ライフサイエンスコーパス: anion exchange

1 be rendered water-insoluble through reverse anion exchange.

2 thelial differentiation, keratinization, and anion exchange.

3 thetic composition tuning through topotactic anion exchange.

4 lication in both heterogeneous catalysis and anion exchange.

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

6 reductive dissociation, which is followed by anion exchange.

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

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

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

10 readily achievable using typical methods of anion exchange.

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

12 The anion-exchange ability of layered double hydroxides (LDH

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

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

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

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

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

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

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

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

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

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

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

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

30 nated purified rat p67 with molecular sieve, anion exchange, and cation exchange chromatographic step

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

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

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

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

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

36 emonstrated for the detection of Tc-99 using anion-exchange beads mixed with scintillating beads and

37 ion; and hexavalent chromium detection using anion-exchange beads with spectroscopic detection.

38 r with negative slopes demonstrating typical anion exchange behavior.

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

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

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

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

43 in a conformation required for regulation of anion exchange by pHi.

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

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

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

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

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

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

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

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

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

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

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

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

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

59 High-pH anion exchange chromatography analysis of the resulting

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

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

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

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

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

65 prefractionation of serum proteins by batch anion exchange chromatography into three fractions: one

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

67 e pea leaf activity is mainly cytosolic, and anion exchange chromatography revealed multiple isoforms

68 Using anion exchange chromatography to fractionate a whole cel

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

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

71 Following purification by anion exchange chromatography using triethylammonium bic

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

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

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

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

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

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

78 essed and then separated by high-performance anion exchange chromatography with pulsed amperometric d

79 igosaccharides have been analyzed by high pH anion exchange chromatography with pulsed amperometric d

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

81 on scheme, preseparation elemental analysis, anion exchange chromatography, ad hoc selective precipit

82 y, endoarabinanase digestion, Dionex high pH anion exchange chromatography, and matrix-assisted laser

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

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

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

86 tized carbon or cellulose cartridge, high-pH anion exchange chromatography, fraction collection, and

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

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

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

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

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 ssing the recombinant VP1 protein using weak anion exchange chromatography.

96 ence of Nonidet P-40 with gel filtration and anion exchange chromatography.

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

98 ctric focusing electrophoresis and cation or anion exchange chromatography.

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

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

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

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

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

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

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

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

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

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

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

110 Here we report an optimized anion-exchange chromatography method with simplified cho

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

112 Anion-exchange chromatography was utilized for speciatio

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 After 5-10 microl serum was injected for anion-exchange chromatography, a stepwise gradient was a

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

117 When supernatants were examined by anion-exchange chromatography, the p-NPPC hydrolase acti

118 on of each polysaccharide can be purified by anion-exchange chromatography, the side group structures

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

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

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

122 be separated into its component proteins by anion-exchange chromatography.

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

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

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

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

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

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

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

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

131 Furthermore, after utilization of this anion-exchanging-column enrichment followed by LC/MS/MS

132 On a variety of commercial anion exchange columns, monovalent ClO4- elutes after do

133 Anion-exchange columns with bed volumes of 100-300 nL we

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

135 ge of the quantum dots is found to induce an anion-exchange effect on the sensor function, and theref

136 Anion exchange experiments confirmed the internal caviti

137 robust in certain cases, as demonstrated by anion-exchange experiments.

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

139 and characterized from LC-MS/MS of selected anion exchange fractions.

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

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

142 ontributes to pH sensor function by studying anion exchange function of AE2 mutants in which these an

143 enopus oocytes confirmed preservation of its anion exchange function.

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

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

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

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

148 alyloligosaccharides have been quantified by anion exchange high-performance liquid chromatography (H

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

150 Anion-exchange high-performance liquid chromatography (A

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

152 droxyproline from gelatin hydrolysates using anion-exchange high-performance liquid chromatography fo

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

154 otide P-diastereomers can be separated using anion exchange HPLC to yield diastereomerically pure pho

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

156 e purified with a three-step procedure using anion-exchange, hydrophobic interaction, and hydroxyapat

157 nclusion bodies and purified with sequential anion-exchange, hydroxyapatite, and size exclusion chrom

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

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

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

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

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

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

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

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

166 Anion exchange is also shown to selectively alter the so

167 h to enhancing the efficacy of liquid-liquid anion exchange is demonstrated.

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

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

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

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

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

173 pA-X support the hypothesis that synergistic anion exchange may be an important regulator in iron del

174 on uptake process, supporting the role of an anion exchange mechanism (SLCO/OATP-like transport) in G

175 ynthesis and core-shell formation through an anion-exchange mechanism was also studied.

176 o remove anionic contaminants mainly through anion exchange mechanisms.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

204 Single-bead anion exchange of plutonium at nanomolar and subpicomola

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

206 400 mum packed with 4 and 7 mum macroporous anion-exchange particles were investigated employing a c

207 has some commonality with the electroneutral anion-exchange pathway.

208 e observed that chromatography on pellicular anion exchange phases, but not on porous anion exchange

209 lar anion exchange phases, but not on porous anion exchange phases, completely resolves oligonucleoti

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

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

212 13.2 mS cm(-1) and represent a new class of anion-exchange polymers and membranes.

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

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

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

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

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

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

219 ransformations by employing either cation or anion exchange processes.

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

221 cies-specific differences in SLC26A6 oxalate/anion exchange properties as expressed in Xenopus oocyte

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

240 in Nhe1-null mice suggesting that increased anion exchange required carbonic anhydrase activity.

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

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

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

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

245 Anion exchange resin treatment is a commonly used techni

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

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

248 F2-Eu) with either TEVA resin or strong base anion-exchange resin (Dowex 1 x 8-400(Cl)).

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

250 l approximately 760 microm diameter AG 1 x 4 anion-exchange resin beads were determined using acousti

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

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

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

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

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

256 on of neutral to basic peptides by the added anion-exchange resin.

257 cation of large amounts of nucleotides using anion-exchanging resin but has shown the promise of enri

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

259 Anion exchange resins are important tools for the remova

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

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

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

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

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

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

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

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

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

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

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

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

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

273 predict the separation of peptides in strong anion exchange (SAX) chromatography using artificial neu

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

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

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

277 lbumin elimination exceeded that after batch anion exchange serum sample prefractionation.

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

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

280 arged sphingolipids were then partitioned by anion exchange solid phase extraction.

281 und-uridine were bottom-line separated on an anion-exchanging solid-phase extraction (SPE) column by

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

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

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

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

286 eads with reversed phase, cation-exchange or anion-exchange surfaces embedded in a Teflon mesh.

287 Unlike previous methods that use anion exchange to alter selectivity or enrich phosphopep

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

289 nomethylarsonic acid (MMA) were separated by anion exchange using carbonate-bicarbonate and NaOH elue

290 Anion exchange was confirmed by X-ray crystallography in

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