Chemistry of phosphorus fluorides. Part III. The reaction of thiophosphoryl-fluoride with dimethylamine and some properties of the dimethylaminothio- phosphoryl fluorides

1968 ◽  
Vol 46 (4) ◽  
pp. 613-621 ◽  
Author(s):  
R. G. Cavell

Dimethylamine reacts with thiophosphoryl fluoride with non-integral stoichiometry to yield the volatile compound dimethylaminothiophosphoryldifluoride and the solid products contained hexafluoro-phosphate and difluorodithiophosphate ions, and an unstable complex ion containing phosphorus and fluorine. The reaction of dimethylaminothiophosphoryldifluoride with dimethylamine to form bis-(dimethylamino)thiophosphorylfluoride has also been studied. The solid residues of this reaction contained hexafluorophosphate and difluorodithiophosphate ions and an unidentified phosphorus-fluoride salt. Dimethylaminothiophosphoryldifluoride did not complex with boron trifluoride but reacted with hydrogen halides to yield the halogenothiophosphoryldifluorides. Physical and spectroscopic data on the alkylaminothiophosphoryl fluorides are reported.

1967 ◽  
Vol 45 (12) ◽  
pp. 1309-1319 ◽  
Author(s):  
R. G. Cavell

Phosphoryl fluoride reacts with dimethylamine in an equimolar ratio to yield volatile dimethylaminophosphoryldifluoride. The residual solid is a mixture of dimethylammonium hexafluorophosphate and dimethylammonium difluorophosphate salts rather than the simple fluoride salt. Dimethylamine reacts slowly with dimethylaminophosphoryldifluoride to yield bis(dimethylamino)phosphorylfluoride and the same complex fluorophosphate anions in the solid products. Physical data are reported on the alkylamino phosphoryl fluorides. The reaction of the difluorophosphoryl compound with hydrogen halides has been studied.


Author(s):  
Gang Li ◽  
Iouli E. Gordon ◽  
Robert J. Le Roy ◽  
Photos G. Hajigeorgiou ◽  
John A. Coxon ◽  
...  

1978 ◽  
Vol 56 (21) ◽  
pp. 2764-2767 ◽  
Author(s):  
S. Brownstein ◽  
G. Latremouille

Complex fluoroanions have been prepared with boron trifluoride and perchlorate, nitrate, nitrite, acetate, formate, azide, cyanide, cyanate, thiocyanate, and thiophenolate ions. The complexes formed from the anions of the strong acids, except the hydrogen halides, do not disproportionate to BF2(anion)2−. Complexes of anions of weaker acids may disproportionate and, or, complex a second molecule of BF3. Regularities in fluorine–boron coupling constants are tabulated.


Author(s):  
Gang Li ◽  
Iouli E. Gordon ◽  
Photos G. Hajigeorgiou ◽  
John A. Coxon ◽  
Laurence S. Rothman

1973 ◽  
Vol 26 (2) ◽  
pp. 333 ◽  
Author(s):  
RK Norris ◽  
S Sternhell

Treatment of five 1,4-benzoquinone dihalides in boron trifluoride etherate gives very high yields of isomeric dihalogenohydroquinones. With the exception of the conversion of 5,6-dichlorocyclohex-2-ene-1,4- dione into 2,3-dichlorohydroquinone, which is a true keto-enol isomerization, these products arise through elimination of hydrogen halides followed by re-addition.


1979 ◽  
Vol 46 ◽  
pp. 65-74 ◽  
Author(s):  
A.C. Fabian ◽  
J.E. Pringle ◽  
J.A.J. Whelan ◽  
J.A. Bailey

Abstract.Recent photometric and spectroscopic observations of the dwarf nova system Z Cha are discussed. Methods for constraining the system parameters are applied and the disc emissivity is deduced as a function of radius. Indications are found that the disc shrinks in size with increasing time after outburst.


1997 ◽  
Vol 90 (3) ◽  
pp. 495-497
Author(s):  
CLAUDIO ESPOSTI ◽  
FILIPPO TAMASSIA ◽  
CRISTINA PUZZARINI ◽  
RICCARDO TARRONI ◽  
ZDENEK ZELINGER

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