Ten 1:1 and 2:1 complexes of [Mn(CO)(3)](+) and [Re(CO)(3)](+) with [Nb6O19
](8-) and [Ta6O19](8-) have been isolated as potassium salts in good yields
and characterized by elemental analysis, O-17 NMR and infrared spectroscop
y, and single-crystal X-ray structure determinations. Crystal data for 1 (t
-Re2Ta6): empirical formula. K4Na2Re2C6Ta6O35H20, monoclinic, space group,
C2/m, a = 17.648(3) Angstrom, b = 10.056(1) Angstrom. c = 13.171(2) Angstro
m, beta = 112.531(2)degrees, Z = 2. 2 (t-Re2Nb6): empirical formula, K6Re2C
6Nb6O38H26, monoclinic, space group, C2/m, a = 17.724(1) Angstrom, b = 10.0
664(6) Angstrom, c = 13.1965(7) Angstrom, beta = 112.067(1)degrees, Z = 2.3
(t-Mn2Nb6): empirical formula, K6Mn2C6Nb6O37H24, monoclinic, space group,
C2/m, a = 17.812(2) Angstrom, b = 10.098(1) Angstrom, c = 13.109(3) Angstro
m, beta = 112.733(2)degrees, Z = 2.4 (c-Mn2Nb6): empirical formula: K6Mn2C6
Nb6O50H50, triclinic. space group, P (1) over bar, a = 10.2617(6) Angstrom,
b = 13.4198(8) Angstrom, c = 21.411(1) Angstrom, alpha = 72.738(1)degrees,
beta = 112.067(1)degrees, gamma = 83.501(1)degrees Z = 2.5 (c-Re2Nb6): emp
irical formula, K6Re2C6Nb6O54H58, monoclinic, space group, P2(1)/c, a = 21.
687(2) Angstrom, b = 10.3085(9) Angstrom, c = 26.780(2) Angstrom, beta = 10
8.787(1)degrees, Z = 3. The complexes contain M(CO)(3) groups attached to t
he surface bridging oxygen atoms of the hexametalate anions to yield struct
ures of nominal C-3v (1:1), D-3d (trans 2:1), and C-2v (cis 2:1) symmetry.
The syntheses are carried out in aqueous solution or by aqueous hydrotherma
l methods, and the complexes have remarkably high thermal, redox, and hydro
lytic stabilities. The Re-containing compounds are stable to 400-450 degree
sC, at which point CO loss occurs. The Mn compounds lose CO at temperatures
above 200 degreesC. Cyclic voltammetry of all complexes in 0.1 M sodium ac
etate show no redox behavior, except an irreversible oxidation process at s
imilar to1.0 V vs Ag/AgCl. In contrast to the parent hexametalate anions th
at are stable only in alkaline (pH > 10) solution, the new complexes are st
able, at least kinetically, between pH 4 and pH similar to 12.