E. Bouwman et al., DOUBLY-HYDRATED HEXAFLUOROACETYLACETONE AS A TETRADENTATE LIGAND - SYNTHESIS, MAGNETOCHEMISTRY, AND THERMAL TRANSFORMATIONS OF A MN(III)2 COMPLEX, Inorganic chemistry, 32(16), 1993, pp. 3463-3470
A convenient synthesis of the doubly-hydrated form of hexafluoroacetyl
acetone (hfacH) is reported, viz. 1,1,1,5,5,5-hexafluoropentane-2,2,4,
4-tetraol (hfptH4; 1), together with the initial employment of the lat
ter as a ligand. A reaction system in CH2Cl2 comprising [Mn3O(OAc)6(py
)3](ClO4), hfacH, hfptH4, and py (py = pyridine) in a 1:6:1.5:9 ratio
leads to a 58% yield of (pyH)2[Mn2(hfpt)(hfac)4] (2). Crystal data for
1 at -171-degrees-C: monoclinic, P2(1)/n, a = 11.108(6) angstrom, b =
5.104(3) angstrom, c = 14.736(8) angstrom, beta = 90.30(2)degrees, Z
= 4, V = 835.44 angstrom3, R (R(w)) = 6.58% (7.42%). Crystal data for
2 at -130-degrees-C: monoclinic, C2/c, a = 17.884(5) angstrom, b = 12.
573(3) angstrom, c = 23.715(7) angstrom, beta = 107.77(1)degrees, Z =
4, V = 5077.62 angstrom3, R (R(w)) = 9.80% (9.37%). The structure of 1
confirms a bis(gem-diol) structure with an extended-chain conformatio
n. The anion of 2 consists of two Mn(hfac)2 fragments bridged by the h
fpt4- group; the latter functions as a bidentate chelate ligand to eac
h Mn(III), employing one alkoxide oxygen atom from each gem-diolate pa
ir. Variable-temperature magnetochemical studies have been performed o
n powdered samples of 2 in the range 5-320 K. The Mn(III) centers are
weakly interacting; the exchange interaction is ferromagnetic, and fit
ting of the data leads to the following values for the variables: J =
+0.21 cm-1 (employing the -2JS1.S2 convention), D = 0.9 cm-1, g = 1.99
. Vacuum thermolysis of 2 in the range 111-150-degrees-C yields (py)Mn
(hfac)3 (3) and lesser amounts of cis-Mn(py)2(hfac)2 (5), Mn(hfac)3 (4
), the tetraol (1), and a manganese(greater-than-or-equal-to IV) oxide
. All but the oxide are volatile and have been characterized in part b
y single-crystal X-ray diffraction. The mechanism of thermolysis is pr
oposed to be initiated by proton transfer from pyH+ to the tetraolate
oxygen to which it is hydrogen bonded; this process facilitates the el
ectrophilic cleavage of C/O bonds, which furnishes hfac- as well as ox
ide for the manganese oxide product. Crystal data for 3 (-175-degrees-
C): a = 10.487(2) angstrom, b = 15.790(4) angstrom, c = 9.356(2) angst
rom, alpha = 101.78(1)degrees, beta = 106.58(1)degrees, gamma = 108.50
(1)degrees with Z = 2 in space group P1BAR. Crystal data for 4 (-159-d
egrees-C): a = 8.879(0) angstrom, b = 12.941(1) angstrom, c = 18.748(1
) angstrom, beta = 91.35(0)degrees with Z = 4 in space group P2(1)/n.
Crystal data for 5: a = 9.112(3) angstrom, b = 16.821(6) angstrom, c =
16.315(5) angstrom, beta = 105.34(5)degrees with Z = 4 in space group
C2/c.