Dergiler / Gazi University Journal of Science / 2014 / Cilt: 27 - Sayı: 2

Spectrophotometric determination of the acidity dissociation constants of symmetric Schiff base derivatives

Sayfa
771–783
Yayın Tarihi
2014-06-27
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The second protonation (pKa2) was found for molecules 2 (-5.384), 8 (-5.165), 5 (-5.028), 7 (-4.775), 4 (-4.518), 1 (-4.111), 6 (-3.866) and 3 (-3.212).

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:In this study, the acidity constants of series symmetric Schiff base derivatives have been determined using the UV-visible spectrophotometric method at a temperature of 25(±0.1) °C.
📊
Temel Bulgular & Veri:The first and the second protonated acidity constants (pKa1 and pKa2) have been found to cause the protonation of the imine nitrogen atom for all molecules.
💡
Sonuç & Katkı:The second protonation (pKa2) was found for molecules 2 (-5.384), 8 (-5.165), 5 (-5.028), 7 (-4.775), 4 (-4.518), 1 (-4.111), 6 (-3.866) and 3 (-3.212).
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Spectrophotometric determination · Symmetric Schiff base · Acidity Dissociation Constants

Abstract

In this study, the acidity constants of series symmetric Schiff base derivatives have been determined using the UV-visible spectrophotometric method at a temperature of 25(±0.1) °C. The deprotonated acidity constants (pKa) have been found to be associated with the deprotonation of phenolate oxygen. The first and the second protonated acidity constants (pKa1 and pKa2) have been found to cause the protonation of the imine nitrogen atom for all molecules. The deprotonated acidity constants (pKa) were found for molecules 5 (9.088), 8 (9.848), 6 (10.243), 2 (10.2569), 3 (10.297), 1 (10.587), 7 (10.692) and 4 (10.804). The first protonation (pKa1) was found for molecules 2 (3.432), 5 (4.207), 8 (4.612), 7 (4.758), 4 (4.995), 1 (5.288), 6 (5.606) and 3 (6.452). The second protonation (pKa2) was found for molecules 2 (-5.384), 8 (-5.165), 5 (-5.028), 7 (-4.775), 4 (-4.518), 1 (-4.111), 6 (-3.866) and 3 (-3.212).

🔖

Bu Makaleye Atıf Yap

TÜRKOĞLU, G., BERBER, H., ÖZKÜTÜK, M. (2014). Spectrophotometric determination of the acidity dissociation constants of symmetric Schiff base derivatives. Gazi University Journal of Science, Cilt: 27 - Sayı: 2, 771–783. https://ajindex.com/articles/254835

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (10)

  1. Calligaris, M., Randaccio, L., In Comprehensive Coordination Chemistry; Wilkinson, G., Ed.; Pergamon: London,Vol. 2, p 715, (1987).
  2. Jia, H.P., Li, W., Ju, Z.F., Zhang, J., “Synthesis, Structure, and Magnetic Properties of a Novel Mixed-Bridged Heterometal Tetranuclear Complex [Mn2Ni2(MeOSalen)2(l1,1-N3)2(N3)2]”, Chem. Commun., 10: 397-400 (2007). Inorg. [3] Cohen, M.D., Schmidt, G.M.J., Flavian, S., “Topochemistry. VI. Experiments on Photochromy and Thermochromy of Crystalline Anils of Salicylaldehydes”, J. Chem. Soc., 2041-2051 (1964).
  3. Lahav, M., Schmidt, G.M.J., “Tophochemistry. XXIII. The Solidstate Photochemistry at 25 Deg of Some Muconic Acid Derivatives”, J. Chem. Soc. B, 312-317, (1967).
  4. Hadjoudis, E., Vitterakis, M., Moustakali-Mavridis, I., “Photochromism and Thermochromism of Schiff Bases in the Solid and in Rigid Glasses”, Tetrahedron, 43: 1345-1360 (1987).
  5. Kaya, I., Yıldırım, M., Avcı, A., “Synthesis and Characterization of Fluorescent Polyphenol Species Derived From Methyl Substituted Aminopyridine Based Schiff Bases: The Effect of Substituent Position on Optical, Electrical, Electrochemical, and Fluorescence Properties”, Synth. Met., 160: 911-920 (2010).
  6. Ramakrishna, D., Bhat, B.R., Karvembu, R., “Catalytic Oxidation of Alcohols by Nickel (II) Schiff Triphenylphosphine in Ionic Liquid: an Attempt towards Oxidation Commun., 11: 498-501 (2010). Containing Process”, Catal. [8] Soltani, N., Behpour, M., Ghoreish i, S. M., Naeimi H., “Corrosion Inhibition of Mild Steel in Hydrochloric Acid Solution by Some Double Schiff Bases”, Corr. Sci., 52: 1351-1361 (2010).
  7. Sabaa, M.W., Mohamed, R.R., Oraby, E.H., “Vanillin–Schiff’s Bases as Organic Thermal Stabilizers and Co-stabilizers for Rigid Poly(vinyl chloride)”, Europ. Poly. J., 45: 3072-3080 (2009). [10] Chakraborty, A., Kumar, P., Ghosh, K., Roy, P., “Evaluation of a Schiff Base Copper Complex Compound as Potent Anticancer Molecule with Multiple Targets of Action”, Europ. J. Pharm., 647: 1-12 (2010).
  8. Kamel, M. M., Ali, H. I., Anwar, M.M., Mohamed, N.A. Soliman, A.M., “Synthesis, Antitumor Activity and Sulfonamide-Schiff's Benzothiazinones Derivatives”, Europ. J. Medic. Chem., 45: 572-580 (2010).
  9. Study of Novel Bases, Thiazolidinones, and Their c-nucleoside [12] Roswadowski, Z., Majewski, E., Dziembowska, T., Hansen, P.E., “Deuterium Isotope Effects On 13C Chemical Hydrogenbonded Schiffs Bases”, J. Chem. Soc. Perkin Trans., 2: 2809 (1999).
  10. Intramolecularly Zgierski, Photochromism of N-salycylidene-R-b