High-Yield Molecular Borazine Precursors for Si−B−N−C Ceramics

Abstract

The synthesis of Si−B−N−C ceramic materials can be accomplished via two different routes using B-tris(trichlorosilylvinyl)borazine ( 2 ) as starting material. This silyl-functionalized ethinylborazine is obtained by Pt-catalyzed hydrosilylation of B, B‘, B‘ ‘-tri-ethynylborazine ( 1) with HSiCl 3 in quantitative yield with a selectivity of 80% β-substituted product. Amminolysis of 2 with methylamine leads to the soluble silazane polymer P3 which contains intact borazine rings connected by CH CH Si NMe linkages. In a second approach, the trichlorosilyl groups of 2 are hydrogenated to yield the B-tris(hydrosilylvinyl)borazine ( 4 ). With polymer P3 or 4, a highly durable Si−B−N−C ceramic is obtained after pyrolysis under inert atmosphere. The composition SiBN 1+ x C 2 of the ceramic material corresponds exactly to the backbone of the precursor molecules 2 or 4, and very compact materials are obtained in each case. The ceramic yield of approximately 94% starting from the silane precursor 4 sets a new standard for this type of ceramics using the pyrolysis of a single site molecular precursor. Conductivity measurements show a semiconductor behavior of the ceramic at about 10 2 (Ωm) - 1 at room temperature. The composition of the ceramic was characterized by laser-ablation ICP-MS, which was used for that purpose for the first time. The very satisfying results demonstrate the high potential of this direct solid sampling technique.