Golchoubian, Hamid’s team published research in Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy in 138 | CAS: 140-28-3

Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy published new progress about 140-28-3. 140-28-3 belongs to catalysis-chemistry, auxiliary class Benzenes, name is N1,N2-Dibenzylethane-1,2-diamine, and the molecular formula is C16H20N2, Formula: C16H20N2.

Golchoubian, Hamid published the artcileHalochromism, ionochromism, solvatochromism and density functional study of a synthesized copper(II) complex containing hemilabile amide derivative ligand, Formula: C16H20N2, the publication is Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy (2015), 913-924, database is CAplus and MEDLINE.

This study investigates chromotropism of newly synthesized 3,3′-(ethane-1,2-diylbis(benzylazanediyl))dipropanamide copper(II) perchlorate complex. The compound was structurally characterized by physico-chem. and spectroscopic methods. X-ray crystallog. of the complex showed that the copper atom achieved a distorted square pyramidal environment through coordination of two amine N atoms and two O atoms of the amide moieties. The pH effect on the visible absorption spectrum of the complex was studied which functions as pH-induced “off-on-off” switches through protonation and deprotonation of amide moieties along with the Cu-O to Cu-N bond rearrangement at room temperature The complex was also observed to show solvatochromism and ionochromism. The distinct solution color changes mainly associated with hemilability of the amide groups. The solvatochromism of the complex was investigated with different solvent parameter models using stepwise multiple linear regression method. The results suggested that the basicity power of the solvent has a dominant contribution to the shift of the d-d absorption band of the complex. D. functional theory, DFT calculations were performed in order to study the electronic structure of the complex, the relative stabilities of the Cu-N/Cu-O isomers, and to understand the nature of the halochromism processes taking place. DFT computational results buttressed the exptl. observations indicating that in the natural pH (5.8) the Cu-O isomer is more stable than its linkage isomer and conversely in alk. aqueous solution

Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy published new progress about 140-28-3. 140-28-3 belongs to catalysis-chemistry, auxiliary class Benzenes, name is N1,N2-Dibenzylethane-1,2-diamine, and the molecular formula is C16H20N2, Formula: C16H20N2.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia