FT-IR, FT-Raman and NMR characterization of 2-isopropyl-5- methylcyclohexyl quinoline-2-carboxylate and investigation of its reactive and optoelectronic properties by molecular dynamics simulations and DFT calculations.
IR@CSIR-CFTRI
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Relation |
http://ir.cftri.com/13582/
http://dx.doi.org/10.1016/j.molstruc.2016.07.096 |
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Title |
FT-IR, FT-Raman and NMR characterization of 2-isopropyl-5- methylcyclohexyl quinoline-2-carboxylate and investigation of its reactive and optoelectronic properties by molecular dynamics simulations and DFT calculations. |
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Creator |
Vidya, V. Menon
Edakot, Fazal Sheena, Mary. Y. Nagarajan, S. |
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Subject |
24 Organic Chemistry
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Description |
The FT-IR and FT-Raman spectra of the synthesized compound, 2-isopropyl-5-methylcyclohexyl quinoline- 2-carboxylate is recorded and analyzed. Optimized molecular structure, wave numbers, corresponding assignments regarding 2-isopropyl-5-methylcyclohexyl quinoline-2-carboxylate has become screened tentatively as well as hypothetically using Gaussian09 program package. Natural bonding orbital assessment has been completed with a reason to clarify charge transfer or conjugative interaction, the intra-molecular re-hybridization and delocalization of electron density within the molecule. The NMR spectral assessment had been made choosing structure property relationship by chemical shifts along with the magnetic shielding effects regarding the title compound. The first and second hyperpolarizabilities were calculated. The calculated first order hyperpolarizability is commensurate with the documented worth of very similar derivatives and could be an interesting object for more experiments on nonlinear optics. Local reactivity properties have been investigated using average local ionization energies and Fukui functions. Investigation of optoelectronic properties encompassed calculations of reorganization energies and hopping rates of charge carriers within the framework of Marcus semiempiric approach. The docked ligand title compound forms a stable complex with CDK inhibitors and gives a binding affinity value of �9.7 kcal/mol and molecular docking results suggest that the compound might exhibit inhibitory activity against CDK inhibitors. |
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Date |
2017
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Type |
Article
PeerReviewed |
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Format |
pdf
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Language |
en
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Identifier |
http://ir.cftri.com/13582/1/Journal%20of%20Molecular%20Structure%201127%20%282017%29%20124e137.pdf
Vidya, V. Menon and Edakot, Fazal and Sheena, Mary. Y. and Nagarajan, S. (2017) FT-IR, FT-Raman and NMR characterization of 2-isopropyl-5- methylcyclohexyl quinoline-2-carboxylate and investigation of its reactive and optoelectronic properties by molecular dynamics simulations and DFT calculations. Journal of Molecular Structure, 1127. pp. 124-137. |
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