Electrochemical Propertics and Oxidation Reaction of Hydrazobenzene by Oxygen Adducted Tetradentate Schiff Base Cobalt(II)(3MeOSED) Activated Catalyst in Aprotic Solvents(I)

비수용매에서 산소첨가된 네자리 Schiff Base Cobalt(II)(3MeOSED) 활성촉매에 의한 Hydrazobenzene의 산화반응과 전기화학적 성질 (제 1 보)

  • Ki-Hyung Chjo (Department of Chemistry, College of Natural Science, Chonnam National University) ;
  • Yong-Kook Choi (Department of Chemistry, College of Natural Science, Chonnam National University) ;
  • Sang-Bock Kim (Department of Chemistry, University of Ulsan)
  • 조기형 (전남대학교 자연과학대학 화학과) ;
  • 최용국 (전남대학교 자연과학대학 화학과) ;
  • 김상복 (울산대학교 자연과학대학 화학과)
  • Published : 1992.04.20

Abstract

Tetradentate Schiff base Cobalt(II)(3MeOSED)$(H_2O)_2$ complexe was synthesized and allowed to react with dry oxygen to form oxygen adducts of Cobalt(III) complexes such as ${\mu}$-peroxo type [Co(III)(3MeOSED)(DMF)]$_2O_2$ and [Co(III)(3MeOSED)(DMSO)]$_2O_2$in DMF and DMSO or superoxo type [Co(III)(3MeOSED)(Py)]$O_2$ in pyridine. The oxygen adducted complex was investigated by cyclic voltammetry and DPP method with glassy carbon electrode in 0.1M TEAP-DMF (-DMSO,-Py) as supporting electrolyte solution. As a result the reduction reaction process occurred to four steps including prewave Of $O_2^-$in 1 : 1 oxygen adducted superoxo type [Co(III)(3MeOSED)(Py)]$O_2$complex and three steps not including prewave of $O_2^-$ in 1 : 2 oxygen adducted ${\mu}$-peroxo type [Co(III)-(3MeOSED)(DMF)]$_2O_2$ and [Co(III)(3MeOSED)(DMSO)]$_2O_2$. A superoxo type [Co(III)(3MeOSED)(L)]$O_2\;(L: CH_3OH)$ was generated with oxygen in methanol. Selectively oxidized hydrazobenzene $(H_2AB)$ to trans-azobenzene(t-AB) and the rate constant k for oxidation reaction of the following equation is $(2.96 {\pm} 0.2)$${\times}$ $10^{-1}$M/sec. $H_2AB$ + Co (II)(3MeOSED)$(L_2)+O_2\;{\rightleftarrow^K}$ [Co(III)(3MeOSED)(L)]$O_2{\cdot}H_2AB{\longrightarrow^K}$ Co(II(3MeOSED)$(L)_2$+t-AB+$H_2O_2 $.

네자리 Schiff base의 착물 Co(II)(3MeOSED)$(H_2O)_2$을 합성하였다. 이 착물의 균일 산화 활성촉매로서 산소첨가 착물은 DMF와 DMSO 용매에서는 ${\mu}$-peroxo형인 [Co(III)(3MeOSED)(DMF)]$_2O_2$와 [Co(III)(3MeOSED)(DMSO)]$_2O_2$이나 pyridine 용매에서는 superoxo형인 [Co(Ⅲ)(3MeOSED)(Py)]$O_2$로 주어진다. 이들의 CV법과 DPP법에 의한 전기화학적인 특성으로 ${\mu}$-peroxo형은 3단계 환원과정으로 일어나지만, superoxo형은 $O_2$의 prewave를 포함한 4단계 환원과정으로 일어난다. 산소가 포화된 메탄올 용액에서 [Co(III)(3MeOSED)(L)]$O_2(L: CH_3OH)$ 의 균일 산화 활성촉매에 의한 hydrazobenzene-$(H_2AB)$의 산화 주생성물은 trans-azobenzene(t-AB)이 선택적으로 다음과 같은 반응식으로 생성되고 이 때 속도상수는 k = (2.96 ${\pm}$ 0.2) ${\times}$ $10^{-1}$M/sec임을 알았다. $H_2AB$ + Co (Ⅱ)(3MeOSED)$(L_2)+O_2\;{\rightleftarrow^K}$ [Co(III)(3MeOSED)(L)]$O_2{\cdot}H_2AB{\longrightarrow^K}$ Co(II(3MeOSED)$(L)_2$+t-AB+$H_2O_2 $.

Keywords

References

  1. Real. Trav. Chim. pays-Bus v.86 H. M. Van Dort;H. J. Guerson
  2. J. Org. Chem. v.34 L. H. Vogt;J. G. Wirth;H. L. Finkbeimer
  3. J. Org. Chem. v.35 D. H. Tomaja;W. H. Vogt;J. G. Wirth
  4. J. Catal. v.41 V. M. Kothari;J. J. Tazuma
  5. J. Am. Chem. Soc. v.103 R. S. Drago;A. Zombeck;B. B. Cordon;J. H. Gaul
  6. J. Chem. Soc. (A) C. Floliani;F. Calderazzo
  7. Bull. Chem. Soc. Japan v.42 A. Misono;S. Koda
  8. Inorg. Chim. Acta. v.5 C. Busetto;C. Neri;N. Palladino;E. Penotti
  9. Chem. Comm. D. Dimente;B. M. Hoffman;F. Basolo
  10. J. Inorg. Nucl. Chem. v.35 E. I. Ochiai
  11. J. Phys. Chem. v.71 J. A. Weil;J. K. Kinnaird
  12. J. Am. Chem. Soc. v.89 M. Mori;J. A. Weil
  13. J. Am. Chem. Soc. v.92 B. M. Hoffman;D. L. Dimento;F. Basolo
  14. J. Am. Chem. Soc. v.92 F. A. Walker
  15. J. Korea. Chem. Soc. v.31 no.6 K. H. Chjo;J. S. Chung;H. S. Ham;S. S. Seo
  16. J. Korea. Chem. Soc. v.33 no.2 K. H. Chjo;J. S. Chung;H. S. Ham;S. S. Seo
  17. J. Korea. Chem. Soc. v.33 no.3 K. H. Chjo;S. S. Seo;D. S. Chon
  18. J. Chem. Educ. v.54 no.7 T. G. Appleton
  19. J. Korea Chem. Soc. v.34 no.6 K. H. Chjo;Y. K. Choi;H. S. Ham;S. S. Seo;S. B. Kim
  20. Purification of Laboratory Chemicals D. D. Perrin;W. L. Armargo;D. R. Perrin
  21. J. Am. Chem. Soc. v.97 no.21 J. H. Burness;T. G. Dillard;L. T. Talor
  22. Iowa state coll. Jour. science v.22 H. Diehl;L. Ligget;C. C. Hach;G. C. Hanrrison;L. Henselmeier;R. W. Schwant;J. Matheewe Jr.
  23. Anal. Chem. v.54 D. T. Sawyer
  24. Chem. Ber. v.101 G. Kaupp;G. A. Russwel
  25. Chem. Rev. v.79 F. Basolo;R. D. Jones;D. A. Summerville
  26. J. General Chem. of the U.S.S.R. v.49 A. V. Savitskii;V. I. Nelyubin
  27. J. Am. Chem. Soc. v.102 R. S. Drago;J. P. Cannady;K. A. Leslie
  28. J. Am. Chem. Soc. v.107 R. S. Drago;B. B. Cordon;R. P. Perito
  29. Ph. D. Thesis, University of East Anglia S. B. Kim