Synthesis and ceramic conversion reactions of pinacolborane- amd diethylborazine-modified poly(vinylsiloxane)s. The development of a processable single-source polymeric precursor to boron-modified silicon carbide

被引:25
作者
Brunner, AR
Bujalski, DR
Moyer, ES
Su, K
Sneddon, LG [1 ]
机构
[1] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
[2] Univ Penn, Res Struct Matter Lab, Philadelphia, PA 19104 USA
[3] Dow Corning Corp, Cent Res & Dev, Rigid Mat Sci Expertise Ctr, Midland, MI 48686 USA
关键词
D O I
10.1021/cm000317y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The design, synthesis, and properties of two new types of poly(borosiloxane) preceramic polymers, diethylborazine- (PVS-DEB) and pinacolborane-modified (PVS-PIN) poly(vinylsiloxane)s, are reported. The polymers are synthesized in excellent yields by the RhH(CO)(PPh3)(3)-catalyzed reactions of poly(vinylsiloxane) (PVS) with either diethylborazine (DEB-H) or pinacolborane (PIN-H). The spectroscopic data for the polymers, along with results of the RhH(CO)(PPh3)(3)-catalyzed hydroboration reactions of diethylborazine and pinacolborane with the model compound vinyltris(trimethylsiloxy)silane, are consistent with predominately anti-Markovnikov hydroboration of the polymer vinyl groups by the boranes. The degree of polymer hydroboration is simply controlled by varying the reactant ratios with the compositions of the PVS-DEB polymer ranging from (MeSiO1.5)(0.42)(PhSiO1.5)(0.37)(ViMe(2)-SiO0.5)(0.17)(DEB(CH2)(2)Me2SiO0.5)(2) to (MeSiO1.5)(0.42)(PhSiO1.5)(0.37)(DEB(CH2)(2)Me2SiO0.5)(0.21) and those of the PVS-PIN polymers from (MeSiO1.5)(0.42)(PhSiO1.5)(0.37)(ViMe(2)SiO(0.5)) Me2SiO0.5)0.03 to (MeSiO1.5)(0.42)(PhSiO1.5)(0.37)(PIN(CH2)(2)Me2SiO0.5)(0.21) The borane-modified polymers are soluble and stable in ethers, acetone, methylene chloride, benzene, and pentane. Molecular weight analyses using SEG with refractive index, viscometry, and light-scattering triple detection show significant; differences in hydrodynamic volume, molecular weight, radius of gyration, and conformation, which indicate that the PVS-PIN and PVS-DEB polymers adopt a more branched and spherical structure compared to the unmodified PVS. Bulk pyrolysis of the modified resins produced SiOCB ceramic chars with boron contents ranging from 0.3 to 0.7% depending upon the percentage of polymer modification. XRD and TEM studies of the 1800 degrees C chars of PVS and PVS-PIN showed significant differences in the degree of grain growth and distribution with the boron-modified char showing both a smaller average crystallite size and a more narrow size range. The PVS-PIN polymers were found to be excellent melt-processable, single-source precursors to small-diameter SiOCB fibers.
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收藏
页码:2770 / 2780
页数:11
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