ライフサイエンスコーパス: selenide

1 MR chemical shift or (1)J(P-Se) of phosphine selenide.

2 venting the activation of trialkyl phosphine selenide.

3 phine chalcogenide such as diphenylphosphine selenide.

4 he synthesis of selenophosphate from ATP and selenide.

5 sors, zinc carboxylate and trialkylphosphine selenide.

6 he reaction is also feasible with an allylic selenide.

7 sible reagent, namely, benzyltrifluoromethyl selenide.

8 ryl-alkyl, aryl-heteroaryl, and diheteroaryl selenides.

9 much more potent than either the sulfides or selenides.

10 trinsically doped p-type polycrystalline tin selenides.

11 f nanoscale oxides, pnictides, sulfides, and selenides.

12 nocrystals of copper and silver sulfides and selenides.

13 cylphosphonate (Cd-ODPA) with alkylphosphine selenides (1, tri-n-octylphosphine selenide; 2, di-n-but

14 Crossover experiments with selenide 12 and its deuterated crotyl analogue 27 indica

15 The oxidation of allyl selenide 12 with hydrogen peroxide produced the correspo

16 phosphine selenides (1, tri-n-octylphosphine selenide; 2, di-n-butylphenylphosphine selenide; 3, n-bu

17 phine selenide; 2, di-n-butylphenylphosphine selenide; 3, n-butyldiphenylphosphine selenide) in recry

18 Selenoxide 8 is not reduced to selenide 6 by PhSH in the presence of H(2)O(2).

19 Although alkaline iron selenide A(y)Fe(1.6+x)Se(2) (A=K, Rb, Cs) superconductor

20 d via selenocysteine lyase (SCLY), producing selenide, a substrate for selenophosphate synthetase 2 (

21 The reversible formation of chloro selenide adducts was unambiguously established by crosso

22 order to determine the metabolic effects of selenide administration, we exposed mice to hydrogen sel

23 We also examined the metabolic effects of selenide administration.

24 mperature before, during, and after hydrogen selenide administration.

25 tissues as silver sulfides (Ag2S) and silver selenide (Ag2Se).

26 s the protective effects of phenylaminoethyl selenides against peroxynitrite-induced DNA damage.

27 Bismuth chalcogenides and lead telluride/selenide alloys exhibit exceptional thermoelectric prope

28 Several selenide analogues were attached to polyethylene glycol

29 radical (C3'(dephos) sugar radical), phenyl selenide and acyl modified sugar and nucleoside derivati

30 m donor, selenophosphate is synthesized from selenide and ATP by selenophosphate synthetase.

31 synthetase, which forms selenophosphate from selenide and ATP, is found in various prokaryotes, eukar

32 vealed the Km values for the two substrates, selenide and ATP, were similar for both enzymes.

33 MP, and orthophosphate in a 1:1:1 ratio from selenide and ATP.

34 d later precipitate as chloride, sulfide, or selenide and be incorporated in bones during the growth.

35 wise, the reaction between trialkylphosphine selenide and cadmium n-octadecylphosphonic acid complex

36 crystals, prepared from tri-n-octylphosphine selenide and cadmium octadecylphosphonate in tri-n-octyl

37 Dimethyl selenide and dimethyl diselenide were detected as the pr

38 no-selenium compounds detected were dimethyl selenide and dimethyl diselenide.

39 Using a combination of triphenylphosphine selenide and diphenyl phosphate as a catalyst, a wide ra

40 ctive selenium 75 in the form of selenite or selenide and measured blood and tissue selenium levels a

41 presence of selenomethionine indicating that selenide and selenomethionine exert their toxicity via d

42 ctant templated, open framework platinum tin selenide and telluride materials assembled using K4SnQ4

43 unterions and have a value of 2.0 eV for the selenides and 3.0-3.1 eV for the sulfides.

44 the electronic interaction between the core selenides and surface in situ generated oxides/hydroxide

45 ing the synergistic effect between the inner selenides and surface oxidation species.

46 using the thiol as the sulfur source, while selenides and tellurides can be accessed upon mixing wit

47 The selenides and tellurides catalyze the oxidation of bromi

48 of diaryl chalcogenides including sulfides, selenides and tellurides has been developed by the react

49 ivity is established across a range of metal selenides and tellurides, showing that conductive materi

50 00-fold catalytically superior to the diaryl selenides and their spirodioxyselenurane counterparts in

51 ony-rich precipitates are endotaxial in lead selenide, and appear remarkably effective in reducing th

52 ding bismuth oxide, bismuth sulfide, bismuth selenide, and bismuth telluride, have been heavily inves

53 hiol, but not t-butylthiol, diphenyl sulfide/selenide, and di-n-butyl sulfide.

54 endent on both Mg(2+) and K(+) and uses ATP, selenide, and water to catalyze the formation of AMP, or

55 Dendrimeric polyphenylsulfides, -selenides, and -tellurides are prepared in high yield us

56 eries (AIBs) in comparison with sulfides and selenides, and has, thus, been nearly abandoned.

57 on metal dichalcogenides including sulfides, selenides, and tellurides of group V and VI transition m

58 ns gives the new structure both the bridging selenide anion sites that connect pairs of Bi(2)O(2) lay

59 characterization revealed the K(m) value for selenide approached levels that are toxic to the cell.

60 imilarly with speciation dominated by organo-selenide ( approximately 61%).

61 f Pb-oleate with tris(diethylamino)phosphine selenide are highly sensitive to the presence of water,

62 These attributes of cuprous selenide are now integrated with a one-dimensional morph

63 Copper selenides are an important family of materials with appl

64 ver, the difference between the sulfides and selenides arises from the change in crystal packing.

65 olic azides (ArN3), sulfides (ArSR, ArSAr'), selenides (ArSePh), alcohols [ArCH(OH)R], amino derivati

66 inactive in the standard in vitro assay with selenide as substrate, was found to exhibit detectable a

67 ted systems, and confirms the appeal of iron selenides as a platform for understanding superconductiv

68 ly change the electronic structure of cobalt selenide, assuring a rapid charge transfer and optimal e

69 In the absence of selenide, ATP is converted quantitatively to AMP and two

70 ppressed in a resonantly pumped Pr(3+)-doped selenide-based chalcogenide fibre amplifier.

71 in a 4.1 mum resonantly pumped Pr(3+)-doped selenide-based chalcogenide glass fibre amplifier of len

72 enhancement of energy-transfer from cadmium selenide-based core-shell quantum dots to gold-iron oxid

73 Five selenide BFA prodrugs were also prepared that are envisi

74 mparable to the commercial bismuth telluride selenide (Bi(2)Te(3-) (x) Se (x) ) but much cheaper.

75 in film of the topological insulator bismuth selenide (Bi2Se3) at room temperature can indeed exert a

76 ray diffraction (XRD) experiments of bismuth selenide (Bi2Se3) have been carried out to pressures of

77 activity of electrocatalysts based on metal selenides, but also sheds light on further surface and i

78 etween cadmium oleate and trialkyl phosphine selenide by binding to cadmium and preventing the activa

79 tronic response of single crystals of indium selenide by means of angle-resolved photoemission spectr

80 We report that the self-assembly of cadmium selenide-cadmium sulfide (CdSe-CdS) core-shell semicondu

81 ing ensembles of near-unity emitting cadmium selenide/cadmium sulfide (CdSe/CdS) core-shell quantum d

82 kinetics of the II-VI semiconductor cadmium selenide can be used to vary the shapes of the resulting

83 nanorod heterostructures composed of cadmium selenide (CdSe) and cadmium sulfide (CdS).

84 The small cadmium selenide (CdSe) dots, with an intraband energy separatio

85 Colloidal quantum rods of cadmium selenide (CdSe) exhibit linearly polarized emission.

86 onductor nanowires (NWs) composed of cadmium selenide (CdSe) have been directly grown on transparent

87 The kinetics of cadmium selenide (CdSe) nanocrystal formation was studied using

88 ntum-confined Stark effect in single cadmium selenide (CdSe) nanocrystallite quantum dots was studied

89 reports the potential application of cadmium selenide (CdSe) quantum dots (QDs) in improving the micr

90 tavidin-linked inorganic crystals of cadmium selenide [(CdSe)ZnS].

91 ic effect of thin-film copper indium gallium selenide cells (CIGS) is conferred by the latter element

92 lfide, CH(3)SeSSCH(3), and dimethyl bis(thio)selenide, CH(3)SSeSCH(3), were synthesized and analyzed

93 n-film PV technologies-copper indium gallium selenide (CIGS) and cadmium telluride (CdTe)-in the Unit

94 tions with silicon and copper indium gallium selenide (CIGS), as well as all-perovskite tandem cells,

95 step electrodeposition of two copper-indium-selenide (CISe) compounds on flexible foil.

96 A series of selenide clusters (undoped supertetrahedral T4-ZnGaSe, S

97 m 1/SeH(-)/L(-) in acetonitrile, a series of selenide clusters [(Tp)(2)Mo(2)Fe(6)S(8)SeL(2)](3)(-) (L

98 ions: whereas copper chalcogenide and silver selenide clusters show a clear tendency to approach stru

99 We show that various sulfide and selenide clusters, when bound to metal ions, yield gels

100 ct fragmentation pattern of the mixed sulfur/selenide compounds allow the tentative differentiation b

101 The lead selenide constituent has a distorted rock salt structure

102 a series of three-dimensional sulphides and selenides containing highly mobile alkali metal cations

103 Diaryl selenides containing o-hydroxymethylene substituents fun

104 em utilizes water cooled chromium doped zinc selenide (Cr(2+):ZnSe) as the gain medium and is pumped

105 rmonic signal versus the thickness of Indium Selenide crystals, in contrast to the quadratic increase

106 A new wurtzite phase of copper tin selenide (CTSe) was discovered, and the resulting nanocr

107 als: a gold nanorod (AuNR) core and a copper selenide (Cu(2-x)Se, x >/= 0) supraparticle shell.

108 m sulfide (CuInS2) and copper indium gallium selenide (Cu(InxGa(1-x))-Se2; CIGS) nanocrystals ranging

109 Herein, a flexible thermoelectric copper selenide (Cu2 Se) thin film, consisting of earth-abundan

110 of a p-type thermoelectric material, copper selenide (Cu2Se), utilizing solution-processing and ther

111 Typically, the formation of copper selenide (CuSe) and indium selenide (InSe) nanocrystals

112 All measurements indicate that selenide decreases metabolism.

113 imilar to NIFS may be involved as an in vivo selenide delivery protein for selenophosphate biosynthes

114 ossibility that this enzyme might serve as a selenide delivery protein for the in vitro biosynthesis

115 nthetase activity in the assay that measures selenide-dependent AMP formation from ATP.

116 clusively into orthophosphate in the overall selenide-dependent reaction indicates that the beta-phos

117 RNA oligonucleotides containing a phenyl selenide derivative of 5-methyluridine were chemically s

118 nyl diselenide, di-n-butyl sulfide, diphenyl selenide, diphenyl sulfide, 1-octadecanethiol, t-butyl d

119 A repair-deficient strains hypersensitive to selenide displayed wild-type growth rate properties in t

120 Dimethyl selenide (DMSe) is one of the major volatile organoselen

121 n and volatilization of selenate to dimethyl selenide (DMSe): (a) uptake of selenate, (b) activation

122 Specificity studies show that with dimethyl selenide, DMSOR yields a species analogous to the DMS sp

123 horizontal lineSe bond in trialkylphosphine selenide during the synthesis of CdSe nanocrystals.

124 was proposed for synthesizing thioethers and selenide ethers from anilines under solvent-free and tra

125 anilines and diselenides, the corresponding selenide ethers were obtained with satisfactory to excel

126 e we show that ultrasmall clusters of copper selenide exhibit a disordered cationic sub-lattice under

127 ocrystal (NC) of the inorganic solid cadmium selenide exhibits strong positive co-operativity in its

128 ons enhance electron-phonon coupling in iron selenide (FeSe) and related pnictides, but direct experi

129 The superconductor iron selenide (FeSe) is of intense interest owing to its unus

130 Films of iron selenide (FeSe) one unit cell thick grown on strontium t

131 The conductivity of lead selenide films, for example, can be manipulated over at

132 tobacter vinelandii NifS protein can replace selenide for selenophosphate biosynthesis in vitro sugge

133 for ORR and various defects in metal oxides/selenides for OER is also provided.

134 ctural analogue, 4-fluorophenyl 2-aminoethyl selenide (FPAESe) as an internal standard.

135 inum-germanium chalcogenide and platinum-tin selenide frameworks were prepared by linking correspondi

136 l strategy for the synthesis of sulfides and selenides from phosphonium salts and thio- or selenesulf

137 administration, we exposed mice to hydrogen selenide gas (0-5 ppm) mixed into air (20.95% oxygen) fo

138 The four polymorphs of layered gallium selenide (GaSe) crystals that result from different laye

139 Gallium selenide (GaSe) is a layered semiconductor and a well-kn

140 c structure of a germanium doped phosphorous selenide glass of composition Ge(2.8)P(57.7)Se(39.5) is

141 n of trace amounts of the vapors of hydrogen selenide (H(2)Se), methylselenol (CH(3)SeH), dimethylsel

142 ne (AsH(3)), phosphine (PH(3)), and hydrogen selenide (H(2)Se), while qualitative detection was obser

143 method for the preparation of unsymmetrical selenides has been developed.

144 pic rearrangement of enantioenriched allylic selenides has been expanded to provide access to three n

145 or quantum dots (zinc sulfide-capped cadmium selenide) have been covalently coupled to biomolecules f

146 Here, we show that mercury selenide (HgSe) nanoparticles in the liver and brain of

147 ed (LB) mercury telluride (HgTe) and mercury selenide (HgSe), with tunable band gap.

148 Heavily electron-doped iron-selenide high-transition-temperature (high-T c) supercon

149 pound, 4-hydroxyphenyl 2-methyl-2-aminoethyl selenide (HOMePAESe), were unsuccessful because of exten

150 e of ADP with ATP observed in the absence of selenide implies the existence of a phosphorylated enzym

151 Because the formation of binary copper selenide impurities seemed to form more readily, two app

152 E. coli NifS-like protein could replace free selenide in the in vitro SPS assay for selenophosphate f

153 n cadmium carboxylate and trimethylphosphine selenide in the presence of an alcohol produces alkoxytr

154 The disappearance of tri-n-octylphosphine selenide in the presence of Cd-OA and Cd-ODPA can be fit

155 yl halides for the synthesis of alkyl phenyl selenides in moderate to excellent yields.

156 to give functionalized arylalkyl and diaryl selenides in moderate to excellent yields.

157 sphine selenide; 3, n-butyldiphenylphosphine selenide) in recrystallized tri-n-octylphosphine oxide w

158 brary of functionalized organo mono- and bis-selenides, including a potent biologically active molecu

159 is the first experimental study to report on selenide incorporation in iron monosulfide by a multi-ed

160 rmation of copper selenide (CuSe) and indium selenide (InSe) nanocrystals precedes the formation of C

161 on the less thermodynamically stable indium selenide (InSe) nanocrystals.

162 ort the superplastic deformability of indium selenide (InSe).

163 mbly systems organizes Fe(2+/3+) and sulfide/selenide into cuboidal [(Tp*)WFe(2)S(3)] or cubane [(Tp*

164 By contacting selenide ions with FeS in suspension, part of Se is loca

165 Specific incorporation of selenide is demonstrated by the formation of [WFe(3)S(3)

166 The phenyl selenide is rapidly converted to an electrophilic, allyl

167 Selenide is used as a surrogate for sulfide in cluster a

168 plane, as well as increased covalency of the selenide lattice which decreases the Ni(II) to Ni(III) o

169 e difference in compressibility in oxide and selenide layers.

170 citations of the heavily electron-doped iron-selenide material Li0.8Fe0.2ODFeSe (T c = 41 K).

171 These mesostructured semiconducting selenide materials are of the general formulae (CP)4-2xM

172 The pores of these sulfide and selenide materials preferentially absorb heavy metals.

173 backbones is described, which is based on a selenide-mediated cleavage of a backbone ester moiety.

174 novel route to fabricating crystalline zinc selenide microcylindrical resonators from our semiconduc

175 lts) and selenocyanates transfer the allylic selenide moiety to thiols giving primary allylic selenos

176 hat serves to passivate and dope the cadmium selenide nanocrystal channel layer.

177 Exposing lead selenide nanocrystal thin films to solutions containing

178 Metallic silver and semiconducting cadmium selenide nanocrystals are deposited to form high-conduct

179 ron transport in arrays of colloidal cadmium selenide nanocrystals capped with the molecular metal ch

180 Cuprous selenide nanocrystals have hallmark attributes, especial

181 t its application to the analysis of cadmium selenide nanocrystals produced in organic solvents.

182 stigated cation exchange reactions in copper selenide nanocrystals using two different divalent ions

183 A solution of cadmium selenide nanocrystals was used to print inorganic thin-f

184 in superlattices of cadmium selenide or lead selenide nanocrystals when the size of the gold nanocrys

185 ed quantum dots (zinc sulfide-capped cadmium selenide nanocrystals) into polymeric microbeads at prec

186 the carboxylate surface ligands from cadmium selenide nanocrystals, oleic acid impurities are first r

187 Here, we show that cadmium selenide nanocrystals, or quantum dots, can be integrate

188 The surface chemistry of cadmium selenide nanocrystals, prepared from tri-n-octylphosphin

189 ions and field-effect transistors on cadmium selenide nanocrystals.

190 the underlying mechanism by preparing copper selenide nanocubes in the presence of Al ions.

191 Stoichiometric copper(I) selenide nanoparticles have been synthesized using the h

192 Cadmium selenide nanoparticles, prepared by known methods, were

193 We demonstrated this concept in cadmium selenide nanorods with gold tips, in which the gold plas

194 ation in a new ferroic beta"-phase of indium selenide nanowires through the application of a direct-c

195 logy to nonstoichiometric copper sulfide and selenide NCs.

196 ype cores [W(2)Fe(6)S(6)Se(3)](1+), in which selenide occupies mu(6)-Se and mu(2)-Se sites.

197 tutional dopants in superlattices of cadmium selenide or lead selenide nanocrystals when the size of

198 Addition of sodium selenide or selenophosphate did not restore the catalyti

199 reduced when compared with the corresponding selenides or halides.

200 amounts of selenium in the form of phosphine selenides or selenoureas.

201 uced into various inorganic forms (selenite, selenide, or elemental Se) or partially incorporated int

202 res of diblock copolymers and either cadmium selenide- or ferritin-based nanoparticles exhibit cooper

203 composites of poly(3-hexylthiophene)-cadmium selenide (P3HT-CdSe) were synthesized by directly grafti

204 ve hot-electron transfer from colloidal lead selenide (PbSe) nanocrystals to a titanium dioxide (TiO2

205 exciton fission, at the interface with lead selenide (PbSe) nanocrystals.

206 current enhancement arising from MEG in lead selenide (PbSe) QD-based solar cells, as manifested by a

207 pt transition of the entire NC to the copper selenide phase, as manifested by a strongly sigmoidal re

208 xtracting indium from copper-indium-gallium- selenide photovoltaic cell (CIGS) leachates under low pH

209 tosis induced by the CH3SeH and the hydrogen selenide pools of selenium metabolites.

210 ly generated in a dinucleotide from a phenyl selenide precursor (4).

211 free, one-pot reaction using a new phosphine selenide precursor.

212 been conducted on materials based on cadmium selenide primarily due to its many years of development

213 structural characterization of three cadmium selenide QDs with uniform compositions (Cd35Se20(X)30(L)

214 from an artificial system--a single cadmium selenide quantum dot at room temperature.

215 of tri-n-octylphosphine oxide-capped cadmium selenide quantum dots (QCdSe) onto indium-tin oxide (ITO

216 he tri-n-octylphosphine oxide capped cadmium selenide quantum dots (QD) Langmuir monolayer.

217 synthesis of a size series of copper indium selenide quantum dots (QDs) of various stoichiometries e

218 structure of the atomically precise cadmium selenide quantum dots Cd35Se20X30L30, Cd56Se35X42L42, an

219 ecular vibrations to bulk phonons in cadmium selenide quantum dots for the first time.

220 e pair states in nearly monodisperse cadmium selenide quantum dots with radii ranging from 1 to 4 nan

221 nganese(II) spins in doped colloidal cadmium selenide quantum dots.

222 Se](2-), and Se(2-) ions, as well as dialkyl selenide (R(2)Se) and dialkyl diselenide (R-Se-Se-R) spe

223 ed benzoselenazolone as a novel bifunctional selenide reagent for both off- and on-DNA C-H selenylati

224 cardiography and observed in all assays that selenide reduced damage to the heart; selenite was not e

225 rconductivity in heavily electron-doped iron-selenide remains unclear.

226 In the present study, the selenide retention by coprecipitation with and by adsorp

227 , but only very scarce studies report on the selenide (Se(-II)) retention.

228 te that, on average, 21% of Se is present as selenide (Se(2-)) in pyrite and sphalerite, 19% of Se is

229 ible to nucleophilic attack and resulting in selenide (Se(2-)) release.

230 ansient absorption spectroscopy that cadmium selenide semiconductor nanoparticles, selectively excite

231 e colloidal synthesis of anisotropic cadmium selenide semiconductor nanorods can be extended to the s

232 Calculations on diethyl selenide show that the Se-Ge dative bond is slightly str

233 The loss spectrum of indium selenide shows the direct free exciton at 1.3 eV and sev

234 ms were transferred to nearby electron-dense selenide sites for H(2) formation and release.

235 00 to 773 kelvin, realized in hole-doped tin selenide (SnSe) crystals.

236 Among existing thermoelectrics, tin selenide (SnSe) has had particularly rapid development o

237 Nanocrystals of phase-pure tin(II) selenide (SnSe) were synthesized via a solution-phase ro

238 Single-crystal tin selenide (SnSe), a record holder of high-performance the

239 everal compositions of manganese-tin-bismuth selenide solid-solution series, Mn(1-x)Sn(x)Bi(2)Se(4) (

240 dot (QD) syntheses, pure tertiary phosphine selenide sources (e.g., trioctylphosphine selenide (TOPS

241 8 K), specifically in the magnesium scandium selenide spinel.

242 nd film of silver on the surface of the zinc selenide substrate.

243 terminates at residue 244, was analyzed for selenide-sulfide and disulfide linkages.

244 Mass spectrometric analysis indicated that a selenide-sulfide bond exists between Sec40 and Cys43.

245 The finding of a selenide-sulfide bond in the shortest isoform is compati

246 alyzed construction of sulfides, disulfides, selenides, sulfoxides and sulfones from unstrained keton

247 ced superconductivity in electron-doped iron selenide superconductor remains unclear.

248 Iron selenide superconductors exhibit a number of unique char

249 comparing the newly discovered alkaline iron selenide superconductors, which exhibit no Fermi-surface

250 Only selenide targets to injured tissue.

251 Selenide targets to reperfusing tissue and reduces reper

252 In contrast, several selenides that afford pincer selenuranes (e.g., 20 and 2

253 gold plasmon was strongly damped by cadmium selenide through interfacial electron transfer.

254 We synthesized thallium selenide (TlSe), which is comprised of intertwined stiff

255 this patterning technique, it is shown that selenide TMDs exhibit lower edge recombination velocity

256 gamma phosphate of ATP is transferred to the selenide to form selenophosphate, while ADP is hydrolyze

257 clooctatetraene (COT) and triphenylphosphine selenide to make (C5Me5)Gd(C8H8), [(C5Me5)2Gd]2Se2, and

258 carboxylate on a Cd(2+)-activated phosphine selenide to produce an acyloxytrialkylphosphonium interm

259 As expected, when oxidation of the selenide to selenoxide was attempted, in situ syn elimin

260 The primary oxidant for converting selenides to selenoxides was "Br(+)" produced initially

261 mpounds and in the oxidation of sulfides and selenides to sulfoxides and selenoxides.

262 ne selenide sources (e.g., trioctylphosphine selenide (TOPSe)) were surprisingly found to be unreacti

263 ested a mechanism whereby cells can overcome selenide toxicity.

264 to occur as a result of the binding between selenide trapped into the organic drop as selenium hydri

265 e oxidation of dimethyl sulfide and dimethyl selenide, two-electron oxidations, proceeds by an S(N)2-

266 is methodology results in vinylic halides or selenides under mild reaction conditions and tolerates a

267 such as CdTe and CIGS (copper indium gallium selenide) used in solar cells in just about a decade.

268 on the silver-catalyzed synthesis of diaryl selenides via a cross-coupling reaction of diaryl disele

269 two closely related metastable tin vanadium selenides via near-diffusionless reactions at low temper

270 ewly synthesized beta-disilanyl sulfides and selenides were determined by photoelectron spectroscopy.

271 Allyl selenides were found to be exceptionally reactive olefin

272 Phenylaminoethyl selenides were found to protect plasmid DNA from peroxyn

273 The selenides were synthesized pure by stoichiometric reacti

274 n-periodic chalcogenide flakes (sulfides and selenides) were considered.

275 ecule and a couple of analogues of bioactive selenides, were obtained in high yields by this protocol

276 conducting ammonia-rich intercalates of iron selenide which reversibly absorb and desorb ammonia arou

277 -VI2 semiconductor materials such as cadmium selenide, which exist as two stable phases, cubic and he

278 of selenium, is metabolized by the liver to selenide, which is the form of the element required for

279 s is in sharp contrast to bismuth doped lead selenide, which reaches a figure of merit of <1.

280 ncreased performance for antimony-doped lead selenide with a thermoelectric figure of merit of ~1.5 a

281 of an oligonucleotide containing the phenyl selenide with amino acids in the presence of mild oxidan

282 ypothesis, we have shown that replacement of selenide with NIFS and L-selenocysteine in the in vitro

283 Parent selenides with 3-hydroxypropyl or 2,3-dihydroxypropyl gr

284 manium or high-tin zeolite-type sulfides and selenides with four different topologies are reported.

285 amily of quasi-one-dimensional ferromagnetic selenides with general formula Fe(x)Pb(4-x)Sb(4)Se(10) (

286 nd subsequent reduction back to the original selenides with glutathione.

287 However, rates of oxidation of the selenides with H(2)O(2) under homogeneous or biphasic co

288 , highly ordered mesostructured platinum tin selenides with hexagonal symmetry were obtained using th

289 ment of the corresponding chloro sulfides or selenides with silver hexafluoroantimonate, followed by

290 ow-temperature synthesis of transition metal selenides with vast applications in nanotechnology, ther

291 ed selenium, selenite, and reduced selenium, selenide, would target to injured heart tissue in myocar

292 Crystalline semiconducting sulfide and selenide zeolite analogs were synthesized that possess f

293 We characterized water-soluble cadmium selenide-zinc sulfide quantum dots for multiphoton imagi

294 ayers (2D-WS2) and a single layer of cadmium selenide/zinc sulfide core/shell 0D-QDs.

295 The performance of cadmium-selenide/zinc-sulfide (CdSe@ZnS) quantum dots (QDs) and

296 Electrochemical detection of cadmium-selenide/zinc-sulfide (CdSe@ZnS) quantum dots (QDs) as l

297 alcium fluoride (CaF(2)) substrates and zinc selenide (ZnSe) prisms, respectively, for subsequent spe

298 ctron volts, are capped by an epitaxial zinc selenide (ZnSe) shell.

299 ed electrode array (IDA) patterned on a zinc selenide (ZnSe) substrate.

300 Fluorocarbon films were deposited onto zinc selenide (ZnSe) waveguides from plasma-polymerized penta