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0032497189
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The variety of sila[1]ferrocenophane functionality was previously restricted to that accessible via alkoxy, aryloxy, or amino substitution of Si-Cl bonds, see: Nguyen, P.; Stojcevic, G.; Kulbaba, K.; MacLachlan, M. J.; Liu, X. H.; Lough, A. J.; Manners, I. Macromolecules 1998, 31, 5977.
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33748500225
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Pt-catalyzed insertion of alkynes into the strained Si-Cp bond of sila[1]ferrocenophanes has been reported. See: Sheridan, J. B.; Temple, K.; Lough, A. J.; Manners, I. J. Chem. Soc., Dalton Trans. 1997, 711.
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note
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See the Experimental Section for details on the GPC procedure.
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48
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29Si NMR spectra. See: ref 18.
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52
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MacLachlan, M. J.; Ginzburg, M.; Coombs, N.; Coyle, T. W.; Raju, N. P.; Greedan, J. E.; Ozin, G. A.; Manners, I. Science 2000, 287, 1460.
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(a) Ceramic yields of 45% (1000 °C, 4 h) have been detected for poly(ferrocenylmethylvinylsilane). See: Petersen, R.; Foucher, D. A.; Tang, B.-Z.; Lough, A.; Raju, N. P.; Greedan, J. E.; Manners, I. Chem. Mater. 1995, 7, 2045.
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(b) The insoluble PFS poly(ferrocenyldihydrosilane) has a ceramic yield of 63% at 1000 °C. See: Pudelski, J. K.; Rulkens, R.; Foucher, D. A.; Lough, A. J.; Macdonald, P. M.; Manners, I. Macromolecules 1995, 28, 7301.
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1H NMR spectroscopy.
-
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60
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Bruker Analytical X-ray Systems: Madison, WI
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SHELXTL\PCV5.1
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Sheldrick, G.M.1
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