How to cite this paper
Shevchenko, D., Horak, Y., Obushak, M., Tischenko, N & Sobechko, I. (2025). Synthesis and thermodynamic properties of 3-(5-phenyl-1-(pyridin-3-yl)-1H-pyrrol-2-yl)propanoic acid in condensed and gaseous states.Current Chemistry Letters, 14(3), 559-566.
Refrences
1. Heravi M. M., and Zadsirjan, V. (2020). Prescribed Drugs Containing Nitrogen Heterocycles: An Overview. RSC Adv., 10 (72), 44247–44311 (DOI: 10.1039/d0ra09198g)
2. Masci D., Hind C., Islam M. K., Toscani A., Clifford M., Coluccia A., Conforti I., Touitou M., Memdouh S., Wei X., La Regina G., Silvestri R., Sutton J. M., and Castagnolo D. (2019). Switching on the Activity of 1,5-Diaryl-Pyrrole Derivatives against Drug-Resistant ESKAPE Bacteria: Structure-Activity Relationships and Mode of Action Studies. Eur. J. Med. Chem., 178 (1), 500–514 (DOI: 10.1016/j.ejmech.2019.05.087).
3. Romagnoli R., Oliva P., Maria Kimatrai Salvador, Manfredini S., Padroni C., Brancale A., Ferla S., Hamel E., Ronca R., Maccarinelli F., Rruga F., Mariotto E., Viola G., and Bortolozzi, R. (2021). A Facile Synthesis of Diaryl Pyrroles Led to the Discovery of Potent Colchicine Site Antimitotic Agents. Eur. J. Med. Chem., 214, 113229–113229 (DOI: 10.1016/j.ejmech.2021.113229).
4. Li Petri G., Spanò V., Spatol, R., Holl R., Raimondi M., Barraja P., and Montalbano, A. (2020). Bioactive Pyrrole-Based Compounds with Target Selectivity. Eur. J. Med. Chem., 208, 112783 (DOI: 10.1016/j.ejmech.2020.112783).
5. Ganesh B., Raj A., Aruchamy B., Nanjan P., Drago C., and Ramani P. (2023). Pyrrole: A decisive scaffold for the development of therapeutic agents and structure‐activity relationship. ChemMedChem, 19 (1) (DOI: 10.1002/cmdc.202300447).
6. Ji Ram V., Sethi A., Nath M., and Pratap R. (2019). Five-Membered Heterocycles. The Chemistry of Heterocycles, 149–478 (DOI: 10.1016/b978-0-08-101033-4.00005-x)
7. Zhao Y., Li Y., Ou X., Zhang P., Huang Z., Bi F., Huang R., and Wang Q. (2008). Synthesis, Insecticidal, and Acaricidal Activities of Novel 2-Aryl-Pyrrole Derivatives Containing Ester Groups. J. Agric. Food Chem., 56 (21), 10176–10182 (DOI: 10.1021/jf802464d)
8. El Mahdy A., Halim S., and Taha H. (2018). DFT and TD-DFT Calculations of Metallotetraphenylporphyrin and Metallotetraphenylporphyrin Fullerene Complexes as Potential Dye Sensitizers for Solar Cells. J. Mol. Struct., 1160, 415–427. (DOI: 10.1016/j.molstruc.2018.02.041).
9. Bulumulla C., Gunawardhana R., Gamage P., Miller J., Kularatne R., Biewer M., and Stefan, M. (2020). Pyrrole-containing semiconducting materials: Synthesis and applications in organic photovoltaics and organic field-effect transistors. ACS Appl. Mater. Interfaces, 12 (29), 32209–32232 (DOI: 10.1021/acsami.0c07161).
10. Rebbah B., El Haib A., Lahmady S., Forsal I., Gouygou M., Mallet-ladeira S., Medaghri-alaoui A., Rakib E., and Hannioui A. (2024). Synthesis, characterization, and inhibition effects of a novel eugenol derivative bearing pyrrole functionalities on the corrosion of mild steel in a hcl acid solution. RSC Adv., 14 (20), 14152–14160 (DOI: 10.1039/d4ra01337a)
11. Kerru N., Gummidi L., Maddila S., Gangu K. K., and Jonnalagadda S. (2020). A review on recent advances in nitrogen-containing molecules and their biological applications. Molecules, 25 (8), 1909 (DOI: 10.3390/molecules25081909)
12. Zhuang X., Song Y., Zhan H., Yin X., and Wu C. (2019). Synergistic Effects on the Co-Combustion of Medicinal Biowastes with Coals of Different Ranks. Renewable Energy, 140, 380–389 (DOI: 10.1016/j.renene.2019.03.070)
13. Sobechko B., Dibrivnyi V., and Gorak Yu. (2022). Enthalpy of formation and combustion of 5-(4-nitrophenyl)furan-2-carbaldehyde and its 2-methyl and 2-oxomethyl derivatives in the condensed state. Chemistry, technology and application of substances, 5 (2), 30–36 (DOI: 10.23939/ctas2022.02.030).
14. P.J. Linstrom and W.G. Mallard, Eds., NIST Chemistry WebBook, NIST Standard Reference Database Number 69, National Institute of Standards and Technology, Gaithersburg MD, 20899, (DOI: 10.18434/T4D303)
15. Electronic resource: http://www.codata.info/resources/databases/key1.html (Accessed on Jan 22, 2025)
16. Acree W., and Chickos J. (2016). Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds. Sublimation, Vaporization and Fusion Enthalpies From 1880 to 2015. Part 1. C1−C10. J. Phys. Chem. Ref. Data, 45, 033101 (DOI: 10.1063/1.4948363).
17. Sobechko I. (2016). Calculation Method of Heat Capacity Change during Organic Compounds Vaporization and Sublimation. Chem. Chem. Technol., 10 (1), 27–33 (DOI: 10.23939/chcht10.01.027).
18. Sobechko I., Horak Y., Dibrivnyi V., Obushak M., Goshko L. (2019). Thermodynamic Properties of 2-Methyl-5-Arylfuran-3 Carboxylic Acids Chlorine Derivatives in Organic Solvents. Chem. Chem. Technol., 13 (3), 280–287 (DOI: 10.23939/chcht13.03.280).
19. Domalski, E. and Hearing, E. (1993). Estimation of the thermodynamic properties of C-H-N-O-S-halogen compounds at 298.15 K. J. Phys. Chem. Ref. Data, 22 (4), 805–1159 (DOI: 10.1063/1.555927)
20. Joback K. and Reid R. (1987). Estimation of pure-component properties from group-contributions. Chem. Eng. Commun., 57 (1-6), 233–243 (DOI: 10.1080/00986448708960487).
21. Benson S. (1965). III-bond energies. J. Chem. Educ., 42 (9), 502. (DOI: 10.1021/ed042p502)
22. Salmon A. and Dalmazzone D. (2007). Prediction of enthalpy of formation in the solid state (at 298.15 K) using second-order group contributions – part 2: Carbon-hydrogen, carbon-hydrogen-oxygen, and carbon-hydrogen-nitrogen-oxygen compounds. J. Phys. Chem. Ref. Data, 36 (1), 19–58 (DOI: 10.1063/1.2435401).
23. Shevchenko D., Horak, Y., Tischenko, N., Pyshna, D., and Sobechko, I. (2024). Thermodynamic properties of 3-(1,5-diphenylpyrrol-2-yl)-Propanoic acid. Chemistry, technology and application of substances, 7 (1), 8–14. (DOI: 10.23939/ctas2024.01.008).
24. Ohlinger W. S., Klunzinger P. E., Deppmeier B. J., Hehre W. J. (2009). Efficient Calculation of Heats of Formation. J. Phys. Chem. A, 113 (10), 2165–2175. (DOI: 10.1021/jp810144q).
25. Rossini F. D. (1956) Experimental Thermochemistry. Interscience Publishers. N. Y.; London, Vol. 2. P. 326.