3,5-diamino-1,2,4-triazole Molekülünün Titreşim Frekanslarının ve Moleküler Parametrelerinin Üzerine Çözücü Etkilerinin bir DFT ve FT-IR Çalışması

Year 2018, , 85 - 93, 31.03.2018

Mustafa Tuğfan Bilkan

https://doi.org/10.21597/jist.407841

Cited By: 3

Abstract

Bu çalışmada, 3,5-diamino-1,2,4-triazole (Guanazole) anti tümör ajanın yapısal ve spektroskopik özellikleri üzerine çözücü etkileri araştırıldı. Çözücü ortamlar içerisinde optimize edilmiş moleküler yapılar elde edildi. Guanazole’nin konformasyonel yapıları gaz fazda incelendi ve nispi nüfus analizleri Boltzmann dağılımı kullanılarak elde edildi. Ayrıca, Guanazole’nin deneysel FT-IR spektrumu kaydedildi. Ek olarak titreşim frekansları ve şiddetler optimize yapılar kullanılarak her bir çözücü ortam için hesaplandı ve deneysel veriler ile kıyaslandı. Hesaplamamalarda Yoğunluk Fonksiyoneli Teorisi ve 6311++G(d, p) temel seti kullanıldı. Saf Guanazole’nin deneysel IR spektrumundan yola çıkılarak, Guanazole’nin katı fazda dimer yapıda olduğu belirlendi. Bu yüzden dimer yapı için detaylı incelemeler yapıldı.

Keywords

Çözücü etkileri, guanazole, titreşim spektroskopisi, yoğunluk fonksiyoneli teorisi

An FT-IR and DFT Study of Solvent Effects on Molecular Parameters and Vibrational Frequencies of 3,5-diamino-1,2,4-triazole

Abstract

In this paper, solvent environments effects on structural and spectroscopic properties of 3,5-diamino-1,2,4-triazole (Guanazole) antitumor agent have been investigated. Optimized molecular structures were obtained in solvent media. Conformational structures of Guanazole in the gas phase were investigated and the relative population distributions of the conformations were obtained using the Boltzmann distribution. Moreover, the experimental FT-IR spectrum of Guanazole were recorded. In addition, vibrational frequencies and its intensities were calculated for each environment by using of optimized structures and they compared with the experimental data. Density Functional Theory and 6311++G (d,p) basis set were used in the theoretical calculations. Based on the solid phase IR spectrum of pure Guanazole, it was seen that Guanazole is dimeric structure in solid phase. For this reason, the dimer structure of Guanazole has been investigated in detail.

Keywords

Density functional theory, guanazole, solvent effects, vibrational spectroscopy

References

• Aurkie R, Mitra S, Rosair GM, 2008. A novel hydroxo-bridged cyclic tetranuclear copper (II) complex using the guanazole ligand: Synthesis, crystal structure and thermal analysis, Inorganic Chemistry Communications 11: 1256-1259.
• Bilkan MT, 2017. Structural and spectroscopic studies on dimerization and solvent-ligand complexes of Theobromine, Journal of Molecular Liquids, 238: 523-532.
• Dave C, Paul MA, Rustum YM, 1978. Studies on the selective toxicity of guanazole in mice, European Journal of Cancer, 14: 33-40. Dennington RD, Keith TA, Millam JM, 2008. GaussView 5, Gaussian, Inc.
• Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Cheeseman JR, Montgomery JA, Jr., Vreven T, Kudin KN, Burant JC, et all, 2004. Gaussian, Inc., Gaussian 03, Revision D.01, Wallingford CT.
• Jamróz MH, 2004. Vibrational Energy Distribution Analysis VEDA 4, Warsaw.
• Guennoun L, Jastimi JE, Guédira F, Marakchi K, Kabbaj OK, Hajji AE, Zaydoun S, 2011. Molecular geometry and vibrational studies of 3, 5-diamino-1, 2, 4-triazole using quantum chemical calculations and FT-IR and FT-Raman spectroscopies, Spectrochimica Acta Part A, 78: 347-353.
• Haixiang Z, Dong Y, Liu H, 2016. Two new luminescent Zn (II) compounds constructed from guanazole and aromatic polycarboxylate ligands, Journal of Molecular Structure, 1105: 112-117.
• Ho JA, Pickens CV, Gamscik MP, Colvin OM, Ware RE, 2003. In vitro induction of fetal hemoglobin in human erythroid progenitor cells, Experimental hematology, 31: 586-591.
• Kumar VK, Keresztury G, Sundius T, Xavier RJ, 2005. Hydrogen bonding and molecular vibrations of 3, 5-diamino-1, 2, 4-triazole, Spectrochimica Acta Part A, 61: 261-267.
• Miertuš S, Scrocco E, Tomasi J, 1981. Electrostatic interaction of a solute with a continuum. A direct utilizaion of AB initio molecular potentials for the prevision of solvent effects, Chemical Physics, 55: 117-124.
• Penglei C, Li X, 2015. Construction of two new Zn (II)-guanazole frameworks via varying organic carboxylate ligands, Journal of Molecular Structure, 1081: 182-186.
• Starova GL, Frank-Kamanetskaya OV., Shibanova EF, Lopyrev VA, Voronkov МG, Makarskii VV, 1979. X-ray diffraction examination of the molecular structure of guanazole (3,5-diamino-ih-i,2,4-triazole), Khimiya Geterotsiklicheskikh Soedinenii, 10: 1422-1423.
• Suter W, Romagna F, 1990. DNA repair induced by various mutagens in rat hepatocyte primary cultures measured in the presence of hydroxyurea, guanazole or aphidicolin, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 231: 251-264.
• Xin Z, Jie Y, Rosenberg MR, Wan J, Zeng S, Cui W, Xiao Y, Li Z, Tu Z, Casarotto MG, Hu W, 2012. Design and synthesis of pinanamine derivatives as anti-influenza A M2 ion channel inhibitors, Antiviral research, 96:91-99.
• Vick JA, Herman EH, 1970. Cardiovascular effects of Guanazole, Toxicology and applied pharmacology, 16:108-119.