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Synthesis and Characterization of Mn(Ⅲ) Chloro Complexes with Salen-Type Ligands

Mn(Ⅲ) Chloro-Salen형 리간드 착물의 합성과 특성

  • 변종철 (제주대학교 자연과학대학 화학과) ;
  • 한충훈 (제주대학교 자연과학대학 화학과) ;
  • 박유철 (경북대학교 자연과학대학 화학과) ;
  • 이남호 (제주대학교 자연과학대학 화학과) ;
  • 백종석 (제주대학교 자연과학대학 화학과)
  • Published : 2002.06.20

Abstract

Aseries of novel salen-type complexes {[Mn(III)($L_{acn}$)CI]: n=1~11} containing CI- ion were obtained by reactions of the Mn(CH$_3$COO)$_2$· 4H$_2$O with the potentially tetradentate compartmental ligand {$H$_2$L_{acn}$} prepared by condensation the of one mole of diamine {ethylenediamine, 1,3-propnediamine, o-phenylenediamine and 2,2-dimethyl-1,3-propanediamine} with two moles of aldehyde {alicylaldehyde, 5-chloro-salicylaldehyde, 3,5-dichlorosalicylaldethyde, and 3,5-di-tert-butyl-2-hydroxy-benzaldehyde} in a methanol solution. The resulting salen-type lignds and their Mn(III) complexes were identified and characterized by elemental analysis, conductivity, themogravimetry and UV-VIS, IR and NMR spectroscopy.

Cl- 이온을 포함하는 일련의 salen형 착물 {[Mn(III)($L_{acn}$)CI]: n=1~11} 들은 $Mn(CH_3COO)_2{\cdot}4H_2O$와 네자리 칸막이 리간드 {$H_2L_{acn}$}로 부터 얻었다. 이 salen형 리간드는 diamine류 {ethylenediamine, 1,3-propnediamine, 2,2-dimethyl-1,3-propanediamine, o-phenylenediamine}와 aldehyde류 {salicylaldehyde, 5-chlorosalicyladehyde, 3,5-dichlorosalicyladehyde, 3,5-di-tert-butyl-2-hydroxybenzaldehyde}를 lmethanol 용액에서 축합반응시켜 합성하였다. 이들 리간드 및 착물들은 원소 분석, 전도도, 열분석법 및 UV-VIS IR, NMR 분광학법 등을 이용하여 확인 고찰하였다.

Keywords

References

  1. Yamamura, T.; Tadokor, M.; Kuroda, R. Bull. Chem.Soc. Jpn. 1993, 66, 1984. https://doi.org/10.1246/bcsj.66.1984
  2. Fallon, G. D.; Gatehouse, B. M.; West, B. O. J. Chem.Soc., Dalton Trans. 1984, 2733.
  3. Canali, L.; Sherrington, D. C. Chem. Soc. Rev. 1999,28, 85. https://doi.org/10.1039/a806483k
  4. Holm, R. H.; Everett, G. W. Prog. Inorg. Chem. 1966,7, 83. https://doi.org/10.1002/9780470166086.ch3
  5. Leung, W. H.; Chan, E. Y. Y.; Chow, E. K. F.; Williams,I. D.; Peng, S. M. J. Chem. Soc., Dalton Trans. 1996,1229.
  6. Yamamura, T.; Tadokoro, M.; Kuroda, R. Chem. Lett.1989, 1245.
  7. Drummond, L. A.; Hendrick, K.; Tasker, P. A. Inorg.Chem. 1982, 21, 3923. https://doi.org/10.1021/ic00141a014
  8. Jaeger, D. A.; Wang, J. J. Org. Chem. 1993, 58, 6745. https://doi.org/10.1021/jo00076a040
  9. Jaeger, D. A.; Su, D. Tetrahedron Lett. 1999, 40, 257. https://doi.org/10.1016/S0040-4039(98)02350-8
  10. Munoz, S.; Gokel, G. W. Inorg. Chim. Acta. 1996,250, 59. https://doi.org/10.1016/S0020-1693(96)05211-5
  11. Fallis, I. A.; Griffiths, P. S.; Winnigton, A. L. J. Chem.Soc., Chem. Commum. 1998, 665.
  12. Hampl, F.; Liska, F.; Tonellato, U. Langmuir 1999, 15,405. https://doi.org/10.1021/la980861+
  13. Davis, J. A.; Watson, P. L.; Liebman, J. F.; Greenberg, A. Selective Hydrocarbon Oxidation. Principles and Progress; Eds.; VCH: New York, 1990.
  14. Simadi, L. I. Dioxygen Activation and HomogeneousCatalytic Oxidation; Ed.; Elsevier: New York, 1991.
  15. Lyons, J. E.; Ellis, P. E. Catal. Lett. 1991, 8, 45. https://doi.org/10.1007/BF00764382
  16. Grinstaff, M. W.; Hill, M. G.; Labinger, J. A.; Gray, H.B. Science 1994, 264, 1311. https://doi.org/10.1126/science.8191283
  17. Grinstaff, M. W.; Hill, M. G.; Gray, H. B. Inorg. Chem.1995, 34, 4896. https://doi.org/10.1021/ic00123a026
  18. Yoon, H.; Burrows, C. J. J. Am. Chem. Soc. 1988, 110,4087. https://doi.org/10.1021/ja00220a086
  19. Zhang, W.; Jacobsen, E. N. J. Org. Chem. 1991, 56,2296. https://doi.org/10.1021/jo00007a012
  20. Katsuki, T. Coord. Chem. Rev. 1995, 140, 189. https://doi.org/10.1016/0010-8545(94)01124-T
  21. Chang, C. J.; Labinger, J. A.; Gray, H. B. Inorg. Chem.1997, 36, 5927. https://doi.org/10.1021/ic970824q
  22. Bohle, D. S.; Zafar, A.; Jaeger, D. A. Inorg. Chem.2000, 39, 712. https://doi.org/10.1021/ic990950p
  23. Stinziano-Eveland, R. A.; Nguyen, S. T. Inorg. Chem.2000, 39, 2452. https://doi.org/10.1021/ic990548a
  24. Aguiari, A.; Bullita, E.; Casellato, U.; Guerriero, P.; Tamburini,S.; Vigato P. A. Inorg. Chim. Acta 1992, 194, 157. https://doi.org/10.1016/S0020-1693(00)82657-2
  25. Aguiari, A.; Tamburini, A.; Tamasin, P.; Vigato, P. A.Inorg. Chim. Acta 1997, 256, 199. https://doi.org/10.1016/S0020-1693(96)05441-2

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