| Yazarlar |
Fikret Karcı
Pamukkale Üniversitesi, Türkiye |
Prof. Dr. İzzet ŞENER
Ankara Üniversitesi, Türkiye |
|
Hasalettin Deligöz
Pamukkale Üniversitesi, Türkiye |
| Özet |
| Twelve new azocalix[6]arenes (1-12) have been synthesized by linking o-, m-, p-chloroaniline, o-, m-, p-nitroaniline, o-, m-, p-toluidine, m-, p-anisidine and aniline to calix[6]arene through a diazo-coupling reaction. The prepared compounds were characterized based on UV-vis, FT-IR and 1H-NMR spectroscopic techniques as well as elemental analysis. The effect of varying pH and solvent upon the absorption ability of azocalixarenes substituted with electron-donating and electron-withdrawing groups at their o-, m-, p-position was examined. Observed results were compared with those found for unsubstituted azocalix[6]arenes. Concentration effects on the visible absorption maxima of the dyes are also reported. © 2004 Elsevier Ltd. All rights reserved. |
| Anahtar Kelimeler |
| calixarene,azocalix[6]arenes,calixarene dyes diazo-coupling reaction,solvent effect,substituent effect,absorption spectra |
| Makale Türü | Özgün Makale |
| Makale Alt Türü | SSCI, AHCI, SCI, SCI-Exp dergilerinde yayımlanan tam makale |
| Dergi Adı | DYES AND PIGMENTS |
| Dergi ISSN | 0143-7208 |
| Dergi Tarandığı Indeksler | SCI |
| Makale Dili | İngilizce |
| Basım Tarihi | 08-2004 |
| Cilt No | 62 |
| Sayı | 2 |
| Sayfalar | 131 / 140 |
| Doi Numarası | 10.1016/j.dyepig.2003.11.017 |
| Atıf Sayıları | |
| WoS | 38 |
| SCOPUS | 29 |
| Google Scholar | 44 |
| Google Scholar | 44 |
