Measurement of the sound velocity in fluids using the echo signals from scattering particles

With conventional methods the sound velocity c in fluids can be determined using the back wall echo. This paper proposes a novel technique, in which the signals reflected by scattering particles suspended in a fluid are analysed instead. The basic idea is that the particles generate the strongest echo signal when being located in the sound field maximum. Therefore the position of the echo signal maximum is a measure for the propagation time to the sound field maximum. Provided that calibration data or sound field simulations for the ultrasonic transducer are available, this propagation time suffices to determine both sound velocity and the location of the sound field maximum. The feasibility of the new approach is demonstrated by different kinds of experiments: (i) Measurements of the sound velocity c in four fluids covering the wide range between 1116 and 2740 m/s. The results show good agreement with values published elsewhere. (ii) Using the dependence of the sound velocity on temperature, it is possible to vary c over the comparatively small range between 1431 and 1555 m/s with increments of less than 10 m/s. The measured statistical variation of 1.4 m/s corresponds to a relative uncertainty not worse than 0.1%. (iii) The focus position, i.e. the distance of the maximum of the sound field from the transducer, was varied by time-shifted superposition of the receive signals belonging to the different elements of an annular array. The results indicate that the novel method is even capable of measuring profiles of the sound velocity along the ultrasonic beam non-invasively.     

Enantioselective Dihalogenation of Alkenes

The dihalogenation of alkenes is one of the classic reactions in organic chemistry and a prime example of an electrophilic addition reaction. The often observed anti-selectivity in this addition reaction can be explained by the formation of a haliranium-ion intermediate. Although dihalogenations have been studied for more than a century, the development of reagent-controlled, enantioselective dihalogenation has proved to be very difficult. Only recently, significant progress has been achieved. In this review, an overview on current method development in enantioselective dihalogenation is provided and mechanistic aspects that render this transformation challenging are discussed.