Complexation behaviour of p-t-butyl-calix[4]arene propoxy derivatives toward alkali metal cations in chloroform
Yazarlar (4)
A. Amiri
Islamic Azad University, İran
Prof. Dr. Majıd MONAJJEMI Islamic Azad University, İran
K. Zare
Islamic Azad University, İran
S. Ketabi
Islamic Azad University, İran
Makale Türü Özgün Makale (ESCI dergilerinde yayınlanan tam makale)
Dergi Adı Physics and Chemistry of Liquids
Dergi ISSN 0031-9104 Wos Dergi Scopus Dergi
Makale Dili İngilizce Basım Tarihi 08-2006
Cilt / Sayı / Sayfa 44 / 4 / 449–456 DOI 10.1080/00319100500502400
Makale Linki http://www.scopus.com/inward/record.url?eid=2-s2.0-33745917420&partnerID=MN8TOARS
Özet
Spectrophotometric technique is used to evaluate the alkali metal ion binding selectivity's of a series of calix[4]arenes in chloroform solution. On the basis of formation constant values calculated, complexation of K+, Na+, and Li+ are favored toward di propoxy (L1), tri propoxy (L2), and bromopropoxy calix[4]arenes (L3), respectively, in agreement with the cavity sizes of the ligands. All ligands have been shown to form exclusively 1 : 1 (metal ion to ligand ratio) complexes with alkali cations in our experimental conditions. Chloroform stabilize endo complexes and the spectrophotometery results predict that in weakly polar solvents endo complexation is preferred. © 2006 Taylor & Francis.
Anahtar Kelimeler
Calixarenes | Molecular recognition | Spectrophotometry