ライフサイエンスコーパス: anion exchange

1 e of energies (1.8-3.1 eV) via postsynthetic anion exchange.

2 en made to address this issue through chiral anion exchange.

3 cyanate, azide, cyanide, phenylsulfinate) by anion exchange.

4 thelial differentiation, keratinization, and anion exchange.

5 lication in both heterogeneous catalysis and anion exchange.

6 es provide insight into the mechanism of the anion exchange.

7 ecord water sorption capacities by employing anion exchange.

8 be rendered water-insoluble through reverse anion exchange.

9 readily achievable using typical methods of anion exchange.

10 thetic composition tuning through topotactic anion exchange.

11 reductive dissociation, which is followed by anion exchange.

12 The separation time of strong anion-exchange (2 mm column, flow rate 380 muL min(-1),

13 In addition, by measuring anion exchange activity of SLC26A1, we demonstrate that

14 By measuring AE1 anion exchange activity or cation leak, it is proposed t

15 tion of actin cytoskeletal reorganization by anion-exchange activity and intracellular pH, independen

16 Red blood cell Ae1-mediated anion-exchange activity and surface polypeptide expressi

17 We propose that reduced basolateral anion-exchange activity in A-ICs inhibits trafficking an

18 three beta-cyclodextrin polymers (CDPs), an anion-exchange (AE) resin, and a cation-exchange (CE) re

19 of mouse immunoglobulin genes using a strong anion exchange (AEX) resin.

20 VA for technetium and UTEVA for uranium) and anion exchange (AGMP-1 M for plutonium and neptunium) ch

21 The minor enrichment due to anion exchange alone (1.4 +/- 0.2 per thousand) was conf

22 etate film functionalized with strong cation/anion exchange and C8 resins, for interacting with both

23 rials with positive frameworks for selective anion exchange and separation or storage and delivery.

24 anions have many applications from sensing, anion exchange and separation, to fast ion conductivity.

25 ed from the latex of Euphorbia neriifolia by anion exchange and size-exclusion chromatography.

26 The aqueous phase was subjected to anion-exchange and cation-exchange/mixed mode chromatogr

27 A mixed-mode column that has both anion-exchange and reversed-phase properties was used in

28 Using anion-exchange and size exclusion chromatography, an inh

29 wo types of edge sites complexes, interlayer anion exchange, and CaMoO4 precipitation.

30 rich yeast using preparative size exclusion, anion exchange, and capillary reverse phase columns coup

31 s consisting of a reversed phase, mixed-mode anion exchange, and mixed-mode cation exchange sorbent c

32 chemistry and the dynamics of cage assembly, anion exchange, and other anion-induced structural trans

33 porating polar embedded reversed phase, weak anion exchange, and strong cation exchange material.

34 , which is contrast to the classical view of anion exchange as the primary retention mechanism.

35 isoforms, which is a major issue when using anion exchange-based resins.

36 and their utilization as a platform for the anion exchange-based separation process.

37 r with negative slopes demonstrating typical anion exchange behavior.

38 Notwithstanding, the anion exchange between CO3(2-)/HCOO(-) and OH(-) was fou

39 ntrations of hypothetical new compounds (via anion exchange between IL and ZDDP) on the fluid surface

40 ased on saponification, apolar adsorption or anion exchange, but most probably an adsorption mechanis

41 zation was also increased with inhibition of anion exchange by 4,4*-diisothiocyanostilbene-2,2*-disul

42 In this work, we show that the controllable anion exchange can be achieved in a dihalomethane soluti

43 te that these pcu MOFs are cationic and that anion exchange can be used to affect the MOF properties.

44 onation, on the basis of charge using strong anion exchange, can subsequently be applied.

45 g P-MOFs whose high stability, porosity, and anion-exchange capability allow immobilization of anioni

46 The typical anion exchange capacities were approximately 20 pequiv/m

47 After AS18 latex coating, the strong base anion exchange capacity was on the order of 10 pequiv/mm

48 maintaining and in some cases increasing the anion exchange capacity.

49 bon, effective cation-exchange capacity, and anion-exchange capacity was evaluated to determine sorpt

50 atographic strategy that uses a long (50 cm) anion-exchange capillary column operating in the electro

51 uding elution of the [(18)F]fluoride from an anion exchange cartridge with a basic solution of K(2)CO

52 was trapped on a quaternary methyl ammonium anion exchange cartridge, then allowed to react with BF3

53 s retained on the quaternary methyl ammonium anion exchange cartridge.

54 suitable for removal of [(18)F]F(-) from the anion-exchange cartridge.

55 [(18)F]F(-) is eluted from small (10-12 mg) anion-exchange cartridges with solutions of tetraethylam

56 mouse cerebral cortex using a combination of anion-exchange, charge-transfer, and size-exclusion chro

57 Here, we show that the anion-exchange chemistry can be precisely controlled in

58 Anion exchange chromatography (AEX) is an orthogonal sep

59 fractions were analyzed by high performance anion exchange chromatography (HPAEC) and were completel

60 A high performance anion exchange chromatography (HPAEC) coupled with pulse

61 High performance anion exchange chromatography (HPAEC) coupled with pulse

62 rates were quantified using high-performance anion exchange chromatography (HPAEC) with pulsed ampero

63 The method utilized a strong anion exchange chromatography (IEC) column in tandem wit

64 Second, monosaccharide analysis by high pH anion exchange chromatography and electrospray ionizatio

65 cLPMO9C were analyzed using high performance anion exchange chromatography and multidimensional mass

66 Following fractionation with sequential anion exchange chromatography and solid phase extraction

67 sing traditional centrifugation steps and/or anion exchange chromatography and their resulting surfac

68 rified from hot extracts by a combination of anion exchange chromatography and TLC, is a very polar a

69 In conclusion, we have demonstrated that anion exchange chromatography in combination with ultrah

70 udies may require removal of such species by anion exchange chromatography prior to mass spectral ana

71 combination of OFFGEL fractionation and weak anion exchange chromatography to separate the charge var

72 , it enables the separation of Cr species by anion exchange chromatography using a mobile phase which

73 Following purification by anion exchange chromatography using triethylammonium bic

74 MeSb) were separated in less than 8min using anion exchange chromatography with a Hamilton PRP-X100 c

75 ctions in plasma and urine were separated by anion exchange chromatography with a salt gradient of 0.

76 Bikunin has been isolated previously by anion exchange chromatography with a salt gradient up to

77 mination was carried out by high performance anion exchange chromatography with conductivity detector

78 In this study high performance anion exchange chromatography with conductometric detect

79 ice samples was examined by high performance anion exchange chromatography with pulsed amperometric d

80 , a high-throughput (5-min) high-performance anion exchange chromatography with pulsed amperometric d

81 hickpea legumin and vicilin were obtained by anion exchange chromatography, and were identified by ma

82 globin and human plasma, enriched using weak anion exchange chromatography, as this trisialylated fra

83 gnificantly less salt than comparable strong anion exchange chromatography, facilitating NMR detectio

84 ered Pichia pastoris broth to homogeneity by anion exchange chromatography, His-Trap affinity chromat

85 ycans in T cells in vivo as shown by high pH anion exchange chromatography, MALDI-TOF mass spectrosco

86 otocol involved several steps including weak anion exchange chromatography, ultrafiltration, and soli

87 purity was increased from 54.5% to 97.1% by anion exchange chromatography, with a recovery of 42.0%.

88 line hydrolysis followed by High Performance Anion Exchange Chromatography-Pulsed Amperometric Detect

89 y tris buffer, and purified and separated on anion exchange chromatography.

90 ctric focusing electrophoresis and cation or anion exchange chromatography.

91 ination of strong cation exchange and strong anion exchange chromatography.

92 NHS)-ester and fractionated the sample using anion exchange chromatography.

93 m sulfate fractionation, gel filtration, and anion exchange chromatography.

94 g DNA and proteins were removed using strong anion exchange chromatography.

95 hy (SEC-ICP-sfMS), with possible addition of anion exchange chromatography.

96 Protein samples are separated by 1D anion-exchange chromatography (AEX) with an eight-step s

97 body was separated into several fractions by anion-exchange chromatography (AEX), which is an importa

98 hilic interaction chromatography (ERLIC) and anion-exchange chromatography (AEX).

99 An accurate high-performance anion-exchange chromatography (HPAEC) method is presente

100 metabolomics workflow was established using anion-exchange chromatography (IC) coupled to high-resol

101 Removal of fibronectin through anion-exchange chromatography abrogated V2-independent g

102 Epitope detection in association with anion-exchange chromatography analysis indicates that in

103 entin matrix protein-1-enriched fractions by anion-exchange chromatography and analyzed by SDS-PAGE,

104 s purified, using fractionation, followed by anion-exchange chromatography and then characterised.

105 nara cardunculus by combining diafiltration, anion-exchange chromatography and ultrafiltration.

106 r plants were separated and quantified using anion-exchange chromatography coupled to inductively cou

107 Using high-performance anion-exchange chromatography coupled with pulsed ampero

108 th a Hyp-Gal standard after high performance anion-exchange chromatography fractionation.

109 A one-step anion-exchange chromatography method (NaCl gradient elut

110 In this report, a high-performance anion-exchange chromatography method with pulsed amperom

111 New anion-exchange chromatography methods linked to inductiv

112 m Phaseolus vulgaris cv. 'King Pole Bean' by anion-exchange chromatography on Q Sepharose and FPLC-ge

113 (XOS), and AXOS by applying high-performance anion-exchange chromatography with pulsed amperometric d

114 High-pH anion-exchange chromatography with pulsed amperometric d

115 ied endoxylanase III and analyzed by high-pH anion-exchange chromatography, only two oligosaccharides

116 High-performance anion-exchange chromatography-pulse amperometric detecto

117 e peaks that overlap in the high-performance anion-exchange chromatography-pulsed amperometric detect

118 vel using ammonium sulfate precipitation and anion-exchange chromatography.

119 a divalent metal chelation disk followed by anion-exchange chromatography.

120 nd arrestin-containing complexes purified by anion-exchange chromatography.

121 tively coupled plasma mass spectrometry with anion-exchange chromatography.

122 ssisted sample preparation with an automated anion exchange column separation and detection using a f

123 tions of oligonucleotides and proteins on an anion exchange column was developed.

124 g fast-protein liquid chromatography with an anion-exchange column and examined the distribution of L

125 High-performance anion-exchange column chromatography revealed HM-3A a gl

126 The Pu recoveries from 400 muL anion-exchange column separation sequences were 89% and

127 , wet ash, iron hydroxide precipitation, and anion-exchange column separations.

128 hy as the first separation step, followed by anion-exchange column separations.

129 The light-controlled anion exchange demonstrated here can be utilized to patt

130 Anion exchange experiments confirmed the internal caviti

131 Here, we introduce the use of an anion-exchange filter paper (as a replacement for standa

132 framework, both materials display reversible anion exchange for a variety of inorganic species.

133 This process is triggered by an anion exchange from 1[SO4] to 1[BF4].

134 Upon undergoing a second anion exchange, from 1[BF4] to 1[SO4], the cage, togethe

135 enopus oocytes confirmed preservation of its anion exchange function.

136 -methyldi-n-octylamine (MDOA) to serve as an anion exchange group.

137 A chromatographic method based on anion exchange has been optimized to separate and quanti

138 A thermochemical analysis of synergistic anion exchange has been provided for the first time, res

139 o RNAi duplex guide strands was coupled with anion exchange high performance liquid chromatography to

140 ted oligosaccharides are confirmed by strong anion exchange high-pressure liquid chromatography, elec

141 Anion-exchange high-performance liquid chromatography (A

142 plementation of EDTA, and rapid analysis via anion-exchange high-performance liquid chromatography co

143 Using anion-exchange high-pressure liquid chromatography (HPLC

144 aphosphates are purified by reverse phase or anion exchange HPLC, yielding triethylammonium or ammoni

145 ysis of the gastrointestinal hydrolysates by anion exchange HPLC-ICP-MS showed that the bioaccessible

146 Inhibitors of pendrin anion exchange identified in a small molecule screen inc

147 Conversely, anion exchange in Bi is rapid (kassoc = 13.1 +/- 0.4 M(-

148 f two distinct mechanisms of exchange during anion exchange in CsPbX3 nanocrystals (NCs), ranging in

149 Anion exchange in Pi is slow, taking days to equilibrate

150 th the protein kinase A inhibitor H89 or the anion exchange inhibitor 4,4'-diisothiocyano-2,2'-stilbe

151 exchange sorbent providing additional strong anion exchange interaction sites (Oasis MAX).

152 We also show that anion exchange is a dynamic process that takes place in

153 This anion exchange is accompanied by a metal-to-insulator cr

154 Anion exchange is also shown to selectively alter the so

155 cal reactions (e.g. anion deintercalation or anion-exchange) is extremely challenging as these low-te

156 We report the quantitative imaging of anion exchange kinetics in individual single-crystalline

157 n tubular ion chromatograph (OTIC) that uses anion exchange latex coated 5 mum radius silica and 9.8

158 s selectively separated and determined using anion exchange LC-ICPMS.

159 c interaction chromatography (ERLIC) with an anion-exchange material, the C-terminus of the peptides

160 e found widespread application as catalysts, anion exchange materials, fire retardants, and nano-fill

161 e often preferentially sorbed by traditional anion-exchange materials.

162 by enrichment of glycopeptides through mixed anion exchange (MAX) method, and then the flow-through p

163 ral (HLB), cation-exchanging (MCX, WCX), and anion-exchanging (MAX, WAX) OASIS polymers have been stu

164 and micrometer sizes can be seen as a simple anion exchange mechanism without dissolution-recrystalli

165 o remove anionic contaminants mainly through anion exchange mechanisms.

166 henesulfonamide, PDSinh-C01, inhibited Cl(-)/anion exchange mediated by mouse pendrin with a 50% inhi

167 d exchange of anions in a candidate alkaline anion exchange membrane (AAEM) material for alkaline fue

168 An anion exchange membrane (AEM) and catalyst layer ionomer

169 By a smart selection of membranes [anion exchange membrane (AEM) with a cation exchange mem

170 in alkaline media is critical for developing anion exchange membrane electrolyzers.

171 ined within the cathode catalyst layer in an anion exchange membrane fuel cell is critical for a func

172 r several electrochemical devices, including anion exchange membrane fuel cells (AEMFCs).

173 In anion exchange membrane fuel cells, catalytic reactions

174 dic chamber from which anions flux across an anion exchange membrane into an anodic chamber, resultin

175 onfocal Raman depth profiles of the AEM/CEM (anion exchange membrane/cation exchange membrane) interf

176 Alkaline anion-exchange membrane (AAEM) fuel cells have attracted

177 nd Tris and ethylenediamine buffers using an anion-exchange membrane (AEM) -based cation suppressor.

178 om suspensions of two soils (low P) using an anion-exchange membrane (AEM) and from a third soil (hig

179 Briefly, CRE diffuses through an anion-exchange membrane (AEM) from a sample contained in

180 study, the preparation of a new, functional anion-exchange membrane (AEM), containing guanidinium gr

181 with a cation-exchange membrane (CEM) and an anion-exchange membrane (AEM), respectively.

182 ) by a cation-exchange membrane (CEM) and an anion-exchange membrane (AEM).

183 s by a cation-exchange membrane (CEM) and an anion-exchange membrane (AEM).

184 d cell that employs an Zn metal anode and an anion-exchange membrane as the separator, which yields a

185 ompared to those of a commercially available anion-exchange membrane bearing conventional quaternary

186 types of cation-exchanger membranes and one anion-exchange membrane were characterized, and potentio

187 aCl supporting electrolytes using a low-cost anion-exchange membrane.

188 Alkaline anion exchange membranes (AAEMs) are an important compon

189 evaluated as a functional group for alkaline anion exchange membranes (AAEMs).

190 Anion exchange membranes (AEMs) find widespread applicat

191 ationic moieties are a critical component of anion exchange membranes (AEMs) in alkaline fuel cells (

192 Here we present the first metal-cation-based anion exchange membranes (AEMs), which were synthesized

193 y has played a prominent role in research on anion exchange membranes for use in alkaline electrochem

194 -opening olefin metathesis route to alkaline anion exchange membranes via the copolymerization of a t

195 n), hydroxide conducting membranes (alkaline anion exchange membranes, AAEMs) have been relatively un

196 The development of polymeric anion-exchange membranes (AEMs) combining high ion condu

197 The development of cationic polymers for anion-exchange membranes (AEMs) with high alkaline stabi

198 ted to construct metallo-polyelectrolytes as anion-exchange membranes in solid-state alkaline fuel ce

199 nt of highly conductive and thermally stable anion-exchange membranes is unambiguously a principal re

200 r to establish the limitations of commercial anion-exchanging membranes, using chronopotentiometry as

201 ated from matrix elements by using either an anion exchange method or solvent extraction, and was ana

202 five sorbent materials: two commercial weak anion-exchange mixed-mode sorbents (Strata X-AW and Oasi

203 e charge inversion on the positively charged anion exchange nanomembrane upon hybridization of negati

204 ange (OTIE) column by coating a monolayer of anion exchange nanoparticle to a 16-20 mum bore polymeth

205 acids based on an ionic diode feature of an anion exchange nanoporous membrane under DC bias.

206 We present here anion-exchange nanospheres as novel titration reagents f

207 ecord capacity and kinetics via the complete anion exchange of a cationic metal-organic framework.

208 replacing oxido donors with sulfido donors), anion exchange of bridging ligands (considering mu-Br(-)

209 introduces a new and convenient way for the anion exchange of viologen systems by utilizing methyl t

210 400 mum packed with 4 and 7 mum macroporous anion-exchange particles were investigated employing a c

211 e have systematically observed a symmetrical anion exchange pathway on the nanoplates with dependence

212 The hydroxide anion exchange polymer is a key component of any solid p

213 ented in this study can be extended to other anion-exchange polymer chemistries and, therefore, offer

214 benzimidazolium hydroxide and its analogous anion-exchange polymer is reported for the first time.

215 ly protected poly(arylimidazolium) hydroxide anion exchange polymers that possess a combination of hi

216 13.2 mS cm(-1) and represent a new class of anion-exchange polymers and membranes.

217 enes constitute a new class of alkali-stable anion-exchange polymers and membranes.

218 al-organic framework composite with flexible anion-exchange polymers threaded within the host cavity

219 en C4P and Aliquat 336 is so pronounced that anion exchange prefers chloride over more extractable ni

220 sed on both hydrophilic interaction and weak anion exchange principles, allowing it to target glycope

221 The column-based anion exchange procedure separates the pertechnetate fro

222 Moreover, an anion exchange process on both CaAl LDHs was followed by

223 ransformations by employing either cation or anion exchange processes.

224 sation of organoalkoxysilanes and subsequent anion exchange produces organosiloxane supramolecular li

225 The anion-exchange properties of SCU-8 were explored with ma

226 performed using cation exchange (silica) and anion exchange (propylamine) guard columns connected in

227 ng domain with the cytoplasmic domain of the anion exchange protein (AE1) and via its spectrin bindin

228 rter) and then GLUT2 and GLUT4, the red cell anion exchange protein (Band 3), asialoglycoprotein rece

229 mediated disruption of the major erythrocyte anion exchange protein, band 3.

230 Herein we present a simple anion-exchange protocol that allows the dissolution in w

231 sess the unique capability of post-synthesis anion exchange providing facile tunability of the optica

232 location of the linkage in the RNA isomer by anion exchange purification and electrospray ionization

233 The high anion exchange rate of (Zn,Cu) hydroxy nitrate HDS drive

234 e growth of a thin oxide shell, we study the anion exchange reaction in the CsPbX(3) perovskites nano

235 t interface through the precisely controlled anion exchange reaction, offering a design protocol for

236 A higher MABr concentration enhances I-Br anion exchange reaction, yielding poorer device performa

237 ptical properties can be readily tuned by an anion-exchange reaction with good morphology preservatio

238 The possibility to perform an anion-exchange reaction within the layer was demonstrate

239 to be the only known system where cation and anion exchange reactions can be sequentially combined wh

240 host-compounds is easily adjusted by simple anion exchange reactions so that the compounds can be ma

241 We demonstrate that, via controlled anion exchange reactions using a range of different hali

242 Additionally, it is able to undergo anion-exchange reactions with small ions such as carbona

243 tion can be independently controlled through anion-exchange reactions.

244 e of intracellular pH in osteoclasts through anion exchange regulates the actin superstructures requi

245 he samples by ion exchange chromatography on anion exchange resin AG 1-X4 with NH4NO3 and measured by

246 Synthesis of scintillating anion exchange resin consisted of diffusing a fluor, 2-(

247 this research was to develop a scintillating anion exchange resin selective for monitoring (129)I at

248 s added to anoxic extractions using a strong anion exchange resin to separate dissolved U(IV) and U(V

249 Anion exchange resin treatment is a commonly used techni

250 lammonium chloride) (polyDADMAC) polymer, or anion exchange resin were examined.

251 nventional TIMS involving Pu purification by anion exchange resin.

252 esin, PPL- and C18 - SPE cartridges, and one anion exchanging resin-diethylaminoethyl (DEAE) -cellulo

253 ists of a packed bed containing a mixture of anion-exchange resin and scintillating plastic beads.

254 )Lmol(-1)cm(-1)), fixed on a Dowex 1-X8 type anion-exchange resin for 10mL, 100mL, 500mL, and 1000mL,

255 Chromate is retained on the anion-exchange resin from water at parts-per-billion lev

256 ped flow-cell system utilizing scintillating anion-exchange resin.

257 he water sample and the concentration on the anion-exchange resin.

258 gnificantly with pertechnetate uptake on the anion-exchange resin.

259 his study examined removal of anionic OCs by anion exchange resins (AXRs) as a promising alternative.

260 Anion exchange resins are important tools for the remova

261 However, spent anion exchange resins are themselves regenerated using b

262 for the pretreatment and appropriate use of anion exchange resins by drinking water utilities and fo

263 ng water utilities and for the production of anion exchange resins by manufacturers.

264 EDTA binding to the anion exchange resins could saturate the resin, decrease

265 In bench-scale batch and column experiments, anion exchange resins from a large, representative group

266 Most importantly, the mixed bed of anion exchange resins is self-regenerated with the rejec

267 an appropriate mixture of self-regenerating anion exchange resins that selectively remove and replac

268 Both strong (Q) and weak (DEAE) anion exchange resins were found to adsorb surprisingly

269 riately designing or tuning the mixed bed of anion exchange resins, the process can be extended to ne

270 Using anion exchange resins, we also found that a significant

271 eters were determined for five commonly used anion exchange resins.

272 helix (TMH) domain, as compared with strong anion exchange (SAX) and strong cation exchange (SCX) St

273 opeptide enrichment strategy based on strong anion exchange (SAX) chromatography (UPAX), which permit

274 g cartridges containing materials for strong anion exchange (SAX) chromatography increased yield and

275 ion separations have been achieved by strong anion exchange (SAX) chromatography on Propac PA1 and ce

276 ared mixture of C18, strong cation (SCX) and anion exchange (SAX) sorbents in the ratio 2/1.5/1.5 (w/

277 Weak anion-exchange (WAX) and strong anion-exchange (SAX) columns were compared, with both pe

278 id chromatography (HILIC), strong cation and anion exchange (SCX, SAX), and mixed-mode separations.

279 quence did not interfere with the subsequent anion-exchange separation when a simple wet ash step was

280 henyl-Hexyl column, to accomplish mixed-mode anion-exchange separations, which results in increased r

281 selectivity are the presence of a rigid weak anion-exchange site and a H-donor site separated from ea

282 Additionally, incorporation of the weak anion-exchange site into a cyclic ring structure provide

283 e conclude that having guanidinium groups as anion-exchange sites improves the selectivity of AEMs.

284 (AEM), containing guanidinium groups as the anion-exchanging sites (Gu-100), is described as well as

285 ical Integrative Sampler (POCIS) with a weak anion exchange sorbent as a receiving phase.

286 face area (Chromabond HR-X) and a mixed-mode anion exchange sorbent providing additional strong anion

287 g a solid-core particle column containing an anion exchange stationary phase.

288 ad in scope, and does not require a separate anion exchange step to install the trifluoroacetate grou

289 DON species, an XAD-8 resin coupled with an anion exchange treatment was employed prior to chemical

290 rformance liquid chromatography (UPLC), weak anion exchange-UPLC, and lectin histochemistry.

291 A weak anion exchange (WAX) chromatography method coupled to on

292 In the present study, weak anion exchange (WAX) is evaluated for the enrichment of

293 raction (RP-SPE) and use of a polymeric weak anion exchange (WAX-SPE) resin.

294 Weak anion-exchange (WAX) and strong anion-exchange (SAX) col

295 Two anion receptors enhance liquid-liquid anion exchange when added to quaternary alkylammonium ch

296 id scintillation counting, and scintillating anion exchange with a flow-cell detection system for a s

297 The subsequent anion exchange with OH(-) further leads to a porous netw

298 Anion exchange with S was performed on ZnO colloidal nan

299 developing a microkinetic description of the anion exchange, with implications not only for understan

300 e varied all the way to CsPbBr3 or CsPbI3 by anion exchange, with preservation of the size and shape