| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5217252 | Tetrahedron | 2014 | 7 Pages |
Abstract
A series of novel chiral 1,2-diaminocyclohexane derivatives bearing heterocyclic units were synthesized via improved methods under ultrasonic irradiation. The photophysical properties of compounds were studied in ethanol, methanol, and chloroform. The sensitivity of these amines toward Cu2+, Cd2+, and Ni2+ was studied by the UV-vis and fluorescent methods. The Ï-electron structure of thiophene and bithiophene containing sensors is the most active toward all above mentioned metal ions and is highly selective for Ni2+ and Cd2+.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Violetta V. Meshkovaya, Alexander V. Yudashkin, Polina Y. Bushueva, Natalya B. Eremeeva, Yuri N. Klimochkin,