Carbonylative Cyclization of Unsaturated Carboxylic Acids by Palladium Complexes with Phosphines(I) Synthesis and Structure of Palladium(O, II) Complexes with Unsaturated Carboxylic Acids

포스핀류가 배위된 팔라듐 착물에 의한 불포화카르복실산의 카르보닐화고리 반응 (제 1 보). 불포화카르복실산이 배위된 팔라듐(0, Ⅱ) 착물의 합성과 구조

  • Myung-Ki Doh (Department of Chemistry, Yeungnam University) ;
  • Maeng-Jun Jung (Department of Chemistry, Yeungnam University) ;
  • Dong-Jin Lee (Department of Industrial Chemistry, Kyungbuk Sanup University) ;
  • Kohtaro Osakada (Research Laboratory of Resources Utilization, Tokyo Institute of Technology) ;
  • Akio Yamamoto (Deppartment of Applied Chemistry, Shool of Science and Engineering. Waseda University)
  • 도명기 (영남대학교 이과대학 화학과) ;
  • 정맹준 (영남대학교 이과대학 화학과) ;
  • 이동진 (경북산업대학교 공업화학과) ;
  • ;
  • Published : 1993.04.20

Abstract

New Palladium(0)-olefin complexes, $(PMe_3)_2Pd{CH_2=C(CH_3)COOH} \;and\;(PMe_3)_2Pd{(CH_3)CH=CHCOOH}$ have been prepared by treating $Pd(PMe_3)_2$(styrene) with methacrylic acid and trans-crotonic acid, respectively. These complexes were characterized by elemental analysis, IR and $^1H-,\;^{13}C-,\;and\;^{31}P$-NMR spectroscopy. The carboxylic acid entity was found non-bonded with palladium while ${\pi}$-bond is formed between the olefin double bond and Pd(0). The results are compared with the metallacycle formation the reaction of Pd(PMe3)2(styrene) with 3-butenoic acid.

$trans-PdEt_2(PMe_3)_2$와 styrene을 반응시켜 얻어진 $Pd(PMe_3)_2$(styrene)에 methacrylic acid와 trans-crotonic acid를 각각 반응시켜 새로운 팔라듐(O)-올레핀착물로서 $(PMe_3)_2Pd{CH_2=C(CH_3)COOH}$(PMe_3)_2Pd{(CH_3)CH=CHCOOH}$를 합성하고, 구조와 특성을 원소분석, IR 및 $^1H-,\;^{13}C-,\;^{31}P-NMR$ 등의 분광학적 방법으로 조사하였다. methacrylic acid 와 trans-crotonic acid에 존재하는 올레핀의 이중결합은 팔라듐(O)에 ${\pi}$-결합을 형성하였고, 카르복실산은 팔라듐에 결합되지 않았음을 알게되었다. 그리고 동일한 반응에서 metallacycle을 형성하는 3-butenoic acid와 비교 검토하였다.

Keywords

References

  1. Principles and Application of Organotransition Metal Chemistry J. P. Collman;L. S. Hegedus;J. R. Nortan;R. G. Finke
  2. Organotransition Metal Chemistry Fundamental Concepts and Applications A. Yamamoto
  3. Phosphine Arsine, and Stibine Complexes of the Transition Elements C. A. McAuliffe;W. Levason
  4. Chem. Rev. v.77 C. A. Tolman
  5. J. Am. Chem. Soc. v.95 S. Otsuka;A. Nakamura;T. Yoshida;M. Naruto;K. Ataka
  6. Organic Synthesis with Palladium Compounds J. Tsuji
  7. Palladium Reagents in Organic Synthesis R. F. Heck
  8. Chem. Commun. R. van der Linde;R. O. De Johgh
  9. J. Am. Chem. Soc. v.94 C. A. Tolman;W. C. Seidel;D. H. Gerlach
  10. J. Organomet. Chem. v.168 F. Ozawa;T. Ito;Y. Nakamura;A. Yamamoto
  11. J. Am. Chem. Soc. v.101 M. J. S. Dewar;G. P. Ford
  12. Inorg. Chem. v.13 N. Rosch;R. Hoffmann
  13. J. Am. Chem. Soc. v.101 T. A. Albright;R. Hoffmann;J. C. Thibeault;D. L. Thorn
  14. Coord. Chem. Rev. v.108 C. A. Tsipis
  15. J. Am. Chem. Soc. v.99 B. Akermark;M. Almemark;J. Almlof;J. Backvall;B. Ross;A. Stogard
  16. Inorg. Chem. v.20 K. Kitaura;S. Sakaki;K. Morokuma
  17. Inorg. Chem. v.18 T. Ziegler;A. Rauk
  18. Shokubai(Catalyst) v.17 A. Nakamura
  19. J. Chem. Soc. Chem. Commun. T. Yamamoto;K. Igarashi;J. Ishizu;A. Yamamoto
  20. J. Chem. Soc. Chem. Commun. v.102 T. Yamamoto;K. Igarashi;S. Komiya;A. Yamamoto
  21. Bull. Chem. Soc. Jpn. v.57 K. Sano;T. Yamamoto;A. Yamamoto
  22. Chem. Letters (Japan) K. Sano;T. Yamamoto;A. Yamamoto
  23. Chem. Letters (Japan) K. Sano;T. Yamamoto;A. Yamamoto
  24. J. Am. Chem. Soc. v.109 C. Yamamoto;K. Sano;A. Yamamoto
  25. Organometallics v.9 K. Osakada;M. K. Doh;F. Ozawa;A. Yamamoto
  26. Pure and Appl. Chem. v.63 no.5 A. Yamamoto;F. Ozawa;K. Osakada;L. Hwang;T. I. Son;N. Kawasaki;M. K. Doh
  27. Organometallics v.2 H. Nakazawa;F. Ozawa;A. Yamamoto
  28. Infrared and Raman spectra of Inorganic and Coordination Compounds K. Nakamoto
  29. J. Korean Chem. Soc. v.37 no.4 M. K. Doh;B. K. Kim;M. J. Jung;Y. D. Song;B. K. Park
  30. J. Organomet. Chem. v.171 T. Yamamoto;J. Ishizu;S. Komiya;Y. Nakamura;A. Yamamoto
  31. J. Am. Chem. Soc. v.102 H. Kurozawa;T. Majima;N. Asada
  32. Specktroskopische Methoden in der Organischen Chemie M. Hesse;H. Meier;B. Zeeh
  33. J. Chem. Soc. L. Malatesta;M. Angoletta
  34. Inorg. Synth v.13 D. R. Coulson
  35. J. Organomet. Chem. v.33 K. Kudo;M. Hidai;Y. Uchida
  36. Bull. Chem. Soc. Jpn. v.50 T. Ito;H. Tsuchiya;A. Yamamoto
  37. 日本化學會 新實驗化學講座(8), 無機化合物 合成(III) 丸善