Sarr, Bougar and Diop, Cheikh A.K. and Melin, Frederic and Sidibe, Mamadou and Hellwig, Petra and Michaud, Francois and Maury, Francis and Senocq, François
and Mbaye, Abdou and Rousselin, Yoann
Non-hydrothermal synthesis and structure determination of two new β-octamolybdate (VI) stabilized with dialkylammonium counterions.
(2018)
Journal of Molecular Structure, 1170. 44-50. ISSN 0022-2860
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(Document in English)
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Official URL: http://doi.org/10.1016/j.molstruc.2018.05.055
Abstract
Two new organiceinorganic materials based on MoePOM, namely (iPr2NH2)2.((CH3)2NH2)2.[Mo8O26] (1) and (Pr2NH2)4$[Mo8O26] (2), have been synthesized by a non-hydrothermal method at room temperature and characterized by single crystal X-ray diffraction, thermal gravimetric analysis (TGA) and vibrational spectroscopy. The compound (1) is a b-[Mo8O26]4- anion which crystallizes as a mixed salt of both dimethylammonium [(CH3)2NH2]þ and diisopropylammonium [iPr2NH2]þ. The interaction between anions and cations leads to an inorganic-organic band structure. Similarly, in compound (2), the interconnection of b-[Mo8O26]4- anions with dipropylammonium [Pr2NH2]þ cations gives an inorganicorganic band structure. In both compounds, the cations interact with two different sites of the cluster: a fundamental site formed by four highly nucleophilic terminal oxo ligands, and a second site which is composed of Ot, m2-O and/or m3-O oxygen groups. A remarkable difference between the two compounds is that in compound (2) interactions between the bands involve only Van der Waals forces, whereas in compound (1) the bands interact also through hydrogen bonds.
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