Slow diffusion in a H-tube at room temperature of a methanolic solution of [VO(acac) 2] (Hacac = acetylacetone) and 1,10-phenanthroline (phen) or 2,2′-bipyridine (bipy) into an aqueous solution of sodium pyrophosphate (Na 4P 2O 7) resulted in the serendipitous formation of X-ray quality crystals of mixed-valent, hexameric oxovanadates of general formula [V 6O 12(OCH 3) 4(L) 4]·solv [L = 1,10-phenanthroline (phen) for 1 · 2CH 3OH · 4H 2O (1a), and 2,2′-bipyridine (bipy) for 2 · 4H 2O (2a)]. These were characterized by single-crystal X-ray diffraction, IR, elemental and thermogravimetric analysis (TGA). A facile, rationalized synthetic route for the isolation of 1a and 2a could be established following structural determination, involving NaOH in place of Na 4P 2O 7 as pH modulator. The use of distilled water (pH 7) as methanolic co-solvent also resulted in crystallization of the two complexes, proving the presence of a base in the reaction scheme is not vital, with slightly pH-depended yields noted for 2a only. A survey of the literature revealed the occurrence of several other procedures, from classical methods to hydrothermal routes, leading to different solvates of 1, the crystal structure of 2 being unreported in any form to date. The precise nature of the molecular assembly in these type of hybrid organic-inorganic poly-vanadates is contradictory in published reports. On the basis of newly acquired high resolution crystal data and supported by magnetic investigation of the samples, we propose herein a formulation as [(V IVO) 2(V VO 2) 4(μ 3-O) 2(μ-OCH 3) 4(L) 4], with two oxovanadyl(IV) and four dioxovanadyl(V) units per molecule. A net ferromagnetic coupling between the two isolated V IV metal centers was measured with literature-consistent J values of +16.1(1) and +19.7(1) cm -1 for 1a and 2a, respectively [H = -JS A·S B + S A·D·S B + βH (g AS A + g BS B)], suggesting that crystal packing forces do not significantly influence the magnetic properties of this class of materials. A facile route toward the synthesis of the fully-oxidized [V V4O 8(CH 3O) 4(bipy) 2] and [V V4O 6(CH 3O) 6(acac) 2] tetraoxovanadates is also reported. © 2011 The Royal Society of Chemistry.

Synthetically persistent, self assembled [V IV2V V4] polyoxovanadates: Facile synthesis, structure and magnetic analysis

Marino, Nadia;
2011

Abstract

Slow diffusion in a H-tube at room temperature of a methanolic solution of [VO(acac) 2] (Hacac = acetylacetone) and 1,10-phenanthroline (phen) or 2,2′-bipyridine (bipy) into an aqueous solution of sodium pyrophosphate (Na 4P 2O 7) resulted in the serendipitous formation of X-ray quality crystals of mixed-valent, hexameric oxovanadates of general formula [V 6O 12(OCH 3) 4(L) 4]·solv [L = 1,10-phenanthroline (phen) for 1 · 2CH 3OH · 4H 2O (1a), and 2,2′-bipyridine (bipy) for 2 · 4H 2O (2a)]. These were characterized by single-crystal X-ray diffraction, IR, elemental and thermogravimetric analysis (TGA). A facile, rationalized synthetic route for the isolation of 1a and 2a could be established following structural determination, involving NaOH in place of Na 4P 2O 7 as pH modulator. The use of distilled water (pH 7) as methanolic co-solvent also resulted in crystallization of the two complexes, proving the presence of a base in the reaction scheme is not vital, with slightly pH-depended yields noted for 2a only. A survey of the literature revealed the occurrence of several other procedures, from classical methods to hydrothermal routes, leading to different solvates of 1, the crystal structure of 2 being unreported in any form to date. The precise nature of the molecular assembly in these type of hybrid organic-inorganic poly-vanadates is contradictory in published reports. On the basis of newly acquired high resolution crystal data and supported by magnetic investigation of the samples, we propose herein a formulation as [(V IVO) 2(V VO 2) 4(μ 3-O) 2(μ-OCH 3) 4(L) 4], with two oxovanadyl(IV) and four dioxovanadyl(V) units per molecule. A net ferromagnetic coupling between the two isolated V IV metal centers was measured with literature-consistent J values of +16.1(1) and +19.7(1) cm -1 for 1a and 2a, respectively [H = -JS A·S B + S A·D·S B + βH (g AS A + g BS B)], suggesting that crystal packing forces do not significantly influence the magnetic properties of this class of materials. A facile route toward the synthesis of the fully-oxidized [V V4O 8(CH 3O) 4(bipy) 2] and [V V4O 6(CH 3O) 6(acac) 2] tetraoxovanadates is also reported. © 2011 The Royal Society of Chemistry.
Hydrogen-Ion Concentration; Models, Molecular; Molecular Conformation; Solvents; Vanadates; Magnetic Phenomena; Inorganic Chemistry
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/20.500.11770/292770
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