George R.
Rossman, F.-D. Tsay, Harry B. Gray Arthur Noyes Laboratory of Chemical Physics California Institute of Technology, Pasadena, CA 91109 |
Several salts
containing the
Mo(CN)74- ion have been studied by a variety of
spectroscopic and magnetic techniques. Infrared and Raman spectral data
together with magnetic susceptibility measurements suggest a
pentagonal-bipyramidal (D5h) structure (2E1
“ –
(e1 “)3 ground state) for Mo(CN)74-
in aqueous solutions of K4Mo(CN)7·2H2O.
Anhydrous K4Mo(CN)7 and solid Cs4Mo(CN)7·xH2O
also appear to contain pentagonal-bipyramidal anions. Solid K4Mo(CN)7·2H2O,
however, exhibits infrared and Raman spectra that differ from the
aqueous
solution results. The esr spectrum of the dihydrate, which can be
observed only
below 150°K, gives g|| = 2.103 and gꞱ
= 1.973. The g values
and a μeff
= 1.73 BM are consistent with a 2A1(a2)2(a1)1
ground state of a monocapped trigonal-prismatic (C2v)
coordination
geometry. Electronic spectral bands at 16,100, 20,900, and 22,500 cm-1
in crystalline K4Mo(CN)7·2H2O
are assigned
respectively to the d-d transitions 2A1 -> 2A2,
2A1 -> 2B2, and 2A1
-> 2B1. The lowest spin-allowed d-d
transition in D5h
Mo(CN)74- occurs
at 24,900 cm-1.