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New insights into the thermal stability of Mn12clusters: The case of complex [Mn12O12(O2CCCH)16(H2O)4]·3H2O and its thermolysis derived [Mn3(O2CCCH)6(H2O)4]·2H2O complex
Author(s) -
Jordi GómezSegura,
Javier Campo,
Inhar Imaz,
Klaus Wurst,
Jaume Veciana,
Philippe Gerbier,
Daniel RuizMolina
Publication year - 2007
Publication title -
dalton transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.98
H-Index - 184
eISSN - 1477-9234
pISSN - 1477-9226
DOI - 10.1039/b700298j
Subject(s) - monoclinic crystal system , crystallography , chemistry , magnetization , thermal decomposition , crystal structure , thermal stability , yield (engineering) , reciprocal lattice , bond length , hysteresis , condensed matter physics , physics , thermodynamics , magnetic field , quantum mechanics , diffraction , optics , organic chemistry
Two novel Mn12 derivatives [Mn12O12(O2CC[triple bond]CH)16(H2O)4] x 3H2O (1) and [Mn12(O2CC[triple bond]CC6H5)16(H2O)4] x 3H2O (2) have been prepared and characterized. Magnetic measurements confirm that both function as single-molecule magnets (SMM), showing frequency-dependent out-of-phase AC susceptibility signals and magnetization hysteresis curves. Thermal stability studies of both complexes were first conducted in the solid state. While complex 1 undergoes a sudden exothermal decomposition at T(onset) = 118 degrees C, complex 2 exhibits a higher stability. Thermolysis reaction of 1 was hence assessed in solution to yield dark red crystals of a two-dimensional Mn(II)-based co-ordination polymer [Mn3(O2CC[triple bond]CH)6(H2O)4] x 2H2O (3), which corresponds to an extended sheet-like structure that crystallizes in the monoclinic space group P2(1)/n; a = 9.2800(2) angstroms, b = 9.4132(2) angstroms, c = 14.9675(3) angstroms, beta = 99.630(1) degrees, and Z = 2. Finally, the magnetic properties of complex 3 have been studied on an oriented single crystal over two different orientations of the reciprocal vector versus the external field.

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