Abstract:This review discusses the recent advances in the syntheses of high explosive energetic materials. Syntheses of some relevant modern primary explosives and secondary high explosives, and the sensitivities and properties of these molecules are provided. In addition to the synthesis of such materials, processing improvement and formulating aspects using these ingredients, where applicable, are discussed in detail.

Transition metal chalcogenides are important materials because of their range of useful properties and applications, including as thermoelectrics, magnetic semiconductors, superconductors, quantum dots, sensors, and photovoltaics. In particular, iron chalcogenides have received renewed attention following the discovery of superconductivity in PbO-type β-FeSe and related solid solutions. This paper reports a low-temperature solution chemistry route to the synthesis of β-FeSe, β-FeTe, FeTe 2 , and several members of the β-Fe(Se,Te) solid solution. The samples were analyzed by powder XRD, TEM, EDS, SAED, SEM with elemental mapping, AFM, and SQUID magnetometry. Consistent with the layered crystal structures, the FeSe, FeTe, and Fe(Se,Te) products are predominantly twodimensional single-crystal nanosheets with thicknesses of approximately 2-3 nm and edge lengths ranging from 200 nm to several micrometers. FeTe 2 forms a mixture of nanosheets and onedimensional sheet-derived nanostructures. None of the samples are superconducting, which could be due to size effects, nonstoichiometry, or low-level impurities.

A family of heteroleptic (C;N)2Ir(acac) and homoleptic fac-Ir(C;N)3 complexes have been synthesized and their photophysical properties studied (where C;N = a substituted 2-phenylpyridine and acac = acetylacetonate). The neutral Delta and Lambda complexes were separated with greater than 95% enantiomeric purity by chiral supercritical fluid chromatography, and the solution circular dichroism and circularly polarized luminescence spectra for each of the enantio-enriched iridium complexes were obtained. The experimentally measured emission dissymmetries (gem) for this series compared well with predicted values provided by time-dependent density functional theory calculations. The discovered trend further showed a correlation with the dissymmetries of ionic, enantiopure hemicage compounds of Ru(II) and Zn(II), thus demonstrating the applicability of the model for predicting emission dissymmetry values across a wide range of complexes.

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