ライフサイエンスコーパス: benzene

1 (dubbed benzpolarene for its relationship to benzene).

2 actor regulators of the cellular response to benzene.

3 sonance energies of organic molecules, e.g., benzene.

4 omoting the adsorption and SERS detection of benzene.

5 ocalization function electronic structure of benzene.

6 yzed dearomative trans-1,2-carboamination of benzene.

7 duction potentials powerful enough to reduce benzene.

8 one, 1-methyl-4-(propa-1,2-dien-1-ylsulfonyl)benzene.

9 tion of functionalized acyclic products from benzene.

10 nations to form dienes and aromatics such as benzene.

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

12 hallenge, even for simple molecules, such as benzene.

13 latively less electron-rich arenes including benzene.

14 t of associated transcriptional response was benzene.

15 t and performing the acetylene conversion to benzene.

16 on-carbon bond formation in the synthesis of benzene.

17 yzed olefin cross-metathesis with homoprenyl benzenes.

18 ursor tetrakis- or hexakis- (trifluoromethyl)benzenes.

19 aled a selective and covalent hNE inhibitor: benzene-1,2-disulfonyl fluoride.

20 Through the combination of Zr(6) -BTB (BTB=benzene-1,3,5-tribenzoate) layers and diverse secondary

21 In this paper, a series of benzene-1,3,5-tricarboxamide (BTA) based supramolecular

22 upramolecular helices composed of an achiral benzene-1,3,5-tricarboxamide (BTA) ligand, coordinated t

23 copolymerization between two derivatives of benzene-1,3,5-tricarboxamide (BTA) monomers: a-BTA and N

24 sponsive, mono acyl hydrazone functionalized benzene-1,3,5-tricarboxamide (m-BTA) monomers that play

25 is a C(3)-symmetric monomer, consisting of a benzene-1,3,5-tricarboxamide core conjugated to a series

26 olecular (co)polymers based on water-soluble benzene-1,3,5-tricarboxamides (BTAs) that form double he

27 hod to locally mix Cu(2+) salt precursor and benzene-1,3,5-tricarboxylate (BTC(3-) ) ligand reagents,

28 had arithmetic mean (and 95% CI) as follows: benzene 17.83 (0.22, 98.05) g/h, toluene 34.43 (1.01, 12

29 90 Gg y(-1)) and is s source of carcinogenic benzene (30-280 Gg y(-1)).

30 ual compounds relative to the enhancement of benzene, a known tracer of fossil fuel in the United Sta

31 (mu(3) -NBn); reaction with mesityl azide in benzene affords a terminally bound imido complex ((tbs)

32 ized two small libraries of 2-OMe or 2-NO(2)-benzene analogues 2a-i and 3a-i containing a wide variet

33 he series of molecules investigated includes benzene and 18 monosubstituted derivatives.

34 d one to see two ion peaks, corresponding to benzene and 2-butanone.

35 Stereoisomers of 4-(1-hydroxyethyl)benzene and 4-(1,2-dihydroxyethyl)benzene moieties were

36 Taken together, we reveal how the ESAA in benzene and 6pai-electron heterocycles trigger photochem

37 reaction between a 1-azido-(2-halogenomethyl)benzene and a phosphine gives different products dependi

38 ubstitution reactions between ortho-difluoro benzene and catechol building units, which form ether li

39 re appears to support an association between benzene and childhood leukemia risk, with no indication

40 has sufficient detoxifying activity against benzene and chloroform to suggest that biofilters using

41 analyze the E(T(1)), E(S(1)), and E(T(2)) of benzene and cyclobutadiene (CBD) as excited-state antiar

42 ulations with phosphate- and dithiophosphate-benzene and dimethyl phosphate- and dimethyl dithiophosp

43 No solvate adduct could be formed between benzene and FeCp(2).

44 power (3.33 V vs. SCE) sufficient to oxidize benzene and halogenated benzenes via single-electron tra

45 hat at 20 GPa CHCF forms tilted columns with benzene and hexafluorobenzene stacked alternatively, and

46 e structures were synthesized by compressing benzene and its derivatives.

47 itions using a combination of (diacetoxyiodo)benzene and K(2)S(2)O(8) is reported.

48 rted iron system that sequentially activates benzene and N(2) to form aniline derivatives.

49 sing low catalyst loadings (<1 mol percent), benzene and other functionalized arenes were selectively

50 eral reaction pathways connecting the eta(2)-benzene and phenyl hydride isomers, due to the relativel

51 g in ReB(6)(-) is compared with that in both benzene and rhenabenzene [(CO)(4)ReC(5)H(5)], and remark

52 actionation associated with the oxidation of benzene and several methylated and methoxylated analogs,

53 hanism involves protonation of excited-state benzene and subsequent rearrangement to bicyclo[3.1.0]he

54 irst few minutes of 1,3,5-tris(4-aminophenyl)benzene and terephthaldehyde polymerization, which yield

55 ders the dihedral angle rotation between the benzene and the diamine ring; this may partially account

56 ))(3)}(2) sites and are superior to those in benzene and THF, and that grafting onto MSN treated at 5

57 adduct that is used to separate a mixture of benzene and thiophene upon crystallization.

58 electrophilic amination of aromatics such as benzene and toluene with methyl- and trifluoromethylamin

59 al reactions occur in the studied mixture of benzene and toluene, all with rather low yield and leadi

60 ed for the synthesis of a variety of alkynyl benzenes and heteroarenes in good to excellent yields.

61 s, and isochroman to afford phosphine oxide, benzene, and 1-isochromanone.

62 on peaks for methyl salicylate, naphthalene, benzene, and 2-butanone.

63 oronene was released from 1 upon addition of benzene, and both the cage and the purified coronene cou

64 IUR) and for the combination of chloroform, benzene, and carbon tetrachloride.

65 ic carcinogens (VOCs), such as formaldehyde, benzene, and chloroform.

66 We show that acrolein, formaldehyde, benzene, and hydrogen cyanide are the dominant contribut

67 hexane, DMSO, acetonitrile, methanol, water, benzene, and toluene using broadband SRS with femtosecon

68 ncluding vinyl chloride, 1,2-dichloroethane, benzene, and toluene.

69 he benzene derivative mixtures consisting of benzene, anisole, and toluene.

70 The use of benzene as a dopant with 2-butanone allowed one to see t

71 enzene (C(6)H(6)) and 1,3-di(trifluoromethyl)benzene, as well as a C-F bond in partially fluorinated

72 aterial of CH stoichiometry synthesized from benzene at high pressure and room temperature by slow so

73 ble of selectively adsorbing high amounts of benzene at low partial pressures, promising for future i

74 pai-chromophoric 1,4-bis(anthracenylethynyl)benzene (BAB)-based highly emissive J-aggregated organog

75 hyde subunits linked together by a diethynyl benzene backbone.

76 ns of alpha-carbonyl sulfoxonium ylides onto benzenes, benzofurans and N-p-toluenesulfonyl indoles in

77 This new assay uses 1,2-diacetyl benzene/beta-mercaptoethanol, which forms a fluorescent

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

79 at the oxidative addition of the C-C bond in benzene by an isolated metal complex is not only possibl

80 )) with benzene (C(6)H(6); X(1)A(1g)) and D6-benzene (C(6)D(6); X(1)A(1g)) were conducted to explore

81 tive (4) selectively activates a C-H bond of benzene (C(6)H(6)) and 1,3-di(trifluoromethyl)benzene, a

82 1-propynyl radical (CH(3)CC; X(2)A(1)) with benzene (C(6)H(6); X(1)A(1g)) and D6-benzene (C(6)D(6);

83 case of the archetypal aromatic hydrocarbon benzene, C-C cleavage is thermodynamically disfavored, a

84 Furthermore, 1,2,4,5-tetrasubstituted benzenes can be used to synthesize tetraimide heteropent

85 The [Cu(OTf)](2) .benzene catalyst that has been standard in this reaction

86 s reveal a similarity to the classic eta(6) -benzene complex (eta(6) -C(6) H(6) )Mo(CO)(3) regarding

87 ations also identified an eta(2)-coordinated benzene complex in which the arene is held more loosely

88 al-free approach for the construction of the benzene core has been developed through self-condensatio

89 o two tridentate ligands (with s-triazine or benzene cores) occurs with high negative allosteric coop

90 hancement ratios of several VCP compounds to benzene correlate well with population density (R(2) ~ 0

91 compared with its non-hemilabile (methylthio)benzene counterpart and demonstrate a previously unexplo

92 C(2)H(4), C(2)H(6)) and larger hydrocarbons (benzene, cyclohexane) both in liquid and vapor phases wa

93 stereochemical reactivity of cyclobutadiene, benzene, cyclooctatetraene, and the [10]- to [14]annulen

94 With benzene-d(6) as the deuterium source, easily reducible f

95 solution of the iron trans-bimetallacycle in benzene-d(6) produced predominantly the cis-cyclobutane

96 erized by measuring the Raman spectra of the benzene derivative mixtures consisting of benzene, aniso

97 ts; while MRL and 2xMRL of Mep-Form promoted benzene derivatives (benzyl alcohol, benzaldehyde, and t

98 penylium-functionalized (DAC-functionalized) benzene derivatives as high-potential catholytes for non

99 We have prepared novel highly functionalized benzene derivatives by regioselective metalation of este

100 system for the dearomative hydroarylation of benzene derivatives has been developed.

101 ation potentials (in CH(3)CN) of various DAC-benzene derivatives will range from +0.96 to +1.64 V vs

102 ntally derived properties of monosubstituted benzene derivatives.

103 nitrogen complex, followed by migration of a benzene-derived aryl group to the nitrogen.

104 -bdc, with four methyl groups decorating the benzene dicarboxylate linker, leads to a smooth transiti

105 extractable organic carbon was identified as benzene dicarboxylic acids, tricarboxylic acids, and tet

106 celerated molecular dynamics simulations for benzene dissociation from the buried cavity of the T4 ly

107 between (bdt)(O)W(VI) and Cu(I)(NHC) (bdt = benzene dithiolate, NHC = N-heterocyclic carbene) sites.

108 and (E)-1,2,3-trimethoxy-5-(4-methoxystyryl)benzene (DMU-212) are synthesized by this single-step ap

109 Coordination of a lithium cation to benzene does not change substantially the electron local

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

111 quinolinium as an excited acceptor and alkyl benzene donors.

112 the reduction of unactivated arenes such as benzene (E(red) < -3.42 V vs SCE).

113 49%, formaldehyde EFs increased by 216%, and benzene EFs increased by 82%.

114 The path observed for benzene egress is a multistep ligand migration from the

115 ns of wild-type T4 lysozyme also reveal that benzene-egress-associated dynamics in the L99A mutant ar

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

117 Benzene exhibits a rich photochemistry which can provide

118 re describing the strong association between benzene exposure and accepted markers of genotoxicity in

119 quantitative relationship between real-life benzene exposure and genetic damage in future risk asses

120 ative evidence on the cytogenetic effects of benzene exposure on CAs and MN respectively.

121 Preconception benzene exposure was associated with 29% (95% confidence

122 In contrast, benzene exposure was positively and approximately linear

123 esults from 7 studies] per parts-per-million benzene exposure.

124 lkyne moieties of 1,3,5-tris(4-ethynylphenyl)benzene (Ext-TEB) precursors adsorbed on Ag(111).

125 acetate also produces carcinogen alkenes and benzene for which the negative long-term medical effects

126 Predicted users' daily average intake of benzene, formaldehyde, acetaldehyde and acrolein were 39

127 ia the barrierless addition of 1-propynyl to benzene forming a low-lying doublet C(9)H(9) intermediat

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

129 stigations into the industrial separation of benzene from gasoline using aliphatic MOF materials.

130 larylisoxazoles, pyrazoles and electron-rich benzenes from the corresponding scaffolds, is suggested.

131 ro- dichloro-, and dinitro- (o-, m-, and p-) benzene guests.

132 ight MeOH molecules and encapsulation of two benzene guests.

133 d linker 1,2,3,4,5,6-hexakis(4-carboxyphenyl)benzene (H(6)cpb) by solvothermal reactions in dimethylf

134 Self-assembly of [1,4-di(1H-tetrazol-5-yl)benzene] (H(2)L(1)) with chiral acceptors (R,R)M and (S,

135 The genotoxicity of benzene has been investigated in dozens of biomonitoring

136 Here by compressing a benzene-hexafluorobenzene cocrystal (CHCF), H-F-substitu

137 ignificantly increase catalyst reactivity in benzene hydride-transfer and n-hexane cracking reactions

138 oxidant capable of effecting cyclohexane and benzene hydroxylation within seconds at -40 degrees C.

139 ion of N-Boc-acrylamides with (diacetoxyiodo)benzene in acetic acid produced 5,5-disubstituted oxazol

140 nitiated nucleophilic addition of solvent to benzene in acidic media leading to substituted bicyclo[3

141 lations demonstrate that the dithiophosphate-benzene interaction is much stronger than the correspond

142 y, as in the case of (4-azido-4-methylpentyl)benzene, intramolecular C-H amination kinetically outcom

143 Benzene is an important organic intermediate, used for t

144 While benzene is aromatic in its ground state, it is antiaroma

145 It is well known that benzene is aromatic in the ground state (the Huckel's ru

146 Current production of benzene is primarily from crude oil processing, but due

147 With 1,4-cyclohexadiene, 0.5 equiv of benzene is produced prior to the formation of an EPR det

148 In these simulations, benzene is released through a previously characterized,

149 e a class of molecules in which a CH unit in benzene is replaced by a functionalized transition-metal

150 e motif affects photochemical reactivity, as benzene is well-known to completely change its aromatic

151 CPOBOP (1,4-Bis [2-(3,5-Dichloropyridyloxy)] benzene) is a constitutive androstane receptor (CAR) ago

152 Three disubstituted benzene isomers ( o-, m-, and p-fluorophenyl piperazine)

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

154 idyne radical to the pai-electron density of benzene leading eventually to a Jahn-Teller distorted tr

155 When the exotridentate tris-pyridyl benzene ligand and ZnCl(2) with appropriate templating m

156 two-dimensional COFs based on a (diarylamino)benzene linker that form a Kagome (kgm) lattice and show

157 haracterize the crown ether solvated complex benzene-lithium Bz-Li-Cro as a superelectrophile.

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

159 tron-donating (4-methoxy-1-(2-ethylhexyl)oxy)benzene (MEH) and electron-accepting benzothiadiazole (B

160 ing methoxy or ethoxy groups on a benzene or benzene-methanol backbone were clustered into one group

161 aline-earth Lewis acid sites yield increased benzene methylation barriers and destabilization of typi

162 l influence on the reactivity of propene and benzene methylations.

163 RMs investigated in comparison with a water-benzene mixture, and the rate constant values depend on

164 thyl phosphate- and dimethyl dithiophosphate-benzene model systems.

165 droxyethyl)benzene and 4-(1,2-dihydroxyethyl)benzene moieties were explored as P2' ligands providing

166 lleagues, which possesses a tetrasubstituted benzene moiety and eight stereocenters.

167 alogues with the polar 4-(1,2-dihydroxyethyl)benzene moiety were less potent, and only the (R)-epimer

168 ivatives, 1 and 2, bearing a monosubstituted benzene moiety.

169 ion of the methylidyne radical (CH) with the benzene molecule (C(6)H(6)) on the doublet C(7)H(7) surf

170 or the irreversible desolvation of entrapped benzene molecules.

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

172 ile hydrocarbons (0.03-0.4 mug/L), including benzene, more hydrocarbons than in any other sample.

173 lar interest to assess how the presence of a benzene motif affects photochemical reactivity, as benze

174 Here, we investigate how a benzene motif influences the photoinduced electrocycliza

175 dging the two thienyl units is replaced by a benzene motif, and show that this compound undergoes ele

176 oichiometric amount of 1-azido-4-(tert-butyl)benzene N(3)(C(6)H(4)-p-(t)Bu) furnished the correspondi

177 ity, and related excited-state properties of benzene, naphthalene, and anthracene could be tuned and

178 ene-in which the arylene pendants are either benzene, naphthalene, or anthracene.

179 r modeled levels of air contaminants such as benzene, nitrogen dioxide, 1,3-butadiene, and particulat

180 e compound possessing -OH and -OMe groups on benzene nucleus along with pyrrolobenzoxazine core moiet

181 the coincidence for experimentally measured benzene off rate and apo protein slow-timescale NMR rela

182 gy for the efficient construction of ethynyl benzene oligomers with specific sequences of aniline and

183 2) -symmetric 1,4-bis(diethylphosphonomethyl)benzene or 4,4'-bis(diethylphosphonomethyl)biphenyl with

184 s used for the treatment of water containing benzene or alkylbenzenes.

185 ely containing methoxy or ethoxy groups on a benzene or benzene-methanol backbone were clustered into

186 In polystyrene glass and in frozen benzene or dibutyl phthalate solution, both 1 and 2 are

187 Applying this approach to simple benzene or other arenes also affords arylation products

188 to the basicity (pK(aH) in water and K(b) in benzene) or nucleophilicity (N Mayr constants) of the te

189 xy, dimethoxy, benzyl ether-substituted iodo-benzenes, other iodoarenes, such as iodo-naphthalene, he

190 or example, 1 shows excellent selectivity of benzene over cyclohexane (20:1 for vapors, 92:1 for liqu

191 about methane dehydroaromatization (MDA) to benzene over ZSM-5-supported transition metal oxide-base

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

193 While compounds with the 4-(1-hydroxyethyl)benzene P2' moiety maintained excellent antiviral potenc

194 i (Psi), if any, negligible, when exposed to benzene, phenol, xylene and 4-nitrophenol as negative co

195 In this study, the benzene/phenyl hydride equilibrium is explored for the {

196 ion kinetics and products of key radicals in benzene photo-oxidation.

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

198 ntiaromaticity (ESAA) triggers a fundamental benzene photoreaction: the photoinitiated nucleophilic a

199 of the F-ring phenol group by (diacetoxyiodo)benzene (PIDA) was employed.

200 e N-oxide and 1,4-bis(2-(4-pyridyl)-ethynyl)-benzene pillars that connect 2D sheets of 9,10-dicarboxy

201 The employed 1,3,5-tris(4-bromophenyl)benzene precursor is comparatively studied on Ag(111) ve

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

203 lly, and it was found that silyl-substituted benzenes provide the most rapid access to bicyclo[3.1.0]

204 our system was further probed by photolyzing benzene/pyridine solutions of 4a under H(2) and D(2) atm

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

206 ith substituents also present on the central benzene ring and show that such substituents generally h

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

208 on-withdrawing or -donor substituents in the benzene ring are higher than that of the unsubstituted p

209 directions, along the molecular plane as the benzene ring bridges two electrodes using anchoring grou

210 lations, or phenalenannulations, transform a benzene ring directly into a substituted pyrene by "wrap

211 delocalization of the oxygen electron to the benzene ring in phenoxides.

212 functionalization was observed in the other benzene ring in the ortho position with respect to the c

213 units to a single appropriately substituted benzene ring inhibits DCvC behavior.

214 s substitutions on the nitrogen atom and the benzene ring of the BTZ nucleus.

215 lfur atom in DMDS by the radical site in the benzene ring of the deprotonated triradical to generate

216 direct contact between the pai system of the benzene ring of the molecules and the Au(111) electrode,

217 ed cycloalkane can be stabilized by fusing a benzene ring on each side, substituted with proper funct

218 d BamBC subunits of class II BCRs accomplish benzene ring reduction at an active-site tungsten cofact

219 lved in the energetic coupling of endergonic benzene ring reduction have remained hypothetical.

220 laminobenzothiazole (or -oxazole), and/or P1-benzene ring with fluorine scan of mono- or bis-fluorine

221 ached to a single, appropriately substituted benzene ring, the resulting diradical system engages in

222 of various groups to the ortho position of a benzene ring.

223 employed to install the methyl group on the benzene ring.

224 +/0), depending upon the substituents on the benzene ring.

225 aromatic cyclobutadiene ring and an aromatic benzene ring.

226 ill interact if they are located on adjacent benzene rings and only after being separated further tha

227 sted to be used as saturated bioisosteres of benzene rings for the purpose of drug discovery projects

228 ctural formula C(33)H(15), consisting of ten benzene rings fused in a triangular fashion.

229 Biphenylene analogues in which one of the benzene rings has been replaced by a different (4n + 2)

230 ene-like compounds with different numbers of benzene rings have been studied, finding out a very good

231 enylene(1-3)-a molecule that consists of two benzene rings joined by a four-membered ring at its core

232 mide bonds and their similar groups and even benzene rings of spicy compounds were fund to be critica

233 a new 2D COF (TFPB-COF) with six unsaturated benzene rings per repeating unit and ordered mesoporous

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

235 e valuable as pharmaceutical bioisosteres of benzene rings, and in particular 1,3-disubstituted BCP m

236 fications such as the numbers of constituent benzene rings, methylation and hydroxylation.

237 g, and ortho-condensed arrangements of fused benzene rings-is revealed.

238 arger number of phenol groups grafted on the benzene rings.

239 sisting, from end-to-end, of 18 and 24 fused benzene rings.

240 This opens up a possibility of controlling benzene's physicochemical behavior in its excited state,

241 rformed to explore the substituent effect on benzene's structure and aromaticity upon excitation to t

242 f 1-(cyclopentylmethyl)-3-(3-phenylpropanoyl)benzene scaffold.

243 ed adsorption preference of cyclohexane over benzene (selectivity up to 5:1).

244 ucture of the nickel(II) octaethylporphyrin/ benzene solvate shows no significant distortion of the c

245 n which organic compounds, mostly methylated benzene species, are trapped.

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

247 therapeutic benefit in mice during trinitro-benzene-sulfonic acid (TNBS)-induced colitis by decreasi

248 elioration of disease activity in a trinitro-benzene-sulfonic-acid model of colitis in humanized NOD/

249 pyridines/pyrazines/pyridazine with 2-chloro benzene sulfonyl chloride followed by a Cu(I)-catalyzed

250 idines/pyrazines/pyridazines on the 2-chloro benzene sulfonyl chloride, followed by Cu(I)-catalyzed i

251 opyridines/pyrazines/pyridazine and 2-chloro benzene sulfonyl chloride.

252 r protease inhibitor AEBSF (4-[2-aminoethyl] benzene sulfonyl fluoride) up-regulated full-length Dice

253 aining side chains of bis(anthracenylethynyl)benzene) supports J-aggregation.

254 that the use of a non-polar solvent such as benzene suppressed formation of the cationic rhodium pro

255 The methylidyne-benzene system represents a benchmark to probe the outco

256 nal imine COFs comprising tris(4-aminophenyl)benzene (TAPB) and a variety of dialdehyde linear buildi

257 h the commonly used 1,3,5-tris(4-aminophenyl)benzene-terephthaldehyde network (TAPB-PDA COF), the mos

258 Hexagonal hexaminophenyl benzene, tetragonal tetrakis(4-aminophenyl) ethane, and

259 ium linked by a trimethylene tether to alkyl benzenes) that proved to be well suited to demonstrating

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

261 le the second involves photorearrangement of benzene to benzvalene followed by protonation and nucleo

262 pt, we demonstrate a four-step conversion of benzene to cyclohexene with varying degrees of deuterium

263 f the stabilizing agent, binding energies of benzene to gold are measured even though only weak Londo

264 The dihapto-coordination of benzene to the pai-basic fragment {TpW(NO)(PMe(3))} (Tp

265 tution with a variety of ortho disubstituted benzenes to yield a series of chromophores.

266 units of conjugated acetylenic polymers from benzene- to thiophene-based.

267 ensity functional theory calculations of the benzene-to-phenyl hydride landscape suggest a single lin

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

269 mance Liquid Chromatography (HPLC-UV), BTEX (Benzene, Toluene, Ethylbenzene and Xylenes) by gas chrom

270 tial reaction between HO(*) or SO(4)(*-) and benzene, toluene, ethylbenzene, and (BTEX) xylene isomer

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

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

273 the first off-site direct flux estimates of benzene, toluene, ethylbenzene, and xylenes from upstrea

274 organic carbon, formaldehyde, acetaldehyde, benzene, toluene, ethylbenzene, and xylenes were measure

275 he homes sampled including xylenes, pinenes, benzene, toluene, ethylbenzene, hexane, pentane, chlorof

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

277 s (2-methylpentane, hexane, heptane, octane, benzene, toluene, m,p-xylene, o-xylene, and ethylbenzene

278 zoic acid, other monocyclic aromatics (i.e., benzene, toluene, salicylic acid, benzyl alcohol, and ph

279 ibuted 45% of SOA formation; BTEX compounds (benzene, toluene, xylenes, and ethylbenzene), 40%; other

280 i(+)-catalyzed Diels-Alder (DA) reactions of benzene toward a series of acetylenes of improved nucleo

281 orted using 2,4,6-trimethoxy-1,3,5-triformyl benzene (TpOMe) as a precursor aldehyde.

282 etrical heterobenzisapphyrins containing one benzene, two pyrroles, one furan, and one thiophene ring

283 imited Methane DehydroAromatization (MDA) to benzene under non-oxidative conditions appears very prom

284 and selectivity (99.9%) for the oxidation of benzene under visible light.

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

286 e considered unacceptable for chloroform and benzene (upper IUR) and for the combination of chlorofor

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

288 ufficient to oxidize benzene and halogenated benzenes via single-electron transfer (SET), resulting i

289 Studies where benzene was the primary genotoxic exposure and that had

290 ene and H(2) pdms=1,2-bis(methanesulfonamido)benzene), was electrochemically synthesised and investig

291 hane, and trigonal 1,3,5-tris(p-formylphenyl)benzene were all joined together by imine linkages to yi

292 While monocyclic aromatics such as benzene were found to disrupt the structure of surfactan

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

294 lychlorinated biphenyls and four chlorinated benzenes were below a factor of 2 in the plant species s

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

296 at the bulky diol 1,4-Bis(2-hydroxy-2-propyl)benzene, which has distant hydroxyl groups, is able to c

297 inter-molecular C-H arylation of unactivated benzenes with aryl halides (Ar-X; X = I, Br, Cl) toward

298 e (i) Vollhardt cyclization of bis(propargyl)benzenes with bis(trimethylsilyl)acetylene, (ii) halo-de

299 cloaddition of 1,4-bis[2-(4-pyridyl)ethenyl]-benzene within a porous coordination polymer (PCP).

300 rototype of a closed-shell aromatic molecule-benzene-yielding nonbenzenoid fulvenallene.