DOI QR코드

DOI QR Code

Preparation of Carbosilane Dendrimers Based on Siloxane Tetramer: Silane Arborols $(VII)^1$

  • Published : 1997.02.20

Abstract

Via hydrosilation-alkenylation approach using hydrosilanes (HSiMeCl2 and HSiCl3) and allylmagnesium bromide with siloxane tetramer (MeCH2=CHSiO)4 as core molecule, noble carbosilane dendrimers with 12, 24, 48 and 96 allylic end groups have been prepared. The reaction path of the repetitive alkenylation and hydrosilation was monitored by means of NMR spectroscopic measurements. Every step for the formation of dendrimer provided almost quantitative yields as pure dendrimers. Based on the observation of UV spectroscopic measurements of Gn (n=1-4) molecules containing allylic end groups, the maximal molal absorption coefficients (εmax) at λmax and the number of double bonds proved an exponentially increased correlation.

Keywords

References

  1. J. Korean Chem. Soc. v.39 Kim, C.;Sung, D. D.;Chung, D. I.;Park, E.;Kang, E.
  2. J. Korean Chem. Soc. v.39 Kim, C.;Park, E.;Kang, E.
  3. Bull. Korean Chem. Soc. v.17 Kim, C.;Park, E.;Kang, E.
  4. Bull. Korean Chem. Soc. v.17 Kim, C.;Park, E.;Kang, E.
  5. J. Korean Chem. Soc. v.40 Kim, C.;Park, E.;Jung, I.
  6. C&EN O'Sullivan D. A.
  7. C&EN Dagani, R.
  8. C&EN Dagani, R.
  9. C&EN Fox, M. A.;Jones Jr, W. E.;Watkins, D. M.
  10. Synthesis Buhleier, E.;Wehner, W.;Vogtle, F.
  11. US-A 4 410 Denkenwalter, R. G.;Kolc, J. F.;Lukasavage, W. J.
  12. J. Org. Chem. v.50 Newkome, G. R.;Yao, Z.-Q.;Baker, G. R.;Gupta, V. K.
  13. Polym. J. v.17 Tomalia, D. A.;Baker, H.;Dewald, J.;Hall, M.;Kallos, G.;Martin, S.;Roeck, J.;Ryder, J.;Smith, P .
  14. US-A 4 507 466 Tomalia, D. A.;Dewald, J. R.
  15. US-A 4 558 120 Tomalia, D. A.;Dewald, J. R.
  16. Advances in Dendritic Marcromlecules, Vol 1 (Ed. Newkome) v.1 Moorefield, C. N.;Newkome, G. R.
  17. Angew. Chem. v.107 Issberner, J.;Moore, R.;Vogtle, F.
  18. Angew. Chem. Int. Ed. Engl. v.33 Issberner, J.;Moore, R.;Vogtle, F.
  19. Top. Curr. Chem. v.165 Tomalia, D. A.;Durst, H. D.
  20. Angew. Chem. v.102 Tomalia, D. A.;Naylor, A. M.;Goddard Ⅲ, W. A.
  21. Angew. Chem. Int. Ed. Engl. v.29 Tomalia, D. A.;Durst, H. D.
  22. Macromolecules v.27 Gitsov, I.;Frecht, J. M.
  23. C&EN Dagani, R.
  24. Macromolecules v.26 Roovers, J.;Zhou, L.-L.;Toporowski, P. M.;van der Zwan, M.;Iatrou, H.;Hadjichristidis, N.
  25. J. Am. Chem. Soc. v.116 Rao, C.;Tam, J. P.
  26. Inorg. Chem. v.35 Lange, P.;Schier, A.;Schmidbauer, H.
  27. J. Am. Chem. Soc. v.114 Denti, G.;Campagna, S.;Serroni, S.;Ciano, M.;Balzani, V.
  28. Inorg. Chem. v.31 Campagna, S.;Denti, G.;Serroni, S.;Ciano, M.;Juris, A.;Balzani, V.
  29. Inorg. Chem. v.30 Campagna, S.;Denti, G.;Serroni, S.;Ciano, M.;Juris, A.;Balzani, V.
  30. Adv. Mater. v.8 Lorenz, K.;Holter, D.;Stuhn, B.;Mulhaupt, R.;Frey, H.
  31. Macromolecules v.28 Lorenz, K.;Mulhaupt, R.;Frey, H.
  32. Chem. unserer Zeit v.30 Frey, H.;Lorenz, K.;Lach, C.
  33. Adv. Mater. v.4 Kim, Y. H.
  34. Adv. Mater. v.5 van der Made, A. W.;van Leeuwen, P. W. N. M.;de Wilde, J. C.;Brandes, R. A. C.
  35. J. Chem. Soc., Chem. Commun. van der Made, A. W.;van Leeuwen, P. W. N. M.
  36. Organometallics v.13 Seyferth, D.;Son, D. Y.;Rheingold, A. L.;Ostrander, R. L.
  37. Organometallics v.14 Seyferth, D.;Kugita, T.;Rheingold, A. L.;Yab, G. P. A.
  38. Macromolecules v.24 Morikawa, A.;Kakimoto, M.;Imai, Y.
  39. Organicum Hazzard, B. Z.
  40. Calculated by ChemSite 2.2 from Pyramid learning