ライフサイエンスコーパス: dimethyl ether

1 to fuel conversion with 79% selectivity for dimethyl ether.

2 recycling of carbon dioxide to methanol and dimethyl ether.

3 olvents containing a hydrogen bond acceptor, dimethyl ether.

4 e for the C-H bonds of methane, methanol, or dimethyl ether.

5 was modeled with Bu(3)Sn-H and prekinamycin dimethyl ether along with prekinamycin itself.

6 Propylene, dimethyl ether, ammonia, R-152a, propane, and HFE-152a a

7 The alkanes and dimethyl ether analyses were performed by headspace-gas

8 del systems (N-methylpyridinium complexes of dimethyl ether and dimethyl phosphate anion) provide qua

9 ed reactions, the dehydration of methanol to dimethyl ether and the total methane oxidation reactions

10 solvent removal, the sodide is dissolved in dimethyl ether and transferred through a frit into a sep

11 The products, methanol, dimethyl ether, and CO2, were desorbed with the passage

12 yclopentane, trifluoroethane, fluoromethane, dimethyl ether, and difluoromethane at ambient temperatu

13 s review examines the potential of methanol, dimethyl ether, and ketene as possible oxygenate interme

14 ed reactions, such as CO(2) hydrogenation to dimethyl ether, and thereby expanding the possibilities

15 transformations into fuels such as methanol, dimethyl ether, and varied products including synthetic

16 and careful tests, we show that methanol and dimethyl ether are apparently unreactive on the two most

17 of CO2 to formate/formic acid, methanol, and dimethyl ether are thoroughly reviewed, with special emp

18 hylene glycol (PEG), and polyethylene glycol dimethyl ether-are evaluated to identify suitable candid

19 iX.E, LiX.2E, and LiX.3E (X = F, Cl, Br; E = dimethyl ether as a model for THF).

20 t 6-31+g(d) using RLi coordinated with three dimethyl ethers as a computational model for RLi in THF.

21 hylene carbonate and tetra (ethylene glycol) dimethyl ether) as catholytes, forming membrane-free bat

22 ed and the reductive lithiation performed in dimethyl ether at -70 degrees C.

23 element of the new ligands is their acyclic dimethyl ether backbone in lieu of the (isopropylidene)

24 this study, we present a highly concentrated dimethyl ether-based electrolyte that appears as a liqui

25 alyst" unduly catalyzes the reduction of the dimethyl ether-based electrolyte, resulting in loose SEI

26 s studied by use of a tetra(ethylene glycol) dimethyl ether-based electrolyte.

27 n a highly convergent synthesis of radicicol dimethyl ether but failed in the removal of the two aryl

28 of C-H activation of methane, methanol, and dimethyl ether by [(N-N)PtMe(TFE-d(3))](+) ((N-N) = ArN=

29 e pendant tetradentate ligand in the masked (dimethyl ether) catechol form, and kinetic pH-rate profi

30 intercalant distribution, and less stable Na-dimethyl ether coordination.

31 angren B trimethyl ether and palodesangren D dimethyl ether could be synthesized in 29 and 18% overal

32 ed through decarboxylative iodination of the dimethyl ether derivative of BINOL-3,3'-dicarboxylic aci

33 arboxylative iodination is effected with the dimethyl ether derivative of BINOL-3,3'-dicarboxylic aci

34 the toxicity of 10% (v/v) diethylene glycol dimethyl ether (DGDME) added as a biodiesel fuel additiv

35 s or even from the air itself to methanol or dimethyl ether (DME) and their varied products can be ac

36 Dimethyl ether (DME) has been considered as a promising

37 ons, the main reactions are the methanol and dimethyl ether (DME) interconversion and the formation o

38 explored in the electrochemical oxidation of dimethyl ether (DME) on platinum.

39 y steps required for catalytic combustion of dimethyl ether (DME) on Pt clusters were determined by c

40 the direct selective oxidation of methane to dimethyl ether (DME) over Pt/Y(2) O(3) .

41 ep controls catalytic carbonylation rates of dimethyl ether (DME) to methyl acetate.

42 diction (ANN-RSM-DOM) to streamline waste-to-dimethyl ether (DME) upcycling using a set of sustainabi

43 for one-step conversion of synthesis gas to dimethyl ether (DME) was imaged simultaneously and in si

44 nation of CO(2)-yielding methanol (CH(3)OH), dimethyl ether (DME), and CO as products.

45 Recycling of CO(2) into methanol, dimethyl ether (DME), and derived fuels and materials is

46 , renewable diesel (RD), bio-oils, methanol, dimethyl ether (DME), ethanol, and ammonia-across 16 fue

47 w surface tension, low boiling point solvent dimethyl ether (DME).

48 This work reports a dimethyl ether-driven fractional crystallization process

49 -O(2) batteries with a tetra(ethylene)glycol dimethyl ether electrolyte.

50 eal solvents (usually in mixtures of THF and dimethyl ether, ether, and 2,5-dimethyltetrahydrofuran).

51 O(2) (formed at >10 wt %) were selective for dimethyl ether formation, while atomically dispersed ReO

52 the isotopologue distribution of the initial dimethyl ether formed when a flow of CH(3)OH was passed

53 associative routes mediate the formation of dimethyl ether from methanol on zeolitic acids at the te

54 nic liquids consisting of triethylene glycol dimethyl ether (G3) and Mg(TFSI)(2) or NaTFSI yield valu

55 4'-hexahydroxy-1,1'-biphenyl-6,6'-dimethanol dimethyl ether [HBDDE]) but not PKC-beta II (LY379196) d

56 ls including syngas, methanol, formaldehyde, dimethyl ether, heavier hydrocarbons, aromatics, and hyd

57 Qaw was calculated from the uptake of dimethyl ether in the anatomic dead space minus the most

58 her or other solvent, and evaporation of the dimethyl ether in vacuo, the alpha-methylstyrene is adde

59 Intact poly(ethylene glycol) dimethyl ether is identified as the electrolyte degradat

60 gy of dimerization of fluoromethyllithium in dimethyl ether is predicted to be -0.9 kcal mol(-)(1), w

61 ouble Baeyer-Villiger reaction of quinizarin dimethyl ether is viable, directly providing the dibenzo

62 It's dehydration product, dimethyl ether, is a diesel fuel and liquefied petroleum

63 by a combination of specific coordination of dimethyl ether ligands on each lithium and "dielectric s

64 t and outlook in synthesis of light olefins, dimethyl ether, liquid fuels, and alcohols through two l

65 oxide ratios being suitable for synthesis of dimethyl ether, methanol and for the Fischer-Tropsch pro

66 f the carbenoid reactions of alpha-lithiated dimethyl ether (methoxymethyllithium) and the intramolec

67 in the lithium dimethylaminoborohydride bis(dimethyl ether) microsolvate.

68 were calculated in the gas phase and for the dimethyl ether microsolvated molecules.

69 and reactions of compounds in which the O of dimethyl ether or acetone has been replaced by NH, PH, o

70 d by the use of microsolvation with explicit dimethyl ether or THF ligands and by the combined use of

71 recedented insight into the carbonylation of dimethyl ether over Mordenite is provided through the id

72 a previous study of idealized disiloxane and dimethyl ether parent species to fully methylated deriva

73 ethyl carbonate (EMC), poly(ethylene glycol) dimethyl ether, poly(ethylene glycol) ethyl methyl ether

74 Dimethyl ether/poly(hydrogen fluoride) (DMEPHF), are sta

75 Dimethyl ether pyrolysis (2% CH3OCH3/Ar) was observed be

76 reliminary monitoring of propane, butane and dimethyl ether residues, in cakes and chocolate after sp

77 rbenoids are studied in the gas phase and in dimethyl ether solvent.

78 f mixtures of water and tetraethylene glycol dimethyl ether (TEGDE), a methyl-terminated derivative o

79 rmolecular interactions with systems such as dimethyl ether, trimethylamine, trimethylphosphine, and

80 Qaw was measured with the dimethyl ether uptake technique, which reflects blood fl

81 ol in this complex undergoing dehydration to dimethyl ether was determined for a series of E with pro

82 Release kinetics of propane, butane and dimethyl ether were measured over one day with sprayed f

83 Reaction of dimethyl ether with 2(TFE) proceeds similarly (K(eq) = 0