Synthesis of p-tert-butylcalix[4]arene dinitrile bonded aminopropyl silica and investigating its usability as a stationary phase in HPLC
Küçük Resim Yok
Tarih
2006
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
TAYLOR & FRANCIS INC
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
The 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.
Açıklama
Anahtar Kelimeler
calixarene, immobilization, aminopropyl silica, HPLC, nucleo bases, nucleosides, aromatic compounds
Kaynak
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY
WoS Q Değeri
N/A
Scopus Q Değeri
Q2
Cilt
A43
Sayı
2
