Restricted rotation about partial C,N double bonds

The restricted rotation about the partial C,N double bond in 2-chloro-6-NR₂-pyran-4-ones is discussed in the light of NMR spectroscopic data and theoretical calculations.Ab initio calculations at the HF/6-31G^* level were carried out using a continuum model to take solvent effects into account. The delocalization of-electron density [described by natural bond orbital analysis (NBO)] was applied to determine the degree of conjugation in the ground state (GS) and in the transition state (TS) for the restricted rotation of the compounds studied. The reason for the different barriers to rotation of the NR₂ substituents (pyrrolidino > dimethylamino > morpholidino > piperidino) at the 2-chloro-pyran-4-one ring appears to be the different steric hindrance of the NR₂ substituents in the GS for the restricted rotation.     

Investigation of gain and hyperfine splitting in the niobium X-ray laser

Neon-like niobium X-ray lasers have been studied using both slab and thin-foil target geometries. Niobium foils of various lengths were irradiated from both sides with two beams of the frequency-doubled Nova laser system using a line focus. We looked for gain by measuring spectrally integrated line intensities at different plasma lengths. Gain was observed in four neon-like niobium lines corresponding to 3s–3p transitions. The line profile of theJ = 0–1 line ( = 145.9 ) shows splitting due to the hyperfine effect. Improved contrast in the hyperfine structure is observed as the plasma length is increased. Hyperfine splitting may be relevant to other 3s–3p transitions in neon-like niobium as well as other neon-like X-ray laser systems.