Research Article
Synthesis, characterization, and quantum chemical studies of new chiral acyclic (O,N,Te) type Schiff base, (R)-1-(((1-((4-methoxyphenyl)tellanyl)propan-2-yl)imino)methyl)naphthalen-2-ol
@INPROCEEDINGS{10.4108/eai.13-11-2024.2355656, author={Rajegowda HR and Padala Ashok and Chethan BS and Raghavendra Kumar P}, title={Synthesis, characterization, and quantum chemical studies of new chiral acyclic (O,N,Te) type Schiff base, (R)-1-(((1-((4-methoxyphenyl)tellanyl)propan-2-yl)imino)methyl)naphthalen-2-ol}, proceedings={Proceedings of the 1st International Conference on Frontiers in Physical and Chemical Sciences: Exploring New Horizons, FPCS 2024, 13-14 November 2024, Bengaluru, Karnataka, India}, publisher={EAI}, proceedings_a={FPCS}, year={2025}, month={8}, keywords={schiff’s base chiral tellurium dft qtaim}, doi={10.4108/eai.13-11-2024.2355656} }- Rajegowda HR
Padala Ashok
Chethan BS
Raghavendra Kumar P
Year: 2025
Synthesis, characterization, and quantum chemical studies of new chiral acyclic (O,N,Te) type Schiff base, (R)-1-(((1-((4-methoxyphenyl)tellanyl)propan-2-yl)imino)methyl)naphthalen-2-ol
FPCS
EAI
DOI: 10.4108/eai.13-11-2024.2355656
Abstract
The reaction of the chiral telluro-amine, (R)-2 with 2-hydroxy-1-naphthaldehyde has produced a new chiral telluro Schiff's base of (O,N,Te) type, (R)-1-(((1-((4-methoxyphenyl)tellanyl)propan-2-yl)imino)methyl)naphthalen-2-ol (R)-3. The SOR, CHN and spectroscopic analysis were used to characterize the structure of (R)-3. The different intermolecular interactions were shown by the fingerprint plots and Hirshfeld surface analysis. To describe the optimal structure, FMO, and reactive characteristics, DFT studies were carried out. Additionally, the RDG-based isosurface analysis conducted to investigate the type and nature of interactions.
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