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Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme

Year 2007, Volume: 20 Issue: 1, 113 - 136, 30.06.2007

Abstract

 Beş monoazo bileşiğinin asitlik sabitleri, pKa, yarı-empirik PM3 yöntemiyle hesaplanmış ve elde edilen asitlik sabitleri ile deneysel olarak elde edilmiş olanlar arasındaki uyum araştırılmıştır. Uyumun en iyi olduğu durumlar seçilerek proton-verme merkezleri ve mekanizmaları saptanmaya çalışılmıştır. Bulunan asitlik sabitleri kullanılarak keto-enol tautomerik denge sabitleri teorik olarak, KT dengeleri, hesaplanmış ve incelenen tüm monoazo bileşikler için enol formlarının daha kararlı olduğu gözlenmiştir. Birinci proton-verme iki hidroksil grubu içeren aromatik halkanın para-konumundaki protonunu vermesi, ikinci proton-verme ise aromatik halkanın orto-konumundaki fenolik hidroksil grubundan olmaktadır. Ancak diğer halkada orto konumunda hidroksil grubu içeren iki molekülün.farklı mekanizma ile proton verdiği gözlenmiştir. 

References

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  • [2] G.S., Kumar, “Azo Functional Polymers: Functional Group Approach in Macromolecular Design”, Tecnomic Publishing Co. Inc.: Lancaster, Basel, 1993.
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  • [6] R.D., Little, and G., Venegas, “A New, mild method for the synthesis of azo compounds”, J. Org. Chem, Vol.43, No. 14, 2921-2923, 1978.
  • [7] A.B., Hashim, A.J., Elie, and C., Noel, “Unusual and efficient (Z)stereoselective peterson synthesis of 2-diethoxyphosphonyl-1-alkoxy-3methylpenta-1,3-dienes. their use in the diels-alder reaction”, Tetrahedron Lett., Vol.37, Issue 17, 2951-2954, 1996.
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  • [23] A., Klamt, G. J. Schueuermann, “COSMO: A New approach to dielectric screening in solvents with explicit expressions for the screening energy and its gradient”, J. Chem. Soc. Perkin Trans. Vol.2, Issue 5 799, 1993.
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  • [26] S., Yarlıgan, C., Öğretir, B., Kaynak, E., Esenoğlu, “A Study on acid-base properties and hydrogen bonding of some 2-substitued benzimidazoles in aquas phase using semi-empirical methods”, Journal of Molecular Structure: THEOCHEM, Vol.586, Issues 1-3, 9-16, 2002.
  • [27] C., Öğretir, T.A., Demir, M., Yaman (Özkütük) And K., Görgün “Quantum chemical studies on prototropic tautomerisation and protonation behaviour of 6-propyl-2-thiouracil”, Journal of Molecular Structure: THEOCHEM, 679, Issues 1-2, 33-43, 2004.

A Theoretıcal Study On Proton-Loss Behavıor Of Some Monoazo Derıvatıves

Year 2007, Volume: 20 Issue: 1, 113 - 136, 30.06.2007

Abstract

The deprotonation acidity constants, (pKa) of five monoazo derivatives were calculated by using the semi-empirical PM3 method and the obtained pKa values were compared with the experimental ones. Taking into account of the best fit results, the deprotonation centers and deprotonation patterns were determined. Using the calculated acidity constants the equlibrium constants, for keto-enol tautomerizm KT, were calculated. The evaluation of the toutomeric equlibrium constant volues revealed that the enol forms are more stable. It was observed that both deprotonation takes place on the aromatic ring which has two phenolic hydroxy groups. Whith the exception two molecules which deprotonates at phenolic hydroxy group located at ortho position of the other aromatic ring. The first deprotonation for all seems to take place at the para positioned phenolic hydroxyl group. 

References

  • [1] H., Zolinger, “Synthesis, Properties and Applications of Organic Dyes and Pigments, Color chemistry” 2 nd ed., VCH, Weinheim, 1991.
  • [2] G.S., Kumar, “Azo Functional Polymers: Functional Group Approach in Macromolecular Design”, Tecnomic Publishing Co. Inc.: Lancaster, Basel, 1993.
  • [3] Z.F., Liu, K., Hashimoto, and A., Fujishima, “Photoelectrochemical information storage using an azobenzene derivative”, Nature, Vol.347, 658660, 1990.
  • [4] H.W., Russ, and H., Tappe, Eur. Pat. Appl., EP. 629, 667, 1994.
  • [5] X.J., Peng, and J.Z., Yang, Chin. Image Sci. Practise, 4, 5, 1998.
  • [6] R.D., Little, and G., Venegas, “A New, mild method for the synthesis of azo compounds”, J. Org. Chem, Vol.43, No. 14, 2921-2923, 1978.
  • [7] A.B., Hashim, A.J., Elie, and C., Noel, “Unusual and efficient (Z)stereoselective peterson synthesis of 2-diethoxyphosphonyl-1-alkoxy-3methylpenta-1,3-dienes. their use in the diels-alder reaction”, Tetrahedron Lett., Vol.37, Issue 17, 2951-2954, 1996.
  • [8] S., Xie, A., Natansohn, and P., Rochon, “Recent developments in aromatic azo polymers research”, Chem. Mater., Vol.5, Issue 4, 403-411, 1993.
  • [9] T.J., Marks, and M.A., Ratner, “Desing, synthesis, and properties of molecule- based assemblies with large second order optical nonlinearities”, Angew. Chem. Int. Ed. Engl., Vol.34, Issue 2, 155-173, 1995.
  • [10] DM., Burland, RD., Miller, and C.H., Walsh, “Second-order nonlinearity in poled-polymer systems”, Chem. Rev., Vol. 94, No. 1, 31-75, 1994.
  • [11] E., Stenberg, and D., Dolphin, “Infrared Absorbing Dyes”, Chapter 15, NewYork:Plenum, USA, 1990.
  • [12] P., Gregory, P., Rev. Prog. Coloration, 24, 1, 1994.
  • [13] J.N., Bair, In: A.R., Gennaro, (ed), “Remington: The science and practice of pharmacy”, Chapter 79, p.1366, Easton, Pennsylvania, 1995.
  • [14] E.D., Huhges, C.K., Ingold, and J.H. Ridd “Nitrosation, diazotization, and deamination Part I. Principles, background and method for kinetic study of diazotization”, J. Chem. Soc. 58-65, 1958.
  • [15] E.D., Hughes, C.K., Ingold, and J.H., Ridd “Nitrosation, diazotization, and deamination Part II. second- and third-order diazotization of aniline in dilute perchloric acid”, J. Chem. Soc. 65-69, 1958.
  • [16] E.D., Hughes, C.K., Ingold, and J.H., Ridd “Part III. Zero-order diazotization of aromatic amines in carboksilic acid buffers”, J. Chem. Soc. 70-76, 1958.
  • [17] E.D., Hughes, C.K., Ingold, and J.H., Ridd “Part IV. Hydrogen-ion catalysis in the diazotization of o-chloroaniline in dilute perchloric acid”, J. Chem. Soc. 77-82, 1958.
  • [18] E.D., Hughes, C.K., Ingold, and J.H., Ridd “Part V. Catalysis by anions of acids the diazotization of aniline and of o-chloroanaline in dilute perchloric acide”, J. Chem. Soc. 82-88, 1958.
  • [19] E.D., Hughes, C.K., Ingold, and J.H., Ridd “Part VI. Comperative discussion of the mechanism of N- and O-nitrosation whit special referance to diazotization”, J. Chem. Soc. 88-98, 1958.
  • [20] E., Ermiş, “Bazı Monoazo Bileşiklerinin Spektrofotometrik Yöntemle Asitlik Sabitlerinin Hesaplanması”, Yüksek Lisans Tezi, Anadolu Üniversitesi Fen Bilimleri Enstitüsü, Eskişehir, 2003.
  • [21] E. Ç. S., Lekesiz, “Bazı Monoazo Bileşiklerinin Spektrofotometrik Yöntemle Asitlik Sabitlerinin Hesaplanması”, Yüksek Lisans Tezi, Anadolu Üniversitesi Fen Bilimleri Enstitüsü, Eskişehir, 2004.
  • [22] J.J.P., Stewart, MOPAC 7.0 QCPE, University of Indiana, Bloomington IN, USA.
  • [23] A., Klamt, G. J. Schueuermann, “COSMO: A New approach to dielectric screening in solvents with explicit expressions for the screening energy and its gradient”, J. Chem. Soc. Perkin Trans. Vol.2, Issue 5 799, 1993.
  • [24] CS Chemoffice Pro for Microsoft Windows, Cambridge Scientific Computing, Inc., 875 Massachusetts Avenue, Suite 61, Cambridge MA 2139, USA.
  • [25] E., Açıkkalp, K., Yıldız, S., Yarlıgan, C. Öğretrir, “Semiempirical gas phase study on tautomerizm of 2-hydroxy amino and mercapto benzimidazoles”, Journal of Molecular Structure: THEOCHEM, Vol.536, Issues 1-3, 155-160, 2000.
  • [26] S., Yarlıgan, C., Öğretir, B., Kaynak, E., Esenoğlu, “A Study on acid-base properties and hydrogen bonding of some 2-substitued benzimidazoles in aquas phase using semi-empirical methods”, Journal of Molecular Structure: THEOCHEM, Vol.586, Issues 1-3, 9-16, 2002.
  • [27] C., Öğretir, T.A., Demir, M., Yaman (Özkütük) And K., Görgün “Quantum chemical studies on prototropic tautomerisation and protonation behaviour of 6-propyl-2-thiouracil”, Journal of Molecular Structure: THEOCHEM, 679, Issues 1-2, 33-43, 2004.
There are 27 citations in total.

Details

Journal Section Research Articles
Authors

Cemil Öğretir This is me

Publication Date June 30, 2007
Acceptance Date December 15, 2006
Published in Issue Year 2007 Volume: 20 Issue: 1

Cite

APA Öğretir, C. (2007). Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme. Eskişehir Osmangazi Üniversitesi Mühendislik Ve Mimarlık Fakültesi Dergisi, 20(1), 113-136.
AMA Öğretir C. Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme. ESOGÜ Müh Mim Fak Derg. June 2007;20(1):113-136.
Chicago Öğretir, Cemil. “Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme”. Eskişehir Osmangazi Üniversitesi Mühendislik Ve Mimarlık Fakültesi Dergisi 20, no. 1 (June 2007): 113-36.
EndNote Öğretir C (June 1, 2007) Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme. Eskişehir Osmangazi Üniversitesi Mühendislik ve Mimarlık Fakültesi Dergisi 20 1 113–136.
IEEE C. Öğretir, “Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme”, ESOGÜ Müh Mim Fak Derg, vol. 20, no. 1, pp. 113–136, 2007.
ISNAD Öğretir, Cemil. “Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme”. Eskişehir Osmangazi Üniversitesi Mühendislik ve Mimarlık Fakültesi Dergisi 20/1 (June 2007), 113-136.
JAMA Öğretir C. Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme. ESOGÜ Müh Mim Fak Derg. 2007;20:113–136.
MLA Öğretir, Cemil. “Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme”. Eskişehir Osmangazi Üniversitesi Mühendislik Ve Mimarlık Fakültesi Dergisi, vol. 20, no. 1, 2007, pp. 113-36.
Vancouver Öğretir C. Bazı Monoazo Türevlerinin Proton-Verme Davranışları Üzerinde Teorik Bir İnceleme. ESOGÜ Müh Mim Fak Derg. 2007;20(1):113-36.

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