ライフサイエンスコーパス: propylene

1 or VOCs emitted were benzene, acetylene, and propylene.

2 , and the ring-cracking products butanol and propylene.

3 e dehydrogenation, but are not selective for propylene.

4 ting to yield gas phase products CO, H2, and propylene.

5 yield [rac-(EBI)ZrCl][MeB(C(6)F(5))(3)] and propylene.

6 elimination to yield Pd[bond]Cl species and propylene.

7 +) species vary in the order VC > ethylene > propylene.

8 hese new catalysts copolymerize ethylene and propylene.

9 ing to higher selectivity for epoxidation of propylene.

10 adium oxide clusters with alkenes (ethylene, propylene, 1-butene, and 1,3-butadiene) are investigated

11 1)H and (13)C NMR spectroscopy, a mixture of propylene, 1-butene, and 2-butenes is formed.

12 h simple terminal olefins, such as ethylene, propylene, 1-hexene, and styrene, selectively at the les

13 Gases such as propane, butane, isobutane, propylene, 2-methylpropene, and 1,3-butadiene even xenon

14 ective hydrogenation of ethylene relative to propylene (25:1) when surface sites are passified by CO.

15 ne acetal (4b), and 5-formyl-2'-deoxyuridine propylene acetal (5b).

16 es to propylene), trifunctional (ethylene to propylene, alkane metathesis, ...).

17 and achieves higher yields than the standard propylene ammoxidation process.

18 semicrystalline blocks and poly(ethylene-co-propylene) amorphous blocks.

19 tandem hydroformylation was also observed on propylene and 1-butene.

20 e elimination at low temperature to generate propylene and 2-butenes, respectively.

21 microchannels formed in fluorinated ethylene propylene and 50-microm fused-silica tubing for use with

22 omplex feedstocks in an increasing amount of propylene and diesel-range fuels.

23 agments of pmoB (spmoB) bind copper and have propylene and methane oxidation activities.

24 re, methanol can be transformed to ethylene, propylene and most of the petrochemical products current

25 osphate in pores of the host membranes, poly(propylene) and poly(ethersulfone).

26 of carbon monoxide (CO) to ethylene, ethane, propylene, and propane.

27 degrees C, under which conditions ethylene, propylene, and water vapor are not significantly capture

28 Propylene- and pentylene-tethered PBIs follow a similar

29 elective molecular exclusion of propane from propylene at atmospheric pressure, as evidenced through

30 -on coordination of acetylene, ethylene, and propylene at the iron(II) centers, while also providing

31 The gelation behavior of a poly(ethylene-alt-propylene)-b-poly(ethylene oxide)-b-poly(N-isopropylacry

32 one)-based grafted membrane compared to poly(propylene)-based membrane.

33 catalyst to achieve high selectivity towards propylene because of facile desorption of the product.

34 otactic polypropylene-block-poly(ethylene-co-propylene)-block-syndiotactic polypropylene and isotacti

35 entrations) completely prevented growth with propylene but had no effect on growth with acetone or n-

36 ic cycle has been demonstrated to react with propylene, but its reactivity has not been extensively i

37 Hydroamination of propylene by p-toluenesulfonamide proceeds with Markovni

38 /mol activation energy) and then reacts with propylene by proximal oxygen abstraction (9.3 kcal/mol a

39 for the transfer of a single oxygen atom to propylene (C(3)H(6)), suggesting the formation of propyl

40 Propylene carbonate (PC) decomposition on a model electr

41 Es) were tested as probes for alkali ions in propylene carbonate (PC) in an oxygen- and water-free en

42 )) phase with the common liquid electrolyte, propylene carbonate (PC), and its Li salt solutions.

43 CDC EDLCs with mixed electrolytes of IL and propylene carbonate (PC), the IL ions were observed ente

44 the propylene oxide/CO2 polymerization, poly(propylene carbonate (PPC) diols are successfully produce

45 We discovered that two solution additives, propylene carbonate and ethylene carbonate, which have h

46 energies of activation determined for cyclic propylene carbonate and poly(propylene carbonate) format

47 g reagents m-nitrobenzyl alcohol (m-NBA) and propylene carbonate at producing highly charged protein

48 tal results for sodium and potassium ions in propylene carbonate by obtaining over 3 orders of magnit

49 ellent capacity retention at high rates in a propylene carbonate electrolyte.

50 heterogeneous catalysts for the synthesis of propylene carbonate from CO2 and propylene oxide under m

51 Addition of 5% m-NBA or 15% propylene carbonate increases the average charge of thre

52 aximum charge state of ubiquitin formed with propylene carbonate is 21+, four charges higher than pre

53 ectrodeposition of lithium from solutions of propylene carbonate producing isotopically light metal d

54 Electroreduction of dissolved SiCl(4) in propylene carbonate using a liquid gallium [Ga(l)] pool

55 ylene glycol)-block-poly(2-methyl-2-carboxyl-propylene carbonate) (PEG-PCC) copolymer using carbodiim

56 ropylene oxide (PO) and CO(2), yielding poly(propylene carbonate) (PPC) with no detectable byproducts

57 e carbonate) where the polyisoprene and poly(propylene carbonate) blocks can be orthogonally removed

58 ined for cyclic propylene carbonate and poly(propylene carbonate) formation were 100.5 and 67.6 kJ.mo

59 ase of PO, the carbonate content of the poly(propylene carbonate) formed was in the range of 92-99% a

60 of polyisoprene-block-polystyrene-block-poly(propylene carbonate) where the polyisoprene and poly(pro

61 The microstructure of the poly(propylene carbonate), PPC, formed in the reactions betwe

62 weight distributions (see picture; PPC=poly(propylene carbonate); PLA=polylactide).

63 hols, dipolar aprotic solvents, ethylene and propylene carbonate, and ionic liquids instantaneously d

64 By use of ethylene carbonate and propylene carbonate, nearly the entire charge state dist

65 Ethylene carbonate, propylene carbonate, o-nitroanisole, m-nitrobenzyl alcoh

66 In the nonaqueous solvent, propylene carbonate, there is evidence for a role for su

67 ylene glycol)-block-poly(2-methyl-2-carboxyl-propylene carbonate-graft-dodecanol; PEG-PCD) to prepare

68 lene glycol)-block-poly (2-methyl-2-carboxyl-propylene carbonate-graft-SMART-graft-dodecanol) (abbrev

69 is an electrocatalyst for water oxidation in propylene carbonate-water mixtures.

70 d by comparing reactions in acetonitrile and propylene carbonate.

71 MR studies is presented for the formation of propylene carbonate.

72 oxide/carbon dioxide produces mostly cyclic propylene carbonate.

73 om theoretical predictions is observed using propylene carbonate.

74 eagents, although this effect is greater for propylene carbonate.

75 fective at producing high charge states than propylene carbonate.

76 y (up to at least 2.0 M) in acetonitrile and propylene carbonate.

77 ylamine, perfluorodecalin, acetonitrile, and propylene carbonate; solvents that swelled PDMS the most

78 so established that hydride migration in the propylene complexes yields exclusively the primary alkyl

79 In both the Rh ethylene and propylene complexes, the transition state for hydride mi

80 Temperature, propylene concentration, and solvent polarity dependence

81 Propylene consumption by cells was largely unaffected by

82 lymer blend of polystyrene, styrene-ethylene/propylene copolymer, and polypropylene that have overlap

83 Results from propylene copolymerizations suggested that chain end con

84 ) detectors for characterization of ethylene-propylene copolymers.

85 A study of cotrimerization of ethylene with propylene correlates with these findings of regioselecti

86 roduction is only modestly anion-sensitive; [propylene] dependence studies reveal enantiofacial propy

87 These results suggest that BES inhibits propylene-dependent growth and epoxide metabolism via ir

88 rain B276 showed that BES is an inhibitor of propylene-dependent growth in this organism as well but

89 BES) was shown to be a specific inhibitor of propylene-dependent growth of and epoxypropane metabolis

90 ally the very high turbidity of one ethylene propylene diene monomer rubber (EPDM) or thermoplastic e

91 Propylene, dimethyl ether, ammonia, R-152a, propane, and

92 the rate and stereochemistry of syndiotactic propylene enchainment by the archetypal C(s)-symmetric p

93 Poly(isobutylene) (PIB) and poly(ethylene-co-propylene) (EPCO) were investigated as sensitive layers

94 ts based on bulk silver surfaces with direct propylene epoxidation by molecular oxygen have not resol

95 Direct propylene epoxidation by O2 is a challenging reaction be

96 We show that propylene epoxidation near a Si-vacancy occurs through a

97 , we report that steady-state selectivity in propylene epoxidation on copper (Cu) nanoparticles incre

98 w microstructural aspects of Ti sites effect propylene epoxidation reactivity and shows that Ti sites

99 s may provide highly efficient catalysts for propylene epoxidation.

100 using a modified Teflon fluorinated ethylene propylene (FEP) dynamic flux chamber (DFC) in a remote,

101 ylether (PTFE-TFM); and fluorinated ethylene propylene (FEP).

102 asoline, as well as an important fraction of propylene for the polymer industry.

103 ptive separation of ethylene from ethane and propylene from propane relative to any known adsorbent,

104 describes the synthesis of 500-4,000 Da poly(propylene fumarate) (PPF) by a two-step reaction of diet

105 , characterize, and evaluate 3D-printed poly(propylene fumarate) scaffolds is proposed for vasculariz

106 ic patterning and are composed of rigid poly(propylene fumarate) segments and stimuli-responsive poly

107 ation of the material into 3D printable poly(propylene fumarate) was utilized to produce thin films a

108 irst synthesis of high molecular weight poly(propylene fumarate).

109 -cigarettes heat and aerosolize the solvents propylene glycol (PG) and glycerol (GLY), thereby afford

110 Ethanol (EtOH), isopropyl alcohol (IPA), and propylene glycol (PG) increase topical drug delivery, bu

111 The influence of choice of flavour solvent, propylene glycol (PG) or triacetin (TA), was investigate

112 s in three different refill "e-liquids" were propylene glycol (PG), glycerin, nicotine, ethanol, acet

113 (EG), ethyl acetate (EA), isopropanol (IPA), propylene glycol (PG), polyethylene glycol-400 (PEG-400)

114 Deuterated water (D2O), propylene glycol (PG-d8), and dimethyl sulphoxide (DMSO-

115 of four treatments: (1) vehicle control (90% propylene glycol + 10% lactated Ringer solution); (2) 20

116 ination of polyethylene glycol 400 0.4 % and propylene glycol 0.3 % (PEG/PG) (n = 72).

117 ctives were a) to document the occurrence of propylene glycol accumulation associated with continuous

118 Propylene glycol accumulation was observed in six of nin

119 dose lorazepam infusion, and the presence of propylene glycol accumulation, as evidenced by a high an

120 Propylene glycol accumulation, as reflected by a hyperos

121 , serum propylene glycol concentrations, and propylene glycol accumulation; and c) to assess the rela

122 This study investigated the propylene glycol alginate (PGA)-induced coacervation of

123 amel matrix (AMEL) suspended in a vehicle of propylene glycol alginate (PGA).

124 ial properties that can be attributed to the propylene glycol alginate vehicle.

125 The electronic cigarette solvents propylene glycol and glycerol are known to produce toxic

126 he main components of e-cigarette e-liquids (propylene glycol and glycerol), while the role of flavor

127 lets of well-chosen miscible liquids such as propylene glycol and water deposited on clean glass are

128 , ethanol, ethylene glycol, isopropanol, and propylene glycol are obtained with greater than 95% sele

129 tios using the volatile lactic acid analogue propylene glycol as a model compound, measured by on-lin

130 mol gap was the strongest predictor of serum propylene glycol concentrations (r =.804, p =.001).

131 ill adults with normal renal function, serum propylene glycol concentrations may be predicted by the

132 een duration of lorazepam infusion and serum propylene glycol concentrations was observed (p =.637).

133 high-dose lorazepam infusion rate and serum propylene glycol concentrations was observed (r =.557, p

134 Serum propylene glycol concentrations were drawn at 48 hrs int

135 e relationship between lorazepam dose, serum propylene glycol concentrations, and propylene glycol ac

136 onship between high-dose lorazepam and serum propylene glycol concentrations.

137 relationship between the osmol gap and serum propylene glycol concentrations.

138 sing vehicle excipient, such as substituting propylene glycol for PEG400, provides an alternative app

139 tability during lactic acid hydrogenation to propylene glycol in the presence of methionine.

140 chirmer test compared to polyethylene glycol/propylene glycol in the treatment of dry eye disease.

141 Administration of 1 mg E2 in propylene glycol produced a CPP.

142 Notably, 1 mg E2 in propylene glycol produced moderate levels of E2 in the n

143 a two-step reaction of diethyl fumarate and propylene glycol through a bis(hydroxypropyl) fumarate d

144 2, ovariectomized rats were SC administered propylene glycol vehicle (n = 11), 10 microg (n = 13), o

145 ), and mephedrone (4-methylmethcathinone) in propylene glycol vehicle using concentrations ranging fr

146 Using polymer interfaces modified with poly(propylene glycol) (PPG) chains, our results indicate tha

147 model is tested with a non-amphiphilic CPE (propylene glycol) and both nonionic and ionic amphiphili

148 tri-, tetra-, penta(ethylene glycol) and tri(propylene glycol) separating the 1,2,5,6-tetrahydropyrid

149 rocarbons, including acetylated sugars, poly(propylene glycol), and oligo(vinyl acetate), have been u

150 SDS) and nonionic poly(ethylene glycol)-poly(propylene glycol)-poly(ethylene glycol) (PEO-PPO-PEO) tr

151 ss and market potential, the bioproducts are propylene glycol, 1,3-propanediol, 3-hydroxypropionic ac

152 ubstrates for NADH biosynthesis, and produce propylene glycol, a precursor of pyruvate derived from g

153 at for the small osmolytes, ethylene glycol, propylene glycol, and glycerol, Deltax(u) scales with th

154 methanol, methylethyl ketone, methylsulfone, propylene glycol, and trimethylsilanol.

155 Using propylene glycol, H-bonding and ionic interactions were

156 e samples was performed, and the presence of propylene glycol, sorbic and benzoic acids was found in

157 d quantification of semi-volatile additives (propylene glycol, sorbic and benzoic acids) in wines.

158 ation ranges 0-250, 0-125, and 0-250mg/L for propylene glycol, sorbic and benzoic acids, respectively

159 of dosing vehicle excipients such as PEG400, propylene glycol, Tween 80, and hydroxypropyl-beta-cyclo

160 applied as a close-to-saturated solution in propylene glycol, was directly observed to crystallise i

161 phoresis-induced spreading of stripes of 1,2 propylene glycol.

162 amolecular isotope ratios in four samples of propylene glycol.

163 and end-group deprotection to form hexa-1,3-propylene glycol.

164 aminant systems, glycerin/diethylene glycol, propylene glycol/diethylene glycol, and lactose/melamine

165 f 1,25-dihydroyvitamin D(3) in 0.1 ml of 95% propylene glycol:5% ethanol vehicle or vehicle only.

166 or 1,8-diazabicyclo [5,4,0] undec-7-ene, in propylene glycol:ethanol (7:3) to hairless mouse skin an

167 y to catalyze the unprecedented formation of propylene (H(2)C = CH-CH(3)) through the reductive coupl

168 rictly vinylidene chain ends, as observed in propylene homopolymerization.

169 gas temperatures during the hydrogenation of propylene in reactors packed with metal nanoparticles an

170 ramolecular proton transfer process in which propylene is eliminated from the isopropoxy group, subse

171 The evolved propylene is oligomerized by rac-(EBI)ZrR(+) as it is fo

172 The evolved propylene is oligomerized by rac-(EBI)ZrR(+).

173 ethyl (2) complexes in the polymerization of propylene is presented.

174 H6, HCN, and CH3CN and for IAA products were propylene, isobutylene, HCN, and CH3CN.

175 led a binding cooperativity of the P3/P4 and propylene-linked beta-d-glucose fragments, stronger in f

176 f sulfur atom from propylene sulfide to form propylene, (log(k(s)/M(-1) s(-1)) = (8.75 +/- 0.91) - (2

177 d the living, isoselective polymerization of propylene ([m4] = 0.73, alpha = 0.94).

178 rder to produce high end-group fidelity poly(propylene maleate).

179 ) are produced as intermediates in bacterial propylene metabolism from the nucleophilic addition of c

180 coenzyme M (CoM) in the bacterial pathway of propylene metabolism.

181 ene] dependence studies reveal enantiofacial propylene misinsertion to be the prevailing mm-generatin

182 M = Ti, Zr), with vinyl chloride (VC) and VC/propylene mixtures have been investigated.

183 ients of methane, ethane, ethylene, propane, propylene, n-butane, and 1-butene in ZIF-8 are reported

184 transient on pH and the presence of phenol, propylene, or acetylene was investigated by double-mixin

185 aining high selectivity towards formation of propylene over by-products.

186 ptionally high separation performance toward propylene over propane.

187 erial metabolism of epoxypropane formed from propylene oxidation uses the atypical cofactor coenzyme

188 eine (d-cysteine) selectively adsorb the (R)-propylene oxide ((S)-propylene oxide).

189 lene (C(3)H(6)), suggesting the formation of propylene oxide (C(3)H(6)O), an important monomer used,

190 astronomical detection of a chiral molecule, propylene oxide (CH3CHCH2O), in absorption toward the Ga

191 the living, alternating copolymerization of propylene oxide (PO) and CO(2), yielding poly(propylene

192 TPD titrations of NEA-modified Pt(111) using propylene oxide (PO) as a chiral probe point to a relati

193 Statistical ethylene oxide (EO) and propylene oxide (PO) copolymers of different monomer com

194 fined alternating copolymers made of CO2 and propylene oxide (PO) or cyclohexene oxide (CHO) were ind

195 erizes lactide (L and rac) dissolved in neat propylene oxide (PO) to yield polylactide (PLA) terminat

196 The metal-free polymerization of propylene oxide (PO) using a special class of alkene-N-h

197 The enantioselective polymerization of propylene oxide (PO) using biaryl-linked bimetallic sale

198 ortant epoxide monomers ethylene oxide (EO), propylene oxide (PO), and butylene oxide (BO).

199 cific equilibrium constants for (R)- and (S)-propylene oxide adsorption on the chiral Au nanoparticle

200 on in the presence of complex 1, coupling of propylene oxide and carbon dioxide was found to occur by

201 Just add water: The copolymerization of propylene oxide and CO2 catalyzed by a cobalt complex is

202 .7H2O with N-methyl formamide as porogen and propylene oxide as initiator.

203 droxy-telechelic isotactic PPO using racemic propylene oxide as the monomer.

204 ar sequence) starting from d-mannose and (S)-propylene oxide as the source of the stereogenic centers

205 xide/ethylene oxide copolymer (predominantly propylene oxide based, PPO/PEO) for polar solvents or wa

206 ificity with 2-butanol exposure suggest that propylene oxide can interact either with a single adsorb

207 exhibits high catalytic activity for the CO2/propylene oxide coupling reaction and can be used as a r

208 ysteine selectively adsorb one enantiomer of propylene oxide from a solution of racemic propylene oxi

209 e enantioselective chemisorption of R- and S-propylene oxide has been measured either on clean Pd(111

210 onoxide and at room temperature in methanol, propylene oxide is converted to methyl 3-hydroxybutanoat

211 Propylene oxide is detected in the gas phase in a cold,

212 Production of the industrial chemical propylene oxide is energy-intensive and environmentally

213 rotation of polarized light by (R)- and (S)-propylene oxide is enhanced by interaction with Au nanop

214 olecule, specifically that the uptake of (S)-propylene oxide is larger than that of (R)-propylene oxi

215 )-propylene oxide is larger than that of (R)-propylene oxide on (S)-2-methylbutanoate adsorbed layers

216 nces in adsorption energetics of (R)- vs (S)-propylene oxide on the (S)-2-methylbutanoate/Pt(111) ove

217 erized in random and triblock ethylene oxide/propylene oxide polyols using LC/CR/MS.

218 as temperature, pressure, and molar ratio of propylene oxide to catalyst have been investigated, and

219 ynthesis of propylene carbonate from CO2 and propylene oxide under mild catalytic conditions; the per

220 rization of tricyclic anhydrides with excess propylene oxide using aluminum salen catalysts.

221 e atactic polymers are produced from racemic propylene oxide using chain shuttling agents and double-

222 ic isotactic PPO is synthesized from racemic propylene oxide with control of molecular weight using e

223 The alternating copolymerization of propylene oxide with terpene-based cyclic anhydrides cat

224 Hydroxy-telechelic poly(propylene oxide) (PPO) is widely used industrially as a

225 chelic supramolecular polymers based on poly(propylene oxide) (PPO), thymine (Thy), and diaminotriazi

226 hthalate and a poly(ethylene oxide) and poly(propylene oxide) block copolymer, and they were implante

227 drophilic-lipophilic balance values and poly(propylene oxide) contaminants, whereas this interaction

228 alyst allows for the preparation of the poly(propylene oxide) in high yields with high turnover (TON>

229 racemic catalyst forms highly isotactic poly(propylene oxide) in quantitative yield.

230 m PLLA/Pluronic-P104 (poly(ethylene oxide-co-propylene oxide) triblock copolymer) blends in attempts

231 dioxide with epoxides (cyclohexene oxide or propylene oxide) using the (salen)Cr(III)Cl complex as c

232 diation, chemical transformation (propene to propylene oxide), wastewater denitrification, as compone

233 n of leptin with poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide), Pluronic P85 (P

234 k copolymer, poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide), was covalen

235 , such as triblock poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) copo

236 phiphilic triblock poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) copo

237 of ethyl ether and poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) or P

238 -cyclodextrins and poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) trib

239 ectively adsorb the (R)-propylene oxide ((S)-propylene oxide).

240 alicyclic (cyclohexene oxide) and aliphatic (propylene oxide).

241 The adsorption of propylene oxide, a chiral molecule, on a Pt(111) single-

242 vity factor (s = k(fast)/k(slow)) of 370 for propylene oxide, allowing enantiomerically pure epoxide

243 H(2))(9)CH(3), and O(2)C(CH(2))(6)CH(3), and propylene oxide, PO, have been studied in CDCl(3) and ha

244 f propylene oxide from a solution of racemic propylene oxide, thus leaving an enantiomeric excess in

245 ing copolymerization of maleic anhydride and propylene oxide, using a functionalized primary alcohol

246 Using enantiopure propylene oxide, we synthesized semicrystalline polyeste

247 eaction of the chiral anion with (S)- or (R)-propylene oxide.

248 y important epoxidation of propylene to form propylene oxide.

249 xposure to enantiomerically pure and racemic propylene oxide.

250 rate) by the carbonylative polymerization of propylene oxide.

251 n-bonding interactions between 2-butanol and propylene oxide.

252 reactions, starting from (R)-citronellal and propylene oxide.

253 ard the adsorption of the two enantiomers of propylene oxide.

254 G), glycerin, nicotine, ethanol, acetol, and propylene oxide.

255 clohexyl carbonate, under similar conditions propylene oxide/carbon dioxide produces mostly cyclic pr

256 se of water as chain-transfer reagent in the propylene oxide/CO2 polymerization, poly(propylene carbo

257 for hydrophobic/low polarity solvents and a propylene oxide/ethylene oxide copolymer (predominantly

258 Comparative studies of the propylene-oxidizing actinomycete Rhodococcus rhodochrous

259 Reaction with ethylene, propylene, perfluoroalkylethylene, vinylidene fluoride,

260 ranes, thereby substantially improving their propylene permeance (that is, flux).

261 ZIF-8 membranes showed a drastic increase in propylene permeance by about four times, with a negligib

262 on system that are in marked contrast to the propylene polymerization by analogous C(s)-ligated catio

263 In comparison to 3-6, propylene polymerization mediated by MAO (2) + 1 in tolu

264 Counteranion effects on propylene polymerization rates and stereoselectivities a

265 luated as catalysts for living, isoselective propylene polymerization upon activation with methylalum

266 effect on the activity and isoselectivity of propylene polymerization.

267 ric precatalyst 2 as an agent of isospecific propylene polymerization.

268 lausible mechanism for the polymerization of propylene, presenting that the polymerization is mainly

269 degrees to +60 degrees C and at 1.0-5.0 atm propylene pressure (at 60 degrees C) reveal that activit

270 also M(w), are least sensitive to increased propylene pressure for FAl(2-C(6)F(5)C(6)F(4))(3)(-), bu

271 splays the highest ethylene/ethane (>25) and propylene/propane (>55) selectivity under relevant condi

272 istics for separation of ethylene/ethane and propylene/propane mixtures at 318 kelvin.

273 about four times, with a negligible loss in propylene/propane separation factor when compared to as-

274 framework, ZIF-8, membranes show impressive propylene/propane separation, their throughput needs to

275 d under nitrogen and doped with arsine and a propylene real sample from a cracker plant were analyzed

276 ies, below 55 and 70 kJ/mol for ethylene and propylene, respectively, indicate that these adsorbents

277 and liquid phases was performed in the real propylene sample.

278 to improve the zeolite structure stability, propylene selectivity and the overall catalyst accessibi

279 vities at TLR7 and TLR8; the C2 dimer with a propylene spacer was maximally antagonistic at both TLR7

280 second generation fluorous reagents bearing propylene spacers instead of the ethylene spacers show e

281 methodology provides access to nonsymmetric propylene styryl/aryl dithioethers, a previously undiscl

282 ixing isotactic, regioregular chains of poly(propylene succinate) synthesized via the copolymerizatio

283 arrier that consists of a diblock polymer of propylene sulfide (PS) and N,N-dimethylacrylamide (poly(

284 and for the abstraction of sulfur atom from propylene sulfide to form propylene, (log(k(s)/M(-1) s(-

285 Propylene sulfide was first polymerized using a thioacyl

286 ymersomes from poly(ethylene glycol)-bl-poly(propylene sulfide) block copolymers.

287 attributed to the negligible diffusivity of propylene through the small-pore zeolite and provide fin

288 st for commercially important epoxidation of propylene to form propylene oxide.

289 VC coordinates more weakly than ethylene or propylene to the simple catalyst (Me(2)bipy)PdMe(+) (Me(

290 sis), bifunctional (1-butene or 2-butenes to propylene), trifunctional (ethylene to propylene, alkane

291 in glass capillaries or fluorinated ethylene propylene tubes.

292 is based on transparent fluorinated ethylene propylene tubing and a household compact fluorescent lam

293 nverts ethylene ( approximately 80%) but not propylene under identical conditions, in contrast to Pt/

294 cells are fabricated in fluorinated ethylene propylene using a novel technique where channels with in

295 which terminates chain growth and precludes propylene/VC copolymerization.

296 e(4)SiMe(2)N(t)Bu)ZrMe][B(C(6)F(5))(4)] with propylene/VC mixtures yields polypropylene containing bo

297 n of racemic alpha-olefins with ethylene and propylene was carried out in the presence of enantiopure

298 enrichment, a thin layer of poly(ethylene-co-propylene) was coated onto the ATR waveguide surface, th

299 This predominantly decomposes to yield propylene, while a smaller portion yields cross-metathes

300 y using either the oxo process starting from propylene (with H2 and CO over a rhodium catalyst) or th