ライフサイエンスコーパス: borate

1 ture TpNi(III)(R)(R(1)) (Tp = tris(pyrazolyl)borate).

2 ment and inhibition by 2-aminoethoxydiphenyl borate).

3 e following order: phosphate > bicarbonate > borate.

4 cked by nifedipine and 2-aminoethoxydiphenyl borate.

5 arbonate, hydroxide, hydrogen phosphate, and borate.

6 erion, i.e. bromide vs tetrakis(1-imidazolyl)borate.

7 ted by PTx, La(3+), or 2-aminoethoxydiphenyl borate.

8 affeine, ryanodine, or 2-aminoethoxydiphenyl borate.

9 riphenylmethylium tetrakis(pentafluorophenyl)borate.

10 tly or after activation to the corresponding borate.

11 r gelation of water by guanosine and lithium borate.

12 idic aryl and alkyl boranes to various alkyl borates.

13 bond in 2-ammoniophenyl(aryl)- or -(alkenyl)borates.

14 e) = hydridotris(3,4,5-trimethylpyrazol-1-yl)borate].

15 he potassium salt of the monoanionic bis(NHC)borate 1 (NHC = N-Heterocyclic Carbene) enables the synt

16 osphate receptors with 2-aminoethoxydiphenyl borate (100 mum), depletion of intracellular Ca(2+) stor

17 yield formation of diphenylterphenylsilylium borate 17[B(C6F5)4].

18 to 1 afforded the alkali metal disilicon(0) borates 1M[BAr4] (M = Li, Ar = C6F5; M = Na, Ar = Ar(F))

19 The inhibitor 2-aminoethoxydiphenyl borate (2-APB) binds to TRPV6 in a pocket formed by the

20 2-Aminoethoxydiphenyl borate (2-APB) elicits potentiation current (Ip) on Ca(2

21 2-Aminoethoxydiphenyl borate (2-APB) has emerged as a useful pharmacological t

22 d during application of 2-aminoethyldiphenyl borate (2-APB) to activate a nonselective cation conduct

23 permeation behavior of 2-aminoethoxydiphenyl borate (2-APB), a broad-spectrum modulator for a number

24 Furthermore, 2-aminoethoxydiphenyl borate (2-APB), a common activator of thermo-sensitive v

25 activation pathway as 2-aminoethoxydiphenyl borate (2-APB), a common agonist for these TRPV channels

26 e-independent manner by 2-aminoethyldiphenyl borate (2-APB), a small molecule with complex pharmacolo

27 nly in the presence of 2-aminoethoxydiphenyl borate (2-APB), irrespective of STIM1.

28 native cells, including 2-aminoethyldiphenyl borate (2-APB), SKF96363, and removal of extracellular C

29 powerful SOC modifier, 2-aminoethoxydiphenyl borate (2-APB), the mechanism of which has eluded recent

30 zing the SOCE modifier 2-aminoethoxydiphenyl borate (2-APB), we demonstrate that 2-APB-activated stor

31 and ryanodine but not 2-aminoethoxydiphenyl borate (2-APB).

32 eparin, caffeine, and 2-aminomethoxydiphenyl borate (2-APB).

33 ctrode with [Fe(tris(3,5-dimetyl-1-pyrazolyl)borate)(2)](+)[FeCl(4)](-).

34 e of an IP3 R blocker (2-aminoethoxydiphenyl borate, 2-APB), or during block of IP3 production by the

35 zation, but La(3+) and 2-aminoethoxydiphenyl borate (a dual inhibitor of inositol 1,4,5-triphosphate

36 receptor blocker, and 2-aminoethoxydiphenyl borate, a nonselective storeoperated Ca(2+) entry channe

37 This assay was also used to evaluate serine-borate, a well-known inhibitor of GGT1, which was 8-fold

38 For the Pu(III) borates, a Pu 6p orbital is observed with delocalized el

39 made from uniaxial birefringent alpha-barium borate (alpha-BBO) or calcite crystals that overcome the

40 ium were attenuated by 2-aminoethoxydiphenyl borate, an inhibitor of store inositol trisphosphate rec

41 well-known "scorpionate" tris(pyrazol-1-yl)-borate and -methane ligands.

42 and bpy are hydridotris(3-methylpyrazol-1-yl)borate and 2,2'-bipyridine, respectively.

43 ral Ni(IV) complex ligated by tris(pyrazolyl)borate and a cationic octahedral Ni(III) complex ligated

44 sium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate and calcium ionophore IV (ETH 5234) or calcium io

45 In this work, we demonstrate novel phenyl borate and carborane-based anions paired with a near-inf

46 ment, where Tp' = tris(3,5-dimethylpyrazolyl)borate and L = neopentyl isocyanide, is used to investig

47 agmas in the early Hadean eon, may have made borate and molydate species available to prebiotic chemi

48 SLC4A11 is a putative Na(+) borate and Na(+):OH(-) transporter.

49 plexes 1-15, where Tp is a N,N,N-tris(azolyl)borate and P is a tertiary phosphine, have been synthesi

50 ibonucleosides stabilized by borate mobilize borate and phosphate from luneburgite, and are then regi

51 by InsP3R inhibitors 2-aminoethoxyldiphenyl borate and xestospongin-C.

52 is of potassium trifluoro(N-methylheteroaryl)borates and their use in cross-coupling reactions with v

53 (Tp(tBu) = hydro-tris(3-tert-butyl-pyrazolyl)borate) and investigated the influence of the trifluoroe

54 b = phenyltris(3-methyl-imidazolin-2-ylidene)borate) and triethylamine as well as N,N-dimethylaniline

55 = phenyltris(3- tert-butylimidazol-2-ylidene)borate), and [Fe(V)(O)(TAML)](-) (5, TAML(4-) = tetraami

56 PM7 blockers Gd(3+) or 2-aminoethoxydiphenyl borate, and by knockdown of TRPM7 channels with small in

57 ing three non-denaturing aqueous (phosphate, borate, and carbonate) buffers at various conditions of

58 of three non-denaturing aqueous (phosphate, borate, and carbonate) buffers at various ionic strength

59 ither Tris, acetate, and EDTA (TAE) or Tris, borate, and EDTA (TBE).

60 he presence of aqueous potassium tetraphenyl borate, and its competence as an intermediate was demons

61 rmeable to Na(+), H(+) (OH(-)), bicarbonate, borate, and NH4 (+).

62 positions relies on the assumption that only borate, and no boric acid, is present.

63 dium tetrakis[3,5-bis(perfluorohexyl) phenyl]borate, and one of four fluorophilic Ag(+)-selective ion

64 odium tetrakis[3,5-bis(perfluorohexyl)phenyl]borate, and one of four fluorophilic H(+)-selective iono

65 als are all involved in bonding in a Cf(III) borate, and that large crystal-field effects are present

66 Depending on conditions, pyro-borates, spiro-borates, and boroxinate species can be generated and the

67 lysts, and these include meso-borates, spiro-borates, and diborabicyclo-borate esters.

68 er of frequency-doubling oxides, phosphates, borates, and fluoride-containing borates were found, no

69 ) self-decay and ferric chloride addition in borate- and phosphate-buffered waters showed that phosph

70 rophic bacteria due to a decrease in oceanic borate anion concentration.

71 nts of HN(NO2 )2 afforded the di-substituted borate anion consisting of two isomers, one with both ni

72 Borate anion is also shown to bind to apo-Mb-FbpA with m

73 that the reaction to form the chiral spiral borate anion is stereospecific, namely, only one of two

74 ng and lipophilic tetrakis(pentafluorophenyl)borate anion stable as a solid and soluble in low polari

75 This ratio of borate anion to ligand is crucial for gelation as it lin

76 th OECs are chemically similar, and that the borate anions do not play an apparent role in the cataly

77 n chemical reductions to their corresponding borate anions.

78 rate); and pftpb = tetrakis(pentfluorophenyl)borate) are oxygen gas sensors.

79 BAr(f) = tetrakis(3,5-trifluoromethylphenyl)borate) are reported.

80 e; [Bc(Me)](-) = dihydrobis(methylimidazolyl)borate) are synthesized and fully characterized to exami

81 rate that a variety of weak acids (silicate, borate, arsenite, cyanide, carbonate, and sulfide) canno

82 electrolyte, using lithium difluoro(oxalato)borate as an electrolyte additive, that has superior per

83 /2+)) paired with tetrakis(pentafluorophenyl)borate as counterion.

84 Using a mixture of phosphate, citrate, and borate as the buffering ions and using a CEM suppressor,

85 acid) (PAA) as the capping ligand and sodium borate as the salt, the borate hydrolyzes rapidly in res

86 from the resulting mixture of diastereomeric borates as a result of differential solubilities.

87 is reaction employs nonsymmetric bis(alkenyl)borates as substrates and appears to occur by a mechanis

88 riphenylcarbenium tetrakis(pentafluorophenyl)borate at -20 degrees C formed the cationic gold (beta,b

89 phosphate buffer at I=0.5 for hazelnut, and borate at I=0.15 for pistachio.

90 resence of Na(+), K(+), Mg(2)(+), Li(+), and borate at soil concentrations lethal to Arabidopsis.

91 er SLC4A11 in corneal endothelium transports borate (B[OH](4)(-)), bicarbonate (HCO3(-)), or hydroxyl

92 the complex with phenyl substituents on the borate backbone.

93 th tetrakis-[3,5-bis(trifluoromethyl)phenyl]-borate (BArF) to enhance catalytic activity and control

94 f the triphenylsulfonium salt of a carbamato borate based on a carbazole function, its establishment

95 We present herein anionic borate-based bi-mesoionic carbene compounds of the 1,2,3

96 , U; [Bp(Me)](-) = dihydrobis(methypyrazolyl)borate; [Bc(Me)](-) = dihydrobis(methylimidazolyl)borate

97 In borate (Bi) and phosphate (Pi) buffers, anions must be d

98 Borate-binding ligands (apiose, dehydroascorbic acid, al

99 The serine-borate-bound hGGT1 crystal structure demonstrates that s

100 es, material is expected to have passed from borate-bound pent(ul)oses to a branched heptulose, which

101 After treatments to promote borate-bridging of RGII, we assessed freeze-induced dama

102 Purified (18)F-SFB was incubated with IL2 in borate buffer (pH 8.5) and ethanol at 50 degrees C for 1

103 tassium hydroxide (KOH, pH = 14) and aqueous borate buffer (pH = 9.5) solutions.

104 0.5 mM hydroxyl propyl-beta-cyclodextrin in borate buffer [80 mM, pH 9.3].

105 Labeling reaction conditions (100mM borate buffer at pH 8.5, labeling reaction time 60min, t

106 mal conditions for the separation were 100mM borate buffer at pH 9.7 and detected at 475nm.

107 25 kV with a background electrolyte of 25 mM borate buffer containing 5.0% (v/v) acetonitrile.

108 re solubilized by heating at 95 degrees C in borate buffer containing detergent (5 min), then labeled

109 C)2](+) complex doped in sol-gel matrix in a borate buffer of pH 9.2.

110 mplex at 645nm after excitation at 400nm, in borate buffer, pH 9.2.

111 CE of fluorescein disodium salt solution in borate buffer.

112 ited 334 nM (18.3 ppb) limit of detection in borate buffer.

113 etry signal carried out at pH 11.0 in a 0.1M borate buffer.

114 ution for filter impregnation is prepared in borate-buffer rather than in water.

115 d with 2-AA within 30-60 min in mild acetate-borate buffered solution.

116 the voltammetric data for water oxidation in borate buffered solutions (pH 9.2) at electrodes functio

117 absorbed by a paper filter impregnated with borate-buffered (pH 9.0) hydroxoaquocobinamide (hereinaf

118 The other one was a borate-buffered dextran gel, which utilized the secondar

119 on matrix and in less than one hour with the borate-buffered dextran gel.

120 1.5-4.7) x 10(-8) M (4.5-13 ng/mL), with the borate capping agent having the best performance.

121 alloy of earth-abundant metals and a cobalt|borate catalyst, respectively.

122 Addition of borate caused a general decrease in (1)H T(1) values, co

123 re we propose the end-of-life utilization of borated CFI as B fertilizer, to decrease societal B cons

124 Consistent with known borate chemistry, the principal alterations in the (1)H

125 le method for the functionalization of closo-borates [closo-B10 H10 ](2-) (1), [closo-1-CB9 H10 ](-)

126 Oxidic Co and Ni borate (Co-B(i) and Ni-B(i)) thin films electrodeposited

127 arable to that of another OER cocatalyst, Co-borate (Co-Bi), in 1 M Na2CO3, reaching 10 mA/cm(2) at a

128 )6, as a soluble model of a cobalt-phosphate/borate (Co-OEC) water splitting catalyst.

129 nd binuclear organoscandium complexes with a borate cocatalyst are active for ethylene + amino olefin

130 greater than any variation introduced by the borate complexation, which had a negligible effect on th

131 The synthesis of the Cu-borate complexes [(6Mes)Cu(HBR3 )] featuring the unusual

132 ive conjunctive cross-coupling between 9-BBN borate complexes and aryl electrophiles can be accomplis

133 would almost certainly have formed as stable borate complexes on the surface of an early Earth beneat

134 xploited for its ability to bind and release borate-containing therapeutics such as BTZ in a pH-depen

135 s of type 1 Cu sites based on tris(pyrazolyl)borate copper thiolates [Cu(II)]-SR to unravel the facto

136 w-temperature reaction of the tris(pyrazolyl)borate copper(II) hydroxide [(iPr2) TpCu]2 (mu-OH)2 with

137 Reaction of tris(pyrazolyl)borate copper(II) thiolates (iPr2)TpCu-SR (R = C6F5 or C

138 eins and functions as an electrogenic sodium borate cotransporter.

139 n the interval from 15 to 60 degrees C using borate cross-linked dextran sieving matrix.

140 ehyde halogenation proceeded most readily in borate cross-linked gels at high ammonium persulfate dos

141 crocycle and a highly charged, electron-rich borate cycle.

142 the technique by measuring the silicate and borate depth profiles in the Pacific Ocean; the silicate

143 rompts reaction with H2 to give a borane-oxy-borate derivative, the product of C-O bond cleavage.

144 gment {WTp(NO)(PMe(3))} (Tp = tris(pyrazolyl)borate), derived from pyridine, are demonstrated to unde

145 treatment to hydrolyse rhamnogalacturonan II borate diester bonds neither affected chains length or b

146 ogalacturonan-II (RG-II) is cross-linked via borate diester bridges, which influence the expansion, t

147 structural model that involves formation of borate dimers and G4.K(+) quartets by G 1 and KB(OH)4.

148 ated as [Fe(14)], Tp(-), hydrotris(pyrazolyl)borate; DMSO, dimethyl sulfoxide), which has a fluctuati

149 stasis in plants is regulated in part by the borate efflux transporter Bor1, a member of the solute c

150 Whereas catalyst films formed in borate electrolyte (CoB(i)) exhibit coherent domains con

151 in film from Ni(aq)(2+) solutions containing borate electrolyte (Ni-B(i)) has been studied by in situ

152 trodeposited from dilute Ni(2+) solutions in borate electrolyte at pH 9.2 (B(i)).

153 xidation in a mixed lithium borate-potassium borate electrolyte.

154 Co(2+) in phosphate, methylphosphonate, and borate electrolytes effects the electrodeposition of an

155 Methylphosphonate and borate electrolytes support catalyst activity comparable

156 Molten alkali metal borates embody a new class of high-temperature liquid-ph

157 pW(NO)(PMe(3))} (Tp = hydridotris(pyrazolyl)-borate) enhances the basicity of the arene ligand to the

158 One borate ester catalyst has two molecules of VANOL and the

159 amides has been developed with two different borate ester catalysts of VANOL.

160 -quadruplex G4K(+) borate hydrogels by using borate ester linkages (Pt-G4K(+)B hydrogel).

161 Yamaguchi union of a C(20-27) vinyl borate ester, possessing the all-trans triene, with an a

162 Borate esters are often in equilibrium, and their struct

163 Borate esters of BINOL have been investigated as chiral

164 The present study examines the structures of borate esters of BINOL that are produced with different

165 so-borates, spiro-borates, and diborabicyclo-borate esters.

166 tetradodecylammonium tetrakis(4-chlorophenyl)borate (ETH-500) and a cation-sensitive membrane without

167 Tp(iPr) = hydrotris(3-isopropylpyrazol-1-yl)borate], exhibits a distorted octahedral geometry with M

168 ), when combined with 0.5 equiv of potassium borate, forms a strong, self-supporting hydrogel with el

169 high soil boron, facilitating the efflux of borate from cells.

170 from the glass standard obtained by lithium borate fusion.

171 eral acids, microwave digestion, and lithium borates fusion in combination with polyethylene glycol (

172 stigated decomposition of samples by lithium borates fusion in combination with salicylic acid.

173 n yielded the expected imidazolethiones, the borates gave the first representatives of new zwitterion

174 cation helps stabilize the anionic guanosine-borate (GB) diesters, as well as the G4-quartets.

175 The guanosine-borate (GB) hydrogel, which was characterized by cryogen

176 creases the stiffness of the Li(+) guanosine-borate (GB) hydrogel.

177 orming (11)B NMR measurements on a soda lime borate glass that has been pressure-quenched at ~0.6 GPa

178 anges in macroscopic properties of soda lime borate glasses compressed up to ~0.6 GPa are not attribu

179 Tb(3+) or Eu(3+) singly-doped borate glasses or CdS-quantum dot (CdS-QD) coated lenses

180 reference materials (SRMs) fused in lithium borate glasses: two sediments as well as a soil and a ro

181 4) = tetrakis[3,5-bis(trifluoromethyl)phenyl]borate; H(3)TEB = 1,3,5-triethynylbenzene; m-H(2)DEB = 1

182 s been incorporated into G-quadruplex G4K(+) borate hydrogels by using borate ester linkages (Pt-G4K(

183 ng ligand and sodium borate as the salt, the borate hydrolyzes rapidly in response to moisture and pr

184 lumns AS16, AS18, and AS23 were studied with borate, hydroxide and carbonate as suppressible eluents.

185 ) (1) afforded the mixed-valent disilicon(I)-borates [(Idipp)(R)Si(II) horizontal lineSi(0)(Idipp)][B

186 e or hydrogen tetrakis(4-methyl-1-imidazolyl)borate in a concentrated ammonium hydroxide solution at

187 reatment with cold dilute HCl or with excess borate in vitro) enhanced the GIPCs' extractability.

188 r addition of external 2-aminoethoxydiphenyl borate inhibited MagNuM currents.

189 t a 1,2-metalate rearrangement of the silver borate intermediate is the key step responsible for the

190 derivative which reacts further via an epoxy-borate intermediate to capture CO, affording a heterocyl

191 dicate, however, that neither bicarbonate or borate is a substrate.

192 Borate is among those synergistic anions tested which su

193 Borate is an antibacterial preservative widely used in c

194 rsenite, arsenate, phosphite, phosphate, and borate is described.

195 room temperature of the new (trinitromethyl)borate is in sharp contrast to the behavior of [BCl3 C(N

196 The stabilization by borate is not, however, absolute.

197 Borate is shown to play two ostensibly antagonistic role

198 The electronic structure of the Ce(III) borate is similar to the Pu(III) complexes in that the C

199 (dimethylamino)pyridine; Tp = tris(pyrazolyl)borate) is described.

200 BA-TBB) and Potassium tetrakis(4-chlorphenyl)borate (KTClpB)).

201 ensional network structures where rare earth borate layers are joined together by BO(3) and/or BO(4)

202 olyl) supported by the anionic bis(phosphino)borate ligand [Ph(2)B(CH(2)P(t)Bu(2))(2)](-) has been is

203 do complex supported by a bulky tris(carbene)borate ligand.

204 ticular geological environment that contains borate, magnesium, sulfate, calcium, and phosphate in ev

205 e), as well as a chemically distinct Bk(III) borate material for comparison.

206 he disruption of membrane components by high borate may account for the phytotoxicity of excess B.

207 nd molecules such as tetrakis(4-chlorophenyl)borate, metergoline, lidocaine, and bromhexine.

208 tion to guiding carbohydrate pre-metabolism, borate minerals in evaporite geoorganic contexts offer a

209 these respects, especially when compared to borate minerals.

210 , namely inhibition by 2-aminoethoxydiphenyl borate, ML-9, and low concentrations of lanthanides.

211 Ribonucleosides stabilized by borate mobilize borate and phosphate from luneburgite, a

212 ent of a branched pentose that is central to borate-moderated cycles that fix carbon from formaldehyd

213 carbenes that contain a weakly coordinating borate moiety (WCA-NHC) was prepared in one step from fr

214 s of carbohydrate premetabolism, showing how borate, molybdate, and calcium minerals guide the format

215 sodium tetrakis[(3,5-trifluoromethyl)phenyl]borate (NaBARF).

216 iodoalkanes to sodium tetrakis(1-imidazolyl)borate (NaBIm(4)).

217 dium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate (NaTFPB), theoretical calculations, and single-cr

218 o Fe-containing Ni-based OECs, namely nickel borate (Ni(Fe)-B(i)) and nickel oxyhydroxide (Ni(Fe)OOH)

219 f water splitting by a self-assembled nickel-borate (NiBi) OEC.

220 1 crystal structure demonstrates that serine-borate occupies the active site of the enzyme, resulting

221 O(3))(2)] and hydrogen tetrakis(1-imidazolyl)borate or hydrogen tetrakis(4-methyl-1-imidazolyl)borate

222 the 3,3'-position will not form either spiro-borates or boroxinate species and thus are not effective

223 ted DUV NLO materials are almost exclusively borates or phosphates.

224 sts (xestospongin D or 2-aminoethoxydiphenyl borate) or a phospholipase C inhibitor (U73122) attenuat

225 (x)H(y) ligands stabilized by tris(phosphine)borate ([PhB(CH(2)PR(2))(3)] = [PhBP(R)(3)]) ligands hav

226 capillary was used for the separation, and a borate-phosphate buffer containing 25 mM cetyltrimethyla

227 inates from Ln(3+) coordination alterations, borate polymerization diversity and soft ligand coordina

228 nuous PEC water oxidation in a mixed lithium borate-potassium borate electrolyte.

229 roxyl and carboxylate groups, the effects of borate preservation in (1)H NMR-spectroscopy-based metab

230 carboxylate functions, it is concluded that borate preservation is "fit-for-purpose" for (1)H NMR-ba

231 ly produce either chiral primary or tertiary borated products.

232 odium tetrakis[3,5-bis(perfluorohexyl)phenyl]borate providing for ionic sites, and bis[(perfluoroocty

233 n be amplified during the crystallization of borates, providing chemical recognition of specific lant

234 e; Tp(Me) = hydridotris(3-methylpyrazol-1-yl)borate; pzTp = tetrakis(pyrazol-1-yl)borate; Tp* = hydri

235 CNR)] (Tp' = hydrotris(3,5-dimethylpyrazolyl)borate; R = CH(2)CMe(3)).

236 the catalysts' activation stage phosphonium borates [R3PH][HB(C6F5)3] (6, R = iPr a, Cy b) are forme

237 Effects of various concentrations of borate (range 0-30 mM) on (1)H NMR spectra of urine were

238 lexation with a neutral coated capillary and borate reversed polarity, led to a robust platform for t

239 The countercation in the borate salt (MB(OH)4) significantly alters the physical

240 ctivation, we have synthesized the stibonium borate salt [Sb(C6F5)4][B(C6F5)4] (3).

241 ay mixes using sodium silicate as binder and borate salt as flux.

242 their respective tetrakis(pentafluorophenyl)borate salt, an example of desmotropy.

243 t conditions to give a tetrahydroisoxazolium/borate salt.

244 ds used in the coupling are water-soluble as borate salts.

245 Tp(R,R'-) = hydrotris(3-R,5-R'-pyrazol-1-yl)borate ("scorpionate") anion (R = tert-butyl, R' = H, Me

246 s from the punched chad in 30 s using 20 muL borate/SDS buffer.

247 ments, reproduced here, show that Mg(2+) and borate sequester phosphate from calcium to form the mine

248 stry and sinter mineralogy were dominated by borates, sodium, thiosulfate, sulfate, sulfite, sulfide,

249 The finding is that BINOL borate species are not necessarily inferior catalysts to

250 Depending on conditions, pyro-borates, spiro-borates, and boroxinate species can be ge

251 as chiral catalysts, and these include meso-borates, spiro-borates, and diborabicyclo-borate esters.

252 s the synthesis and isolation of the bis(NHC)borate-stabilized chlorogermyliumylidene precursor 2 in

253 (polypyrrole) and a dynamic network (polyol-borate), strong and flexible polymer films were develope

254 Moreover, supplementation experiments with borate suggest that the function of boron in plants migh

255 The bis(NHC)borate-supported thorium-bis(mesitylphosphido) complex (

256 n of the carbohydrate cis-hydroxyl groups by borate suppresses the long-range hydration shell detecte

257 etrabutylammonium tetrakis(pentafluorophenyl)borate [TBATFAB]) was utilized to elucidate the diffusio

258 incorporates the tetrakis(pentafluorophenyl)borate (TFAB(-)) anion, which is also present as a lipop

259 The tetrakis[3,5-bis(triflouromethyl)phenyl]borate (TFPB(-)) membrane dopant in the polymer ISE was

260 the tetrakis[3,5-bis(trifluoromethyl)phenyl]borate (TFPB(-)) weakly coordinating (or "superweak") an

261 TpIr(III) complex (Tp = hydrotris(pyrazolyl)borate) that also features a labile ligand (i.e., 2-THF)

262 catalytic species (a boroxinate and a spiro-borate) that give opposite asymmetric inductions.

263 etroses form extremely stable complexes with borate, they are not accessible by pathways plausible un

264 We describe a bis(NHC)borate thorium-bpy complex (1) that is capable of reduct

265 ([M + Na]+) analyte molecules with trimethyl borate (TMB) in a modified linear quadrupole ion trap ma

266 f protonated sulfone analytes with trimethyl borate (TMB) that yields a diagnostic product ion, adduc

267 Addition of alkali metal borates to 1 afforded the alkali metal disilicon(0) bora

268 he oxidative coupling of different tetraaryl borates to give biaryls.

269 bitors (citric acid, oxalic acid, and sodium borate) to aqueous extraction solutions to aid pigment r

270 ylcarbenium (trityl) tetra(pentafluorophenyl)borate totally inhibits the reaction, producing the corr

271 [Cu(MeCN)(6)](2+) and hydrotris(pyrazol-1-yl)borate (Tp(-)) affords the zigzag chain compound (Bu(4)N

272 silver complexes bearing hydrotris(pyrazolyl)borate (Tp(x)) ligands have been investigated from a mec

273 [where Tp(R) = Tp, hydridotris(pyrazol-1-yl)borate; Tp(Me) = hydridotris(3-methylpyrazol-1-yl)borate

274 ol-1-yl)borate; pzTp = tetrakis(pyrazol-1-yl)borate; Tp* = hydridotris(3,5-dimethylpyrazol-1-yl)borat

275 ; Tp* = hydridotris(3,5-dimethylpyrazol-1-yl)borate; Tp*(Me) = hydridotris(3,4,5-trimethylpyrazol-1-y

276 tested for three such agents: novel enzymes, borate-transferring ligands and cationic 'chaperones' th

277 The borate triplet state is deactivated further via a second

278 ogen structure, which helps formation of the borate triplet state.

279 y reaction with alkyl orthosilicates or aryl borates, under aerobic conditions in the presence of sil

280 The stability of the borate unit allows chemoselective halogenation of the he

281 ch utilized the secondary equilibrium of the borate-vicinal diol complexation to enhance resolution.

282 After re-absorption, aminobenzene borate was linked to the surface of the sensor by boric

283 A tri-substituted borate was tentatively identified by NMR in the reaction

284 sium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate was used as an ion exchanger in a poly(vinyl chlo

285 (sodium tetrakis[(3,5-trifluoromethyl)phenyl]borate) was found to catalyze reactions of (Phebox)Ir(II

286 ) (2) (Tp* = hydrotris(3,5-dimethylpyrazolyl)borate), was synthesized by salt metathesis from Tp*(2)U

287 phosphates, borates, and fluoride-containing borates were found, no transition-metal silicate with us

288 en atoms contrasting the Am(III) and Cm(III) borates, where a basal O 2p orbital delocalizes to the A

289 ) = hydrotris(3-tert-butyl-5-methylpyrazolyl)borate), whereas the analogous reaction with sulfur stop

290 2 (Tp(Me2) = hydrotris(3,5-dimethylpyrazolyl)borate), which contains a labile molecule of water and a

291 3)-N,N',N"-hydridotris(3,5-dimethylpyrazolyl)borate), which incorporate a ptSi atom in addition to tw

292 capping agents-such as tannate, citrate, and borate-which does not seem to have been done previously

293 Mo, W; Tp* = hydrotris(dimethylpyrazol-1-yl)borate], which are readily obtained via the successive t

294 d the channel blocker, 2-aminoethoxydiphenyl borate, widely used reagents for disruption of Ca(2+)-de

295 asible for very weak acids like silicate and borate with a dedicated element specific detector like a

296 )] (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate) with primary phosphines PH2R (R = Ph, Cy) afford

297 (CH3)H (1a, Tp' = tris(3,5-dimethylpyrazolyl)borate) with substrates containing B-H, Si-H, C-F, and C

298 )4 = tetrakis[3,5-bis(trifluoromethyl)phenyl]borate) with the oxygen atom transfer (OAT) reagent 2-te

299 study has shown that the phosphonium hydrido borate zwitterion 10 is formed exergonically in solution

300 temperature to yield the phosphonium/hydrido borate zwitterion 5.