Au ENM were spiked into DI H2O and synthetic and natural

158 ction of diazonium reagents, then a Ti(2 nm)/Au top contact was applied to complete a solid-state mol

159 on dark field measurements from different np-Au surfaces.

160 fibroblasts cultured on nanoporous gold (np-Au) as a model nanostructured material system.

161 er the fluorescence intensity depended on np-Au feature size, complementing the findings with reflect

162 splay different levels of fluorescence on np-Au, planar gold, and glass, suggesting different levels

163 The M134E could specifically nucleate Au precursor (Gold (III) chloride), which enable the eff

164 ance of 0.203-0.213 nm, forming an Au-O-Au-O-Au structure.

165 distance of 0.203-0.213 nm, forming an Au-O-Au-O-Au structure.

166 Taken together, the yolk-shell Fe3 O4 @Au NPs can be regarded as an ideal magnetic-plasmonic th

167 ansporter towards uptake and accumulation of Au in plants.

168 ows us to quantify the increased affinity of Au-catalysts to the Bergman cyclization transition state

169 erase (BChE), could cause the aggregation of Au NPs and the corresponding recovery of FRET-quenched f

170 rate coordination, although trace amounts of Au(delta)(+) are observed.

171 lized as a template to guide the assembly of Au nanoparticles, forming intriguing nanoparticle thread

172 have focused on the established capacity of Au(I) and Pt(0) complexes to act as Lewis acidic and bas

173 migration, the intraparticle coalescence of Au satellites at QD surfaces transforms individual HNCs

174 on boosting of the valence electron count of Au nanoparticles.

175 ational modeling, based on a redox couple of Au(I)-Au(III) species.

176 ity, size of Au-NPs, and surface coverage of Au-NPs.

177 the agglomeration and possible dewetting of Au NPs.

178 Thermal dewetting of Au, which is sandwiched between the yolk and shell, lead

179 al dewetting strategy for the fabrication of Au nanocups with tunable diameter, height, and size of c

180 e reported in Pt determined as a function of Au and Ir spacer layers in Pt/Co/Au,Ir/Pt.

181 The size growth of Au nanoparticles involves two different size-evolution p

182 e vesicle shell is composed of two layers of Au-Fe3 O4 NPs in opposite direction, and the orientation

183 vantage simultaneously of the strong LSPR of Au and the catalytic activity of Fe toward N2 dissociati

184 Despite the myriad of Au(I)-catalyzed reactions of alkynes, the mono Au(I)-cat

185 n opposite direction, and the orientation of Au or Fe3 O4 in the shell can be well controlled by expl

186 The intensity ratio between plasmon peak of Au nanoparticles and in-plane dipolar peak of Ag@Au NPLs

187 The catalytic power of Au(I) in BC stems from a combination of two sources: ste

188 whose activity correlates with the ratio of Au(I):Au(III) present.

189 Ps) were fabricated by one-step reduction of Au(3+) ion using Tyr as a reducing and capping agent und

190 he top, bridge and threefold hollow sites of Au(111).

191 clude heating time, laser intensity, size of Au-NPs, and surface coverage of Au-NPs.

192 clude the surface plasmon resonance (SPR) of Au nanoparticles, low overpotential of Pt nanoparticles,

193 store fluorescence of Tyr on the surfaces of Au NPs.

194 We demonstrate the synthesis of Au nanostar dimers with tunable interparticle gap and co

195 by chemical vapor deposition (CVD) on top of Au(111) surfaces.

196 of the dative Au<--N bond into a new type of Au-N contact.

197 Here, we show the self-assembly on Au(111) of an expanded aza-porphyrin, namely, an "expand

198 lymer brushes of different hydrophilicity on Au and Fe3 O4 surfaces separately.

199 re an individual dibutyl sulfide molecule on Au(111), we show that the differences arise when the rel

200 a self-assembled monolayer (SAM) of OPDs on Au.

201 the facet- and potential-dependent 4e-ORR on Au in alkaline solutions.

202 bonate enhances the rate of CO production on Au by increasing the effective concentration of dissolve

203 clization and covalent coupling reactions on Au(111) according to scanning tunneling microscopy (STM)

204 emistry performed at microfluidic volumes on Au pads directly at the PCB surface with improved limit

205 both the monomer and polymer monolayer onto Au(111).

206 Bimetallic catalysts, such as Pd-Au, show superior performance in various catalytic react

207 nanoscale thermocouples and a heated planar Au substrate that were both subjected to various surface

208 superparamagnetic Zn0.2Fe2.8O4 and plasmonic Au nanocrystals.

209 diluted serum using Anti-TNF-alpha/FNAB/PMMA/Au reveal that system can detect TNF-alpha in 100pg/ml t

210 catalysis mediated by planar polycrystalline Au surfaces.

211 within a hollow cavity encircled by a porous Au outer shell are designed.

212 ctive electrodes (ISEs), the surfaces of Pt, Au, and GC electrodes were coated with 0.1, 1.0, 2.0, an

213 e transition metal (TM = Co, Fe, Cu, Pd, Pt, Au)-based photocatalyst (PC) has led to the dramatic acc

214 -SLs) self-assembled from quantum-dot-Au (QD-Au) satellite-type HNCs.

215 f Pt(II) and their drastically more reactive Au(III) congeners.

216 A 6 x 6 recessed Au nanoring-ring electrodes microarray was fabricated ov

217 In this process, hydrazine reduces Au(III) ions, which attach to the existing nanoparticles

218 Remarkably, Au electrodes modified with 4-pyridinylethanemercaptan s

219 Fe-N-C and especially Ni-N-C catalysts rival Au- and Ag-based catalysts.

220 These new 3D RVC-Au electrodes showed great promise for improving the pow

221 In particular, a 3D RVC-Au sponge provides a large accessible surface area for i

222 of power generation, the EFC device with RVC-Au electrodes provided high volumetric power density of

223 Interestingly, a Cd(S-Au-S)3 "paw-like" surface motif is observed for the firs

224 a junction which connects three monomeric -S-Au-S- motifs.

225 corporate trace elements such as Co, Ni, Se, Au, and commonly As.

226 substituted [6]carbohelicenes by sequential Au-catalyzed intramolecular hydroarylation of diynes.

227 Several Au(III) coordination compounds were tested for their abi

228 We present a systematic study of core-shell Au/Fe3O4 nanoparticles produced by thermal decomposition

229 spensions containing gold-silver core-shell (Au@Ag) NPs in EPA moderately hard water (MHW) and MHW co

230 athematical formula for magic number shells: Au@Au12@Au42@Au92@Au54, which is further protected by a

231 perature, we observed the formation of small Au nanoparticles (NPs; 1-2 nm) from subnanometer Au spec

232 alysis since it was observed that very small Au nanoparticles (NPs) and other noble metal NPs are ext

233 tecting modules of Ag NPs by the incoming SR-Au(I)-SR modules, giving rise to a core-shell [Ag32@Au12

234 nit supported by ultraflat template-stripped Au and contacted by a eutectic alloy of gallium and indi

235 anoparticles (NPs; 1-2 nm) from subnanometer Au species.

236 ability compared to the 3DOM Co3O4-supported Au-Pd and Pd-CoO nanocatalysts.

237 Deactivation of the 3DOM Co3O4-supported Au-Pd, Pd-CoO, and Au-Pd-xCoO nanocatalysts resulting fr

238 We believe that the supported Au-Pd-xCoO nanomaterials are promising catalysts in prac

239 anocluster, in which two neighboring surface Au atomic sites "coalesce" into one Cd atomic site and,

240 , preventing inward diffusion of the surface Au atoms.

241 For symmetrical Au clusters, of varying sizes, the most positive VS,max

242 In this paper, we show that Au nanoparticles (AuNPs) stabilized with either citrate

243 The Au nanostar@Raman Reporter@silica sandwich nanoparticles

244 The Au-Pd-0.40CoO/3DOM Co3O4 sample performed the best (T90%

245 The Au-Pd-xCoO/3DOM Co3O4 nanocatalysts exhibited better the

246 The Au/Fe3O4 core-shell structure was demonstrated by high a

247 The Au/graphene/h-BN heterostructures enable us to explore t

248 In solutions below pH 3.0, the Au NPs aggregate in solution and attach to the electrode

249 ary source of carbon in the CO formed at the Au electrode by a combination of in situ spectroscopic,

250 To induce metallicity by bringing the Au atoms closer together under ambient conditions, we ex

251 on of metallic Lewis adducts and confers the Au(I)/Pt(0) pair a remarkable capacity to activate dihyd

252 The approach used here to fabricate the Au/CdSe NCs is suitable for the construction of other pl

253 l oxidation prior to diffusing away from the Au electrode into the bulk solution.

254 Plasmon resonance energy transfer from the Au NPs to the CdSe QDs, which enhances charge-carrier ge

255 With strong scattering in near infrared, the Au nanocups exhibit superior efficiency as contrast agen

256 In this manner the Au-NPs act as nanoheaters that result in a highly locali

257 As such, a better alignment of the Au Fermi level to the molecular orbital of silane that m

258 The magnetite shell grown on top of the Au nanoparticle displayed a thermal blocking state at te

259 a novel nanocomposite film consisting of the Au nanoparticles/graphene-chitosan has been designed to

260 red with the structure and reactivity of the Au nanostructures prepared in the presence of M134E.

261 In the presence of catalytic amounts of the Au(I) cation [Au(PPh3)](+), a large variety of (Z)-beta-

262 dramatic (>10(12)-fold) acceleration of the Au(I)-catalyzed reaction compared to that of the noncata

263 The structural features of the Au-DNs and their interfacing mechanism with ITO electrod

264 t of the antigen-antibody interaction of the Au/GO-COOH chip cause this chip to become four times as

265 Furthermore, it is also shown that on the Au(111) surface this sigma-bond metathesis can be combin

266 Together, these results clearly reveal the Au uptake capability of COPT2 in yeast and Arabidopsis.

267 The metal measurement data showed that the Au level was increased in COPT2, expressing yeast cells

268 upling of the oligophenylene backbone to the Au electrodes, consistent with experimental transport da

269 When the Au NPs are attached to the electrode from a solution wit

270 ng-standing puzzle remains unsolved: why the Au surfaces with {100} sub-facets were exceptionally cap

271 e 140 h experiment, the solar cells with the Au electrode experience a dramatic, irreversible efficie

272 igh sensitivity of SP-ICP-MS, along with the Au@Ag NPs, enabled us to track the NP transformations in

273 ndings leads to the demonstration that these Au clusters are also effective in selective oxidation of

274 We demonstrate that these Au/C catalysts are supported analogs of single-site homo

275 onjugated Quantum dots (QDs) are adsorbed to Au nanoparticles (AuNPs) due to interaction of aptamers

276 oxylic diimide (PTCDI) molecules attached to Au-electrodes, in the dark and under illumination, and s

277 the enhanced reactivity that they impart to Au(I)-centers after coordination.

278 y in ctr1Deltactr3Delta mutants and leads to Au sensitivity in yeast, which is comparable to Cu in gr

279 d increase in formate production relative to Au foil.

280 ) U.mL(-1) for CA 19-9 by using such tunable Au nanotriangular arrays, a great improvement compared t

281 coupling between sharp tips and cores of two Au nanostars in the wide conjunction region allows the a

282 rimer units are noncovalently packed via two Au(I)cdots, three dots, centeredCu(I) metallophilic inte

283 , tyrosine-protected gold nanoparticles (Tyr-Au NPs) were fabricated by one-step reduction of Au(3+)

284 analytes, confirming the aggregation of Tyr-Au NPs induced by spermine and spermidine, which results

285 surface plasmon resonance (SPR) band of Tyr-Au NPs was red-shifted to 596 and 616nm and the emission

286 The Tyr-Au NPs were successfully used as a dual probe for colori

287 accumulated in the root of Arabidopsis under Au exposure.

288 n the transcript accumulation of COPT2 under Au exposure.

289 PLs) and polyvinylpyrrolidone (PVP) by using Au nanoparticles as concentration reference.

290 Biosensor electrode was constructed using Au-DNs modified electrode for nitrite ions and found imp

291 They can be formed from various Au sources.

292 ands within 65-200 cm(-1), assignable to vCu-Au as validated by both the Harvey-Gray method of crysta

293 tions suggest that the reaction proceeds via Au(I)-catalyzed hydrofunctionalization of the enol ether

294 Superlattices containing 3-20 vol % Au are found to have an elastic modulus of approximately

295 ved from 6-thioguanosine that complexes with Au(I) ions to form a wire-like material that can also in

296 tly n-type doped MAPbI3 single crystals with Au/MAPbI3/Ag configuration based on interface dependent

297 lectrodes is lower than the ones formed with Au and Ag electrodes, again in contrast to the trends in

298 er than the conductance of those formed with Au electrodes.

299 The organic cations (MA(+)) interact with Au atoms, forming positively charged coordination comple

300 The complexation reaction with Au(I) ions spontaneously assembles luminescent one-dimen