Decomposition of Dinuclear Manganese Complexes for the Preparation of Nanostructured Oxide Materials

The crystal structures of several dinuclear complexes of manganese are reported, and the decomposition and analysis of the nanostructured products derived from them are presented. 1,4,7,10-Tetraazacyclododecane (cyclen) forms dinuclear complexes 1−4 containing doubly oxo-bridged or oxo−acetato bridging ligands depending on the manganese salt used for the reaction. Doubly oxo-bridged 1 crystallizes in the orthorhombic space group Pnma, a = 22.3850(14) Å, b = 9.1934(5) Å, c = 13.2424(10) Å, V = 2725.2(3) Å3. 2, containing [Mn(SCN)5]3− conteranions, crystallizes in monoclinic space group I2/a with a = 18.2699(10) Å, b = 11.2384(6) Å, c = 18.6432(9) Å, α = 90.00°, β = 114.510(6)°, γ = 90.00°, V = 3483.0(3) Å3. Oxo−acetato-bridged 3 crystallizes in orthorhombic space group Pca21, a = 13.9322(11) Å, b = 16.2332(13) Å, c = 14.6794(8) Å, V = 3320.0(4) Å3. Compound 4 consists of a templated quasi-one-dimensional manganese oxalate crystallized in the triclinic space group P1̅, a = 9.5442(11) Å, b = 10.3758(10) Å, c = 21.851(2) Å, α = 83.720(12)°, β = 80.106(13)°, γ = 85.457(13)°, V = 2114.9(4) Å3. Compounds 1, 3, and 4 decompose to nanostructured oxide materials, which may be isolated in bulk as lamellar-structured particles or microspheres or deposited on substrates.