ライフサイエンスコーパス: boron

1 awing on the unique and varied reactivity of boron.

2 lting temperature above the melting point of boron.

3 ore substituents as well as substitutions at boron.

4 s an exploration of possible one-dimensional boron.

5 ntly increased after 2 and 3 hours of tracer boron ((10)B) treatment.

6 ed to those with the natural distribution of boron (20 at% (10)B and 80 at% (11)B).

7 the silicon(II) atom and the LUMO has mainly boron 2p character.

8 pared with a nearly stoichiometric amount of boron (4.5) as W0.668Ta0.332B4.5.

9 plexes; 96.2% Z selectivity is observed with boron-activated Mo(NC6F5)(CHR')(OHIPT)(Cl)(PPhMe2).

10 Fifteen years of boron addition to a tropical forest increased plant-avai

11 quantum yields are dramatically improved by boron alkylation, whereas alkylation in the meso-methyl

12 ual net [2+2] cycloaddition reaction between boron alkylidenes and unactivated alkenes.

13 Foliar boron did not correlate with soil boron along a local scale gradient of boron availability

14 to the development of a remarkable family of boron, aluminium and gallium [(18)F]-fluoride anion comp

15 Especially in the case of boron, an enhanced reactivity toward O2 dissociation is

16 The compounds are the first examples of boron analogues of diazoalkanes (R2CNN) and ketenes (R2C

17 itution patterns, along with a wide range of boron and alkenyl nucleophiles that couple under palladi

18 in the area of low-coordinated compounds of boron and group-14 atoms C-Sn in the last decade is pres

19 new combinations of light elements including boron and hydrogen, leading to complex hydrides with ext

20 other elements source (sulphur, phosphorus, boron and iron), and porous g-C3N4 as both template and

21 al honeycomb lattices made of strongly bound boron and nitrogen atoms.

22 cts with Group 13 Lewis acids using both its boron and nitrogen sites.

23 w insight into the stability mechanism of 2D boron and open new ways for the control of the lattice s

24 Boron and strontium exceeded background values of 100 an

25 inorganic geochemistry indicators, including boron and strontium isotope ratios, along with groundwat

26 sphonate that contain amine substitutions at boron and the incorporation of these derivatives into th

27 ing greater orbital interactions between the boron and transition metal atoms than those observed wit

28 Despite the many reports on boron- and nitrogen-doped graphenes, the possible synerg

29 work (ICOF), which contains sp(3) hybridized boron anionic centers and tunable countercations, was co

30 s to organoboranes rely on the reactivity of boron as an electrophile.

31 f the sources and processes that control the boron atmospheric cycle.

32 Mean annual dust and dissolved boron atmospheric depositions are comparable in size (13

33 time series allows the determination of the boron atmospheric inputs to this forest ecosystem and co

34 bis(boranils) differently substituted at the boron atom and iminophenyl groups were synthesized from

35 dissociation products are observed where the boron atom bridges the two systems by forming very stabl

36 In both of these compounds the boron atom is in the formal oxidation state +I which con

37 fic interaction of its nitrile-N center with boron atom of the boronic acids, leading to chemoselecti

38 H atoms were selectively abstracted from the boron atoms by t-butoxyl radicals and this enabled borir

39 ase, the reactions are capable of connecting boron atoms in unusual ways, leading to unprecedented bo

40 metal (BB)-carboryne complex containing two boron atoms of the icosahedral cage connected to a singl

41 tructures of 3 and 4 showed tetracoordinated boron atoms with semiplanar skeleton ligands.

42 s that contains a boroxinate core with three boron atoms, and these have proven to be effective catal

43 rbon vacancies that are randomly occupied by boron atoms.

44 of the bond order between the two metalated boron atoms.

45 g covalent interactions with the surrounding boron atoms.

46 and interact almost symmetrically with both boron atoms.

47 h soil boron along a local scale gradient of boron availability.

48 High boron (B) concentration is toxic to plants that limit pl

49 tions were performed with 0.5-2.5 mol % of a boron-based catalyst, generated in situ from a readily a

50 access azaborininones (carbonyl-containing, boron-based heterocyclic scaffolds) using simple reagent

51 we report that readily available silyl- and boron-based Lewis acids in combination with chiral coppe

52 heory-combined with an efficient sequence of boron-based synthetic transformations, which allowed an

53 tory insertion of the alkene into the carbon-boron bond, similar to the mechanism for hydroboration.

54 arinus (Rma cyt c) were found to form carbon-boron bonds in the presence of borane-Lewis base complex

55 n to elicit the oxidative cleavage of carbon-boron bonds.

56 that the dibora[2]ferrocenophane is prone to boron-boron double bond cleavage reactions.

57 ported fluorescent copper(I) pi-complexes of boron-boron double bonds, the Cun-pi-diboryne compounds

58 ted the first pi-complexes of compounds with boron-boron triple bonds with transition metals, in this

59 ruthenium carbonyl has demonstrated that the boron-bound carbon atoms of all of these reaction produc

60 up, enabling functionalization of one of the boron-bound oxygen atoms by a second electrophile.

61 ferrocenophane containing an unsaturated two-boron bridge, isoelectronic with a C=C double bond, was

62 a tropical forest increased plant-available boron by 70% but did not significantly change tree produ

63 solutes contradicts a control of atmospheric boron by dissolution of seasalts.

64 CNTs can be considered to be a novel form of boron carbide consisting of boron doped, distorted multi

65 e we report the directional amorphization in boron carbide polycrystals.

66 num nanoparticles supported on graphite-rich boron carbide show a 50-100% increase in activity in aci

67 rystalline, porous COFs from light elements (boron, carbon, nitrogen, oxygen, and silicon) that are c

68 ), epitaxially embedded in a two-dimensional boron-carbon-nitrogen alloy.

69 Indeed, the boron center in PhBCO is isoelectronic with the carbene

70 ecause of its electron-rich sp(3)-hybridized boron center.

71 dy demonstrates the first example of tunable boron chemistry in a folded nonnative protein, which off

72 ing boron in cells could expand the scope of boron chemistry in living systems.

73 met need to develop chemoselective access to boron chemotypes, we report herein the synthesis of alph

74 The structure and bonding of a Pr-doped boron cluster (PrB7(-) ) are investigated using photoele

75 odecacarboranyl-1-thio)propanoic acid (3), a boron cluster amino acid that exhibits self-assembly to

76 Two bismuth boron cluster anions, BiB2 O(-) and Bi2 B(-) , containin

77 noccupied orbital delocalized throughout the boron cluster core.

78 e that this review will be of great value to boron cluster scientists and researchers working in the

79 coordination polymers containing icosahedral boron clusters in the last few decades, which have recei

80 was converted to its corresponding difluoro boron complex, and the extent of pi-conjugation was exte

81 cle reports the synthesis of four-coordinate boron complexes based on the unexplored 7-(azaheteroaryl

82 opening the door to design main-group metal-boron complexes with multiple bonding.

83 An electron-rich monovalent boron compound is used as a Lewis base to prepare adduct

84 The boron compounds 3 and 4 have shown low cytotoxicity acti

85 onstrate how the interactions of sugars with boron compounds can be combined with transition metal ca

86 ture Database counts 1253 entries for binary boron compounds!), it is surprising that the application

87 Boron concentrations and isotopic compositions of atmosp

88 ot significantly change tree productivity or boron concentrations in live leaves, wood or leaf litter

89 , Zinc, Iron, Manganese, Copper, Sulphur and Boron concentrations under salinity were also mapped.

90 their carbon isosteres that changed based on boron connectivity.

91 acterization of a novel series of main-chain boron-containing conjugated polymers (CPs), boron "doped

92 h represent the first examples of main-chain boron-containing CPs without aromatic moieties within th

93 witch and the formation of a six-pi-electron boron-containing heteroaromatic system.

94 ods that enhance the heteroatom diversity of boron-containing molecules within a limited set of scaff

95 d electronic properties of this new class of boron-containing polymers.

96 ing a nitrogen-based donor, as well as a new boron-containing radical.

97 on of low cytotoxicity, amphiphilicity, high boron content, high cellular uptake, and moderate BBB pe

98 respect to both the transition metal and the boron content.

99 The notable high boron contents (190-390 mug.g(-1)) of the dust samples a

100 ingle-crystal boron-doped diamond (BDD) with boron contents ranging from 50-3000 ppm.

101 25 degrees C), enabled by facile changes in boron coordination.

102 lomb (de)stabilization originating from the "boron core" and "halogen shell" and the extension of the

103 e most positively charged region, viz., the "boron core" for X = F, Cl, and the surrounding "halogen

104 In this series of MCAs, comprising a "boron core" surrounded by a "halogen shell", the sign of

105 ization of rhamnogalacturonan-II (RG-II) via boron cross-links contributes to the assembly and biophy

106 Instead, the boron data from this study are consistent with a Rayleig

107 ropical tree species revealed no evidence of boron deficiency or toxicity at concentrations likely to

108 thaliana) boron efflux transporter displayed boron deficiency phenotypes.

109 oil, and is therefore sufficient to preclude boron deficiency.

110 rmeability renders these compounds promising boron delivery agents for the BNCT of brain tumors.

111 ntly lower HER activity, indicating a strong boron-dependency of these borides for the HER.

112 followed by an intramolecular version of the boron deprotection reaction can be applied to access the

113 n of two new fluorescent molecular rotors of boron derived from Schiff bases: (2,4,8,10-tetra-tert-bu

114 Boron-derived Lewis acids have been shown to effectively

115 Foliar boron did not correlate with soil boron along a local sc

116 Indeed, it has been reported that boron difluoride dipyridylmethene (DIPYR) is nonemissive

117 pyridylmethene, boron diquinolylmethene, and boron diisoquinolylmethene.

118 sical properties of three simple DIPYR dyes: boron dipyridylmethene, boron diquinolylmethene, and bor

119 rin, chlorin, bacteriochlorin), chromophore (boron-dipyrrin, perylene, terrylene), and attachment sit

120 Boron dipyrromethene (BODIPY) derivatives have found wid

121 Boron-dipyrromethene (BODIPY) chromophores have a wide r

122 Relying on the boron-dipyrromethene (BODIPY) core, all the probes as we

123 as menadione (a quinone redox center), to a boron-dipyrromethene (BODIPY) fluorophore (a lipophilic

124 igand-photosensitizer construct, IYIY-diiodo-boron-dipyrromethene (IYIY-I2-BODIPY) and its scrambled

125 Three furan fused boron dipyrromethenes (BODIPYs) with a CF3 group on the

126 e simple DIPYR dyes: boron dipyridylmethene, boron diquinolylmethene, and boron diisoquinolylmethene.

127 We conclude that boron does not influence tree species distributions in P

128 a novel form of boron carbide consisting of boron doped, distorted multiwalled carbon nanotubes (MWC

129 boron-containing conjugated polymers (CPs), boron "doped" polyacetylenes (BPAs), which represent the

130 It is based on boron-doped diamond (BDD) electrodes and a competitive m

131 HOBr) oxidants was evaluated on Ti-IrO2 and boron-doped diamond (BDD) electrodes using a suite of tr

132 ed but well-separated glassy carbon (GC) and boron-doped diamond (BDD) electrodes.

133 ge (HV > 80 GPa) by examining single-crystal boron-doped diamond (BDD) with boron contents ranging fr

134 ng electrodes, including glassy carbon (GC), boron-doped diamond (BDD), and screen-printed graphitic

135 seemingly catalytically inactive electrode, boron-doped diamond (BDD), is found to be active for CO2

136 l production activity (6.6 x 10(-14) M) with boron-doped diamond (BDD, 7.4 x 10(-14) M) electrodes.

137 Although boron-doped diamond anodes mineralized haloacetic acids

138 e amperometry with a cathodically pretreated boron-doped diamond electrode, using 0.30molL(-1) H2SO4

139 which is significantly higher than that for boron-doped diamond.

140 ith hydride elimination to afford the doubly boron-doped dibenzo[g,p]chrysene Li2[1].

141 A boron-doped graphene quantum dot (B-GQD) as a metal-free

142 Transition-metal-boron double bonding is known, but boron-metal triple bo

143 log of an Arabidopsis (Arabidopsis thaliana) boron efflux transporter displayed boron deficiency phen

144 1 plays a key role in tolerance to high soil boron, facilitating the efflux of borate from cells.

145 A unique nanoheterostructure, a boron-filled hybrid carbon nanotube (BHCNT), has been sy

146 ed good chelating abilities toward trivalent boron fragments such as BF2 or BPh2 to yield the corresp

147 which showed typical reactions of an oxygen/boron frustrated Lewis pair.

148 rrent with advances in the synthesis of pure boron fullerenes and atom-thin layers, motivates an expl

149 rious rings in fused ring systems built upon boron heterocycles.

150 may be drawn with the oxidative addition of boron-hydrogen and silicon-hydrogen bonds to transition

151 se complexes, through carbene insertion into boron-hydrogen bonds.

152 ygen and radical scavengers, we propose that boron-imidates form under the basic reaction conditions

153 ccounts for a considerable proportion of the boron in annual litterfall and is similar to the pool of

154 l that Bi forms triple and double bonds with boron in BiB2 O(-) ([Bi identical withB-B identical with

155 This tunable method for manipulating boron in cells could expand the scope of boron chemistry

156 The annual input of boron in rainfall accounts for a considerable proportion

157 nd is similar to the pool of plant-available boron in the soil, and is therefore sufficient to preclu

158 The synthetic utility of the boron incorporated product has been demonstrated by orth

159 acent carbon resulting in formation of ortho boron-incorporated coupled products.

160 agon concentration in the ground state of 2D boron increases to 1/7 from 1/8 in its charge-neutral st

161 the operative mechanistic pathway is through boron-induced activation of the alkyne followed by elect

162 tic tool for the incorporation of polyhedral boron into novel organic structures.

163 nown wet deposition marine derived elements: boron, iodine, and selenium.

164 antioenriched alkylboronate esters, in which boron is bound to a stereogenic carbon, and we highlight

165 t atomic layer of the as-deposited amorphous boron is the dominant factor leading to the formation of

166 Plant-available boron is uniformly low in tropical forest soils of Panam

167 Despite its electron deficiency, boron is versatile in forming multiple bonds.

168 ining corrugated layers of covalently bonded boron, is a superhard metallic compound with a microhard

169 Here, we use orbitally resolved, boron isotope CO2 data to show that the glacial to inter

170 Here we present boron isotope data-a proxy for seawater pH-that show tha

171 nergy and electronic bandgap varied with the boron isotope mass, the latter due to the quantum effect

172 onal boron nitride crystals with nearly pure boron isotopes ((10)B and (11)B) compared to those with

173 Boron isotopes in dissolved depositions show a clear sea

174 Boron isotopes in dust differ from dissolved inputs, wit

175 istics made by depositing an atomically thin boron layer at a relatively low temperature where no dop

176 etween the n-silicon and the atomically thin boron layer.

177 contains only the more active graphene-like boron layers) by a 5-times increase of its surface area.

178 Two different boron layers, flat (graphene-like) and puckered (phospho

179 omega) in the selected example structures of boron layers.

180 amines are more chemically stable than their boron-linked counterparts, making them more promising fo

181 gradual decomposition of the preformed metal-boron (M-B, M=Fe, Co, Ni, NiCo) composite nanospheres wh

182 s that the predicted unusual behaviors of 1D boron may find powerful applications in nanoscale electr

183 urrent density of 100 A/cm(2), is above the boron melting point (2350 K).

184 ion-metal-boron double bonding is known, but boron-metal triple bonds have been elusive.

185 additional ligand; in other words, they are boron metallomimics.

186 It was recently proposed that boron might be the most important nutrient structuring t

187 d theory, we show that nanoalloying Pt7 with boron modifies the alkene-binding affinity to reduce cok

188 However, using pinacol boronic esters, the boron moiety migrates to the adjacent carbon resulting i

189 Boron nanostructures are easily charged but how charge c

190 Progress in the synthesis of boron nanostructures suggests that the predicted unusual

191 lled carbon nanotubes (MWCNTs) encapsulating boron nanowires.

192 gh incompressibility and a three-dimensional boron network that withstands shear.

193 accomplished by an in-plane rotation of the boron network, which maximizes the in-plane hybridizatio

194 Crystalline 2D hexagonal boron nitride (2D-hBN) nanosheets are explored as a pote

195 One of the low-dimensional Boron Nitride (BN) forms, namely, cubic-BN (c-BN) nanodo

196 actuator made of carbon nanotubes (CNTs) and boron nitride (BN) is developed that can withstand high

197 y pass through interlayer spaces in hydrated boron nitride (BN) membranes.

198 Atomically thin boron nitride (BN) nanosheets are important two-dimensio

199 based on graphene-like 2D materials, such as boron nitride (BN), graphite-carbon nitride (g-C3N4), tr

200 s for the large-scale synthesis of hexagonal boron nitride (h-BN) by chemical vapour deposition (CVD)

201 Herein, hexagonal boron nitride (h-BN) films are prepared from chemical va

202 pattern in highly aligned graphene/hexagonal boron nitride (h-BN) heterostructures is a lateral super

203 heterostructures with graphene and hexagonal-boron nitride (h-BN) inks, and use them to fabricate all

204 The controlled exfoliation of hexagonal boron nitride (h-BN) into single- or few-layered nanoshe

205 ication of individual nanopores in hexagonal boron nitride (h-BN) with atomically precise control of

206 Two-dimensional (2D) hexagonal boron nitride (h-BN), which has a similar honeycomb latt

207 0 nuclear spins in atomically thin hexagonal boron nitride (h-BN).

208 ul growth of MoSe2 on single-layer hexagonal boron nitride (hBN) on the Ru(0001) substrate using mole

209 ted from atomic defects in layered hexagonal boron nitride (hBN), but controlling inhomogeneous spect

210 ime through isotopic enrichment of hexagonal boron nitride (hBN).

211 We report a CVD hexagonal boron nitride (hBN-) assisted transfer method that enabl

212 y the unoccupied band structure of graphite, boron nitride and their heterostructures using angle-res

213 We demonstrate that graphene and boron nitride bands do not interact over a wide energy r

214 lamellar compounds by synthesizing hexagonal boron nitride crystals with nearly pure boron isotopes (

215 pothesis in which oxygen-terminated armchair boron nitride edges are proposed to be the catalytic act

216 ormance is enabled by epitaxial growth on 2D boron nitride for chemical-free transfer to a soft, flex

217 Pristine graphene encapsulated in hexagonal boron nitride has transport properties rivalling suspend

218 trate a device in which a graphene/hexagonal boron nitride heterostructure is suspended over a gold n

219 monolayer graphene and multilayer hexagonal boron nitride heterostructures, we discuss the potential

220 Hexagonal boron nitride is a model lamellar compound where weak, n

221 oxidation of atomically thin two-dimensional boron nitride is studied.

222 eter-thin molybdenum disulfide and hexagonal boron nitride microcrystals, the most-promising van der

223 gh quality, 2-dimensional single crystalline boron nitride nanosheets (BNNSs) at a low substrate temp

224 om restacking of liquid exfoliated hexagonal boron nitride nanosheets (BNNSs) is reported.

225 cles assembled on vacancy-abundant hexagonal boron nitride nanosheets and their use as a model cataly

226 omposites with silver nanoparticle-deposited boron nitride nanosheets as fillers could effectively en

227 composite with silver nanoparticle-deposited boron nitride nanosheets outperforms the one with boron

228 o the lower thermal contact resistance among boron nitride nanosheets' interfaces.

229 nitride nanosheets outperforms the one with boron nitride nanosheets, owning to the lower thermal co

230 ng connections of silver nanoparticles among boron nitride nanosheets.

231 feature of Pt after assembling on hexagonal boron nitride nanosheets.

232 ctural stability and mechanical integrity of boron nitride nanotubes (BNNTs) in high temperature envi

233 Boron nitride nanotubes (BNNTs) were successfully synthe

234 t that iron (Fe) quantum dots functionalized boron nitride nanotubes (QDs-BNNTs) can be used as the f

235 eport atmospheric oxygen induced cleavage of boron nitride nanotubes at temperatures exceeding 750 de

236 page in carbon nanotubes, and no slippage in boron nitride nanotubes that are crystallographically si

237 orphological and chemical transformations in boron nitride nanotubes under high temperature atmospher

238 in few-layer InSe encapsulated in hexagonal boron nitride under an inert atmosphere.

239 Brx), incorporating GaN, monolayer hexagonal boron nitride, and graphene aerogel.

240 ogenide, graphitic carbon nitride, hexagonal boron nitride, and phosphorene) are emerging extraordina

241 t defects emerging in graphene and hexagonal boron nitride, as probed by atomically resolved electron

242 o the emergence and development of hexagonal boron nitride, black phosphorus, and transition metal di

243 In hexagonal boron nitride, low-loss infrared-active phonon-polariton

244 iquids, such as those (e.g., carbon nitride, boron nitride, metal-organic frameworks, covalent organi

245 ted effect with phonon-polaritonic hexagonal boron nitride, plasmonic super-lattices and hyperbolic m

246 ngle-layer graphene, and few-layer hexagonal boron nitride, respectively, are utilized to design high

247 ion in a host of materials such as hexagonal boron nitride, silicon carbide, and others.

248 ase of aligned or nearly-aligned graphene on boron nitride, the graphene lattice can stretch and comp

249 anomaterials (e.g. graphitic carbon nitride, boron nitride, transition metal dichalcogenides, and tra

250 as well as on exfoliated flakes of hexagonal boron nitride.

251 f high-quality BLG encapsulated in hexagonal boron nitride.

252 uctor/insulator/metal layers (WSe2/hexagonal boron nitride/graphene) in a semifloating gate field-eff

253 ructures consisting of dual-gated, hexagonal-boron-nitride-encapsulated bilayer graphene.

254 The intramolecular boron-nitrogen coordination bonds played a key role in r

255 ns allowing for directly anchoring it to the boron of the subphthalocyanine.

256 orine, 14 containing bromine, one containing boron, one containing selenium.

257 al copolymerization of styrene with designer boron or phosphorus containing monomers.

258 preferred structure of two-dimensional (2D) boron, or "borophene", on charge doping controlled by a

259 Both pure and boron- or nitrogen-doped graphene are interfaced with th

260 onding, the hybridization among out-of-plane boron orbitals is crucial for determining the relative s

261 correlate to the hybridization states of the boron orbitals that form the B-B bonds and to the streng

262 herto longest periacene analogue with oxygen-boron-oxygen (OBO) segments along the zigzag edges, that

263 (1) there is an absence of dynamics but the boron pairs are crystallographically equivalent or (2) t

264 e crystallographically equivalent or (2) the boron pairs are crystallographically inequivalent but ar

265 Recently discovered two-dimensional (2D) boron polymorphs, collectively tagged borophene, are all

266 time as removable protecting groups for the boron position of 1,2-azaborines during reactions that a

267 found that samples prepared with a metal to boron ratio of 1:11.6 to 1:9 have similar hardness value

268 DABCO as the catalyst and H-Bpin as both the boron reagent and stoichiometric hydride source has been

269 ic studies via UV-vis spectroscopy with this boron reagent found second-order kinetics, supporting th

270 (18)F-fluorination for a representative aryl boron reagent, and on the labeling of more than 50 (hete

271 e copper-mediated (18)F-fluorination of aryl boron reagents with (18)F-fluoride as a model reaction.

272 mide layer may reduce selectivity, e.g., for boron rejection.

273 gh-like evolution of the atmospheric gaseous boron reservoir with possible but limited anthropogenic

274 The interplay between metals and the boron results in even more varied material's properties,

275 With both electrodes made from the same boron-rich alloy, we found that the arc operation unstab

276 ion and arc synthesis were achieved with the boron-rich anode and the cathode made from a refractory

277 ly synthesized by a dc arc discharge using a boron-rich anode as synthesis feedstock in a nitrogen ga

278 ted as resulting from localized spreading of boron-rich fertilizers, thus indicating a significant lo

279 er 2D materials have been suggested based on boron, silicon, germanium, phosphorus, tin, and metal di

280 ommercially available external electrophilic boron source (B-chlorocatecholborane) in good to high yi

281 of the metal and the simultaneous release of boron species.

282 mpounds featuring multiply and singly bonded boron spin pairs.

283 wever, is limited by the behaviour of common boron starting materials as archetypal Lewis acids such

284 Here we characterize the nanotwins in boron suboxide (B6O) with twin boundaries along the {011

285 For the luminescent material boron subphthalocyanine chloride, the photovoltage deter

286 es, which would trigger 1,2-migration of the boron substituent, creating the new C-C bond.

287 ve 1,1-diboration provided products with two boron substituents that exhibit differential reactivity.

288 Experimental manipulation of boron supply to seedlings of three tropical tree species

289 triggering the 1,2-migration of the group on boron to carbon giving a dearomatized bromoallene interm

290 rearranges via a 1,2-fluorine migration from boron to carbon.

291 s of the transfer of the organic moiety from boron to palladium in the key transmetalation step.

292 Boron transport and homeostasis in plants is regulated i

293 indeed involved in both influx and efflux of boron transport.

294 lamines by triethylsilane in the presence of boron trifluoride etherate is studied and found to incre

295 acted with excess pyrrole in the presence of boron trifluoride etherate to give a tripyrrane analogue

296 Solid Phase Extraction (SPE), methylated by boron trifluoride in methanol, and injected into GC-FID

297 es the formation of B-O and B-N bonds at all boron vertices (B(2), B(4), B(5), and B(9)) of meta-carb

298 For variable boron WBx, it was found that samples prepared with a met

299 ride alloys with a variable concentration of boron were prepared by arc-melting and investigated for

300 ODIPYs with PEG substituents attached to the boron, whereas in the second series, PEG substituents ar