Palladium-catalyzed dehydrogenative polymerization between hydrosilanes and quinones or hydroquinone

Chemistry Letters

Volumn , Issue 3, 2000, Pages 250-251

  Reddy, Poreddy Narsi ^b   Chauhan, Bhanu Pratap Singh ^a   Hayashi, Teruyuki ^a   Tanaka, Masato ^a  

^a NATL INST OF MAT AND CHEM RES   (Japan)

^b JAPAN CHEMICAL INNOVATION INSTITUTE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0034354292     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2000.250     Document Type: Article

References (24)

1. a) "Inorganic and Organometallic Polymers," ACS Symposium Series 360, ed by M. Zeldin, K. J. Wynne, and H. R. Allcock, American Chemical Society, Washington, D.C. (1988).
2. b) "Silicon Chemistry," ed by E. R. Corey, J. Y. Corey, and P. P. Gaspar, Ellis Horwood, Chichester (1988).
3. c) "Silicon-Based Polymer Science," Advances in Chemistry Series 224, ed by J. M. Zeigler and F. W. G. Fearon, American Chemical Society, Washington, D.C. (1990).
4. a) R. Corriu, D. Leclercq, P. H. Mutin, H. Samson, and A. Vioux, J. Polym. Sci., A, Polym. Chem., 32, 187 (1994).
5. b) R. E. Burks, Jr., E. R. Covington, M. V. Jackson, and J. E. Curry, J. Polym. Sci., Polym. Chem., 11, 319 (1973).
6. c) P. R. Dvornic and R. W. Lenz, J. Polym. Sci., Polym. Chem., 20, 951 (1982).
7. d) E. A. Williams, J. H. Wengrovius, V. M. Van Valkenburgh, and J. F. Smith, Macromolecules, 24, 1445 (1991).
8. a) S. A. Nye and S. A. Swint, J. Polym. Sci., A, Polym. Chem., 32, 131 (1994).
9. b) J. E. Curry and J. D. Byrd, J. Appl. Polym. Sci., 9, 295 (1965).
10. H. Krimm and H. Schnell, Ger. 1136114 (to Farben-fabriken Bayer A. -G.): Chem. Abstr., 59, 11732g (1963).
11. a) H. Yamashita, N. P. Reddy, and M. Tanaka, Macromolecules, 26, 2143 (1993).
12. b). H. Yamashita, N. P. Reddy, and M. Tanaka, Organometallics, 16, 5223 (1997).
13. N. P. Reddy, H. Yamashita, and M. Tanaka, J. Am. Chem. Soc., 114, 6596 (1992).
14. 8
15. A. Purkayashtha and J. B. Baruah, the 12th International Symposium on Organosilicon Chemistry, Sendai, May 24, 1999, Abstr., No. P171.
16. Almost the same result was obtained when 1a and 2a were used in a 1 : 1 ratio.
17. The quantity of hydrogen generated in the reaction of 1a with 2a was finally 0.51 mmol.
18. 2Si: C 72.70: H 4.57%.
19. Bakola-Christianopoulou, J. Mol. Catal., 65, 307 (1991).
20. a) Y. Tamai and K. Itoi, Japan. Kokai 73-91024 (to Kuraray Co., Ltd.); Chem. Abstr., 80, 145798c (1974).
21. b) A. S. Berenblyum, A. G. Knizhnik, S. L. Mund, and I. I. Moiseev, J. Organomet. Chem., 234, 219 (1982).
22. a) L. H. Sommer and J. E. Lyons, J. Am. Chem. Soc., 91, 7061 (1969).
23. b) Y. Li and Y. Kawakami, Macromolecules, 32, 3540 (1999).
24. 6)] synthesized according to a literature. See B. Rezzonico and M. Grignon-Dubois, Organometallics, 17, 2656 (1998).