Abstract
The previously known staphylonuclear
halides, Nb6Cl14,7H2O;
Nb6Brl4,7H2O (in
trifling yield) ; Ta6Cl14,7H2O
; and Ta6Br14,7H2O
have been prepared, but intended studies of these have been frustrated by their
instability and insolubility. It has been possible, however, to obtain
approximate molar conductivities in water and ethanol which support the
formulation of (Nb6Cl12)Cl2,7H2O as a 2 : 1 electrolyte, and
evidence by pH titration of the existence of the complex ion [(Nb6Cl12)(OH)4- (H2O)p]2-
in alkaline solution.
The absorption spectra of the four halides
have been obtained over the range 8-50 kK in neutral
and alkaline aqueous solution and in the solid state. It is proposed that the
very strong bands in the visible and infrared region result from transitions
from metal-to-metal bonding to metal-to-metal anti-bonding levels. Excellent
agreement can be obtained between the experimental frequencies of the (Nb6Cl12) group and those predicted
from the molecular orbital energy diagram of Cotton and Haas.
It is proposed that Harned's
brown chloride is a similar material to the green Nb6Cl14,7H2O
but additionally contains μ-hydroxo derivatives of the type [Nb6Cl(12-n)(OH)n]Cl2, resulting from the mode of preparation of
the material.
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