Binding energies for aluminum atom association complexes with dimethyl ether, diethyl ether and tetrahydrofuran

1988 ◽  
Vol 92 (13) ◽  
pp. 3869-3874 ◽  
Author(s):  
J. Mark Parnis ◽  
S. A. Mitchell ◽  
David M. Rayner ◽  
Peter A. Hackett
Keyword(s):  
Dimethyl Ether ◽  
Diethyl Ether ◽  
Aluminum Atom ◽  
Binding Energies

Numerical analysis of spray characteristics of dimethyl ether and diethyl ether fuel

2017 ◽  
Vol 185 ◽  
pp. 1403-1410 ◽  
Author(s):  
Balaji Mohan ◽  
Wenming Yang ◽  
Wenbin Yu ◽  
Kun Lin Tay
Keyword(s):  
Numerical Analysis ◽  
Dimethyl Ether ◽  
Diethyl Ether ◽  
Spray Characteristics

scholarly journals Gaseous Diffusion Coefficients of Dimethyl Ether and Diethyl Ether into Air, Nitrogen and Oxygen

Netsu Bussei ◽  
2006 ◽  
Vol 20 (2) ◽  
pp. 83-86 ◽  
Author(s):  
Naoki Matsunaga ◽  
Morio Hori ◽  
Akira Nagashima
Keyword(s):  
Dimethyl Ether ◽  
Diethyl Ether ◽  
Diffusion Coefficients ◽  
Gaseous Diffusion

POTASSIUM DERIVATIVES OF FLUORENE AS INTERMEDIATES IN THE PREPARATION OF C9-SUBSTITUTED FLUORENES: II. COMPARATIVE REACTIVITIES OF THE ALKALI METALS, LITHIUM, SODIUM, AND POTASSIUM, WITH FLUORENE IN GLYCOL DIMETHYL ETHER, GLYCOL DIETHYL ETHER, TETRAHYDROFURAN, AND DIOXANE

1960 ◽  
Vol 38 (12) ◽  
pp. 2450-2456 ◽  
Author(s):  
G. W. H. Scherf ◽  
R. K. Brown
Keyword(s):  
Dimethyl Ether ◽  
Diethyl Ether ◽  
Organometallic Compound ◽  
Alkali Metals ◽  
Organometallic Compounds ◽  
Lithium Amide ◽  
Glycol Dimethyl Ether ◽  
Derivatives Of ◽  
Sodium And Potassium

In the solvents 1,2-dimethoxyethane (DME), 1,2-diethoxyethane (DEE), tetrahydrofuran (THF), and dioxane, potassium reacts much more readily with fluorene than does sodium or lithium. Lithium is generally more reactive than is sodium. The order of effectiveness of the ethers is DME > DEE ≈ THF > dioxane. Although practically no reaction of these metals with fluorene occurs in toluene, the addition of small amounts of these ethers to toluene does accelerate such reaction. All three organometallic compounds are soluble in refluxing and cold (22°) DME, THF, and DEE except the 9-fluorenyllithium, which precipitates largely from cold DEE. The results are explained in terms of the relative electropositivities of the metals, their size, and the structure of the ethers. It is suggested that these ethers actually participate in the formation of the organometallic compound from the metal.Sodamide and lithium amide react as readily as or more readily than the metals with fluorene in DME to produce the organometallic compounds.Diphenylmethane and triphenylmethane react reasonably well with potassium in DME, but too slowly with lithium and sodium to be useful.

A comparative theoretical study of dimethyl ether, diethyl ether, isopropyl methyl ether and their perfluorinated analogues

1993 ◽  
Vol 300 ◽  
pp. 607-617 ◽  
Author(s):  
Michèle Fontaine ◽  
Joseph Delhalle ◽  
Mireille Defranceschi ◽  
Jean-Michel M. Bourin
Keyword(s):  
Dimethyl Ether ◽  
Diethyl Ether ◽  
Methyl Ether ◽  
Theoretical Study

Binding energies for aluminum atom association complexes with simple alkenes and arenes

1988 ◽  
Vol 92 (6) ◽  
pp. 1655-1664 ◽  
Author(s):  
S. A. Mitchell ◽  
B. Simard ◽  
D. M. Rayner ◽  
P. A. Hackett
Keyword(s):  
Aluminum Atom ◽  
Binding Energies
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