Robust, alkali-stable, triscarbonyl metal derivatives of hexametalate anions, [M6O19{M'(CO)(3)}(n)]((8-n)-) (M = Nb, Ta; M' = Mn, Re; n=1, 2)

Citation
Mh. Dickman et Mt. Pope, Robust, alkali-stable, triscarbonyl metal derivatives of hexametalate anions, [M6O19{M'(CO)(3)}(n)]((8-n)-) (M = Nb, Ta; M' = Mn, Re; n=1, 2), INORG CHEM, 40(11), 2001, pp. 2582-2586
Citations number
32
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
INORGANIC CHEMISTRY
ISSN journal
00201669 → ACNP
Volume
40
Issue
11
Year of publication
2001
Pages
2582 - 2586
Database
ISI
SICI code
0020-1669(20010521)40:11<2582:RATMDO>2.0.ZU;2-6
Abstract
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.