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An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
Abstract A tetrameric cluster composed entirely of (aryl)Sn units, [DMPSn] 4 (DMP=2,6‐dimesitylphenyl), has been prepared by reduction of [DMPSnCl] 2 with a variety of reductants. This cluster was characterized in solution by multinuclear NMR spectroscopies, as well as in the solid‐state by single crystal X‐ray diffraction analysis. This species is stereochemically nonrigid in solution and possesses a cyclo ‐Sn 4 core whose DMP substituents are equivalent at higher temperatures. The solid‐state molecular structure is remarkably unsymmetrical and possesses a nearly planar cyclo ‐Sn 4 core. The DMP substituents are arranged such that three are approximately coplanar, while one is nearly perpendicular to the cyclo ‐Sn 4 core. Density functional theory calculations for a [PhSn] 4 model system show that this distorted geometry about the cyclo ‐Sn 4 core maximizes σ‐bonding between the Sn centers in a manner reminiscent of trans ‐bent bonding in the heavy group 14 analogues of alkenes and alkynes.
Siliceous mesostructured cellular foams (MCFs) with well-defined ultralarge mesopores and hydrothermally robust frameworks are described. The MCFs are templated by oil-in-water microemulsions and are characterized by small-angle X-ray scattering, nitrogen sorption, transmission electron microscopy, scanning electron microscopy, thermogravimetry, and differential thermal analysis. The MCFs consist of uniform spherical cells measuring 24−42 nm in diameter, possess BET surface areas up to 1000 m2/g and porosities of 80−84%, and give, because of their pores with small size distributions, higher-order scattering peaks even in the absence of long-range order. Windows with diameters of 9−22 nm and narrow size distribution interconnect the cells. The pore size can be controlled by adjusting the amount of the organic swelling agent that is added and by varying the aging temperature. Adding ammonium fluoride selectively enlarges the windows by 50−80%. In addition, the windows can be enlarged by postsynthesis treatment in hot water. The MCF materials resemble aerogels, but offer the benefits of a facilitated synthesis in combination with well-defined pore and wall structure, thick walls, and high hydrothermal stability. The open system of large pores give MCFs unique advantages as catalyst supports and separation media for processes involving large molecules, and the high porosities make them of interest for electrical and thermal insulation applications.
A sensitive search for intrinsically faint Seyfert nuclei in the 500 brightest northern galaxies is being conducted with the Hale 5.08 m telescope. The primary aim is to extend the luminosity function of active galactic nuclei (AGNs) to lower luminosities. Thus far, we have detected Hα emission having full-width near zero-intensity (FWZI) ≳ 4000 km s −1 in a significant fraction (≳10%) of nearby galaxies. Moreover, the narrow emission lines in a given nucleus often have markedly different widths, as shown in detail for M81. Those associated with high critical densities are generally the broadest, indicating that a very wide range of densities is present in the narrow-line region. The relative intensities of the lines can readily be explained with models in which clouds of gas having n e ≈ 10 2 to 10 7 cm −3 are photoionized by nonstellar radiation such as that produced by QSOs and luminous Seyfert 1 galaxies.
Abstract Densities, excess volumes and heats of mixing, heat capacities, refractive indices and viscosities of various N‐methyl‐2‐pyrrolidinone (NMP)‐water mixtures are reported. The excess volumes and heat of mixing are negative and show their greatest deviations from ideality at 0.3 ‐ 04 mole fraction NMP. The viscosity of the system passes through a maximum in the same region of solvent composition. These data indicate strong interaction between NMP and water and suggest the existence of transient polymeric species of the type — (NMP · 2H 2 O)n̄.