Related Experiment Video
Updated: Sep 10, 2025

HKUST-1 as a Heterogeneous Catalyst for the Synthesis of Vanillin
Published on: July 23, 2016
Synthesis of Vanillin derivative Schiff's bases from threonine, and valine: Structural study and multiscale
R Karthika1, S Nandhini1, S Suriya2
1Department of Chemistry, Nadar Saraswathi College of Arts and Science for Women, (Autonomous), Affiliated to Mother Teresa Women's University Kodaikkanal, Theni, Tamil Nadu, India.
None:
Addressing the escalating global challenge of antimicrobial resistance, this study reports the synthesis, comprehensive structural characterization, and multiscale computational modeling of two novel vanillin-derived Schiff's bases, 1 (from threonine) and 2 (from valine). Spectral analyses confirmed their successful formation. Antimicrobial assays revealed significant activity against a panel of Gram-negative (Escherichia coli, Pseudomonas aeruginosa), Gram-positive (Bacillus subtilis, Staphylococcus aureus), and fungal (Candida albicans, Aspergillus flaves) strains. Notably, compound 1 exhibited potent inhibition against B. subtilis (18 mm zone), while compound 2 demonstrated superior broad-spectrum efficacy, with inhibition zones of 20 mm against P. aeruginosa and 19.6 mm against S. aureus, often surpassing respective control antibiotics (amikacin: 17-18 mm, nystatin: 16-18 mm). Computational investigations, including Natural Bonding Orbital (NBO) and Non-Covalent Interactions (NCI) analyses, elucidated intramolecular stabilization and reactivity profiles. Drug-likeness and pharmacokinetic evaluations (SwissADME) indicated favorable solubility, high gastrointestinal absorption, and synthetic accessibility. Insights into tautomeric equilibria (SwissParam) and potential biological targets (SwissTargetPrediction), such as proteases and lyases, underscore their therapeutic relevance. This integrated experimental and theoretical approach highlights the promising potential of these novel Schiff's bases as effective antimicrobial agents, providing a robust foundation for future drug development efforts.
Related Concept Videos
Molecular Models
Structures of Carboxylic Acid Derivatives
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the...
Structures of Aldehydes and Ketones
In aldehydes (Figures 1a and 1b),...
Molecular Structure and Acidity
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
Chemical Shift: Internal References and Solvent Effects
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous...

