Tripyridinium cis-tetrachloridodioxidomolybdate(VI) chloride.

Abstract

In the title compound, (C(5)H(6)N)(3)[MoCl(4)O(2)]Cl, the pyridinium cations are N-H⋯Cl hydrogen bonded to the anionic [MoCl(4)O(2)](2-) complexes and to the two crystallographically independent chloride anions (located on C2 axes). The Mo(6+) centre adopts a highly distorted octa-hedral geometry, being surrounded by four chloride and two terminal oxide groups. The oxide ligands are mutually cis.

Fernandes Jose A.; Gomes Ana C.; Figueiredo Sonia; et al.


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Bis(mu-4-phenylpyridine N-oxide-kappa(2)O:O)-bis[bis(1,1,1,5,5,5-hexafluoropentane2,4-dionato)copper(II)].

Abstract

The asymmetric unit of the title compound, [Cu(2)(C(5)HF(6)O(2))(4)(C(11)H(9)NO)(2)], contains one half of the centrosymmetric dinuclear complex. The coordination geometry of the Cu(II) atom is octa-hedral, exhibiting a typical Jahn-Teller distortion. One trifluoro-methyl group is rotationally disordered between two orientations in a 1:1 ratio.

Ramos Ana I.; Fernandes Jose A.; Silva Patricia; et al.


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Diaquobis(1,2-ethanediamine-k2N,N’) copper(II) Bis(4-phenylbenzoate) 2.66 hydrate.

Abstract

In the title complex, [Cu(C2H8N2)(2)(H2O)(2)](C13H9O2)(2)center dot 2.66H(2)O,the Cu-II centre (located at an inversion centre) is coordinated by two bidentate ethylenediamine (en) ligands and two water O atoms in a typical Jahn-Teller distorted octahedral geometry. The amino groups and the water molecules are disordered over two distinct crystallographic positions with occupancies of 1/3 and 2/3. In the crystal, the cations and anions are disposed in alternating layers. One of the water molecules of crystallization is disordered and the other has a fractional occupation. In the 2/3 occupancy component, water molecules are organized into a chain composed of hexameric units interconnected by carboxylate bridges.

José A. Fernandes, Ana Ramos, Patrícia Silva, Susana S. Braga, Paulo Ribeiro-Claro, João Rocha and Filipe A. Almeida Paz.


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Crystal Structure Landscapes from combined Vibrational Spectroscopy and ab initio Calculations: 4-(dimethylamino) benzaldehyde.

Abstract

In this work, the usefulness of the Pairs in Molecular Materials (PiMM) approach to elucidate unknown structures of molecular crystals is assessed. This methodology aims to assist the prediction of probable crystal structures from the vibrational spectra, through the identification of the most relevant motifs in the potential energy landscape of the crystal. The method is successfully applied to the elucidation of 4-(dimethylamino)benzaldehyde crystal structure, considered to be “unknown” to illustrate the applicability of the PiMM approach. The proposed crystal structure, based on weak CH⋯O hydrogen bonding and π-stacking interactions, is in full agreement with the recently reported crystal structure.

M Nolasco, P. Vaz, Paulo Ribeiro-Claro.


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3D-2D-0D Stepwise Deconstruction of a Water Framework Templated by a Nanoporous Organic-Inorganic Hybrid Host.

Abstract

The supramolecular salt [H2pip]3[Ge(hedp)2]⋅14 H2O (1) [H2pip2+=piperazine cation C4H12N22+; hedp5−=deprotonated form of etidronic acid, C2H3P2O75−) is reported. This consists of an organic–inorganic hybrid hydrogen-bonded nanoporous framework, the internal surface of which acts as a template for the three-dimensional (3D) clustering of water molecules. The structure and molecular dynamics of this material are characterised by single-crystal X-ray diffraction, thermogravimetric analysis, Raman (H/D isotopic substitution) spectroscopy, and 2H solid-state (wide-line and MAS) NMR spectroscopy. Material 1 is shown to be unusual because 1) few nanoporous materials exhibit a well-organised 3D framework of water molecules, 2) it provides a unique opportunity to follow experimentally and to rationalise the deconstruction of a 3D water framework and 3) despite the fact that the hybrid framework is a supramolecular salt, the structure does not collapse after dehydration and the final material is crystalline.

João Rocha, Fa-Nian Shi, Filipe A. Almeida Paz, Luís Mafra, Mariana Sardo, Luís Cunha-Silva, Paulo Ribeiro-Claro, Tito Trindade.


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