Investigation of Structural, Electronic, and Thermodynamic Properties of The Carvacrol Molecule in Gas Phase and Different Solvents

Authors

  • Fatma Genç Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Istanbul Yeni Yuzyil University, Istanbul, Turkey
  • Fatema Tayfour Biomedical Engineering Department, Faculty of Engineering & Architecture, Kastamonu University, Kastamonu, Turkey
  • Fatma Kandemirli Biomedical Engineering Department, Faculty of Engineering & Architecture, Kastamonu University, Kastamonu, Turkey

DOI:

https://doi.org/10.58564/IJSER.4.3.2025.321

Keywords:

Carvacrol properties, Frontier Orbitals, MP2/6-311G(d,p), Thermodynamic Properties

Abstract

The electronic structure and some thermodynamic properties of Carvacrol molecule were investigated in detail with calculations at MP2/6-311G(d,p) level in environments such as gas, n-octanol, acetone, ethanol, acetonitrile, DMF, water. The effects of different environments on electron-filled HOMO, HOMO-1, HOMO-2, HOMO-3, and electron-empty LUMO, LUMO+1, LUMO+2, LUMO+3, which are close to the frontier orbitals, and also on polarizability, hyperpolarizability, and thermodynamic parameters of the molecule were investigated. It was observed that highly polar solvents significantly affected the electron density and stability of Carvacrol molecule. It was found that the electronic structure and optical properties of Carvacrol molecule were affected by the solvent environment. Findings about NLO properties and electronic properties of Carvacrol molecule in different environments provide important information in optoelectronic and pharmaceutical applications.

References

[1] T. Hasanvand, M. Mohammadi, F. Abdollahpour, B. Kamarehie, A. Jafari, A. Ghaderpoori, M. A. Karami, “A comparative study on antibacterial activity of carvacrol and glutaraldehyde on Pseudomonas aeruginosa and Staphylococcus aureus isolates: an in vitro study,” J Environ Health Sci Eng, vol. 19, no. 1, pp. 475-482, 2021,

doi: 10.1007/s40201-021-00620-1.

[2] M. V. Garg, and B. D. Sahu, “Carvacrol and its effect on cardiovascular diseases: From molecular mechanism to pharmacological modulation,” Food Biosci, vol. 57, p. 103444, 2024,

doi: 10.1016/J.FBIO.2023.103444.

[3] J. Michiels, J. Missotten, D. Fremaut, S. De Smet, and N. Dierick, “In vitro dose–response of carvacrol, thymol, eugenol and trans-cinnamaldehyde and interaction of combinations for the antimicrobial activity against the pig gut flora,” Livest Sci, vol. 109, no. 1-3, pp. 157-160, 2007,

doi: 10.1016/J.LIVSCI.2007.01.132.

[4] K. Kachur and Z. Suntres, “The antibacterial properties of phenolic isomers, carvacrol and thymol,” Crit Rev Food Sci Nutr, vol. 60, no. 18, pp. 3042–3053, 2020,

doi: 10.1080/10408398.2019.1675585.

[5] P. Shinde, H. Agraval, A. K. Srivastav, U. C. S. Yadav, and U. Kumar, “Physico-chemical characterization of carvacrol loaded zein nanoparticles for enhanced anticancer activity and investigation of molecular interactions between them by molecular docking,” Int J Pharm, vol. 588, p. 119795, 2020,

doi: 10.1016/j.ijpharm.2020.119795.

[6] F. E. Öztürkkan, G. B. Akbaba, and P. Aksu Kılıçle, “In silico Investigation of the Interactions of Thymol and Carvacrol on the Spike Protein of Omicron Variant and MPro Enzyme of Coronavirus,” Karadeniz Fen Bilimleri Dergisi, vol. 14, no. 3, pp. 997–1005, 2024,

doi: 10.31466/kfbd.1338012.

[7] A. Singh, K. Singh, K. Kaur, A. Sharma, P. Mohana, J. Prajapati, U. Kaur, D. Goswami, S. Arora, R. Chadha, P. M. S. Bedi, “Discovery of triazole tethered thymol/carvacrol-coumarin hybrids as new class of α-glucosidase inhibitors with potent in vivo antihyperglycemic activities,” Eur J Med Chem, vol. 263, p. 115948, 2024,

doi: 10.1016/J.EJMECH.2023.115948.

[8] M. Badr Amira, Naglaa F. El-Orabi, Yasmen F. Mahran, Amul M. Badr, Nervana Mustafa Bayoumy, Hanan Hagar, Elshaymaa I. Elmongy, Reem T. Atawia “In vivo and In silico evidence of the protective properties of carvacrol against experimentally-induced gastric ulcer: Implication of antioxidant, anti-inflammatory, and antiapoptotic mechanisms,” Chem Biol Interact, vol. 382, p. 110649, 2023,

doi: 10.1016/J.CBI.2023.110649.

[9] A. Akhlaq, M. Ashraf, M. O. Omer, and I. Altaf, “Carvacrol-Fabricated Chitosan Nanoparticle Synergistic Potential with Topoisomerase Inhibitors on Breast and Cervical Cancer Cells,” ACS Omega, vol. 8, no. 35, pp. 31826–31838, 2023,

doi: 10.1021/acsomega.3c03337.

[10] X. Farto-Vaamonde, L. Diaz-Gomez, A. Parga, A. Otero, A. Concheiro, and C. Alvarez-Lorenzo, “Perimeter and carvacrol-loading regulate angiogenesis and biofilm growth in 3D printed PLA scaffolds,” Journal of Controlled Release, vol. 352, pp. 776–792, 2022,

doi: 10.1016/J.JCONREL.2022.10.060.

[11] P. Wang, Q. Luo, H. Qiao, H. Ding, Y. Cao, J. Yu, R. Liu, Q. Zhang, H. Zhu, L. Qu, “The Neuroprotective Effects of Carvacrol on Ethanol‐Induced Hippocampal Neurons Impairment via the Antioxidative and Antiapoptotic Pathways,” Oxid Med Cell Longev, vol. 2017, no. 1, 2017,

doi: 10.1155/2017/4079425.

[12] A. Mahal, A. M. Almaamuri, S. S. Noori, S. Chandra, A. Elawady, A. J. Obaidullah, M. H. Shuhata Alubiady, S. H. Zain Al-Abdeen, R. Zainul “Effectiveness of B12N12 Nanocage as a Stabilizer and Delivery Carrier for Thymol and Carvacrol Essential Oils and their Influence on Escherichia coli and Staphylococcus aureus Bacteria: A Comprehensive Analysis using DFT, QTAIM, Multiwfn, and Molecular Docking,” Russian Journal of Inorganic Chemistry, vol. 69, no. 9, pp. 1407–1422, 2024,

doi: 10.1134/S0036023624601235.

[13] Z. Mohammedi, “Carvacrol: An Update of Biological Activities and Mechanism of Action”, Open Access Journal of Chemistry, vol. 1, no. 1, pp. 53-62, 2017,

doi: 10.22259/2637-5834.0101008.

[14] H. Chen, P. Michael Davidson, and Q. Zhong, “Impacts of sample preparation methods on solubility and antilisterial characteristics of essential oil components in milk,” Appl Environ Microbiol, vol. 80, no. 3, pp. 907–916, 2014,

doi: 10.1128/AEM.03010-13.

[15] A. Hajibonabi, M. Yekani, S. Sharifi, J. S. Nahad, S. M. Dizaj, and M. Y. Memar, “Antimicrobial activity of nanoformulations of carvacrol and thymol: New trend and applications,” 13, 2023, Elsevier Inc.

doi: 10.1016/j.onano.2023.100170.

[16] T. Alagöz, F. G. Çalişkan, H. G. Bilgiçli, M. Zengin, M. Sadeghi, P. Taslimi, İ. Gulçin, “Synthesis, characterization, biochemical, and molecular modeling studies of carvacrol‐based new thiosemicarbazide and 1, 3, 4‐thiadiazole derivatives”, Archiv der Pharmazie, vol. 356 no. 12, pp. 2300370, 2023,

doi:10.1002/ardp.202300370.

[17] B. R. Salunkhe, E. Soorya, S. S. Pingale, R. Bendre,S. Waghmode, S. Gad, ., “Computational and Experimental Studies on Carvacrol‐Derived Transition Metal Complexes: Structure, Stability, and Biological Activity”, ChemistrySelect, vol. 10, no. 28, e00759. 2025,

doi:10.1002/slct.202500759.

[18] M. R.Đorđević Zlatković, N. S. Radulović, M. Dangalov & N. G. Vassilev, “Conformation Analysis and Stereodynamics of Symmetrically ortho-Disubstituted Carvacrol Derivatives”, Molecules, vol. 29, no. 9, pp. 1962, 2024), doi:10.3390/molecules29091962.

[19] H. Boulebd, “DFT study of the antiradical properties of some aromatic compounds derived from antioxidant essential oils: C–H bond vs. O–H bond”, Free Radical Research, vol. 53, no. 11-12, pp. 1125-1134, 2019,

doi:10.1080/10715762.2019.1690652.

[20] F. Genç, S. G. Kandemirli, & F. Kandemirli, “Theoretical B3LYP study on electronic structure of contrast agent Iopamidol”, Acta Chimica Slovenica, vol. 68, no. 2, pp. 320–331, 2021,

doi: 10.17344/acsi.2020.6233.

[21] F. Genç & F. Kandemirli, “Quantum Chemical Calculations of Some Benzene Derivatives”, Journal of Amasya University Institute of Sciences and Technology, vol. 1, no. 2, pp. 127–141, 2020,

[22] J. Tomasi, B. Mennucci, & R. Cammi, “Quantum mechanical continuum solvation models”, Chemical reviews, vol. 105, no. 8, pp. 2999-3094, 2005,

doi: 10.1021/cr9904009

[23] S. G. Kandemirli, F. Genç, F. Kandemirli, & M. Evecen, “Solvent effects on the contrast agent iomeprol with density functional theory”, Avrupa Bilim ve Teknoloji Dergisi, vol. 20, pp. 351-359, 2020,

doi:10.31590/ejosat.732239.

[24] P. W. Atkins, J. De Paula, & J. Keeler, “Atkins' physical chemistry”, Oxford university press. 2023.

[25] Y. Chen, H. Zhang, & Q. Liu, “FT-IR spectroscopy combined with DFT calculation to explore solvent effects of vinyl acetate”, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol. 126, pp. 122-128, 2014,

doi:10.1016/j.saa.2014.01.105.

[26] L. Chan, G. M. Morris, & G. R. Hutchison, “Understanding conformational entropy in small molecules” Journal of Chemical Theory and Computation, vol. 17, no. 4, pp. 2099-2106, 2021,

doi:10.1021/acs.jctc.0c01213.

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Published

21-10-2025

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How to Cite

Investigation of Structural, Electronic, and Thermodynamic Properties of The Carvacrol Molecule in Gas Phase and Different Solvents. (2025). Al-Iraqia Journal for Scientific Engineering Research, 4(3), 21-33. https://doi.org/10.58564/IJSER.4.3.2025.321

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