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Synthesis of p-tert-butylcalix[4]arene dinitrile bonded aminopropyl silica and investigating its usability as a stationary phase in HPLC

Journal of Macromolecular Science Pure and Applied Chemistry · Mart 2006

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.
28 atıf Mart 2006 DOI
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YÖKSİS Kayıtları
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Makale Bilgileri

Toplam Atıf 28 atıf · Scopus
ISSN10601325
Yayın TarihiMart 2006
Cilt / Sayfa43 · 221-231

Kurumlar

Selçuk Üniversitesi
Selçuklu Turkey

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Bu makaleye, sistemimizdeki Scopus veritabanında bulunan 0 makale atıf yapmıştır. Scopus genel atıf sayısı: 28.

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Scimago Dergi (ISSN Eşleşmesi)
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry
Q3
SJR Skoru0,364
H-Index64
YayıncıTaylor and Francis Ltd.
ÜlkeUnited States
Ceramics and Composites (Q3)
Chemistry (miscellaneous) (Q3)
Materials Chemistry (Q3)
Polymers and Plastics (Q3)
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28
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