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1 ectively adsorb the (R)-propylene oxide ((S)-propylene oxide).
2 alicyclic (cyclohexene oxide) and aliphatic (propylene oxide).
3 reactions, starting from (R)-citronellal and propylene oxide.
4 te nucleophile that ring-opens the activated propylene oxide.
5 G), glycerin, nicotine, ethanol, acetol, and propylene oxide.
6 eaction of the chiral anion with (S)- or (R)-propylene oxide.
7 y important epoxidation of propylene to form propylene oxide.
8 xposure to enantiomerically pure and racemic propylene oxide.
9 rate) by the carbonylative polymerization of propylene oxide.
10 n-bonding interactions between 2-butanol and propylene oxide.
11 ard the adsorption of the two enantiomers of propylene oxide.
12 e Ring-Opening Copolymerization of CO(2) and Propylene Oxide.
13 ides, which have larger sizes as compared to propylene oxide.
19 cific equilibrium constants for (R)- and (S)-propylene oxide adsorption on the chiral Au nanoparticle
20 vity factor (s = k(fast)/k(slow)) of 370 for propylene oxide, allowing enantiomerically pure epoxide
23 Cr(III)-catalyzed system for the coupling of propylene oxide and carbon dioxide reveal that although
24 on in the presence of complex 1, coupling of propylene oxide and carbon dioxide was found to occur by
25 a second order rate law, first order in both propylene oxide and catalyst concentrations, and zeroth
27 suggests that cobalt serves both to activate propylene oxide and to stabilize the catalytic intermedi
28 he bipyridine ligands are "tailed" with poly(propylene oxide) and poly(ethylene oxide) oligomers.
31 ar sequence) starting from d-mannose and (S)-propylene oxide as the source of the stereogenic centers
32 mers, a class of poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) (PEO-PPO-PEO) tr
33 n of leptin with poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide), Pluronic P85 (P
34 xide/ethylene oxide copolymer (predominantly propylene oxide based, PPO/PEO) for polar solvents or wa
35 hthalate and a poly(ethylene oxide) and poly(propylene oxide) block copolymer, and they were implante
36 k copolymer, poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide), was covalen
37 inal and internal epoxides was investigated (propylene oxide, butylene oxide, isobutylene oxide, and
38 lene (C(3)H(6)), suggesting the formation of propylene oxide (C(3)H(6)O), an important monomer used,
39 ificity with 2-butanol exposure suggest that propylene oxide can interact either with a single adsorb
40 alicyclic (cyclohexene oxide) and aliphatic (propylene oxide) carbon dioxide coupling is thought to b
41 clohexyl carbonate, under similar conditions propylene oxide/carbon dioxide produces mostly cyclic pr
42 that acetoacetate is the primary product of propylene oxide carboxylation and that beta-hydroxybutyr
43 astronomical detection of a chiral molecule, propylene oxide (CH3CHCH2O), in absorption toward the Ga
45 ence in the two concurrent reactions for the propylene oxide/CO(2) process (33 kJ.mol(-1)) accounts f
46 se of water as chain-transfer reagent in the propylene oxide/CO2 polymerization, poly(propylene carbo
47 drophilic-lipophilic balance values and poly(propylene oxide) contaminants, whereas this interaction
48 exhibits high catalytic activity for the CO2/propylene oxide coupling reaction and can be used as a r
49 tep is calculated as the ring opening of the propylene oxide (DeltaG(calc)(*) = +22.2 kcal mol(-1));
50 catalyzed the CO2-dependent carboxylation of propylene oxide (epoxypropane) to form acetoacetate and
51 for hydrophobic/low polarity solvents and a propylene oxide/ethylene oxide copolymer (predominantly
52 ysteine selectively adsorb one enantiomer of propylene oxide from a solution of racemic propylene oxi
53 f (R)-3-methylcyclohexanone and (R)- and (S)-propylene oxides from the Cu(643)(R) and Cu(643)(S) surf
55 e enantioselective chemisorption of R- and S-propylene oxide has been measured either on clean Pd(111
56 alyst allows for the preparation of the poly(propylene oxide) in high yields with high turnover (TON>
59 onoxide and at room temperature in methanol, propylene oxide is converted to methyl 3-hydroxybutanoat
62 rotation of polarized light by (R)- and (S)-propylene oxide is enhanced by interaction with Au nanop
63 olecule, specifically that the uptake of (S)-propylene oxide is larger than that of (R)-propylene oxi
64 antioselective chemisorption of (S)- and (R)-propylene oxide is measured on a Pd(111) surface chirall
65 an form the open intermediate with CO(2) and propylene oxide more feasibly than the other three epoxi
66 )-propylene oxide is larger than that of (R)-propylene oxide on (S)-2-methylbutanoate adsorbed layers
67 nces in adsorption energetics of (R)- vs (S)-propylene oxide on the (S)-2-methylbutanoate/Pt(111) ove
68 the living, alternating copolymerization of propylene oxide (PO) and CO(2), yielding poly(propylene
69 TPD titrations of NEA-modified Pt(111) using propylene oxide (PO) as a chiral probe point to a relati
71 fined alternating copolymers made of CO2 and propylene oxide (PO) or cyclohexene oxide (CHO) were ind
73 erizes lactide (L and rac) dissolved in neat propylene oxide (PO) to yield polylactide (PLA) terminat
77 contains poly(ethylene oxide) (EO) and poly(propylene oxide) (PO) units with an approximate molecula
78 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
79 opylacrylamide and poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (known as poloxame
80 , such as triblock poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) copo
81 phiphilic triblock poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) copo
82 of ethyl ether and poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) or P
83 -cyclodextrins and poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) trib
84 olymer of the form poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) helps seal electro
88 chelic supramolecular polymers based on poly(propylene oxide) (PPO), thymine (Thy), and diaminotriazi
89 gel based on poly(ethylene oxide) (PEO)-poly(propylene oxide) (PPO)-PEO poloxamers, capable of contro
90 to the catalytic cycle of carbon dioxide and propylene oxide ring-opening copolymerization is present
92 ncy of a synthetic poly(ethylene oxide)/poly(propylene oxide) side chain-based bottlebrush block copo
93 f propylene oxide from a solution of racemic propylene oxide, thus leaving an enantiomeric excess in
94 as temperature, pressure, and molar ratio of propylene oxide to catalyst have been investigated, and
95 acnacMg](2) 3, react with two equivalents of propylene oxide to generate dinuclear Mg complexes of ge
96 m PLLA/Pluronic-P104 (poly(ethylene oxide-co-propylene oxide) triblock copolymer) blends in attempts
97 ynthesis of propylene carbonate from CO2 and propylene oxide under mild catalytic conditions; the per
99 e atactic polymers are produced from racemic propylene oxide using chain shuttling agents and double-
100 he industrially relevant clean production of propylene oxide using cumene hydroperoxide as an oxidant
101 dioxide with epoxides (cyclohexene oxide or propylene oxide) using the (salen)Cr(III)Cl complex as c
102 ing copolymerization of maleic anhydride and propylene oxide, using a functionalized primary alcohol
103 diation, chemical transformation (propene to propylene oxide), wastewater denitrification, as compone
105 ic isotactic PPO is synthesized from racemic propylene oxide with control of molecular weight using e