Resonance radiation trapping effects in copper and manganese pure metals and their halides as laser materials have been investigated using Holstein’s theory of resonance radiation trapping. Theoretical calculations have been performed for determining the laser-starting and optimum temperatures, and dissociation levels in the metal halides. The results are found to be in excellent agreement with the reported experimental values. A detailed discussion of the results has been presented.

Twenty-five inclusion complexes formed by fe(N-alkyiimidazolidine-2-thione)cuprous halides with the small, chlorine-containing guest molecules CC1 4 , CHC1 3 , CH 2 C1 2 , CH 3 CC1 3 or C 2 H 2 C1 2 , have been prepared. Their 63 Cu and 35 C1 NQR spectra have been measured over the temperature range 77-300 K. For the corresponding bromides the 79 Br and/or 81 Br spectra have also been investigated. The studies reveal the number and symmetry of different inclusion site. The onset of rapid reorientation of the guest molecules is indicated by the fading out of their NQR signals between 77 and 300 K, whereas the resonances from the host molecules usually persist throughout this temperature range. However, as evidenced by discontinuities in the temperature-dependence of the NQR frequencies of the hosts, sixteen of the complexes show one or more phase-changes in this temperature-range.

Unlike chlorination fluorination of ammine complexes of platinum(IV) in aqueous solution does not lead to haloamido complexes. Instead, the triammine complexes [Pt(NH3)3Cl3]Cl and [Pt(NH3)3(NCl2)2Cl]Cl yield no definite main product, and the tetrammine and pentammine complexes trans-[Pt(NH3)4C12]C12, [Pt(NH3)4(NCl2)Cl]Cl2, [Pt(NH3)5Cl]Cl3, and [Pt(NH3)5(OH)]Cl3 form the sparingly soluble complex trans -[Pt (NH3 )4C12] (H2F3 )2 • 2 H-20 as the main product.

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