RESUMEN
Hybrid lead halides are a diverse family of compounds, of interest for their optoelectronic properties, that vary in the dimensionality and connectivity of their inorganic substructures. The great majority of these compounds are based on lead-centered octahedra, with few examples featuring inorganic architectures containing higher coordination numbers. Here, we report the synthesis and characterization of a pyridinium lead bromide phase that is based on seven-coordinate Pb(II) centers. Through edge- and face-sharing, the polyhedra form a corrugated, two-dimensional inorganic substructure. Electronic structure calculations were used to examine the band structure and the role of the stereoactive lone pair in the inherently asymmetric, seven-coordinate Pb(II) geometry. For reference, we have visualized the role of the lone pair in the binary halide PbBr2, which also has a seven-coordinate inner ligand sphere. A comparison of the new structure with the limited number of existing hybrid lead halides with similar inorganic architectures highlights the templating role of the organic cation for these compounds. We also contribute characterization and discussion of isomorphic pyridinium lead chloride, which had been deposited in the Cambridge Structural Database but never, to our knowledge, addressed in the literature. The compounds were synthesized using solution conditions and structures determined with single-crystal X-ray diffraction. The materials were also characterized via powder X-ray diffraction, combustion elemental analysis, and diffuse reflectance UV-vis spectroscopy. While the structures reported here are centrosymmetric, the seven-coordinate, capped trigonal prismatic geometry that we have identified is a source of local asymmetry that could be used as a component in designing globally noncentrosymmetric structures.
RESUMEN
Reactions of carboxylic acids with lead play an important role in the atmospheric corrosion of lead and lead-tin alloys. This is of particular concern for the preservation of lead-based cultural objects, including historic lead-tin alloy organ pipes. Two initial corrosion products, Pb(3)O(2)(CH(3)COO)(2)·0.5H(2)O (1) and Pb(2)O(HCOO)(2) (2), had been identified through powder diffraction fingerprints in the Powder Diffraction File, but their structures had never been determined. We have crystallized both compounds using hydrothermal solution conditions, and structures were determined using laboratory and synchrotron single-crystal X-ray diffraction data. Compound 1 crystallizes in P1, and 2 in Cccm. These compounds may be viewed as inorganic-organic networks containing single and double chains of edge-sharing Pb(4)O tetrahedra and have structural similarities to inorganic basic lead compounds. Bond valence sum analysis has been applied to the hemidirected lead coordination environments in each compound. Atmospheric exposure experiments contribute to understanding of the potential for conversion of these short-term corrosion products to hydrocerussite, Pb(3)(CO(3))(2)(OH)(2), previously identified as a long-term corrosion product on lead-rich objects. Each compound was also characterized by elemental analysis, thermogravimetric analysis and differential scanning calorimetry (TGA-DSC), and Raman spectroscopy.
RESUMEN
Ligand-exchange reactions involving octahedral W6S8 clusters and a family of pyridine-based ligands (isonicotinic acid, isonicotinamide, 4-hydroxypyridine, 4-aminopyridine, 4-pyridineacetamide) have been explored with the goal of preparing compounds that crystallize in hydrogen-bonded arrays. Two new compounds, W6S8(4-pyridineacetamide)6.DMF.4-pyridineacetamide (1) and W6S8(4-aminopyridine)6.4DMF (2), were isolated and characterized by single-crystal X-ray diffraction. Both compounds crystallize in the P2(1)/c space group with a = 16.461(1), b = 33.08(2), c = 13.165(10) A, beta = 103.270(15) degrees for 1 and a = 13.8988(5), b = 13.2791(5), c = 15.6293(6) A, beta = 108.5410(10) degrees for 2. Each compound was further characterized by 1H NMR spectroscopy, elemental (CHN) analysis, and thermogravimetric analysis. Examination of the structures shows that 1 forms a three-dimensional hydrogen-bonded network in which each 4-pyridineacetamide ligand interacts with ligands on neighboring clusters or with the free ligand of crystallization. This is the first hydrogen-bonded network formed from W6S8 clusters. In 2, the amino groups act as hydrogen-bond donors toward DMF molecules of crystallization, but an extended array is not formed. In addition, the binding strengths of these pyridine-based ligands to the W6S8 cluster were studied through quantitative 1H NMR studies of ligand-exchange reactions. A qualitative relationship was found between ligand binding strengths and Hammett substituent constants for this group of ligands.