Asymmetric Organocatalysis and Analysis on a Single Microfluidic Nanospray Chip
Asymmetric Organocatalysis and Analysis on a Single Microfluidic Nanospray Chip
复制标题
DOI:
10.1002/anie.201102331
复制
发表时间:
2011-01-01
影响因子:
16.6
通讯作者:
Belder, Detlev
中科院分区:
文献类型:
--
作者:
Fritzsche, Stefanie;Ohla, Stefan;Belder, Detlev
The miniaturization of chemical processes onto so-called labon-a-chip devices has gained significant importance in different fields of chemistry. Besides the advantages of enhanced portability, reduced reagent consumption, and improved safety, a characteristic feature of miniaturized platforms is the possibility to achieve higher reaction and analysis rates.[1] From their roots in analytical sciences, microfluidic systems have received much attention over the past decade. At present, microfluidics is becoming increasingly popular in inorganic and organic chemistry, as syntheses are performed on chip-based microreactors [2] or capillary-based microflow reactors.[3] While diverse reactions have been performed in microfluidic chip devices with impressive results,[4] the analytical characterization is, however, usually carried out off-chip by conventional macroscopic instruments. However, this approach does not exploit the promise and the full potential of chip technology, namely, the integration of different functionalities such as chemical synthesis and analysis on one single device. Thus, it is desirable to develop, in analogy to microelectronics, integrated chemical circuits [5] as new chemical tools, for example, for catalyst screening [6] or for online monitoring of biological processes.[7] In previous work we demonstrated a first approach for integrating chemical reactions and analysis on a single microchip for the screening of enantioselective biocatalysts.[8] Nevertheless, this system was limited to aqueous media and native fluorescent molecules.[9] Therefore we intended to develop an advanced chip system with a wider applicability in synthetic chemistry, including the utilization of non-aqueous reaction media and a more general detection system. In this context, the coupling to mass spectrometry appears to be very attractive,[10] as it provides additional structural information for substance identification.