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Jarvas, Gabor,Guttman, Andras,Mię,kus, Natalia,Bą,czek, Tomasz,Jeong, Sunkyung,Chung, Doo Soo,Pä,toprstý,, Vladimir,Masá,r, Mariá,n,Hutta, Milan,Datinská,, Vladim Elsevier 2020 Trends in analytical chemistry Vol.122 No.-
<P><B>Abstract</B></P> <P>By coupling a sample pretreatment technique of sample clean up and enrichment power with capillary electrophoresis (CE) of high-performance separation, the task of analyzing trace analytes in a complex matrix such as a biological sample can be carried out successfully with ease. This review aims for providing an overview of strategies to couple sample pretreatment techniques with capillary and related microscale (e.g., microchip) electrophoresis, practically adoptable in an automatic manner, without requiring serious modification of existing instruments to install sophisticated interfaces. In-line sample pretreatment techniques based on liquid phase microextraction performed before sample injection and on-line sample preconcentration techniques performed during or after sample injection are discussed with emphasis on the applicability to samples of high conductivity, commonly encountered for biological samples. An overview of the recent developments in microfluidic immobilized enzymatic microreactors which fit excellently to microchip CE is also given.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Recent advances and major trends in sample pretreatment for capillary electrophoresis are summarized. </LI> <LI> In-line and on-line sample pretreatment techniques are discussed with emphasis on biological samples. </LI> <LI> We provide an overview of strategies to couple sample pretreatment techniques with capillary and microchip electrophoresis. </LI> </UL> </P>
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Purc, Anna,Koszarna, Beata,Iachina, Irina,Friese, Daniel H.,Tasior, Mariusz,Sobczyk, Krzysztof,Pę,dziń,ski, Tomasz,Brewer, Jonathan,Gryko, Daniel T. Royal Society of Chemistry 2017 ORGANIC CHEMISTRY FRONTIERS Vol.4 No.5
<▼1><P>Benzofuran has been proven to be the versatile substituent for tuning the optics of diketopyrrolopyrroles.</P></▼1><▼2><P>An in-depth investigation of the reaction of substituted salicylaldehydes with chloroacetonitrile led to the development of new conditions for the synthesis of 2-cyanobenzofurans. The crucial improvement lies in the use of phase-transfer catalysis in the second step, <I>i.e.</I>, intramolecular aldol type condensation. In a two-step process, the reactants were transformed into a library of 3,6-bis(benzofuran-2-yl)diketopyrrolopyrroles. We show that the presence of a methyl group in a position adjacent to the cyano functionality only slightly decreased the yield of diketopyrrolopyrroles (to 30–57%). An analysis of the relationship between the degree of polarization/planarization of aryl-diketopyrrolopyrroles and their one- and two-photon spectroscopic properties is reported. Careful design of the desired dyes and enhanced control of their ability to assume a planar molecular structure resulted in interesting photophysical properties, such as absorption and emission in the so-called biological window. Despite having less promising linear spectroscopic properties, the deplanarized molecules possess pretty strong two-photon absorbing properties. Placing methyl groups at adjacent positions to the linkage between benzofuran and the DPP core caused the formation of yellow-emitting dyes with almost quantitative fluorescence quantum yield, moderate Stokes shift and reasonable two-photon absorption cross-sections.</P></▼2>
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