DOI QR코드

DOI QR Code

Synthesis, Reactions and Catalytic Activities of Water Soluble Rhodium and Iridium-Sulfonated Triphenylphosphine Complexes. 1. Polymerization of Terminal Alkynes

  • Published : 1997.12.20

Abstract

Polymerization of terminal alkynes (phenlacetylene and 4-ethynyltoluene) catalyzed by water soluble rhodium (Ⅰ) complex, RhCl(CO)(TPPTS)2 (TPPTS=m-P(C6H4SO3Na)3) (1) selectively produces cis-transoid polymers at room temperature in homogeneous solution of H2O and MeOH as well as in biphasic solutions of H2O and CHCl3. The rate of polymerization is higher in H2O/MeOH than in H2O/CHCl3. The iridium analog, IrCl(CO)(TPPTS)2 (2) shows catalytic activity for the polymerization of phenylacetylene only at elevated temperature to give trans-polymers. The polymerization rate increases significantly when the trimethylamine N-oxide (Me3NO) was added to the reaction mixtures. The electronic absorption spectra of the cis-transoid polymers show three absorption bands whereas the trasn-polymers show only one absorption band. It seems that the electronic absorption bands depend on the configuration of the polymers.

Keywords

References

  1. J. Am. Chem. Soc. v.113 Wakatsuki, Y.;Yamazaki, H.;Kumegawa, N.;Satoh, T.;Satoh, J. Y.
  2. J. Am. Chem. Soc. v.114 Lambregts, M. J.;Munson, E. J.;Kheir, A. A.;Haw, J. F.
  3. Organometallics v.13 Bianchini, C.;Frediani, P.;Masi, D.;Peruzzini, M.;Zanobini, F.
  4. Organometallics v.15 Slugovc, C.;Mereiter, K.;Zobetz, E.;Schmid, R.;Kirchner, K.
  5. Angew. Chem. Int. Ed. Engl.. v.32 Schafer, M.;Mahr, N.;Wolf, J.;Werner, H.
  6. Organometallics v.10 Heeres, H. J.;Teuben, J. H.
  7. Bull. Korean Chem. Soc. v.15 Chin, C. S.;Won, G.;Song, J.
  8. J. Am. Chem. Soc. v.117 Van der Linden, A.;Schaverien, C. J.;Meijboom, N.;Ganter, C.;Orpen, A. G.
  9. Rend. Accad. Nazl. Lincei Rend. Classe Sci. Fis. Mat. Nat. v.25 Natta, G.;Mazzanti, G.;Corradini, P.
  10. J. Polym. Sci. Polym. Chem. Ed. v.15 Simionescu, C. I.;Perecec, V.;Dumitrescu, S.
  11. J. Polym. Sci. Polym. Symp. v.64 Simionescu, C. I.;Dumitrescu, S.;Perecec, V.
  12. J. Polym. Sci. Polym. Lett. Ed. v.17 Simionescu, C. I.;Perecec, V.
  13. J. Polym. Sci. Polym. Part A v.7 Kern, R. J.
  14. Macromolecules v.8 Masuda, T.;Sasaki, N.;Higashimura, T.
  15. Acc. Chem. Res. v.17 Masuda, T.;Higashimura, T.
  16. J. Am. Chem. Soc. v.106 Katz, T. J.;Ho, T. H.;Ying, N.-Y.;Stuart, I. W.
  17. J. Am. Chem. Soc. v.116 Kishimoto, Y.;Eckerle, P.;Miyatake, T.;Ikariya, T;Noyori, R.
  18. J. Chem. Soc., Chem. Commun. Goldberg, Y.;Alper, H.
  19. J. Polym. Sci. Part A: Polym. Chem. v.32 Tabata, M.;Yang, W.;Yokota, K.
  20. J. Polym. Sci. Part A: Polym. Chem. v.34 Lee, S.-I.;Shim, S.-C.;Kim, T.-J.
  21. J. Polym. Sci. Part A: Polym. Chem. v.27 Furlani, A.;Napoletano, C.;Russo, M. V.
  22. J. Poly. Bull. v.16 Furlani, A.;Napoletano, C.;Russo, M. V.;Feast, W.
  23. J. Polym. Sci. Part A: Polym. Chem. v.24 Furlani, A.;Napoletano, C.;Russo, M. V.
  24. Polym. J. v.23 Zhao, J.;Yang, M.;Shen, Z.
  25. Chem. Commun. Shim, S. C.
  26. Macromolecules v.28 Yashima, E.;Huang, S.;Matsushima, T.;Okamoto, Y.
  27. Macromolecules v.25 Le Moigne, J.;Hilberer, A.;Strazielle, C.
  28. J. Organomet. Chem. v.452 Yuan, Z.;Stringer, G.;Jobe, I. R.;Kreller, D.;Scott, K.;Koch, L.;Taylor, N. J.;Marder, T. B.
  29. J. Am. Chem. Soc. v.119 Chen, J.;Alper, H.
  30. Chemtech Kuntz, E. G.
  31. Inorg. Chem. v.33 Darensbourg, D. J.;Joo, F.;Kannisto, M.;Katho, A.;Reibenspies, J. H.;Daigle, D. J.
  32. Nature v.373 Chaudhari, R. V.;Bhanage, B. M.;Deshpande, R. M.;Delmas, H.
  33. Angew. Chem. Int. Ed. Engl. v.34 Cornils, B
  34. J. Organomet. Chem. v.502 Cornils, B.;Kuntz, E. G.
  35. J. Organomet. Chem. v.480 Monteil, F.;Queau, R.;Kalck, P.
  36. Bull. Korean Chem. Soc. v.18 Chin, C. S.;Chang, W.-T.;Yang, S.;Joo, K.-S.
  37. Organometallics v.13 Yang, K.;Bott, S. G.;Richmond, M. G.
  38. J. Am. Chem. Soc. v.114 Yeh, W. Y.;Liu, L. K.
  39. Coord. Chem. Rev. v.53 Albers, M. O.;Coville, N. J.
  40. J. Am. Chem. Soc. v.103 Shapley, J. R.;Sievert, A. G.;Churchill, M. R.;Wasserman, H. J.
  41. Inorg. Chem. v.32 Chin, C. S.;Yoon, J.;Song, J.
  42. Chem. Commum. Marder, T. B.;Zargarian, D.;Calabrese, J. C.;Herskovitz, T. H.;Milstein, D.
  43. Chem. Commun. Chow, P.;Zagarian, D.;Taylor, N. J.;Marder, T. B.
  44. Organometallics v.7 Bianchini, C.;Laschi, F.;Ottaviani, F.;Pereuzzini, M.;Zanello, P.
  45. Organometallics v.9 Bianichini, C.;Mas, D.;Meli, A.;Pereuzzini, M.;Ramirez, J. a.;Vacca, a.;Zanobini, F.
  46. Organometallics v.10 Boese, W. T.;Goldman, A. S.
  47. Chem. Commun. Schafer, M.;Wolf, J.;Werner, H.
  48. Organometallics v.11 Esteruelas, M. A.;Lahoz, F. J.;Lopez, J. A.;Oro, L. A.;Schlunken, C.;Valero, C.;Werner, H.
  49. Organometallics v.15 Esteruelas, M. A.;Lahoz, F. J.;Onate, E.;Oro, L.;Rodriguez, L.;Steinert, P.;Werner, H.
  50. Inorg. Synth. v.11 Vrize, K.;Collman, J. P.;Tears Jr., C. T.;Kubota, M.
  51. Inorg. Synth. v.11 Evans, D.;Osborn, J. A.;Wilkinson, G.
  52. Inorg. Synth. v.19 Giordana, G.;Crabtree, R. H.
  53. J. Organomet. Chem. v.389 Hermann, W. A.;Kulpe, J. A.;Konkol, W.;Bahrmann, H.
  54. J. Organomet. Chem. v.389 Hermann, W. A.;Kellner, J.;Riepl, H.