期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 10, 期 8, 页码 1553-1564出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1ob06304a
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资金
- Department of Science and Technology, New Delhi, India
- CSIR
- Fast Track scheme [SR/FTP/CS-70/2006]
Substituted 1,2,3,4-tetrahydroquinoxaline, benzo-annulated unsymmetrical chiral [9]-N-3 peraza, and [12]-N-4 peraza-macrocycles have been synthesized employing an inter-and intramolecular Mitsunobu reaction from an amino acid derived common synthetic intermediate 3. The metal complexation study of these macrocycles has been investigated by UV-visible spectroscopic technique with binding constant (K-b) value 1.84 x 10(3) dm(3) mol(-1) using the Benesi-Hildebrand equation and a Gibbs free energy (Delta G) -19.4 kJ mol(-1) at 35 degrees C for 14d with Co2+. The binding properties of the metal were dependent on the structure of polyaza-macrocycles that were confirmed by the DFT optimized structure of two macrocycles. A detailed investigaton of UV-visible spectra of macrocycles and their complete interpretation with the help of TD-DFT along with the frontier molecular orbital calculations are presented.
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