Anion binding by p-aminoazobenzene-derived aromatic amides: spectroscopic and electrochemical studies

作者:Lukasik Natalia*; Wagner Wysiecka Ewa*
来源:Photochemical and Photobiological Sciences, 2017, 16(10): 1570-1579.
DOI:10.1039/c7pp00245a

摘要

The synthesis and complexing properties of p-aminoazobenzene-derived mono-, bis-, and trisamides were described. Ligands 3 and 4 bind anions, including fluorides, chlorides, bromides, acetates, benzoates, dihydrogen phosphates, hydrogen sulfates, and p-toluenesulfonates, in chloroform forming 1 : 1 complexes. The highest value of stability constant was evaluated for the 4-F- complex (log K = 5.63 +/- 0.21). On the basis of H-1 NMR, and FTIR spectroscopy, the possible nature of the ligand-anion interactions was proposed. The E reversible arrow Z isomerization process of tripodal amide 4 in chloroform was studied. The effect of anions on Z to E thermal back isomerization was investigated.

  • 出版日期2017-10-1