486994-77-8Relevant academic research and scientific papers
Inclusion complexation of phenoxyaliphatic acid derivatives of 3,3′-bis(indolyl)methanes with β-cyclodextrin
Antony Muthu Prabhu,Suresh Kumar
, p. 925 - 931 (2014)
The inclusion complexation behavior of phenoxyaliphatic acid derivatives of 3,3′-bis(indolyl)methane (BIMs 1-5) with β-cyclodextrin (β-CD) were investigated in both solution and solid state by means of UV-Visible, fluorescence spectroscopy, FT-IR and sup
In situ Bronsted-Lowry acid catalyzed syntheses, characterization, single crystal XRD, electronic spectral-, DPPH radical scavenging-, and DNA protection studies of aryl-3,3′-bis(indolyl)methanes
Suresh Kumar,Antony Muthu Prabhu,Seethalaksmi,Bhuvanesh,Kumaresan
supporting information, p. 249 - 256 (2014/01/23)
A series of novel aryl-3,3′-bis(indolyl)methanes (BIMs) were synthesized using indole and formylphenoxyaliphatic acid(s) in water in the absence of any catalyst. The formylphenoxyaliphatic acid behaves as an in situ Bronsted-Lowry acid catalyst in water. UV-Visible and fluorescence spectra of the compounds were recorded in selected solvents. The gas phase geometry optimization of the compounds were achieved using DFT calculations at B3LYP/3-21G(*) level of theory. The electronic properties, such as HOMO-LUMO energies were calculated using the above method based on the optimized structure. Compounds have better DPPH radical scavenging activity and reduction of oxidative damage of DNA.
