Complex fluoroanions in solution. IX. BF3–anion complexes and their disproportionation

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.

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.


1971 ◽  
Vol 26 (8) ◽  
pp. 1346-1356
Author(s):  
V. Devarajan ◽  
S. J. Cyvin

A complete normal coordinate analysis for the complex acetonitrile-boron trifluoride has been carried out for the first time. Mean amplitudes of vibration, Bastiansen-Morino linear shrinkages, and the most important Coriolis coupling constants have also been determined


1970 ◽  
Vol 48 (24) ◽  
pp. 3856-3859 ◽  
Author(s):  
T. Chivers

The reaction of boron trifluoride with o-CF3C6H4SnMe3 in carbon tetrachloride gives o-CF3C6H4BF2, which with aqueous potassium fluoride is converted to K[o-CF3C6,H4BF3]. Boron trichloride and o-CF3C6H4SnMe3 undergo halogen exchange to give, after hydrolysis, o-CCl3C6H4B(OH)2. Halogen exchange also occurs between boron trichloride and o-CF3C6H4Y (Y = H, SiMe3) to give boron trifluoride and o-CCl3C6H4Y. The long range HF and FF nuclear magnetic resonance (n.m.r.) coupling constants observed for o-CF3C6H4-derivatives are briefly discussed.


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.


1976 ◽  
Vol 54 (21) ◽  
pp. 3477-3482 ◽  
Author(s):  
Paul A. Giguère ◽  
Sylvia Turrell

We have re-examined the infrared absorption between 4000 and 800 cm−1 of aqueous solutions of the four hydrogen halides at concentrations up to saturation, and under better experimental conditions than heretofore. The new spectra confirm definitely our previous assignment of the three broad bands around 2900, 1730, and 1200 cm−1 to fundamental vibrations of the H3O+ ion. Other proposed interpretations are shown to be untenable; in particular that of Ackermann, based on alleged similarities in the spectra of strong acids and bases. In hydrofluoric acid, hydrogen-bonded ion pairs are responsible for the shifts of the H3O+ frequencies. There is no evidence in the spectra for higher species, such as H5O2+. We conclude that the H3O+ ion has an appreciably longer lifetime in concentrated aqueous acids than in water. It also forms much stronger hydrogen bonds than H2O because of its ionic charge.


1997 ◽  
Vol 91 (5) ◽  
pp. 897-907 ◽  
Author(s):  
SHEELA KIRPEKAR ◽  
THOMAS ENEVOLDSEN ◽  
JENS ODDERSHEDE ◽  
WILLIAM RAYNES

1997 ◽  
Vol 7 (11) ◽  
pp. 1299-1304 ◽  
Author(s):  
P. Weinberger ◽  
C. Sommers ◽  
U. Pustogowa ◽  
L. Szunyogh ◽  
B. Újfalussy

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