Mixed chloride/amine complexes of dimolybdenum(II,II). 3. Preparation, characterization, and crystal structure of Mo2Cl4(NH2R)(4) (R = Et, Pr-n, Bu-t, Cy): First quadruply-bonded dimolybdenum compounds with primary amine ligands
Fa. Cotton et al., Mixed chloride/amine complexes of dimolybdenum(II,II). 3. Preparation, characterization, and crystal structure of Mo2Cl4(NH2R)(4) (R = Et, Pr-n, Bu-t, Cy): First quadruply-bonded dimolybdenum compounds with primary amine ligands, INORG CHEM, 38(11), 1999, pp. 2649-2654
Four new quadruply-bonded dimolybdenum(II) complexes of the formula Mo2Cl4(
NH2R)(4) (R = Et (1), Pr-n (2), Bu-t (3), Cy (4)) have been prepared in exc
ellent yield by reduction of the dimolybdenum(III) complex MO2Cl6(THF)(3) w
ith 2 equiv of sodium amalgam in the presence of the appropriate primary am
ine. The molecular structures of 2-4 have been investigated by X-ray crysta
llography. Crystal data are as follows: for 2, orthorhombic space group Ccc
a with a = 13.328(3) Angstrom, b = 26.639(5) Angstrom, c = 6.774(2) Angstro
m, and Z = 4; for 3, monoclinic space group P2(1)/c with a = 19.165(1) Angs
trom, b = 20.858(1) Angstrom, c = 14.1400(8) Angstrom, beta = 99.002(5)degr
ees, and Z = 8; for 4, tetragonal space group P4(2)2(1)2 with a 15.556(4) A
ngstrom, c = 6.9368(8) Angstrom, and Z = 2. All of the non-centrosymmetric
molecules 2-4 possess the same structure characterized by a Mo2Cl4N4 core w
ith D-2d virtual symmetry and slight deviation from the eclipsed geometry.
The Mo-Mo bond lengths for 2, 3, and 4 are 2.118(2), 2.1322(6), and 2.117(1
) Angstrom, respectively, which are consistent with the Mo-Mo quadruple bon
d. In addition to the structural data, IR, UV-vis, and H-1 NMR spectroscopy
have been used to characterize the complexes 1-4. Without amalgam, the rea
ctions of the starting material with amines also produce the reduced specie
s but with low yields (not exceeding 25%). The main products of these inter
actions have been found to be mononuclear molybdenum(III) complexes MoCl3(N
H2R)(3) This has been confirmed by a single-crystal X-ray diffraction study
for mer-MoCl3(NH2Prn)(3). 1/6THF (2a(.)1/6THF) with the following crystal
data: triclinic space group P (1) over bar, a = 12.370(2) Angstrom, b = 17.
977(2) Angstrom, c = 25.498(6) Angstrom, alpha = 95.32(1)degrees, beta = 10
3.21(2)degrees, gamma = 103.48(1)degrees, and Z = 12.