No abstract

A simple optical multiple reflection system is developed with two cylindrical concave mirrors at an appropriate spacing. The two cylindrical mirrors have different focal lengths and their principal sections are orthogonal. The alternate focusing of the two cylindrical mirrors at different direction keep the reflecting spots small. The reflecting spots fall on Lissajous patterns on the cylindrical mirrors. The mathematics for this optical system is described and the calculated coordinates of beam spots are very close matches of the experimental observations. The cylindrical mirror optical system is easy to construct and align, with a suitable method for obtaining long optical paths and a large number of passes in small volumes. In a photoacoustic spectrometer the beam family enhance the effective power in the photoacoustic cell and thus the signal-to-noise ratio of photoacoustic signal. An experimental result for photoacoustic spectrum of HDSe gas is given.

Summary Mononuclear metal-peroxo species are invoked as the key intermediates in metalloenzymatic or synthetic catalysis. However, either transience or sluggishness reactivity of synthetic analogs of metal-peroxo species impedes our understanding of oxygen activation mechanism. Herein, we designed and characterized a dioxygen-derived mononuclear osmium-peroxo complex, in which the peroxo ligand is stabilized by internally aromatic metallacycle. We demonstrate that the osmium-peroxo species shows catalytic activity toward promoterless alcohol dehydrogenations. Furthermore, computational studies provide a new mechanism for the osmium-peroxo-mediated alcohol oxidation, starting with the concerted double-hydrogen transfer and followed by the generation of osmium-oxo species. Interestingly, the internally aromatic metallacycle also plays a vital role in catalysis, which mediates the hydrogen transfer from osmium center to the distal oxygen atom of Os–OOH moiety, thus facilitating the Os–OOH→Os=O conversion. We expect that these insights will advance the development of aromatic metallacycle toward aerobic oxidation catalysis.

By using a modified coimpregnation method, a multicomponent Pd&Bi(1.4)/TiO2‐N catalyst with hierarchical metal–metal oxide interfaces was prepared that showed a better activity and stability for low‐temperature CO oxidation than Pd/TiO2‐N and Pd/P25. The structural characterization and catalytic activity results proved that an appropriate amount of Bi species has a clear promoting effect on the Pd‐based catalyst. Particularly, the catalyst can be mass‐produced conveniently, which may be beneficial for versatile reactions and practical applications.

No abstract