Gezici, OTabakci, MKara, HYilmaz, M2020-03-262020-03-2620061060-1325https://dx.doi.org/10.1080/10601320500437060https://hdl.handle.net/20.500.12395/20703The chromatic separation of adenine, adenosine, cytosine, phenol, benzene, and toluene were investigated by using 5,11,17,23-tert-butyl-25,27-bis(cyanomethoxy)-26-(chloroformyl)-28-hydroxy-calix[4]arene bonded aminopropyl silica (CDBAPS) as a stationary phase. The separation ability of the stationary phase was observed to be good for target species. The effect of non-polar calix[n]arene network was observed in chromatographic processes, and it was thought that, thanks to the relatively polar nitrile groups, further selectivity would be obtained in various chromatographic separations.en10.1080/10601320500437060info:eu-repo/semantics/closedAccesscalixareneimmobilizationaminopropyl silicaHPLCnucleo basesnucleosidesaromatic compoundsSynthesis of p-tert-butylcalix[4]arene dinitrile bonded aminopropyl silica and investigating its usability as a stationary phase in HPLCArticleA432221231Q2WOS:000235411500003N/A