Biomedical subjects
Publications and source records attributed to K Seppelt.
The molecular structures of [(CH3)5MoOCH3], [(CH3)4Mo(OCH3)2], [(CH3)5WCl], and [(CH3)3WCl(OCH3)2] are reported. The first three structures are based on trigonal-prismatic geometry, the last one on octahedral geometry.
The first metal-xenon compound with direct gold-xenon bonds is achieved by reduction of AuF(3) with elemental xenon. The square planar AuXe(4)2+ cation is established by a single-crystal structure determination, with a gold-xenon bond length of approximately 274 picometers. The bonding between gold and xenon is of the final sigma donor type, resulting in a charge of approximately 0.4 per xenon atom.
The PF3H+ ion is prepared as PF3H+.SbF6-.HF by protonation of PF3 with HF/SbF5 at low temperatures in anhydrous HF. Crystals are obtained directly from this solvent. A crystal structure determination shows the presence of a pseudo-tetrahedral PF3H+ ion with a mean P-F distance of 148.7(2) pm, a P-H distance of 122(4) pm, and a mean PF2 angle of 106.1(1) degrees. Raman spectra were recorded of PF3H+SbF6-.HF and PF3D+.SbF6-.DF and assigned with the help of ab initio calculations. AsF3 does not react with HF/SbF5, whereas SF4 forms SF3+SbF6-.HF, which is isostructural with PF3H+SbF6-.HF.
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Strongly bent at the nitrogen atom (130.7 degrees ), the OCNCO(+) ion (see structure) is the closest relative to carbon suboxide OCCCO. According to calculations the linear OCNCO(+) ion is only a few kJ mol(-1) higher in energy.