Perfluoralkyljod-verbindungen: Darstellungen und eigenschaften von CF3JO,CF3JOF2 und CF3JO2

Perfluoroalkyl iodine compounds: preparations and properties of CF₃IO, CF₃IOF₂, and CF₃IO₂. The trifluoromethyl iodine compounds CF₃IO, CF₃IOF₂, and CF₃IO₂ are formed from the reactions of CF₃I, CF₃IF₂ or CF₃IF₄ with ozone or silicon dioxide respectively. Their preparartions, properties, ¹⁹F-nmr spectra, and ir spectra are described.     

Zur komplexchemie von 4-zentren-π-systemen : XII. Glyoxaldiiminkomplexe: 1H-nmr-spektren und long range-kopplungen

Glyoxaldiimines (I) RN=CHCH=NR show in the NMR a downfield shift of glyoxalic protons (H_gly) when complexed to

(II: M = Mo, W), but increasing high field shifts when going to

(III) and

complexes (IV). In the tungsten complexes II H_glyW coupling satellites are resolved (J(WH) ≈4–6 Hz); in the phosphine compounds III, IV long range PH_gly coupling is clearly visible. Mechanisms of spinspin interaction are briefly discussed in connection with the EPR results on monoanionic radicals of II–IV.     

Zur komplexchemie von 4-zentren-π-systemen : VIII. ESR-untersuchungen an heterobutadien-chelaten. I. Kalium-(diazabutadien-tetracarbonyl-metallate)

Glyoxal- and diacetyl-bis(imine)metal tetracarbonyls (RNCR′CR′NR)M(CO)₄ (M = Cr, Mo, W) are reduced with potassium in DME to give paramagnetic mono-anions. Their high-resolutior, ESR spectra show the hyperfine splittings of the magnetically active ligand atoms as well as the satellites of the metal isotopes ⁵³Cr,^95,97Mo and ¹⁸³W. The coupling constants are discussed with respect to π-bonding mechanisms.     

Subterahertz superlattice parametric oscillator

We report a superlattice parametric oscillator (SPO), with a GaAs/AlAs superlattice as the active element. The SPO was pumped by a microwave field (power 4 mW) and produced third harmonic radiation at subterahertz frequencies (near 300 GHz; 0.1 mW). We attribute the parametric gain to the nonlinearity of the miniband transport.     

Crystal chemistry of the Tl2−xBa2Ca n Cu n+1O2n+6 (n=0, 1, 2) high-T c superconductors

We report on a comparative crystal chemical study of the Tl_2–xBa₂Ca _n Cu _n+1O_2n+6(n=0, 1, 2) high-T _c superconductors. Superconducting properties were determined by DC-conductivity and-susceptibility measurements. An X-ray diffraction analysis reveals the nonstoichiometry of the compounds as a link between structural and superconducting behavior. A comparison of the different structures gives evidence that T1 deficiency in the TlO double layers increases with increasingn; this deficiency causes apparent Cu valences larger than 2+in the superconducting phases thus maintaining the charge balance. By extracting appropriate chemical formulas and performing a bond strength calculation we obtained the mixed-valent oxidation state of copper for the superconducting tetragonal phases as being 2.17+(n=0), 2.25+(n=1) and 2.31+(n=2) respectively; for the non-superconducting orthorhombic phase Tl_2–xBa₂CuO_6–y a Cu valence of about 2+is suggested.