ライフサイエンスコーパス: benzene

1 as volatile (non-polar) VOC molecules (i.e., benzene).

2 id glass processed from 1,3,5(triethoxysilyl)benzene.

3 oximity to gasoline stations and exposure to benzene.

4 r in situ reductive dechlorination of MCB to benzene.

5 mination sequence starting from 2-fluoro-SF5-benzene.

6 termediate that is more highly oxidized than benzene.

7 best practices should include monitoring for benzene.

8 tadiene (OR = 3.15; 95% CI: 1.57, 6.32), and benzene.

9 degradation of daughter products, especially benzene.

10 shown to undergo an arylation reaction with benzene.

11 affinity for Ab dropped only slightly versus benzene.

12 ated for the production of benzaldehyde from benzene.

13 dent chemical shift value lower than that of benzene.

14 henylethynyl bromide or 1,4-bis(bromoethynyl)benzene.

15 ith very low level exposure to environmental benzene.

16 he reactions of MeTAD with other substituted benzenes.

17 ve hindered their application to substituted benzenes.

18 ed hydroxylations and nitrohydroxylations of benzenes.

19 lco sparverius) were exposed to a mixture of benzene (0.6 ppm), toluene (1 ppm), nitrogen dioxide (NO

20 VOCs studied here include aromatics such as benzene (1.03 pptv/ppbv CO), toluene (3.10 pptv/ppbv CO)

21 These diversely functionalized benzenes (1,2-teraryls or 1,3-teraryls), bearing naphthy

22 O(-CO2)6 secondary building units (SBUs) and benzene-1,3,5-tri-beta-acrylate, BTAC.

23 (HCO2)6] secondary building units (SBUs) and benzene-1,3,5-tribenzoate (BTB) bridging ligands is repo

24 2.5 mol %), both possessing a complementary benzene-1,3,5-tricarboxamide (BTA) central unit, were in

25 between two slightly structurally different benzene-1,3,5-tricarboxamide (BTA) monomers functionaliz

26 ation of different disc-shaped cores such as benzene-1,3,5-tricarboxamides (BTAs), perylenes bisimide

27 ing structure and disorder for four columnar benzene-1,3,5-trisamides by total X-ray scattering and D

28 AB = 4-aminobenzoate), which was linked with benzene-1,4-dialdehyde using imine condensation reaction

29 This study discloses that benzene-1,4-diboronic acid (BDBA) was effective in drivi

30 ation of a new MOF [Yb2(BDC)3(DMF)2]H2O (BDC=benzene-1,4-dicarboxylate and DMF=N,N-dimethylformamide)

31 ty (IUPAC name (E)-2-(2-quinolin-2-yl-vinyl)-benzene-1,4-diol HCl) hereafter designated Q8.

32 For the ligand 4-(trifluoromethyl)benzene-1-carboximidamide binding to the protein trypsin

33 n for the reporter ligand 4-(trifluoromethyl)benzene-1-carboximidamide.

34 of homoleptic Ta(0) complexes are known, Ta(benzene)2 and Ta(dmpe)3 , dmpe=1,2-bis(dimethylphosphano

35 he P2X antagonist pyridoxal phosphate-6-azo (benzene-2,4-disulfonic acid (PPADS) but not by the 5-HT3

36 Here we show that phenanthrene, a PAH with a benzene 3-ring structure, is the key moiety disrupting t

37 (eta(2)-PhCF3) (5) and TpMo(NO)(DMAP)(eta(2)-benzene) (3) is described.

38 es is higher for diesel BC (62-85%) than for benzene (38-71%), reflecting the difference in these pol

39 utyldibenzo[d,h][1,3,6,2]dioxazaboronin-6-yl)benzene (4), as well as the free ligand 2-[[(3,5-di-tert

40 parent absence of aromatic compounds such as benzene, a lack of sulfur-bearing species, and very low

41 res and jobs have 1 common chemical exposure-benzene, a recognized cause of acute leukemia in adults-

42 e XB acceptor, the association in deuterated benzene/acetone/methanol 70:30:1 at 283 K reaches Ka =(2

43 OO)(L)], (H3btb = 1,3,5-tris(4-carboxyphenyl)benzene acid, L = methanol, water, or ethanol), has been

44 nation if exposed to H2 at 1 atm pressure in benzene, affording the silane borane 5-H2 , L(H2 )Si-R-B

45 is allowed to stand, clean conversion to the benzene analogue 3 occurs, and this complex may be preci

46 ine and pyridazine derivatives, close to the benzene analogues and significantly higher than thiophen

47 ff reaction between 1,3,5-tris(4-aminophenyl)benzene and 1,3,5-benzenetricarbaldehyde building blocks

48 On the other hand the systems with fused benzene and a six-membered ring formed atropisomers sepa

49 e studied by photoreaction of 1 in C6F6 with benzene and another substrate (HBpin, PhSiH3, or pentafl

50 alone is often insufficient: the carbons of benzene and cyclobutadiene, or those of diamond, graphen

51 lo-polycondensations of tetrakis(bromomethyl)benzene and dipiperidines under mild conditions.

52 e, thermodynamics prevents the production of benzene and favors formation of the carbene.

53 o be photoactive, enabling the activation of benzene and formation of a new benzoyl complex.

54 pound Specific Isotope Analysis to determine benzene and monochlorobenzene (MCB) stable carbon isotop

55 Rate studies of the isotopic exchange of benzene and monosubstituted arenes with weakly activatin

56 We predict strengths of favorable urea-benzene and N-methylacetamide interactions from experime

57 to C2 (ethylene and acetylene) and aromatic (benzene and naphthalene) products, at the tested conditi

58 diarylethenes of furanone series containing benzene and oxazole derivatives as aryl residues has bee

59 ugh supramolecular chain collapse, to expose benzene and perfluorobenzene motifs that promote a hairp

60 Next, we use benzene and polychlorinated biphenyls as examples to ill

61 The cycloadditions of benzene and ten different azabenzenes (pyridine, three d

62 ncer ancillary such as 2,6-diimidazolylidene benzene and the 6-pyrazolyl-2-phenoxylpyridine chromopho

63 Complex 2 reacted with benzene and toluene to make (C5Me5)2YPh, 7, and (C5Me5)2

64 For benzene and toluene, a reduction in the ion-neutral coll

65 s of detection are 137 ppbv and 401 ppbv for benzene and toluene, respectively.

66 oxidized by an acridinium catalyst, such as benzene and toluene, thus supporting a reactive amine ca

67 efficiently absorb the aromatic hydrocarbons benzene and toluene.

68 , and analysis of delta(13)C for chlorinated benzenes and ethenes.

69 d included occupational and household use of benzenes and solvents, traffic density, and traffic-rela

70 mug/L (MTBE, BTEX, chlorinated ethenes, and benzenes) and 60-97 mug/L for delta(2)H (MTBE and BTEX).

71 th traffic-related environmental exposure to benzene, and additional data are needed.

72 e repair facilities may be another source of benzene, and in 3 studies assessing these sources, we id

73 stribution maps of, e.g., nitrogen monoxide, benzene, and oxygen concentrations were obtained at a ne

74 ix molecules), pi-ligands (alkenes, alkynes, benzene, and substituted benzenes), miscellaneous inorga

75 enzene at room temperature under hydrogen in benzene, and the turnover frequency (TOF) was higher tha

76 rated for regular and perdeuterated acetone, benzene, and toluene as well as toluene-(13)C7 in nitrog

77 3-butadiene (OR = 2.23; 95% CI: 1.28, 3.88), benzene, and toluene; and with IQR increases in exposure

78 ides rapid access to 1,2,3,4-tetraoxygenated benzenes, and has been exploited by application to the t

79 cal groups, that is, carbohydrates, phenols, benzenes, and lignin phenols, together accounting for 62

80 aromatic, rigid, sigma,pi-macrocyclic carbo-benzene archetypes of various substitution patterns, wit

81 tron-deficient and electron-rich substituted benzenes are successfully alkylated.

82 al types of non-aromatic references of carbo-benzenes are then considered, i.e. freely rotating sigma

83 with a substituted 1,6-cyclodecadiyne using benzene as a solvent at room temperature as well as stud

84 Using Kekule benzene as a suitable reference, the AIs of 30 mono- and

85 the BN core, further endorsing the inorganic benzene as a versatile aromatic scaffold for engineering

86 alcium hydride-react with protio and deutero benzene at 60 degrees C through nucleophilic substitutio

87 Inhalation of benzene at levels below the current exposure limit value

88 hyl ketone (MEK), isobutyl alcohol (i-BuAl), benzene (B), toluene (T), p-xylene (p-X), m-xylene (m-X)

89 on timescales congruent with known rates for benzene binding.

90 Et3)4L2 superatoms that are bridged with L = benzene bis-1,4-isonitrile to form polymer strands.

91 Since the discovery of the first "inorganic benzene" (borazine, B3N3H6), the synthesis of other nonc

92 s consisting of 1,4-bis[2-(4-pyridyl)ethenyl]benzene (BPEB) and PdCl2 of variable thicknesses (0-13.4

93 lamine redox centers that are connected to a benzene bridge via alkyne spacers at para- and meta-posi

94 d in para- or in meta-positions to a central benzene bridge, we investigated three series of mixed va

95 anomalous solubility (it is only soluble in benzene but not in other common solvents).

96 the branching ratio of SO4(*-) reacting with benzene, but inversely correlated with that of HO(*) or

97 second singlet excited states (S1 and S2) of benzene (C6H6) and square cyclobutadiene (C4H4) are inve

98 We argue that benzene can be viewed as a molecular "Dr Jekyll and Mr H

99 Formation of the benzene cation is demonstrated in AIMD simulations of ac

100 products including the aromatic ring of the benzene cation.

101 PCDD/F precursors, involving all chlorinated benzenes (CBz) and chlorinated phenols (CPh).

102 ,6-TriCPh), but have detected no chlorinated benzenes (CBzs).

103 of the bis(imino)pyridine molybdenum eta(6)-benzene complex ((iPr)PDI)Mo(eta(6)-C6H6) ((iPr)PDI, 2,6

104 e isomers and three halogenated, substituted benzene compounds.

105 of S2O8(2-) decomposition increasing as the benzene concentration increased.

106 ees C, pH 6, and 500 mg L(-1) of the initial benzene concentration.

107 About 83% of Tehran's surface had benzene concentrations above air quality standard of 5 m

108 Benzene concentrations in a few bars approached the 8-h

109 tion of MeOTf to 1 results in elimination of benzene concomitant with the formation of the phosphonio

110 om the market (n=170) further confirmed that benzene content is significantly correlated to the prese

111 NPA thermolysis in 1,3-cyclohexadiene and/or benzene-d6 are consistent with a model of unimolecular f

112 eters, i.e., alkalinity, pH, and chloride on benzene degradation via heterogeneous persulfate activat

113 ed the rates of persulfate decomposition and benzene degradation, which was associated with the forma

114 etized from 1,3,5-trihydroxybenzene or other benzene derivatives through dehydration and polymerizati

115 Permeation studies using benzene derivatives whose kinetic diameters differ by le

116 unts of monoterpenes, aliphatic alcohols and benzene derivatives, were released using pectinolytic pr

117 allowing the formation of 1,2-di(heteroaryl)benzene derivatives.

118 it to identify D-Cycloserine and furan-based benzene-derived compounds with known Mur ligase inhibiti

119 decorated tetraphenylethylene and one of two benzene dicarboxylate species.

120 rdination sites were connected via a ditopic benzene-dihydroxamate linker.

121 f two passive tracers--tetramethylsilane and benzene--dissolved in an organic solution of active Grub

122 t trapping of the cationic intermediate with benzene does not proceed via a Friedel-Crafts-type react

123 Benzene emissions ranged between 51 +/- 4 and 60 +/- 4 k

124 talytic system for the C-H bond arylation of benzene enables the formation of biaryl compounds in the

125 th extremely low dielectric constants (e.g., benzene, epsilon of 2.27, or cyclohexane, epsilon of 2.0

126 region when this indicator was combined with benzene estimates.

127 oton transfer (SET-PT) mechanisms of 5CQA in benzene, ethanol, and water solutions.

128 The direct and single-step conversion of benzene, ethylene, and a Cu(II) oxidant to styrene using

129 butadiene; TFA is trifluoroacetate] converts benzene, ethylene, and Cu(II) acetate to styrene, Cu(I)

130 aluated the association between occupational benzene exposure and NHL among 73,087 women enrolled in

131 evidence for a positive association between benzene exposure and NHL risk.

132 emia with occupational and household product benzene exposure and traffic-related pollution.

133 a and several different potential metrics of benzene exposure.

134 benzoic acid (which is a known precursor of benzene formation).

135 MoC3 clusters, whose presence coincides with benzene formation.

136 e number of four-coordinate carbon atoms per benzene formula unit as the degree of saturation, a set

137 t with the rates of reductive elimination of benzene from a series of isoelectronic Ir(III) phenyl hy

138 ethane is lost with concomitant formation of benzene from an unstable phosphorus(V) intermediate, yie

139 so been associated with parental exposure to benzene, gasoline, motor vehicle-related jobs, painting,

140 derived from (3,3,3-trifluoroprop-1-yn-1-yl)benzene give access to functionalized ring-opening alkyn

141 ight MeOH molecules and encapsulation of two benzene guests.

142 f CoCl2 with 1,3,5-tri(1H-1,2,3-triazol-5-yl)benzene (H3BTTri) in N,N-dimethylformamide (DMF) and met

143 Women ever exposed to benzene had a significantly higher risk of NHL [hazard r

144 Eight of nine samples containing benzene had groundwater ages >2500 years, indicating the

145 Recently, a direct arylation of unactivated benzene has been achieved in the presence of base (tBuOK

146 amended incubations confirmed that alkylated benzene hydrocarbons were metabolized via known anaerobi

147 rch on Cancer (IARC) working group evaluated benzene in 2009 and noted evidence for a positive associ

148 well as oxidize cyclohexadiene substrates to benzene in a formal H2-transfer process.

149 ble peripheral aromatic rings around central benzene in hexaarylbenzene (HAB) derivatives create a ve

150 From these, the benzene in its solvate form acts as rotation stopper, as

151 the transient mixing dynamics of toluene and benzene in the fingerprint region (200-1500 cm(-1)) with

152 artitioning coefficients were determined for benzene in water/supercritical CO2 over the range 35-65

153 classical UV-vis electronic spectra of carbo-benzenes in solution (lambdamax = 445.5 +/- 1 nm, epsilo

154 dearomatization reagent TpW(NO)(PMe3)(eta(2)-benzene), in which the 1,3-dimethoxybenzene (DMB) analog

155 trated to be reactive with added substituted benzenes, including anisole.

156 We observed a dose-dependent increase in benzene-induced chromosomal damage and estimated a bench

157 DO mice may provide additional insight into benzene-induced genotoxicity.

158 odine](+) and [1,2-bis((pyridine-2-ylethynyl)benzene)iodine](+) BF4(-) complexes substituted with ele

159 Benzene is an established cause of adult leukemia, but i

160 Benzene is an established cause of adult leukemia, but w

161 In contrast, the electron-rich pi-system of benzene is highly resistant to reactions with electron-r

162 hilic aromatic substitution of a C-H bond of benzene is one of the archetypal transformations of orga

163 between Naph(+*)(Pyr) and Bz(+*)(Pyr) (Bz is benzene) is understood by energy decomposition analysis.

164 H, H3BTTri =1,3,5-tris(1H-1,2,3-triazol-5-yl)benzene)), is found to be highly selective in the adsorp

165 hing features from its carbonaceous isostere benzene: its ability to serve as an NH hydrogen bond don

166 iodine(III) reagent, [hydroxy(tosyloxy)iodo]benzene (Koser's reagent), has been developed.

167 Linear alkyl benzenes (LAB) are global chemicals that are produced by

168 tered radicals has been achieved by treating benzene-linked allene-ynes with aryldiazonium tetrafluor

169 ](H2O) (L = 1,2,4,5-tetrakis(phosphonomethyl)benzene, Ln = La, Ce, Pr, Nd, Sm, Eu, Gd) have been synt

170 of phenol only accounted for 30%-60% of the benzene lost in the presence of O2.

171 Flash vacuum pyrolysis of 1,3-bis-iodomethyl-benzene (m-C8H8I2) produces m-C8H8 in gas phase; we used

172 s, molecular units of alpha-graphyne ('carbo-benzene' macrocycles) can be inserted between two anilin

173 ecent victories in the C....._ C cleavage of benzene made possible by a four-pronged iridium gig that

174 pies for these compounds and caffeic acid in benzene, methanol, and water were used for thermodynamic

175 (alkenes, alkynes, benzene, and substituted benzenes), miscellaneous inorganic ligands, and biologic

176 ine/3,3',5,5'-tetrachloro-1,4-bis(pyridyloxy)benzene model of HCC.

177 in saturation of a one-dimensional stack of benzene molecules by enumerating the partially saturated

178 or the irreversible desolvation of entrapped benzene molecules.

179 an convert polycrystalline or single-crystal benzene monomer into single-crystalline packings of carb

180 of terephthalaldehyde and tris(4-aminophenyl)benzene monomers on top of a poly(ether sulfone) (PES) u

181 zation of prochiral 1,3,5-tris(3-bromophenyl)benzene (mTBPB) directly on the surface using an Ullmann

182 racterization of p-dialkyl-tetraphenyl-carbo-benzenes (n = 2, 8, 14, 20) are thus presented and compa

183 n of (iii) cumene from its major impurities (benzene, n-propylbenzene, and diisopropylbenzene) highli

184 examples like molecular nitrogen and oxygen, benzene, naphthalene and their azaderivatives, porphyrin

185 ril tetramer backbone and terminal aromatic (benzene, naphthalene) sidewalls, to act as solubilizing

186 diene, indene, azulene, cycloheptatriene, or benzene, new families of porphyrin-like macrocycles were

187 urban enhancement emission ratios of TEX-to-benzene on a seasonal basis, two potential source signat

188 duced cyclization of 1,2-bis(2-phenylethynyl)benzene on Au(111) using scanning tunneling microscopy a

189 avity surface openings large enough to admit benzene on timescales congruent with known rates for ben

190 elaxometry experiments demonstrate that pure benzene or xylene confined in isoreticular metal-organic

191 hermore, the yields of two major products of benzene oxidation, i.e., phenol and aldehyde, were posit

192 e reactivity of soluble Fe(III) toward known benzene photooxidation products that include fumaric (tr

193 ature mediated by [bis(trifluoroacetoxy)iodo]benzene (PIFA) and N-bromosuccinimide (NBS) using cyanam

194 es linked by eight 1,4-bis(diphenylphosphino)benzene pillars.

195 for two complementary PyC molecular markers, benzene polycarboxylic acids (BPCAs) and polycyclic arom

196 rsistent organic pollutants: polychlorinated benzenes, polychlorinated biphenyls, polychlorinated dib

197 t each of the four possible positions of the benzene portion of the 3-(3',4',5'-trimethoxyanilino)ben

198 ials, here we show that by using 1,3,5 silyl benzene precursors, the connectivity of a silicon atom w

199 n product is also obtained in the absence of benzene, presumably from a tricationic intermediate.

200 Benzene, pyrimidine, and pyridazine derivatives exhibit

201 hrough the carbonization of hypercrosslinked benzene, pyrrole, and thiophene.

202 ric efficiency, as determined by the loss of benzene relative to the loss of persulfate, approached t

203 study introducing an Aspergillus strain for benzene removal and these results highlight that the dev

204 activity, substitutions at position 4 of the benzene ring A were associated with higher transcription

205 reas a new pathway yielding oxidation of the benzene ring after the cleavage of the piperazine ring (

206 model and an archetypal example of the para-benzene ring and are shown to be robust under a weak dis

207 5 to strengthen the interaction between this benzene ring and the agonist's quaternary ammonium (QA)

208 on the organic chemistry of an eta(2)-bound benzene ring are explored using the complex TpW(NO)(PMe3

209 arley straw adsorbent and pi* carbon atom in benzene ring attached to fluorine of levofloxacin was in

210 c transformations which include instances of benzene ring contraction to cyclopentadiene or the forma

211 ped coronene derivative in which the central benzene ring has been replaced by a borazine core is des

212 roxide might whiten HA-AAAs by oxidizing the benzene ring in AAAs.

213 chiral open-shell hydrocarbon, in which one benzene ring is fused to [5]helicene, forming a phenalen

214 Introduction of a para-nitro group into the benzene ring of the diene enabled separation of the Z,E

215 on conditions, the central and most strained benzene ring of the p-terphenyl systems was susceptible

216 ion and excited state antiaromaticity of the benzene ring should be reflected in its photochemical re

217 a deamination reaction at position C4 of the benzene ring to substitute the amino group with an hydro

218 how heteroaromatic ring substitution of the benzene ring will change the odour percept of acetopheno

219 of aryl rings in the linkages to the central benzene ring, coupled with the presence of only one meso

220 the porphyrins are arranged around a central benzene ring.

221 O)6 complex bonded to the para position of a benzene ring.

222 hat noncovalent interactions with associated benzene rings (a simple model of aromatic amino acid sid

223 Replacing benzene rings in arenes by thiadiazoles thereby provides

224 ndings demonstrate that directly linking the benzene rings of PIs with a single C-C bond is a viable

225 al calculations to explore how the fusion of benzene rings onto aromatic chameleonic units represente

226 rd pi-quartets or octets, enabling the outer benzene rings to adapt closed-shell singlet Clar pi-sext

227 somers with linear connectivity of the fused benzene rings to those with cis- or trans-bent connectiv

228 an even number of carbons (22, in six fused benzene rings), it is not possible to draw Kekule-style

229 irst examples of direct pi-stacking of carbo-benzene rings, with inter-ring distances very close to c

230 ally decorating functional groups on the two benzene rings.

231 rbon nanotubes that consist of n para linked benzene rings.

232 y for the detection of odorants that contain benzene rings.

233 tuted triangulene that consists of six fused benzene rings.

234 ssure were shown to have dramatic impacts on benzene's partitioning behavior.

235 markably reactive, hydroxylating methane and benzene selectively at low temperature to form methanol

236 Benzene showed the lowest processing factor (15%), where

237 mined to be 0.05 wt % 1,4-bis(2-methylstyryl)benzene singlet fluorophore and 0.28 wt % Ir(3+), respec

238 When a benzene solution of 5 is allowed to stand, clean convers

239 activity studies indicated the importance of benzene substituted as 2- or 4-methyl, or 4-fluoro, and

240 s of ATX derived by lead optimization of the benzene-sulfonamide in silico hit compound 3.

241 nsive structure-activity relationship of the benzene-sulfonamide scaffold that yielded a series of hi

242 mmon constituents of detergent (linear alkyl benzene sulphonate).

243 and 3,3',5,5'-tetrachloro-1,4-bis(pyridyloxy)benzene (TCPOBOP).

244 One sample contained benzene that could be from a surface release associated

245 or the formation of phenol from oxidation of benzene (the *OH probe used), but a value of about 10 kJ

246 Relative to benzene, the phenyl radical has a substantially larger C

247 of the first pnictogen-silicon congeners of benzene, the triarsa- and the triphospha-trisilabenzene

248 The bis(arylethynyl)arenes were composed of benzene, thiophene, or thieno[3,2-b]thiophene moieties,

249 ing reaction between 4-fluoroiodobenzene and benzene through an outer sphere electron transfer pathwa

250 ar triangle (T) [L1 = 1,4-di(4-pyridylureido)benzene; tmen = N,N,N',N'-tetramethylethane-1,2-diamine]

251 ctivity toward 1,2-addition of a C-H bond of benzene to form 3.

252 position of 1,2,4,5-tetrakis(4-carboxyphenyl)benzene to form supramolecular heterostructures.

253 ,N-diethylaniline, naphthalene, and even [D6]benzene to yield the compounds [Re2(CO)8(mu-H)(mu-eta(1)

254 Anthropogenic activities contribute benzene, toluene, and anisole to the environment, which

255 roxies for oxygenated aromatics derived from benzene, toluene, and anisole) react at the air-water in

256 elta(2)H) of methyl tert-butyl ether (MTBE), benzene, toluene, ethylbenzene, and o-xylene (BTEX), and

257 matic compounds, including the BTEX mixture (benzene, toluene, ethylbenzene, and the regioisomers of

258 tream in a production plant for detection of benzene, toluene, ethylbenzene, and the three structural

259 ative to methane were determined for hexane, benzene, toluene, ethylbenzene, and xylene (BTEX compoun

260 atic hydrocarbon content (largely made up of benzene, toluene, ethylbenzene, and xylene (BTEX)) was a

261 (PN) (over 5.6 nm); black carbon (BC); NO2; benzene, toluene, ethylbenzene, and xylene (BTEX); carbo

262 land sediments caused by the introduction of benzene, toluene, ethylbenzene, and xylenes (BTEX) and e

263 exposed to vehicle emissions, with combined benzene, toluene, ethylbenzene, and xylenes (BTEX) conce

264 ds emissions between PFI and GDIs, including benzene, toluene, ethylbenzene, and xylenes (BTEX).

265 nd volatile organic compounds (VOCs, such as benzene, toluene, ethylbenzene, and xylenes, or BTEX), a

266 We advanced LUR models for benzene, toluene, ethylbenzene, p-xylene, m-xylene, o-xy

267 um (crude oil/fuel) often involve monitoring benzene, toluene, ethylbenzene, xylenes (BTEX), and styr

268 The presence of BTEXS (benzene, toluene, ethylbenzene, xylenes and styrene) in

269 urements of CO2, CO, NOx, black carbon (BC), benzene, toluene, ethylbenzene-xylenes (BTEX), and size-

270 ganic compounds (four aromatic hydrocarbons (benzene, toluene, p-xylene, and styrene), six C2-C5 vola

271 It is further demonstrated by benzene TPD studies that the sensitivity of the REMPI-TO

272 works by auxiliary DCDPS/TCPP linkers (BTB = benzene tribenzoate, DCDPS = 4,4'-dicarboxydiphenyl sulf

273 OF consisting of Cu(II) centers connected by benzene-tricarboxylates (BTC) is prepared by thermoinduc

274 nyl-3,4-tetrahydroisoquinoline-1H-2-carbonyl)benzenes ulfonamide (30) exhibited a remarkable inhibiti

275 irm that benzaldehyde does indeed degrade to benzene under heating conditions, and especially in the

276 ion of the alkene and ortho cyanation of the benzene unit.

277 The AI confirms Clar's rule of disjoint benzene units in many cases, but corrects it in those ca

278 tic strategy starting from ortho-substituted benzene units to construct five-membered rings in this w

279 nvolves a change in the distance between the benzene units, which is common for azobenzene derivative

280 purposes, a comparably high contamination of benzene (up to 4.6mug/L) has been detected in cherry-fla

281 atistatin and (+)-7-deoxypancratistatin from benzene using an enantioselective, dearomative carboamin

282 ns, a sequence for the photocarbonylation of benzene using CO2 as the feedstock was constructed and d

283 a benchmark concentration limit of 0.205 ppm benzene using DO mice.

284 The synthesis of the first tin-bridged bis(benzene) vanadium and trovacene sandwich compounds and t

285 paternal exposure, in studies that assessed benzene versus all solvents, and in studies of gestation

286 icating that SO4(*-) preferentially oxidized benzene via pathways involving fewer hydroxylation steps

287 Benzene was always at lower concentrations than MCB, wit

288 Benzene was detected at low concentrations (<0.15 mug/L)

289 groundwater ages >2500 years, indicating the benzene was from subsurface sources such as natural hydr

290 s ranging from 0.64 for p-xylene to 0.70 for benzene were mainly driven by traffic-related variables

291 Methacrylic acid and vinyl benzene were used as functional monomers.

292 All alkyl-carbo-benzenes were also found to be highly crystalline.

293 es with a volatility equal to or lesser than benzene when employed in conjunction with TFME membranes

294 s was developed for efficient degradation of benzene, which can overcome the potential risk of leakag

295 ule published his theory of the structure of benzene, which he later reported had come to him in a da

296 luding a 2,000-fold decrease in emissions of benzene, which lowered health risks for response workers

297 Substitution of a CH group in benzene with nitrogen has a little effect on its aromati

298 tion metal-catalyzed persulfate oxidation of benzene with pure iron- and manganese-containing mineral

299 These reactions produce the n-alkyl benzenes with regeneration of the calcium hydride.

300 ctions were affected by the concentration of benzene, with rates of S2O8(2-) decomposition increasing