ライフサイエンスコーパス: borate

1 BArF4- = tetra[3,5-di(trifluoromethyl)phenyl]borate).

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

3 ment and inhibition by 2-aminoethoxydiphenyl 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 tly or after activation to the corresponding borate.

10 r gelation of water by guanosine and lithium borate.

11 e following order: phosphate > bicarbonate > 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 (8)(PEt(3))(4)] (1; Tp = hydrotris(pyrazolyl)borate(1-)) with hydrosulfide affords the clusters [(Tp)

17 isoquinolinium hydroxytris(pentafluorophenyl)borate, 1, and phenanthridium hydroxytris(pentafluorophe

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

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

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

21 eceptor (IP3R) blocker 2-aminoethoxydiphenyl borate (2-APB) and the phospholipase C blocker U73122 bu

22 2-Aminoethoxydiphenyl borate (2-APB) elicits potentiation current (Ip) on Ca(2

23 2-Aminoethoxydiphenyl borate (2-APB) has emerged as a useful pharmacological t

24 e nonselective agonist 2-aminoethoxydiphenyl borate (2-APB) have not been universally reproduced in o

25 2-Aminoethyldiphenyl borate (2-APB) is a widely used experimental tool that a

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

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

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

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

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

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

32 CaM can be reversed by 2-aminoethoxydiphenyl borate (2-APB), resulting in rapid, store-independent ac

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

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

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

36 ynthesized a series of 2-aminoethoxydiphenyl borate (2-APB, 2,2-diphenyl-1,3,2-oxazaborolidine) analo

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

38 phenanthridium hydroxytris(pentafluorophenyl)borate, 2, in either CH2Cl2 or CH3CN resulted in C6F5 tr

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

40 to two TRPV3 agonists, 2-aminoethoxydiphenyl borate (2APB) and heat.

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

42 bserved affinity of certain siderophores for borate, a common chemical species in the marine but not

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

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

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

46 GC(ZrMe2)2; C1-Zr2], in combination with the borate activator/cocatalyst Ph3C+ B(C6F5)4- (B1).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

61 ium tetrakis-[3,5-bis(trifluoromethyl)phenyl]borate) and the same concentration of the chromoionophor

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

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

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

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

66 vation, sensitivity to 2-aminoethoxydiphenyl borate, and low concentrations of lanthanides, and large

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

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

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

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

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

72 methane thiosulfonate, 2-aminoethoxydiphneyl borate, and trinitrophenol, compounds that are known to

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

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

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

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

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

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

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

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

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

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

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

84 n chemical reductions to their corresponding borate anions.

85 a nanochannels filled with a gel-free sodium borate aqueous buffer.

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

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

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

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

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

91 /2+)) paired with tetrakis(pentafluorophenyl)borate as counterion.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

107 0.5 mM hydroxyl propyl-beta-cyclodextrin in borate buffer [80 mM, pH 9.3].

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

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

110 excess of derivatizing agent in 0.1 M sodium borate buffer at pH values ranging from 8.5 to 10.

111 25 kV with a background electrolyte of 25 mM borate buffer containing 5.0% (v/v) acetonitrile.

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

113 and a mixture of fluorescein and ROX dyes in borate buffer is utilized as a model sample system.

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

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

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

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

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

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

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

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

122 1.5-4.7) x 10(-8) M (4.5-13 ng/mL), with the borate capping agent having the best performance.

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

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

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

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

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

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

129 )6, as a soluble model of a cobalt-phosphate/borate (Co-OEC) water splitting catalyst.

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

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

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

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

134 de through cationization and the aldopentose-borate complexes in the negative mode.

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

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

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

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

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

140 C4A11, which encodes a membrane-bound sodium-borate cotransporter, cause loss of function of the prot

141 eins and functions as an electrogenic sodium borate cotransporter.

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

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

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

145 etection and quantification of the furanosyl borate diester (BAI-2) subclass of autoinducer 2 (AI-2),

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

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

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

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

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

158 Borate esters are often in equilibrium, and their struct

159 Borate esters of BINOL have been investigated as chiral

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

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

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

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

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

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

166 from the glass standard obtained by lithium borate fusion.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

184 e3; R = Ph or Me; Tp = hydridotris(pyrazolyl)borate] initiate C-H activation of benzene.

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

186 idazolium group, while anions are based on a borate ion with spiral structure and chiral substituents

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

188 Borate is among those synergistic anions tested which su

189 Borate is an antibacterial preservative widely used in c

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

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

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

193 Borate is shown to play two ostensibly antagonistic role

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

195 (2) (Tp' = hydridotris(3,5-dimethylpyrazolyl)borate) is examined herein.

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

197 2-PhN=L) [Tp' = tris-(3,5-dimethyl pyrazolyl)borate, L = CNCH(2)CMe(3)] to form the coordinatively un

198 ]4[O3SCF3]4 (1) [(pzTp) = tetra(pyrazol-1-yl)borate; L = 1-S(acetyl)tris(pyrazolyl)decane], were cova

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

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

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

202 containing "third generation" poly(pyrazolyl)borate ligands.

203 nium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate [LutH(+)B(ArF)(4)(-)], containing a weakly coordi

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

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

217 ) (TpiPr = hydrotris(3-isopropylpyrazol-1-yl)borate), new models for molybdenum hydroxylases, have be

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 by the channel blocker 2-aminoethoxydiphenyl borate or a TRPC5 ion-pore mutant.

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

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

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

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

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

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

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

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

237 n process was followed to recover the excess borate reagent from the resins/product.

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 e solutions of their tetrakis(4-chlorophenyl)borate salts.

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

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

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

249 nses were inhibited by 2-aminoethoxydiphenyl borate, SKF-96365 (1-2-(4-methoxyphenyl)-2-[3-(4-methoxy

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

251 The isopropoxide-protected borate species were obtained from a boronate or in situ

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

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

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

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

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

257 PMe3)X fragments {Tp = hydridotris(pyrazolyl)borate} suggest opportunities for the development of new

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

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

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

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

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

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

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

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

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

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

268 t of glioma cells with 2-aminoethoxydiphenyl borate to inhibit IP(3)Rs negated the effect of methyl-b

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

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

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

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

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

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

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

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

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

278 The borate triplet state is deactivated further via a second

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

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

281 Me, Ph, or NHPh; Tp = hydridotris(pyrazolyl)borate) undergo regioselective hydrogen-deuterium (H/D)

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

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

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

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

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

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

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

297 )4 = tetrakis[3,5-bis(trifluoromethyl)phenyl]borate) with the oxygen atom transfer (OAT) reagent 2-te

298 of the form [(Tab)M(PH3)2X]q (Tab = tris-azo-borate; X = OH, NH2; q = -1 to +2; M = TcI, Re(I), Ru(II

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.