ライフサイエンスコーパス: anion

1 more than 20 times faster than the chloride anion.

2 e lactam ring, hydrogen bond to the chloride anion.

3 d state for the 19e(-) derivatized ferrocene anion.

4 tributor to the antidiabetic effects of this anion.

5 2,3-dimethyl-2-butene from a pinacolatoboryl anion.

6 case of the aromatic, but not the aliphatic, anion.

7 ation of the unpaired spins over the radical anions.

8 level understanding of specific effects for anions.

9 arallel beta-sheet dimer that binds chloride anions.

10 lting in decreased removal of the target oxo-anions.

11 ptors that can differentiate between the two anions.

12 y selectively, even in the presence of other anions.

13 strains the outward migration of bulk oxygen anions.

14 fers zwitterionic compounds over cations and anions.

15 of CH(4) and CO(2) mediated by single atomic anions.

16 s-often helical-that incorporate one or more anions.

17 amidal geometry with two coordinated nitrate anions.

18 quasi-permanent reorientations of PS(4)(3-) anions.

19 hment spectroscopies of cryogenically-cooled anions.

20 Upon incorporation of anions able to interact preferentially with some library

21 (1)) knot are found to selectively transport anions across phospholipid bilayers.

22 beta-elimination reaction, wherein the azide anion acted as the leaving group.

23 ne of the few inorganic materials with large anion adsorption capacity that stems from the presence o

24 ID) of the resulting demethylated PC product anions allows for the determination of the lipid fatty a

25 Recently, a series of isolable aluminium(I) anions ("aluminyls") have been reported, which offer an

26 An ion-exchange-HPLC (with anion and cation exchange columns) and an ICPMS/MS syste

27 t reduction in hydrogen peroxide, superoxide anion and malondealdehyde contents under stress conditio

28 nfestation significantly increase superoxide anion and malondialdehyde production to two-folds as com

29 Here we demonstrate that by using an anion and metal ion template, woven molecular 'tiles' ca

30 lecular polymers composed of custom-designed anion and receptor monomers and demonstrates the utility

31 the pentagonal bipyramidal [Mo(CN)(7) ](4-) anion and the Mn(II) unit with a tridentate ligand resul

32 ong interaction between the O(2-) of Li-salt anion and the surface oxygen vacancies of each oxide and

33 GSH because of increased availability of the anion and, depending on the electrophile, increased reac

34 ters (FNTs) selectively transport monovalent anions and are found in prokaryotes and lower eukaryotes

35 inity concentrations by detecting monovalent anions and cations.

36 In this protocol, metal-containing anions and layered double hydroxides are employed to con

37 polymers (IUPs) with high-density inorganic anions and narrowly distributed ultramicroporosity is re

38 es confirmed the involvement of aryl radical anions and proceeded via a single-electron-transfer (SET

39 the two framework-forming units, polyatomic anions and pyrazines, govern both diffusion and separati

40 enables the determination of cations and/or anions and the use of multiple detectors, which further

41 r cation), sulfate (a stabilizing Hofmeister anion), and urea (a neutral denaturant) alter the foldin

42 the radical anion to give a cyclohexadienyl anion, and finally regioselective protonation.

43 e data imply that glasses containing complex anions, and in which covalent network formation is minim

44 mistries and identify the effect of cations, anions, and Li/Na content on moisture stability.

45 PR/UV-Vis spectral studies revealed that the anion-anion bonding led to the formation of crystals com

46 velopment of the supramolecular chemistry of anion-anion dimers has led to applications in hierarchic

47 al Review will present evidence showing that anion-anion dimers of protic hydroxyanions can form read

48 ty of emerging functional materials based on anion-anion linkages.

49 xometalates (POMs) are molecular metal-oxide anions applied in energy conversion and storage, manipul

50 s in functional foldamers that bind a single anion are examined, including: induced chirality, stimul

51 Small anions are conducted through narrow tunnels in the intra

52 e electronic landscape when both cations and anions are considered as mobile.

53 Polysulfide anions are endowed with unique redox properties, attract

54 batteries (DIBs), in which both cations and anions are involved in the electrochemical redox reactio

55 ting versatility of the 9-borataphenanthrene anion as a ligand.

56 ic couplings for the highly delocalized P3DT anions as enabling the inverted behavior: The presence o

57 Thiocyanate anions at positively charged surface sites and negativel

58 synthesis of a cyclic (alkyl)(amino)aluminyl anion based on a five-membered framework.

59 ined were redistributed in favor of the best anion binders.

60 Anion binding by receptor molecules is a central field o

61 rucial: the demetalated catenane exhibits no anion binding in solution nor any transmembrane ion tran

62 olecular switch involving a highly conserved anion binding site in CK1.

63 light on the allosteric linkage between two anion binding sites that dynamically regulate kinase act

64 n we present the synthesis and evaluation of anion-binding properties of 12 new receptors from the un

65 For each mechanism, the oxo-anions, both target and competitors, are ranked in terms

66 The HE anion can be easily prepared in situ by reaction of the

67 Uncoupling protein 2 (UCP2), a mitochondrial anion carrier, is thought to separately modulate inflamm

68 A structure of the murine voltage-dependent anion channel (VDAC) was determined by microcrystal elec

69 ondrial membrane channels, voltage-dependent anion channel 1 and the mitochondrial calcium uniporter,

70 gulation of ATP release and volume-regulated anion channel activity and provide critical links among

71 nchoe fedtschenkoi, we found that guard cell anion channel activity, recorded under voltage clamp, fo

72 Here, using the human voltage-dependent anion channel as our template scaffold, we designed and

73 This particular anion channel gating mechanism predicts the existence of

74 anion pore and demonstrate the existence of anion channel gating processes outside the EAAT uptake c

75 We conclude that the diurnal cycle of anion channel gene transcription, rather than the physio

76 s Transmembrane Conductance Regulator (CFTR) anion channel is essential for epithelial salt-water bal

77 xistence of mutant transporters with changed anion channel properties, but without alteration in glut

78 chondrial DNA content, and voltage-dependent anion channel protein expression.

79 ctance regulator (CFTR) is a plasma membrane anion channel that plays a key role in controlling trans

80 rc8a) functionally encodes a swell-activated anion channel that regulates PI3K-AKT, ERK1/2, mTOR sign

81 ne product bestrophin-1, a Ca(2+) -dependent anion channel, interacts with Ca(V) 1.3 Ca(2+) channels

82 nductive pathway involving voltage-dependent anion channel-1 (VDAC-1) and by exocytosis of ATP locali

83 a, INSR interacts with the voltage-dependent anion channel-1 (VDAC1) in mitochondria and that INSR kn

84 ant OMM transporter is the voltage-dependent anion channel.

85 udies strongly suggest that EcYfdC is not an anion channel.

86 , an essential component of volume-regulated anion channels (VRAC), as a vital regulator of hypotonic

87 c channels, better known as volume-regulated anion channels (VRAC), as widely expressed cGAMP transpo

88 L46 is a pore-forming residue of the EAAT2 anion channels at the cytoplasmic entrance into the ion

89 uantify absolute open probabilities of EAAT2 anion channels from ratios of anion currents by glutamat

90 fibrosis transmembrane conductance regulator anion channels or proinflammatory cytokines might alter

91 Here, we examined the contribution of anion channels to cGAMP transfer and anti-viral defense.

92 ter increase ATP release by volume-regulated anion channels under hypotonic conditions.

93 described, this is most likely based on fast anion channels.

94 ased absolute open probability of L46P EAAT2 anion channels.

95 d unitary current amplitudes in mutant EAAT2 anion channels.

96 s was not affected by the presence of common anions (Cl(-), Br(-), NO(2)(-), NO(3)(-), SO(4)(2-), and

97 nsfer-independent nucleophilic ferric peroxo anion (compound 0, i.e. Fe(3) (+)O(2) (-)).

98 pHensor, reporting the dynamics of cytosolic anion concentration and pH to monitor the activity of At

99 s uniquely provided by the AOT approach: the anion concentration ratio from the spontaneous Raman spe

100 hese results reveal the potential of spatial anion control in transition-metal catalysis for the func

101 ueous solution has been studied depending on anion coordination and recognition by a larger host-cucu

102 the electron-poor aromatic ring to a radical anion, coupling of the radical and the radical anion to

103 nhancing cathode reversibility by preventing anion cross-over in aqueous electrolytes.

104 p recordings, we observed larger macroscopic anion current amplitudes for L46P than for WT EAAT2.

105 e found that extracellular Mal inhibited the anion current of Kalanchoe guard cells, both in wild-typ

106 ities of EAAT2 anion channels from ratios of anion currents by glutamate uptake currents.

107 ses prepared by topochemical reactions (e.g. anion deintercalation or anion-exchange) is extremely ch

108 4) compounds (as well as various cations and anions derived from these) are accessible in good yields

109 Their electrophilicity permits anion detection through addition reactions that disrupt

110 r the counter cation, indicating cations and anions diffused together to maintain charge neutrality.

111 While anion dimers are difficult to identify unequivocally in

112 stabilized by the configurational entropy of anion disorder across the terminal and bridging sites.

113 whereas the second encapsulated a series of anions, due to electronic and geometric effects.

114 ally overlapping cytosolic Ca(2+), H(+), and anion dynamics, but except for GSSG, only weakly affecte

115 tion of exocytosis compared with kosmotropic anions (e.g., Cl(-)).

116 With stimulation of chaotropic anions (e.g., ClO(4)(-)), the expansion and closing time

117 al-organic frameworks using a combination of anion effects and surface chemistry.

118 l characteristics of the three metal bromide anions enabled the single-crystalline "host-guest" syste

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

135 posing HCO(3) (-) efflux via the basolateral anion exchanger AE2; and (3) inhibits NaCl reabsorption

136 ncoded by SLC26A3, a key intestinal chloride anion exchanger, has recently been identified as a novel

137 on of the enriched population of [CL - H](-) anions facilitates the assignment of individual fatty ac

138 had reduced extracellular proton (H(+)) and anion fluxes, reduced cytosolic pH, reduced tip-to-shank

139 Anion foldamers are defined as single- or multistrand co

140 The emphasis of this review is on helical anion foldamers in solution, and many of the beautiful c

141 Back-electron transfer from the DCA radical anion followed by barrierless intramolecular proton tran

142 d in the [Ru(PPh(3))(C(6)H(4)PPh(2))(2)H](-) anion following the trend 2 (no interaction) < 1 < 3 < 4

143 o their potential to compete with target oxo-anions for sorption sites resulting in decreased removal

144 ctive radical cyclization event, followed by anion formation and quenching to produce a range of comp

145 intra- and extracellular superoxide radical anion ([Formula: see text]).

146 The distance between the anion framework and K(+) resembles a frustrated Lewis pa

147 tively charged electrode surface repels salt anions from the inner layer and results in an inner SEI

148 urinary or blood ketoacids; and 'A', a high anion gap metabolic acidosis.

149 negative ion mode, CID of mass-selected GPL anions generates fatty acyl carboxylate anions via fragm

150 on, adhesion, thrombus formation, superoxide anion generation, and surface activation marker expressi

151 The presence of three anions gives the new structure both the bridging selenid

152 In brief, deprotonated GSL anions, [GSL-H](-), and terpyridine-magnesium complex di

153 nkers, M(2) X(2) (BBTA) (M=metal, X=bridging anion, H(2) BBTA=1H,5H-benzo(1,2-d:4,5-d')bistriazole),

154 Moreover, the bromide anion had a clear catalytic template effect in the macro

155 ion reaction, and surprisingly, the chloride anion had a negative template effect in opposition to th

156 yet biologically critical hydrochalcogenide anions (HCh(-)).

157 s of carbon materials as the cation host and anion host are further revisited by elaborating the elec

158 lfide can lead to the formation of thiolated anions; however, their contributions to total element co

159 pecies, including singlet oxygen, superoxide anion, hydrogen peroxide, and hydroxyl radicals, to affo

160 lices exhibited reduced browning, superoxide anion, hydrogen peroxide, electrolyte leakage and malond

161 itterionic organocatalysts based on an amide anion/iminium cation charge pair were found to be effect

162 tial or simultaneous redox of the cation and anion in a transition metal oxide based cathode for a Li

163 hes a limiting description as a "free" boryl anion in the condensed phase.

164 ort the isolation of a derivatized ferrocene anion in the solid state as part of an isostructural fam

165 als a formal oxidation state of -2 for ozone anions in CaO(3).

166 re phase transitions, where the chalcogenide anions in the channels experience a distortion in the fo

167 anced HS(-) selectivity over other competing anions in this system.

168 The receptors strongly bind anions, in particular carboxylates, even in a highly com

169 0 mediated transport of picloram and several anions, including nitrate and chloride.

170 etal readily affords the corresponding tetra-anion instead of the expected aromatic dianion.

171 sustained by multiple [C-H...pai] and [C-H...anion] interactions in addition to hydrophobic effects.

172 ning the modified alpha-MoO(3) anode with an anion-intercalation graphite cathode, operating well ove

173 Carbonate radical anion is a potent one-electron oxidant capable of genera

174 The 9-borataphenanthrene anion is easily accessed by deprotonation of a 9,10-dihy

175 thesis of a bottleable nucleophilic aluminyl anion is feasible, a handful of derivatives have been de

176 Instead, carbonate radical anion is formed from the Fenton reaction under cellular

177 ermining step, in which the chiral phosphate anion is involved in stereoinduction.

178 crystallography, the highly contorted tetra-anion is stabilized by coordination of two internally bo

179 t 3d-metal SIM based on a nonlacunary Keggin anion is the foundation for a new research area in POM c

180 , and SrNi(4+) O(3) with holes on adjacent O anions is stabilized as a perovskite at the single-unit-

181 he solvent facilitated close approach of the anions leading to their mutual polarization.

182 re pyridine-initiated and p-toluenesulfinate anion-mediated activation of the allenyl sulfone analogo

183 s from Lambda-(S,S)-1(3+) 3Cl(-) by standard anion metathesis recipes (90-98% overall).

184 bilization between the alkane ligand and the anion microenvironment.

185 t was lined on the inner core with phosphate anions, {Mo(132)PO(4)}.

186 ing network polymer with weakly coordinating anion nodes that functions as a high-performing single-i

187 Overproduction of superoxide anion (O(2) (.-) ), the primary cellular reactive oxygen

188 ions, H(3)O(+), NO(+), and O(2)(+*), and the anions, O(-*), O(2)(-*), OH(-), and NO(2)(-), are discus

189 bis(silylene)-stabilized N(I) complex as an anion of 3 with the nido-C(2) B(10) cluster cage.

190 ecoil (8.7 angstrom) of Br observed from the anion of PeBr.

191 t shorter lifetime of the repulsive aromatic anion of PhBr is consistent with the observation of shor

192 produced by nano-ESI where A represents the anion of the electrolyte.

193 cited state of an isolated model chromophore anion of the photoactive yellow protein.

194 These were for ET from radical anions of polydecylthiophene (P3DT) to a series of accep

195 hat the peculiarities of the formation of DB anions of XS(-) can also be characteristic of many hundr

196 However, the nucleophilic attack of the anion on carbonates induces an oxidative breakdown at hi

197 ognized inhibitory effect by the carboxylate anion on the catalytic cycle, whereas 2-ethyl hexanoate

198 % and 92% in DMSO-d(6), respectively), their anions, on the other hand, preferred the anti conformer

199 identical and is not affected by the type of anion or by solution versus the surface chemistry.

200 liquid-free ionoelastomers, in which either anions or cations are fixed to an elastomer network and

201 petitive adsorption between co-occurring oxo-anions, overestimating realistic pollutant removal poten

202 ) complex also serves as a single phosphorus anion (P(-)) transfer reagent towards metal carbonyls an

203 The anion [P(4)O(11)](2-), employed as its bis(triphenylphos

204 tion between each target and competitive oxo-anion pair is classified.

205 roven valuable in sequencing oligonucleotide anions, particularly because it can retain modifications

206 Anion permeability depends both on how well CFTR channel

207 Glycine receptors (GlyRs) are anion-permeable pentameric ligand-gated ion channels (pL

208 netic) product for the three combinations of anions ((PF(6))(-)/(AsF(6))(-), (PF(6))(-)/(SbF(6))(-),

209 cessible following the discovery that chiral anion phase transfer catalysis by C(2)-symmetric phospho

210 ization of difluoroalkenes enabled by chiral anion phase-transfer catalysis.

211 Five "competing" co-occurring oxo-anions (phosphate, sulfate, bicarbonate, silicate, and n

212 [H(3)C-Pt-H(CO(2))](-) by a synergy between anion photoelectron spectroscopy and quantum chemical ca

213 Anions play a vital role in a broad range of environment

214 (6)(SO(4))(2) clusters, where the templating anion plays an integral structure-defining role.

215 portant determinant of the diameter of EAAT2 anion pore and demonstrate the existence of anion channe

216 ence the crucial role of specific asymmetric anion positioning on the lowering of the symmetry.

217 ly transformed at rates that depended on the anions present into colorless crystals with a blue emiss

218 Two of three known groups of anion pumps, the archaeal halorhodopsins (HRs) and bacte

219 produced, which then react with the luminol anion radical and significantly amplify the luminol ECL

220 tive radical species, we report that sulfite anion radical efficiently substitutes the three carboxyl

221 lphonic acid) (ABTS) to green color ABTS(.-) anion radical in the presence of hydrogen peroxide.

222 erties, photocatalytic ability in superoxide anion radical-mediated coupling of (arylmethyl)amines an

223 ly charged species, tetraiodo-p-benzoquinone anion radicals (I(4) Q(-.) ) and iodide anions, was obse

224 crystals comprising 2D layers of I(4) Q(-.) anion radicals linked by iodides and separated by Et(4)

225 ghly efficient transport of diverse types of anions, rather than cations, across lipid membranes.

226 ion for the design and development of future anion receptors and organocatalysts.

227 Supramolecular anion receptors can be used to study the molecular recog

228 ons for practical applications, carbon-based anion receptors have dominated this field, with main gro

229 the thermodynamic conformer of many of these anion receptors is not the dual-hydrogen-bond-facilitati

230 omers, which can be bound by photoswitchable anion receptors to form large bridged assemblies of appr

231 ctrochemical techniques can be used to study anion recognition processes (e.g., binding constant dete

232 the underlying features and relationship for anion redox and cationic redox to occur reversibly.

233 Oxygen-anion redox in lithium-rich layered oxides can boost the

234 he Fe-S interactions, followed by reversible anion redox: 2 S(2-)/(S(2))(2-).

235 In NbOFFIVE-1-Ni, (NbOF(5))(2-) anion reorientation locates propane away from the window

236 apping (tethering) mediated by the recursive anion(s) derived from pyrazolones.

237 he BNB-phenalenyl 7 (BMes, NMe), the radical-anion salt K[7(*)] was generated through chemical reduct

238 nging ability, reducing activity, superoxide anion scavenging ability, linoleic acid and plasma lipid

239 ids against oxidation and superoxide radical anion scavenging activity.

240 Ca(2+)-activated Cl(-) channel activity and anion secretion in human bronchial epithelial (HBE) cell

241 ransmembrane conductance regulator)-mediated anion secretion is an attractive therapeutic approach fo

242 lutamate/Na(+)/H(+)/K(+) transporters and as anion-selective channels.

243 etative insight into motif design for future anion-selective supramolecular receptors and highlight t

244 The anion selectivity of PAC is determined by the positively

245 on supramolecular chemistry, electrochemical anion sensing has received considerable attention in the

246 -N-arylsulfonamides with Hantzsch ester (HE) anion serving as the visible-light-absorbing reagent and

247 To concentrate the [CL - H](-) anion signal, multiple iterations of ion accumulation an

248 the new structure both the bridging selenide anion sites that connect pairs of Bi(2)O(2) layers in Bi

249 ctrolytes by designing a micro-heterogeneous anion solvation network.

250 mechanism by which NIS transports different anion substrates with different stoichiometries has rema

251 rongly basic NHC ligands and noncoordinating anions such as BAr(F)(4) catalyze the cis haloalkynylati

252 ity of GAC for glutamine, whereas activating anions such as P(i) increased this affinity.

253 Scavengers of superoxide radical anion (superoxide dismutase), hydrogen peroxide (catalas

254 Spurred on by significant developments in anion supramolecular chemistry, electrochemical anion se

255 rbonate is demonstrated as a beta-aminoethyl anion synthetic equivalent.

256 nylhydrazine serves as a beta-hydrazinoethyl anion synthetic equivalent.

257 e-bound state (QBS) in the tetracyanobenzene anion (TCNB(-)) using both photoelectron and photodetach

258 molecular strands within a discrete layer by anion-template metal-ion coordination opens the way for

259 ling more bis(trifluoromethanesulfonyl)imide anion (TFSI(-) ) to coordinate with Li(+) ions.

260 ion of the photocatalytic cycle generates an anion that undergoes a polar Truce-Smiles rearrangement,

261 Perchlorate and tosylate are minimally basic anions that are nevertheless suitable for removal of [(1

262 rmations via thiyl and disulfide monoradical anions that resemble a primary step of MCR's catalytic c

263 ge organic ligands, such as cyclopentadienyl anions, that tend to become embedded in the deposit duri

264 ion, coupling of the radical and the radical anion to give a cyclohexadienyl anion, and finally regio

265 responsible for high energy barriers for the anions to enter EcYfdC.

266 Using anions to induce molecular structure is a rapidly growin

267 ompetition between target and competitor oxo-anions to sorb on commonly used, nonselective, metal (hy

268 that the process requires tetrafluoroborate anions to template the assembly of the interwoven grid b

269 Advances in anion transport by synthetic supramolecular systems are

270 Anion transport experiments in POPC-based large unilamel

271 mics, fluorescence changes, organocatalysis, anion transport, and halogen bonding.

272 6 nm in helical height, exhibits the highest anion-transport activities for iodide (EC(50) =0.042 mum

273 Organic anion transporter 1 (OAT1), expressed at the basolateral

274 identified was SLC22A9 that encodes organic anion transporter 7 (OAT7).

275 e view of developing selective transmembrane anion transporters, a series of phosphonium boranes of g

276 The multispecific organic anion transporters, OAT1 (SLC22A6) and OAT3 (SLC22A8), t

277 xy)imines generates a delocalized 2-azaallyl anion-type nucleophile that engages in dearomative C-C b

278 ect the formation of an intermediate radical anion upon reaction of photogenerated holes with an elec

279 dary phases upon oxidation, thereby creating anion vacancies.

280 h tailored chemical treatments that mitigate anion vacancy formation and improve the performance of C

281 eve strain-induced creation and switching of anion-vacancy patterns in perovskite films.

282 ifying simple perovskite oxides with tunable anion-vacancy patterns through epitaxial lattice strain.

283 GPL anions generates fatty acyl carboxylate anions via fragmentation of ester bonds linking the fatt

284 none anion radicals (I(4) Q(-.) ) and iodide anions, was observed and characterized for the first tim

285 Weakly coordinating anions (WCAs) are generally tailored to act as spectator

286 as a major E,E,E isomer, while other studied anions were ineffective in this reaction.

287 -Glu) and an opportunistic ligand, a citrate anion, were determined.

288 deprotonation and exists as IO(3)(-)-IONO(2) anion, whereas the HIO(2)-IONO(2) complex does not exhib

289 d QDs strongly spin polarize the NDI radical anion, which is interpreted in the context of both the r

290 tion to the [RSNO-B(C(6) F(5) )(3) ] radical anion, which is susceptible to N-N coupling prior to los

291 ations are highly selective for the fluoride anion, which is transported more than 20 times faster th

292 Noncoordinating anions, which generally play a subordinate role in coord

293 nd more strongly to the host framework S(2-) anions, which in turn modulates the Li(+) ion potential

294 oduce a family of uranium-oxysulfate cluster anions whose hierarchical assembly in water is controlle

295 on, showing a unique chemical recognition of anions with low charge density.

296 The formation of DB anions with the cage structure has principal features, c

297 concentration bis(fluorosulfonyl)imide (FSI) anions, with sodium bis(trifluoromethanesulfonyl)imide (

298 the recognition of bromide and iodide halide anions, with the chalcogen bonding heteroditopic recepto

299 orters conduct or transport various kinds of anions, with the exception of fluoride, which acts as an

300 Upon the transition from XS to the DB anions XS(-), the unusual shortening of the internuclear