ライフサイエンスコーパス: anion

1 d) or stepwise manner (weak acid then strong anion).

2 using an ionic liquid having a preorganized anion.

3 7 degrees C or in the presence of superoxide anion.

4 nate, and activated water in the imidazolate anion.

5 ion of the stable radical to its diamagnetic anion.

6 of virus, type of salts in solution (cation, anion.

7 oavailability by forming toxic peroxynitrite anion.

8 luding an ammonium cation group and a halide anion.

9 gen radical moiety Fe(III)-N. and a phenoxyl anion.

10 M without any interference from other tested anions.

11 by the crystal chemistries of the available anions.

12 intained a high selectivity for cations over anions.

13 of the binding units in the presence of the anions.

14 ts ability to bind alpha,omega-dicarboxylate anions.

15 arbanions, e.g., Meldrum's acid and dimedone anions.

16 kable progress in the binding and sensing of anions.

17 rs and are therefore rather inaccessible for anions.

18 cept of "dipole-discriminating electrophilic anions."

19 on of the neutral forms led first to radical anions (2(*-) and 3(*-)) and then to a bis(radical anion

20 ide 4, and sulfonyl-substituted chloromethyl anion 5.

21 couple that recombines either as a peroxide anion 7' to afford the aldehyde-to-carboxylic acid produ

22 including KCC2, and extracellular impermeant anions ([A]o) of the extracellular matrix are both propo

23 These robust asymmetric anion-accelerated amino-Cope enabled cascades open the d

24 Patients with lactic and unmeasured anions acidosis, but not those with hyperchloremic acido

25 compressibility, suggesting that the hydride anions act as pi-blockers.

26 he thiyl radical generated from the thiolate anion adsorbed on a CdSe QD plays a key role by abstract

27 We described the observations in terms of anion adsorption and surface oxidation/reduction.

28 ichael acceptors and their calculated methyl anion affinities, particularly when solvation by dimethy

29 in the relationship between pKa and chloride anion affinity of these receptors that will be important

30 the different hydrophilic characters of the anions allied to the hydration of the binding units in t

31 chemical diversity offered by the additional anion allows the integration of two common structural un

32 ogen bond-stabilization of the pyrazine (Pz) anion, an unstable anion in isolation due to its neutral

33 with a trifunctional column, combining RPLC, anion and cation exchange, which allows the simultaneous

34 Our results demonstrate how control of anion and cation order at the nanoscale can be utilized

35 ed on the vibrational modes of a coordinated anion and compare reactivities of various iron(IV)-oxo c

36 FVPY) were found able to scavenge superoxide anion and hydroxyl radicals, organic nitro-radicals (ABT

37 Finally, the chemically generated radical anion and polyanion states, Xn-Hex(*-) and Xn-Hex(n(*-))

38 annihilation of the electrogenerated radical anion and radical cation.

39 n the oxidized photocatalyst and the bromide anion and thus the ability to realize a controlled radic

40 d along the pore that interact with permeant anions and affect anion selectivity, as well as seven po

41 atile sulphur compounds, mercaptans, metals, anions and cations.

42 The NSP4 VPD was selective for cations over anions and channel activity was observed to have both we

43 l X-ray structures of three of their radical anions and of three of their dianions were obtained.

44 through its reconfigurable network of mobile anions and restrict polysulfide diffusion from mesoporou

45 s all predict linear geometries for both the anions and the neutral radicals.

46 tion between the H-bonding properties of the anions and the pKa values of the conjugate acids.

47 quantifying 53 metals, 12 organic acids, 14 anions, and 3 sugars.

48 The SICA effect is primarily determined by anions, and cations exhibit a secondary effect that modu

49 ortality of patients with lactic, unmeasured anions, and hyperchloremic metabolic acidosis with that

50 binding toward the spherical F(-) and Cl(-) anions, and the linear CN(-) (log Kass = 3.46, 3.50, and

51 elf-templated strategy, including sequential anion- and cation-exchange reactions, integrates two dis

52 of complexes formed from anti-electrostatic anion-anion homodimers of organophosphates and cyanostar

53 [Cs(crypt)](+) salts of the [Sc(NR2 )3 ](-) anion are formed, respectively.

54 nd multiple active sites in the preorganized anion are the driving force for the superior CO2 capacit

55 All of the anions are highly energetic.

56 These computational results reveal that PFOS anions are immobilized in SCU-8 by driving forces includ

57 phingomyelin (SM) cations with dicarboxylate anions are shown to charge-invert the positively charged

58 Superoxide anion as a primary member of reactive oxygen species, ha

59 /or sodium-driven transport of (14C)-citrate anion, as well as the organic monovalent cation, ethidiu

60 the transferability of H-bond parameters for anions between different solvents and different HBD part

61 uted compounds where the complex borohydride anion, BH4(-), is replaced by another anion, i.e. a hali

62 However, their potential in solution-phase anion binding applications is only just beginning to be

63 putational studies demonstrate that fluoride anion binding is assisted by the formation of a C-HF hyd

64 e-step process, and was investigated for its anion binding properties by (1)H NMR titrations, 2D NOES

65 Anion binding studies reveal that 2 readily binds a fluo

66 , unprecedented charge-assisted ChB-mediated anion binding was also studied in aqueous solvent mixtur

67 h a strong, localized positive potential for anion binding.

68 gen = Se, Te) motif as a novel ChB donor for anion binding.

69 The anion-binding catalysis results from a pair of triazoliu

70 The aminocatalysis and anion-binding catalysis sites of the dual-function rotax

71 part of the heavy chain, the gamma-loop, and anion-binding exosite 1, the main allosteric binding sit

72 tive sites of C1s and MASP-2, as well as the anion-binding exosites of the enzymes via sulfotyrosine

73 rylene diimide (PDI) unit and two triazolium anion-binding motifs, mechanically bonded with two small

74 rtantly, unprecedented solvent-dependent and anion-binding-induced circumrotatory motion in a hetero[

75 was also found to bind two dianionic sulfate anions bridged by two water molecules in the solid state

76 udies reveal that 2 readily binds a fluoride anion by formation of a unique B-FH-O-B hydrogen bond.

77 The recognition of anions by designed receptors has attracted much attentio

78 Trifluoroacetate (TFA) is a strong anion byproduct of solid-phase peptide synthesis.

79 strate, for the first time, that the TcO4(-) anion can be incorporated into the sodalite structure.

80 The high selectivity of Cl(-) anions can be attributed to the higher binding constant

81 then discuss a number of processes by which anions can be created and destroyed in these environment

82 The coordinated anions can drastically affect the reactivity of the comp

83 Advances in the design of small molecule anion carriers are reviewed in addition to advances in t

84 For certain substrate classes, the chiral anion catalysts were modulated to minimize the formation

85 their diverse applications in catalysis; as anion, cation, and neutral substrate receptors; as ligan

86 A new family of mixed anion cesium rare earth silicates exhibiting intense sci

87 athways (NPP) including a Plasmodium surface anion channel (PSAC).

88 ABSTRACT: The volume-regulated anion channel (VRAC) is the ubiquitously expressed verte

89 inducer, overexpression of voltage-dependent anion channel 1 (VDAC1) induced Parkin translocation to

90 lycine directly bounded to voltage dependent anion channel 1 (VDAC1) on the mitochondrial outer membr

91 ns, including the abundant voltage-dependent anion channel and the cation-preferring protein-conducti

92 smembrane conductance regulator (CFTR) is an anion channel evolved from an ATP-binding cassette trans

93 The QUAC1/ALMT12 anion channel heterologous expressed in oocytes was gate

94 the ubiquitously expressed vertebrate Cl(-) /anion channel that is composed of proteins belonging to

95 d ligand in the IMP, mouse voltage-dependent anion channel-1 (mVDAC1), and top-down MS confirmed a si

96 ion of iChS by chemical modifications favors anion channeling at the expense of substrate transport,

97 Natural anion channelrhodopsins (ACRs) discovered in the cryptop

98 s appear, including with the plasma membrane anion channels and H(+)-ATPase and with the tonoplast TP

99 Twelve subunits are predicted to form anion channels gated by gamma-aminobutyric acid (GABA),

100 malate transporters (ALMTs) form a family of anion channels in plants, but little is known about most

101 ion and the molecular constituents of native anion channels in vivo.

102 the first identified auxiliary subunits for anion channels.

103 ition to advances in the design of synthetic anion channels.

104 applied for the electrochemical detection of anions (Cl(-), SO4(2-), and Br(-)) in a highly diluted w

105 used a case study focused on the perchlorate anion (ClO4(-)) to highlight the value of the AOP framew

106 this process produces polycation-surfactant anion coacervates that entrain the agent and enhance its

107 the TOTA(+) making pi-contact with cyanostar-anion complexes.

108 charge density and/or mobile cation (and/or anion) concentrations alter the localization and functio

109 r study thus reveals the structural basis of anion conduction in a TMEM16 channel and it defines the

110 her, these results clarify the basis of CaCC anion conduction.

111 of enteroids from human small intestine and anion current in enteroid monolayers.

112 Here we investigate the effects of anion delocalization on electron transfer using zinc mes

113 d product selectivity resulted from a chiral anion dependent lowering of the activation barrier for t

114 d electric conductivity and a nonzero cation-anion diffusion coefficient.

115 This pi-conjugated anion displayed pronounced redox activity, undergoing fa

116 ral observations that show that the fluoride anion does not act as a one-electron reducing agent towa

117 aO, which facilitates the transport of O(2-) anions, drastically improves the reaction kinetics, and

118 spite of the undoped-PPy preference for pure anion dynamics.

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

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

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

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

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

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

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

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

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

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

129 readily achievable using typical methods of anion exchange.

130 be rendered water-insoluble through reverse anion exchange.

131 thetic composition tuning through topotactic anion exchange.

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

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

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

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

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

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

138 Anion exchanger 1 (AE1) mediates Cl(-)/HCO3(-) exchange

139 reaction inside red blood cells, and band 3 [anion exchanger 1 (AE1)] provides a passage for HCO3(-)

140 ABSTRACT: The anion exchanger AE3, expressed in hippocampal (HC) neuro

141 H(+) secretion is removed by the basolateral anion-exchanger AE1.

142 The anion exclusion effect in HM is thus more pronounced tha

143 f less hydrophilic trifluoromethanesulfonate anions for hydrophilic sulfate; the resulting water-solu

144 (2(*-) and 3(*-)) and then to a bis(radical anion) for 2(2-) but a dianion for 3(2-).

145 active site of the enzyme in their phenolate anion form.

146 r the first time, it is reported that dimsyl anion, formed from a strong base and DMSO (solvent), is

147 ructure translates into a tunable density of anion Frenkel disorder while cations remain ordered.

148 e important conduits for dissipating lactate anions from glycolytic PDAC cells.

149 different cooperativity in binding pairs of anions from the fullerene-free parent: in one case, posi

150 ynthesis and characterization of the cluster anions [Ge18Pd3{Si(i)Pr3}6](2-) (1) with a core of face-

151 Soluble Si(IV) -O anions generated from solid SiO2 are electrodeposited on

152 de capacity and to understand details of the anion-graphite intercalation mechanism.

153 ondissociated acid form, and the carboxylate anion group, representing the dissociated form, over a w

154 ered hydroxides with inheritance of included anion groups (OH(-) , NO3(-) , CO3(2-) ).

155 photoelectron spectroscopy of the vinylidene anions H2CC- and D2CC- and quantum dynamics calculations

156 o the loosely coordinating superweak TFPB(-) anion has been achieved.

157 in interstitial spaces periodically serve as anions-have attracted broad attention for their exotic p

158 rent work, we report a self-assembled triple anion helicate (host 2) featuring a cavity resembling th

159 Moreover, the anion helped partition Gnd(+) to the polymer surface.

160 utral organic HBAs, and the non-coordinating anion hexafluorophosphate is the weakest acceptor, with

161 lexes at Au/MAPbI3 interface, whereas iodine anions (I(-)) can react with Ag contacts, leading to int

162 ydride anion, BH4(-), is replaced by another anion, i.e. a halide or amide ion; and metal borohydride

163 dissociative photochemistry of the triiodide anion (I3(-)) in single-crystal tetra-n-butylammonium tr

164 ed the coherently formed tetraiodide radical anion (I4(*)(-)) as a reaction intermediate.

165 , including a compound containing the PCO(-) anion in an unprecedented mu(2) :eta(2) ,eta(2) -binding

166 Since glutamate is the major monovalent anion in E. coli, these results suggest that SSB likely

167 tion of the pyrazine (Pz) anion, an unstable anion in isolation due to its neutral counterpart having

168 ctronic effect between the central metal and anion in the complex.

169 ceptors (TLR) induce an influx of superoxide anion in the ensuing endosomes.

170 organic solvent (reaction with arene radical anions in glyme).

171 zed fluoride anions substituted the hydroxyl anions in hydroxyapatite crystals.

172 this article, we review the observations of anions in interstellar clouds, circumstellar envelopes,

173 he abundance, distribution, and chemistry of anions in the interstellar medium.

174 properties of SCU-8 were explored with many anions including small oxo anions like ReO4(-) and Cr2O7

175 sment of a large number of different counter anions, including those that are synthetically challengi

176 nionic ligands X revealed that the nature of anion influences the reactivity more than the spin state

177 ation of a naphthalene diimide (NDI) radical anion is presented.

178 The role played by NOx anions is examined in this investigation.

179 Fluoride, nature's smallest anion, is capable of covalently coordinating to eight si

180 xplored with many anions including small oxo anions like ReO4(-) and Cr2O7(2-) as well as anionic org

181 We present a layered three-anion material, Bi4O4Cu1.7Se2.7Cl0.3, which adopts a new

182 We present a study of halide-->OH anion metathesis of (Ar)Pd(II) complexes using vinylBPin

183 de diffusion from mesoporous carbon hosts by anion metathesis, which we show is selective for higher

184 s of two ligand modifications followed by an anion metathesis.

185 had considered some processes through which anions might form in interstellar clouds and circumstell

186 Salt cations and anions migrate in opposite directions from the sample so

187 to the dynamics of both cation-molecule and anion-molecule reactions studied with this method.

188 st due to the unique features of the hydride anion, most notably the absence of valence p orbitals.

189 ction of an alkyl iodide (R-I) with an azide anion (N3(-)) to reversibly generate the corresponding a

190 o the presence of a remote basic site in the anion namely, OH of bicarbonate, NH of prolinate, and ac

191 vels of lipid peroxidation and of superoxide anion (O2(* horizontal line )) were higher in Prdx6 (-/-

192 e in class I b RNRs that requires superoxide anion (O2(.-) ), rather than dioxygen (O2 ), to access a

193 Until a decade ago, the only anion observed to play a prominent role in astrophysics

194 and energetics of o-, m-, and p-quinonimide anions (OC6H4N(-)) and quinoniminyl radicals have been i

195 tion state than carboxylate that produces an anion of similar stability.

196 Here we study the effect of Hofmeister anions on gramicidin A channels in lipid membranes.

197 Here we show via a high-pressure study of anion-ordered strontium vanadium oxyhydride SrVO2H that

198 ementing a highly hydrophobic perfluorinated anion (perfluorooctanesulfonate, PFOS(-)) as doping ion

199 mic pH as a read-out, indicated that lactate anions permeate gap junctions faster than highly-buffere

200 yl acrylates that is facilitated by a chiral anion phase transfer (CAPT) process is presented.

201 Herein, we present a combined anion photoelectron spectroscopic and density functional

202 cular layers, and thus interact with the PAH anion pi systems.

203 This report focuses on the remote control of anion-pi catalysis by electric fields.

204 Exposed to increasing electric fields, anion-pi catalysts show an increase in activity and an i

205 We have synthesized and immobilized anion-pi catalysts to explore the addition reaction of m

206 to the pi-electron-deficient ClBDPPV through anion-pi electronic interactions is strongly corroborate

207 re of cylindrical nanofibers leads to strong anion-pi interactions between both components.

208 Anion-pi interactions on fullerenes are about as poorly

209 shorter than standard pi-pi interactions and anion-pi interactions on planar surfaces, and alternativ

210 and charge-delocalized enolate tautomers by anion-pi interactions.

211 f neuronal [Cl(-)]i - cytoplasmic impermeant anions, polyanionic extracellular matrix (ECM) glycoprot

212 usually achieved by mixing NCs with reactive anion precursors.

213 identified four new channel activities: two anion-preferring channels and two cation-preferring chan

214 ation which leads to Ca(2+) rise, superoxide anion production, ATP drop and late NADP(H) depletion as

215 tinuous wave pump field, and detects radical anion products via SERS.

216 The reaction of dichloro ketones with azide anions provides acyl azides, through in situ formation o

217 nthetic electron transfer, detoxification of anion radicals, citrate cycle, and tetrapyrrole biogenes

218 [Ta6Br12(H2O)6]@2CD}(2+) and the Dawson-type anion, react together to give a three-component, well-or

219 simple nucleophiles, such as azido or cyano anions, react with unexpected stereo- or regioselectivit

220 (EIE) for the aryl CH...Cl(-) interaction of anion receptor 1H/1D is reported.

221 he higher binding constant of Cl(-) with the anion receptor and the stronger electronic effect betwee

222 omplexes with Cu(II) or Co(II) and a dipodal anion receptor functionalized with dipyrromethene.

223 that will be important for designing future anion receptors and organocatalysts.

224 ging field in the design of highly selective anion receptors.

225 , which revealed considerable differences in anion recognition behavior in comparison with chalcogen-

226 BD partners, allowing reliable prediction of anion recognition properties in other scenarios.

227 ative study of 1,2,3-triazole and triazolium anion recognition units containing sulfoxide, sulfone, a

228 mics simulations are used to investigate the anion recognition- and solvent-dependent dynamic propert

229 of [2]rotaxanes to achieve enantioselective anion recognition.

230 perties arise from a strong coupling between anion redox and cation migration.

231 al oxide positive electrodes offer access to anion redox at high potentials, thereby promising high e

232 Mo-S (a-MoSx) electrocatalytic materials and anion-redox chalcogel battery materials.

233 This finding together with the observed anion reduction as the redox center is of broad interest

234 s finding demonstrates a general paradigm of anion-regulated evolution of distinctive TMSs, providing

235 ey synthetic transformations include Type II Anion Relay Chemistry (ARC) to construct the polyol chai

236 tone enolates as the initial nucleophile for anion relay chemistry (ARC).

237 electronic structure of the para-quinonimide anion require both an accurate account of electron corre

238 h steric and electrostatic forces, where the anions reside in equidistant "clefts" between coordinati

239 d spectral diffusion of the linear triatomic anion, SeCN(-), in poly(ether sulfone) (PES) membranes a

240 in the limit of detection of potentiometric anion-selective electrodes aiming at determining nutrien

241 unded by a repeating sequence of cation- and anion-selective hydrogel membranes.

242 ophyte species, showing that all of them are anion-selective, and thus expanded this protein family t

243 hat interact with permeant anions and affect anion selectivity, as well as seven pore-lining residues

244 ique and sophisticated mechanism for optical anion sensing in competitive protic organic and aqueous-

245 s examined as an initial example of this new anion sensing platform for measurements of fluoride leve

246 photoelectron spectrum of the m-quinonimide anion shows that the ion undergoes several different rea

247 ch individual seesaw-shaped tin (II) bromide anions (SnBr4(2-) ) are co-crystallized with 1-butyl-1-m

248 hydroxyl radical ((*)OH) and sulfate radical anion (SO4(*-)) were measured from ultrasonic activation

249 than (18)F-BF4(-) The ability of a range of anions, some containing fluorine, to block (99m)TcO4(-)

250 ect detection of the 4,4'-bipyridine radical anion species localized in the plasmonic hot spots of in

251 C-terminus and causes aggregation of citrate anion-stabilized silver nanoparticles (AgNPs) in the abs

252 r and nonpolar solvents without changing the anion structure and properties.

253 We further explore the effects of anion structures and functional groups on both device pe

254 hich suggested that small localized fluoride anions substituted the hydroxyl anions in hydroxyapatite

255 dride derivatives have also been discovered: anion-substituted compounds where the complex borohydrid

256 Here, an effective strategy combining anion substitution, defect engineering, and the dopant e

257 lectivity for chloride over major lipophilic anions such as salicylate ( [Formula: see text] ) and th

258 owth method for the targeted growth of mixed anion systems.

259 taining macrocycles, is constructed using an anion template synthetic methodology.

260 Anion-templated aqueous self-assembly resulted in the fo

261 Synthesised by a chloride anion templation strategy, the [3]rotaxane host recognis

262 ic organic cation and inorganic (or organic) anion that loosely fit together, is extending the proper

263 They are the only known examples of cage anions that contain a noble-gas element.

264 With the appropriate urea anions, the polymerizations reached high conversions ( a

265 the composition of the Th-nitrato monomeric anions themselves.

266 ng can also proceed in a cooperative (strong anion then weak acid) or stepwise manner (weak acid then

267 zes the H2O2-dependent oxidation of chloride anion to generate hypochlorous acid, a potent antimicrob

268 ngbone packings by reorienting the molecular anions to create multiple potassium sites within initial

269 Electron transfer from F(-) anions to the pi-electron-deficient ClBDPPV through anio

270 Anion transport by the human sodium-iodide symporter (hN

271 Our results demonstrate that anion transport in polyILs occurs through a mechanism in

272 have a 7 + 7 inverted repeat structure with anion transport initiated by chloride binding at the int

273 8del-CFTR activity, as indicated by enhanced anion transport through the plasma membrane.

274 CNTPs block anion transport, even at salinities that exceed seawater

275 thus inserts into lipid bilayers to turn on anion transport, which can then be turned off through ad

276 clude two "drug" transporters of the organic anion transporter (OAT) family: OAT1 (SLC22A6, originall

277 GLUT1, the glucose transporter; SLC4A1, the anion transporter; RhAG, the Rh-associated glycoprotein;

278 deled, based on structural data from related anion transporters (SLC26Dg and UraA), to have a 7 + 7 i

279 Anion transporters play a vital role in cellular process

280 The application of anion transporters to the potential future treatment of

281 ext of recent findings on the selectivity of anion transporters.

282 s were determined in wild-type (WT), organic anion transporting polypeptide (OATP) knockout mice (lac

283 Here, we investigated the role of organic anion transporting polypeptide (OATP) transporters to th

284 The organic anion-transporting polypeptides represent an important f

285 .5)1 thin film superlattices possessing both anion-vacancy order and Sr and Ca chemical order at the

286 formation is obtained from modified SM lipid anions via amide bond cleavage.

287 f chloride, nitrate, bicarbonate and sulfate anions via hydrogen bonding.

288 Aa1, whereas dual selectivity (to cations or anions) was observed for the pores formed by the trypsin

289 The nucleophilic reactivities of barbiturate anions were compared with those of structurally related

290 In addition, increased unmeasured anions were the leading cause of metabolic acidosis.

291 t act together to CH-hydrogen-bond to halide anions when the macrocycle is located on an alternative

292 and decarboxylation to form an aryl radical anion which is then oxidized by the [4Fe-4S](+2) cluster

293 oduced a mono-substituted [BH3 N(NO2 )2 ](-) anion, which contains a B-N connected dinitramido ligand

294 Reactions of the BH4(-) anion with equimolar amounts of HN(NO2 )2 or of BH3 THF

295 ion-state dynamics by the photodetachment of anions with an equilibrium geometry similar to the neutr

296 ble cage is flexible and able to encapsulate anions with volumes ranging from 35 to 219 A(3) via hydr

297 of a C-based nucleophile, namely the phenyl anion, with the ferric heme nitrosyl [(OEP)Fe(NO)(5-MeIm

298 o host concurrently two dihydrogen phosphate anions within a relatively large internal cavity.

299 of convenient sources of nucleophilic boryl anions would open up a wealth of opportunity for the dev

300 The isostructural chloroxenate anions (Xe-Cl bond lengths, 2.9316(2) to 3.101(4) A) wer