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The crystal of a new tetrachlorocobalt(II) anion salt, [BzPy]2[CoCl4] (1) ([BzPy]+ = benzyl pyridinium), was grown by the slow evaporation solution growth method at room temperature. The salt 1 crystallizes in the monoclinic space group P2(1)/c and consists of two [BzPy]+ cations and one [CoCl4]2− anion in which the Co(II) ion is coordinated by four Cl atoms in a close to tetrahedral geometry. The crystal packing is stabilized by electrostatic interactions and C − H···Cl hydrogen bonds between [BzPy]+ cations and [CoCl4]2− anions. Powder XRD diffraction study confirms the crystalline nature and purity of the title compound. The Fourier transform infrared (FT-IR) spectrum was recorded and analyzed with the aid of DFT calculations in order to make a suitable assignment of the observed bands. The thermal stability of the hybrid crystal was analyzed by TG-DTA techniques revealing that the title crystal was stable up to 195 °C. The title salt exhibits violet and cyan fluorescence emissions upon excitation at 345 nm and weak antiferromagnetic interactions in the temperature range 2-300 K. The nonlinear optical (NLO) effect of this compound was predicted using DFT, suggesting that the title crystal is a good material for NLO applications. [ABSTRACT FROM AUTHOR]

In this article, we present the syntheses, crystal structures, vibrational spectra, optical and antibacterial properties of two new organic-inorganic hybrids, [Py(CH2)3TPP][CoCl4]·H2O (1) and [Py(CH2)3TPP][CuCl4] (2), where [Py(CH2)3TPP]2+ was 1-(1′-pyridyl-propyl)-3-triphenyl phosphonium. Two hybrids were crystallized in the monoclinic space group P21/n. The hybrids consisted of a [Py(CH2)3TPP]2+ cation and a tetrahedral [CoCl4]2−/[CuCl4]2− anion, where the crystal structure was stabilized by C−H···Cl, O−H···Cl, and C−H···O hydrogen bonds due to the presence of a water molecule in 1, and the crystal structure of 2 was stabilized by C−H···Cl hydrogen bonds. Experimental vibrational bands (IR and Raman) have been discussed and assigned. The intermolecular energy, the energy gap between HOMO and LUMO orbitals, as well as the first hyperpolarizabilities were predicted based on DFT calculations. The low energy gaps (1.26 eV for 1 and 1.20 eV for 2) were responsible for the charge transfer interactions that eventually occur between the cation and anion. The first hyperpolarizabilities (βtot) of 1 and 2 were 82 and 237 times as high as that of the standard KDP crystal, respectively, indicating that the as-prepared hybrids were excellent materials for NLO applications. Furthermore, it was found that both salts exhibit good bactericidal activity against Escherichia coli and Staphylococcus aureus. [ABSTRACT FROM AUTHOR]

The hydrothermal reaction of rare earth nitrates, CuCN, 2,7-naphthalenedisulfonate (2,7-nds), and isonicotinic acid (Hina) affords a new family of 3-D heterometallic 3d–4f coordination polymers, [Ln2Cu(2,7-nds)2(ina)4(H2O)4]·4H2O (Ln = Nd (1), Sm (2), Eu (3), Gd (4); 2,7-nds = 2,7-naphthalenedisulfonate, Hina = isonicotinic acid). Complexes1–4are structurally characterized by single crystal X-ray diffraction, elemental analysis, FT-IR spectroscopy (IR), powder X-ray diffraction, and thermogravimetric analyses. X-ray crystal structure analyses reveal that1–4are isomorphous with dinuclear subunit [Sm2(ina)4] binding Cu ions to generate 2-D networks. Such 2-D networks are pillared by linking 2,7-nds ligands to result in the 3-D layer-pillared Ln(III)–Cu(II) coordination architectures. The valence of Cu salts changed in the reaction. In addition, the luminescence properties of1–3and the magnetic properties of3and4have also been investigated. [ABSTRACT FROM PUBLISHER]