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
Islamic Azad University, İran
Prof. Dr. Majıd MONAJJEMI Islamic Azad University, İran
K. Zare
Islamic Azad University, İran
Islamic Azad University, İran
S. Ketabi
Islamic Azad University, İran
Islamic Azad University, İran
| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | Physics and Chemistry of Liquids (Q3) | ||
| Dergi ISSN | 0031-9104 Dergi Bilgileri (2006) | ||
| 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 | ||
| UAK Araştırma Alanları |
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| 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 |
Science Direct
Complexation behaviour of p-t-butyl-calix[4]arene propoxy derivatives toward alkali metal cations in chloroform
BM Sürdürülebilir Kalkınma Amaçları
| Atıf Sayıları | |
| Web of Science | 10 |
| Scopus | 26 |