ライフサイエンスコーパス: alkane

1 termed intrinsic (rare gases) and extrinsic (alkanes).

2 compounds (for example, linear and branched alkanes).

3 eractions in the 2,4-positions of the linear alkane.

4 es as a necessary constituent to convert the alkane.

5 less entropy is lost upon protonation of the alkane.

6 ce, which exhibits limited chemotaxis toward alkane.

7 l(OR(f))4] (15) in the presence of the added alkane.

8 e reacting mixture, leading to aromatics and alkanes.

9 is given for the hydration shells on linear alkanes.

10 converting raw lignocellulose into valuable alkanes.

11 bonds are shorter and stronger than those in alkanes.

12 unusual isotopic distribution in deuterated alkanes.

13 activators of C-H bonds, including those of alkanes.

14 rapid and efficient access to 1-azaspiro[4.n]alkanes.

15 ric oxide, dinitrogen, white phosphorus, and alkanes.

16 , including monitoring H2, H2S, N2, CO2, and alkanes.

17 rocyclic aromatic compounds, and halogenated alkanes.

18 h that it is comparable with the C-C bond in alkanes.

19 he fastest-growing bacteria used short-chain alkanes.

20 ation, dehydrogenation, and fragmentation of alkanes.

21 as catalysts for partial oxidations of light alkanes.

22 elective dehydrogenation of alkyl groups and alkanes.

23 n shells produce the hydration energetics of alkanes.

24 Linear alkanes (8 +/- 1%), branched alkanes (11 +/- 2%), and cycloalkanes (37 +/- 12%) domin

25 The system is selective for higher alkanes: 30% ethane conversion with 98% selectivity for

26 A total of 10 alkanes, 5 ester, 3 alcohol, 13 aldehyde, 8 ketone and 2

27 sis, although lag phases were shorter with n-alkanes (~650-1675 and ~170 days, respectively).

28 Linear alkanes (8 +/- 1%), branched alkanes (11 +/- 2%), and cy

29 opes, indicating that the chemotaxis-related alkane accumulation in A. baylyi is dependent on the car

30 c alkane complexes of the type [(HEB)Re(CO)2(alkane)][Al(OR(f))4] (HEB = eta(6)-hexaethylbenzene; alk

31 emarkable structure-directing influence of n-alkane and ethyleneoxy side chains in polymer self-assem

32 results indicated a significant increase in alkane and methane content, and decrease in alcohol, ald

33 of the incubation, the changes in the total alkane and PAH contents in the NAPL residue were quantif

34 ep plume waters of the spill that assimilate alkane and polycyclic aromatic hydrocarbons during stabl

35 ture for headspace extraction of mixtures of alkanes and alcohols on the sputtered fibers were optimi

36 can catalytically dehydrogenate unactivated alkanes and alcohols under near-UV irradiation at room t

37 nd delta(13)C values for plant wax-derived n-alkanes and alkanoic acids indicate sustained and system

38 The recent identification of C15-C17 alkanes and alkenes in microalgal species suggests hydro

39 include halogenation and oxyhalogenation of alkanes and alkenes, dehydrogenation of alkanes, convers

40 They also synthesize C15-C19 alkanes and alkenes, which results in substantial produc

41 uticular waxes are predominantly composed of alkanes and alkenes.

42 nd free fatty acids, fatty alcohol, sterols, alkanes and aromatic acid derivatives, being palmitic ac

43 rmation of nonolefinic byproducts, including alkanes and aromatics.

44 hydroxide-mediated cleavage of ketones into alkanes and carboxylic acids has been reinvestigated and

45 s two chemical classes (unspeciated branched alkanes and cyclic compounds) in 11 retention-time-based

46 bulk components of petroleum samples such as alkanes and does not deliver a comprehensive view but on

47 nd emissions from oil wells were enriched in alkanes and isotopically depleted relative to natural ga

48 uction of fatty-acid-derived fatty alcohols, alkanes and olefins up to 700%.

49 e strain VM552 grew by utilizing the bulk of alkanes and PAHs in the fuel; however, biofilm formation

50 Second, for many alkanes and polycyclic aromatic hydrocarbons biodegradat

51 lls confirms the presence of these shells on alkanes and supports Kauzmann's 1959 mechanism of protei

52 enantioselective C-H functionalization of n-alkanes and terminally substituted n-alkyl compounds.

53 biotic Cycloclasticus to degrade short-chain alkanes and those of free-living Cycloclasticus that blo

54 onding neutral alkane complexes [(HEB)W(CO)2(alkane)] and [CpRe(CO)2(alkane)] (Cp = eta(5)-cyclopenta

55 nd's molecular structure (n-alkane, branched alkane, and cycloalkane) and its propensity to produce h

56 nonoxygenated (e.g., normal alkane, branched alkane, and cycloalkane) organic compounds.

57 for siloxane, in comparison with silane and alkane, and show that the large conductance decay is int

58 cies including CO, medium-heavy HC, alkenes, alkanes, and NOx and their concentration influence the c

59 Many indigenous microbes metabolize alkanes, and the chemotaxis and accumulation in some str

60 xclusive conversion of vicinally chlorinated alkanes, and tolerance to short-term oxygen exposure is

61 rocarbon cycle within the upper ocean, where alkanes are continually produced and subsequently consum

62 A wide number of electron-poor polyarylated alkanes are easily accomplished through this route by ju

63 tween ionic species produced from individual alkanes are established.

64 Alkanes are found to be much more hydrophobic than rare

65 iso-Alkanes are major components of petroleum and have been

66 Alkanes are one of the most widespread contaminants in t

67 Our results suggest that, although n-alkanes are the simplest hydrocarbons, their dynamic pro

68 n-Alkanes are the textbook examples of the odd-even effect

69 Partially fluorinated alkanes, arenes, and alkenes can be transformed by a var

70 synthesis of hydrocarbons, including liquid alkanes, aromatics, and oxygenates, with carbon numbers

71 methanotroph that can utilize a short-chain alkane as an alternative to methane.

72 irable transformation given the abundance of alkanes as well as the use of olefins as building blocks

73 g the ionic complex 15 and a small amount of alkane at low temperature (183 K).

74 nsted acid be prepared that can protonate an alkane at room temperature?

75 nated intermediates for the autooxidation of alkanes at 500-600 K builds upon prior observations made

76 By protonating alkanes at room temperature, the reactivity of H(CHB11 F

77 n-Alkane average chain length values are positively correl

78 y competent for breaking strong C-H bonds of alkanes (BDE approximately 100 kcal.mol(-1)) through a h

79 late hydrocarbons, predominantly C15 and C17 alkanes, between 0.022 and 0.368% of dry cell weight.

80 y displacing the bound alkane ligand, as the alkanes bind in preference to the HFCs to the organometa

81 roach to characterize the chemotaxis-related alkane bioaccumulation, and has immense potential for fa

82 A lengthy incubation (>6 years) revealed iso-alkane biodegradation after lag phases of 900-1800 and ~

83 he organic compound's molecular structure (n-alkane, branched alkane, and cycloalkane) and its propen

84 , and ester) and nonoxygenated (e.g., normal alkane, branched alkane, and cycloalkane) organic compou

85 pollutants, NO2, total hydrocarbons (THC), n-alkanes, branched alkanes, saturated cycloalkanes, aroma

86 e for the majority of mixing ratios of C2-C8 alkanes, but accounted for a small proportion of alkene

87 that, using this unique platform, selective alkane C-H activation occurs, as probed by H/D exchange

88 ples have been reported in the activation of alkane C-H bonds, many C(sp(3))-H activation/C-C and C-h

89 ivity of a metal oxide surface in activating alkane C-H bonds.

90 oil, glyceride trioleate, oleic acid and the alkane, C16 .

91 d product measurements of a series of normal-alkanes (C18, C20, C22, and C24) to distinguish between

92 arbon and hydrogen isotope compositions of n-alkane C29 show significant correlation with climatic pa

93 ly, 2-D separation of 50 analytes, including alkane (C6-C12), alkene, alcohol, aldehyde, ketone, cycl

94 , approximately 100% of lower molecular mass alkanes (C9-C21) were removed within 10 min of magnetic

95 e bonding between the metal fragment and the alkane can be best characterized as a three-center, two-

96 mics of polymerized monolayers of functional alkanes can be controlled to modify surface wetting and

97 tantly by van der Waals interactions between alkane carbon and water oxygen atoms.

98 rt the transfer-dehydrogenation of gas-phase alkanes catalyzed by solid-phase, molecular, pincer-liga

99 y more stable than their corresponding sigma-alkane cations, suggesting that the solid-state motif ha

100 lysis, we conclude that the lack of membrane alkanes causes higher CEF, perhaps for maintenance of re

101 Though choice in alkane chain length is not often discussed as a way in w

102 and in three others, they are linked via an alkane chain.

103 t CPs are persistent chemicals regardless of alkane-chain lengths.

104 spectral alterations were only found for the alkane chemo-attractant bacteria Acinetobacter baylyi AD

105 eparated analyte signal of a polychlorinated alkanes (chlorinated paraffins) technical mixture that c

106 Free radical alkane chlorination is an important industrial process f

107 y environments where methane and short-chain alkanes co-occur.

108 ma* orbital concerted with C-Cl breakage) in alkanes compared to stepwise OS-SET (SET to a pi* orbita

109 erent isotopomers/isotopologues of the sigma-alkane complex result, as characterized by single-crysta

110 re long-lived than the corresponding neutral alkane complexes [(HEB)W(CO)2(alkane)] and [CpRe(CO)2(al

111 The other alkane complexes exhibit solid-state (31)P NMR data cons

112 etal-alkane complexes, we generated cationic alkane complexes of the type [(HEB)Re(CO)2(alkane)][Al(O

113 The alkane complexes were generated in a hydrofluorocarbon (

114 These observations connect sigma-alkane complexes with their C-H activated products, and

115 suggested to operate via intermediate sigma-alkane complexes, such transient species are difficult t

116 eking to create more-stable transition metal-alkane complexes, we generated cationic alkane complexes

117 ion of single-crystals of well-defined sigma-alkane complexes.

118 is and characterization of a number of sigma-alkane complexes: [Rh(R2P(CH2)nPR2)(eta(2),eta(2)-C7H12)

119 The [(HEB)Re(CO)2(alkane)](+) complexes are more long-lived than the corre

120 ations showed its feasibility in quantifying alkane concentration in environmental samples.

121 nship between Raman spectral alterations and alkane concentrations showed its feasibility in quantify

122 hemotaxis-related affinity, and quantify the alkane concentrations via spectral alterations.

123 sed as complex mixtures of polychlorinated n-alkanes containing thousands of isomers, leading to dema

124 n of alkanes and alkenes, dehydrogenation of alkanes, conversion of alkyl halides, and oxidation of h

125 D3 receptor (D3R) analogues with diazaspiro alkane cores were synthesized.

126 mplexes [(HEB)W(CO)2(alkane)] and [CpRe(CO)2(alkane)] (Cp = eta(5)-cyclopentadienyl), with samples of

127 biomass can be fermented to alcohols or even alkanes, creating a liquid fuel in which carbon released

128 versity of the key marker gene for anaerobic alkane cycling and outline the need for greater understa

129 es suggested that diverse taxa contribute to alkane cycling in geothermal environments.

130 [Al(OR(f))4] (HEB = eta(6)-hexaethylbenzene; alkane = cyclopentane (16) or pentane (17-19); OR(f) = p

131 reanalysis of the available leaf wax deltaDn-alkane dataset from modern plants in the Northern Hemisp

132 the most up-regulated pathways is related to alkane degradation and beta-oxidation of fatty acids.

133 microbial community size (16S rRNA gene) and alkane degradation capacity (alkB gene) by qPCR indicate

134 The potential for alkane degradation could be shown for several genera and

135 Alkane degradation genes were ubiquitous in the assemble

136 ison with genome scaffolds of uncultivated n-alkane degrading 'Smithella' spp. are consistent with th

137 s high activity in olefin polymerization and alkane dehydrogenation (M = Cr) or efficient luminescenc

138 first example of a homogeneous and selective alkane dehydrogenation reaction using a base-metal titan

139 xplored for the industrially important light alkane dehydrogenation reaction.

140 remely high rates and turnover numbers for n-alkane dehydrogenation, and yields of terminal dehydroge

141 lds of alpha-olefin from pincer-Ir catalyzed alkane dehydrogenation, proceeds via two mechanistically

142 surface area (ASA), whereas the HY values of alkanes depend on special hydration shells.

143 However, we found that gamma for a set of alkanes differed from that for four configurations of de

144 itionally, gamma(att) and gamma(rep) for the alkanes differed from those for the decaalanines, implyi

145 ificantly altered after 1-h exposure to pure alkanes (dodecane or tetradecane) and alkane mixtures (m

146 rnal activation dynamics at the surface of n-alkane droplets is established during the evaporation/co

147 ansfer (HAT) from the aliphatic C-H bonds of alkane, ether, alcohol, amide, and amine substrates to t

148 l fashion for selective functionalization of alkane, ether, alcohol, and amide (or amine) substrates

149 o selectively functionalize the C-H bonds of alkane, ether, and alcohol substrates in the presence of

150 We found that odd-numbered n-alkanes exhibit up to 30 times slower dynamics than even

151 Factor contributions of light SVOC and n-alkane factors were more consistent for "predicted-total

152 Using n-alkane fingerprinting data, both linear discriminant ana

153 Reductive elimination of alkane followed by alkene binding completes the catalyti

154 The n-alkane fraction was constituted mainly of n-alkanes in t

155 ion provides efficient access to fluorinated alkanes from a pool of starting materials that are ubiqu

156 C35, although only those most abundant (15 n-alkanes, from 21 to 35 carbon No.) were used as original

157 -H chlorination are among the most selective alkane functionalizations known, providing a unique tool

158 e, the photodriven dehydrogenation of cyclic alkanes gave an excellent apparent quantum efficiency of

159 occupancy, also observed in synthetic-host, alkane-guest systems, suggest general principles for the

160 Examples include long-chain alkanes, halogenated aromatics, and cyclic volatile meth

161 shown to be capable of oxidizing a series of alkanes having C-H bond dissociation energies ranging fr

162 olycyclic aromatic hydrocarbons (PAHs) and n-alkanes, higher fractions of organic carbon (OC) and wat

163 probably explains why NMR efforts to detect alkane hydration shells have failed.

164 Jorgensen et al. for the number of waters in alkane hydration shells.

165 perature hydrogen-deuterium exchange with an alkane hydrocarbon reagent, including one zeolite moiety

166 h intrinsic hydrogen content of liquid-range alkane hydrocarbons (including diesel) offers a potentia

167 entify highly elevated levels of atmospheric alkane hydrocarbons with enhanced rates of C2-C5 nonmeth

168 t its applications in olefin polymerization, alkane hydrogenolysis, depolymerization of branched poly

169 in strong inhibition by H2, also observed in alkane hydrogenolysis.

170 The rebound mechanism for alkane hydroxylation was invoked over 40 years ago to he

171 egarding the relative abundance of four main alkanes in bell pepper fruit water, has proven effective

172 arbon and hydrogen isotope compositions of n-alkanes in extra virgin olive oils from eight Mediterran

173 ynes to expeditiously synthesize bis(indolyl)alkanes in moderate to high yields is described.

174 l difficulty of combining ionic species with alkanes in solution without the solvent molecules rapidl

175 data and the artificially added signal of 31 alkanes in that sample.

176 Analyses of short-chain alkanes in the environment of the Campeche Knolls symbio

177 -alkane fraction was constituted mainly of n-alkanes in the range C8-C35, although only those most ab

178 lational diffusional dynamic properties of n-alkanes in their liquid states.

179 ch as alcohols, alkyl esters, aldehydes, and alkanes in their waxes.

180 nazine has been discovered that undergoes an alkane-induced shift in the solid state from a disordere

181 The dehydrogenation of unactivated alkanes is an important transformation both in industria

182 ccounting for the preferred antipodes of the alkanes is proposed and relies on the subtle influence o

183 on of molecular ion information; [M](+*) for alkanes, ketones, FAMEs, aromatics, [M-H](+*) for chloro

184 The epitaxially grown alkane layers on graphene are prepared by a simple drop-

185 tion capturing the scaling of permeance with alkane length and density.

186 aster curve with an unexpected dependence on alkane length.

187 luxional processes associated with the sigma-alkane ligand are identified using variable-temperature

188 lvent molecules rapidly displacing the bound alkane ligand, as the alkanes bind in preference to the

189 C-H activated products, and demonstrate that alkane-ligand mobility, and selective C-H activation, ar

190 of the protein interior has much more liquid-alkane-like properties than previously appreciated.

191 experimental observations for a number of n-alkane may be reproduced using a hybrid framework TST an

192 ed in H2-rich fluid inclusions, and higher n-alkanes may likely be derived from the same source.

193 , and suggest that the ability to metabolize alkanes may play a role in elastic film formation at oil

194 diagnosis and that several compounds, mainly alkanes, may be significantly associated with asthma inf

195 seems to be uniquely involved in short-chain alkane metabolism suggests that such metabolic flexibili

196 Ti and W and indicates that the key step of alkane metathesis (C-H bond activation followed by beta-

197 horizontal lineCH2)Me2], which are active in alkane metathesis and comparable to the previously repor

198 ween Zr and W suggests that the slow step of alkane metathesis is the C-H bond activation that occurs

199 face tantalum carbene as the intermediate in alkane metathesis.

200 species interactions salient to methanogenic alkane mineralization.

201 Temperature-ramped separations of a simple alkane mixture using the RTIL-coated second-dimension ((

202 o pure alkanes (dodecane or tetradecane) and alkane mixtures (mineral oil or crude oil), but not mono

203 Pure alkanes or alkane mixtures exhibited different limits of detection

204 re molecular diffusion rates, typically at n-alkane-modified planar silica surfaces, which serve as m

205 i enhancing the affinity and accumulation of alkane molecules on cell membranes or cellular internali

206 ber of different chemical classes (including alkanes, monoaromatics, alcohols, aldehydes, ketones, an

207 sed of a complex suite of lipids including n-alkanes, n-alkanoic acids and fatty acyl wax esters.

208 0 times slower dynamics than even-numbered n-alkanes near their respective melting points.

209 effect was not observed for sp(3)-hybridized alkanes, nor for smaller diamondoid molecules.

210 s 2-methylbutane (isopentane), the analogous alkane of the potent inhibitor isoamyl alcohol (isopenta

211 Peak widths for n-alkanes of 30-40 ms at half height were obtained.

212 These molecules yield conductance lower than alkanes of the same length and the largest length-depend

213 otonic dependence of the boiling points of n-alkanes on the chain length.

214 (DeltaHads-H+ and DeltaSads-H+) of gas-phase alkanes onto Bronsted protons.

215 NaH either by hydride addition to re-form an alkane or by deprotonation to form an alkene and H2 .

216 Pure alkanes or alkane mixtures exhibited different limits of

217 ely delivers plant hormones, based on cyclic alkanes or aromatic structures, to regulate plant physio

218 ith sigmoidal kinetics but could not degrade alkanes or the bulk of PAHs.

219 ly more important than hydroxyl radicals for alkane oxidation and were also important for methane and

220 For example, almost all partial alkane oxidations, regardless of the metal oxide, follow

221 n a MoVTeNb oxide (M1 phase) catalyst during alkane oxidative dehydrogenation is reported.

222 The yield of formate and alkane per reduced PetF approaches its theoretical upper

223 pecies have the capacity to produce 2-540 pg alkanes per mL per day, which translates into a global o

224 ly in use as replacements for perfluorinated alkanes (PFCs) and poly-ether heat transfer fluids, whic

225 The n-alkanes present in corn, grapeseed, hazelnut, olive, pea

226 nsertion that is unproductive for generating alkane product but accounts for the unusual isotopic dis

227 Furthermore we show that cyanobacterial alkane production is likely sufficient to sustain popula

228 n-Alkane profiles established by gas chromatography-mass s

229 ond iodination of various cyclic and acyclic alkanes providing iodoalkanes in good yields.

230 ural gas production varied in delta(13)C and alkane ratio composition, with deltaD-CH4 representing t

231 Here, we compare stable isotopic and alkane ratio tracers of natural gas, agricultural, and u

232 e between extra-lattice Al-OH species and an alkane reagent.

233 e evaluated using the delta(2)H values and n-alkanes relative composition as variables.

234 on and bromination, the direct iodination of alkanes represents a great challenge.

235 by using a Grob test mixture, and saturated alkanes, revealing good correlation between previously r

236 otal hydrocarbons (THC), n-alkanes, branched alkanes, saturated cycloalkanes, aromatics, aldehydes, h

237 O2 surface toward the well-ordered and rigid alkane self-assembled layers.

238 uction of isovolatility curves for reference alkane series in GC x GC.

239 Alkane shells are stabilized importantly by van der Waal

240 opposing energetics for forming or releasing alkane shells confirms the presence of these shells on a

241 )C-(2)C and (2)C-(1)C bonds, irrespective of alkane size (C2-C8) or cyclic/acyclic structure.

242 periodic packing of odd- and even-numbered n-alkane solids results in odd-even variation of their mel

243 Detailed chiroptical studies performed in alkane solvents with different molecular structures reve

244 rs are alternatives for low molecular weight alkane solvents.

245 ded by rapidly evolved multitandem genes for alkane storage and transfer.

246 rease in kH as compared to the unsubstituted alkane substrate.

247 symbionts use propane and other short-chain alkanes such as ethane and butane as carbon and energy s

248 arylation of hydrocarbons, including simple alkanes such as methane.

249 rocarbons are ubiquitous in the ocean, where alkanes such as pentadecane and heptadecane can be found

250 el against the known hydration energetics of alkanes, the energetics should be based on the Ben-Naim

251 eparation of a 11-component mixture of C1-C6 alkanes, the hierarchical phase outperforms the structur

252 igned to afford the homologue 1-azaspiro[5.n]alkanes, thereby illustrating the higher versatility of

253 than those prepared by the chemisorption of alkane thiolated compounds.

254 ces of the helicity in linear perfluorinated alkanes through analysis of natural bond orbitals and cl

255 Selectively converting linear alkanes to alpha-olefins under mild conditions is a high

256 s given here that the transfer energetics of alkanes to cyclohexane measure the release of these shel

257 studied for the aerobic oxidations of C1-C4 alkanes to form olefins and oxygenates.

258 nitially studied for the conversion of light alkanes to liquid products, but they have been used (and

259 ing catalytic processes that transform small alkanes to value-added products.

260 in this area, the dehydrogenation of simple alkanes to yield alkenes (specifically monoenes) with hi

261 For the heavier alkanes (undecane-hexadecane), the 2.0 mum sputtered fib

262 dative transformation of semivolatile normal-alkanes under laboratory conditions is largely controlle

263 st that can mediate fluorinations of certain alkanes upon activation with visible light.

264 promoted catalytic dehydrogenation of liquid alkanes using Fe and Ni particles supported on silicon c

265 uses for the differences in leaf wax deltaDn-alkane values among different plant life forms remain po

266 Additionally, variations of leaf wax deltaDn-alkane values and the epsilonwax-p values in gymnosperms

267 his study, we observed that leaf wax deltaDn-alkane values between major high plant lineages (eudicot

268 Leaf wax deltaDn-alkane values have shown to differ significantly among p

269 icant effect on controlling leaf wax deltaDn-alkane values in higher plants.

270 ctor (epsilonwax-p) between leaf wax deltaDn-alkane values of major angiosperm lineages and precipita

271 cADO) converts long-chain fatty aldehydes to alkanes via a proposed diferric-peroxo intermediate that

272 for the conversion of alkenes to 1,2-dibromo alkanes via oxidative bromination using HBr paired with

273 he controlled catalytic functionalization of alkanes via the activation of C-H bonds is a significant

274 lomics (using target aliphatic aldehydes and alkanes) was carried out using solid-phase microextracti

275 2-Methylpentane and both n-alkanes were completely depleted during ~2400 days of in

276 Interestingly, branched-alkanes were ionized with lower excess internal energy,

277 Elevated mixing ratios of methane and C2-C8 alkanes were observed in areas with the highest density

278 omologous bis-alpha,omega-azidoethylammonium alkanes were prepared, where the number of methylene gro

279 n time to 40 min, greater than 67% of C22-25 alkanes were removed.

280 f 560 reference compounds, including 8 odd n-alkanes, were analyzed and experimental linear retention

281 ignificantly more rapidly than [(HEB)Re(CO)2(alkane)](+) when present in the same solution.

282 of coeluting isomers, particularly for the n-alkanes, which are routinely measured by 1D GC/MS and ma

283 voked a decrease in the content of cuticular alkanes, which as an important fraction of cuticular hyd

284 Synechocystis sp. PCC 6803 that produces no alkanes, which grew poorly at low temperatures.

285 egrading bacteria can consume cyanobacterial alkanes, which likely prevents these hydrocarbons from a

286 ntation broths and the hydroisomerization of alkanes with 18-30 carbon atoms encountered in petroleum

287 f cycloalkanes to cyclic alkenes, and linear alkanes with chain lengths of C4 to C8 to terminal olefi

288 ally and electronically diverse polyarylated alkanes with excellent yields and selectivities at room

289 le ligand systems catalyzed the oxidation of alkanes with H2 O2 as the oxidant with high efficiency i

290 on of water-insoluble bio-oil to mixtures of alkanes with high carbon yield.

291 hemicellulose-derived oligomers into liquid alkanes with high efficiency and yield.Bio-oil is a pote

292 hydrodeoxygenation of raw woods into liquid alkanes with mass yields up to 28.1 wt% over a multifunc

293 We incubated defined mixtures of iso- or n-alkanes with mature fine tailings from two tailings pond

294 o generate fatty acid ethyl esters and fatty alkanes with tailored chain length.

295 e of sampling and desorbing C5 through C11 n-alkanes with uniform efficiency.

296 SCCPs are complex mixtures of chlorinated alkanes with variable chain length and chlorination leve

297 ogenative carboxylation (ODC) of unactivated alkanes with various substituted benzoic acids to produc

298 e reaction of OH with a series of C10 (cyclo)alkanes, with 0-3 rings, in order to better understand t

299 araffin, acetylene/ethylene, linear/branched alkanes, xenon/krypton, etc.

300 most abundant petrochemical feedstock beyond alkanes, yet their use in commodity chemical manufacture