journal article·2004-02-01

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

Jörg Haberecht, Frank Krumeich, Hansjörg Grützmacher, Reinhard Nesper

Chemistry of Materials· Volume 16· Issue 3
Publisher page

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.
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Research context

OpenAlex topics: Advanced ceramic materials synthesis · MXene and MAX Phase Materials · Boron and Carbon Nanomaterials Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Laboratory of Inorganic Chemistry, ETH Zurich, W.-Pauli-Strasse 10, CH-8093 Zurich, Switzerland

References (43)

Show source-provided references
1. Baldus H. P. · Angew. Chem., Int. Ed. Engl. · 1997 · 36 · 32910.1002/anie.199703281 ↗
2. Jansen M. · 1992
3. Riedel R. · Nature · 1996 · 382 · 79610.1038/382796a0 ↗
4. Kroke E. · Mater. Sci. Eng. · 2002 · 26 · 9710.1016/S0927-796X(00)00008-5 ↗
5. Yajima S. · Nature · 1976 · 261 · 68310.1038/261683a0 ↗
6. Takamizawa M. · 1986
7. Komeya K. · Mater. Sci. Technol. · 1994 · 11 · 517
8. Jansen, M.; Jaeschke, T.; Jaeschke, B. InHigh-Performance Non-OxideCeramics I; Jansen, M., Ed.; Springer-Verlag: Berlin, Heidelberg, 2002; Vol. 101, p 137.
9. Seifert, H. J.; Aldinger, F. InHigh Performance Non-Oxide Ceramics I; Jansen, M., Ed.; Springer-Verlag: Berlin, Heidelberg, 2002; Vol. 101, p 1.
10. Muetterties E. L. · 1975
11. Schleyer P. v. R. · J. Am. Chem. Soc. · 1997 · 119 · 1266910.1021/ja9719135 ↗
12. Kiran B. · Inorg. Chem. · 2001 · 40 · 361510.1021/ic001394y ↗
13. Fowler P. W. · J. Phys. Chem. A · 1997 · 101 · 140910.1021/jp9637946 ↗
14. Chem. Mater. · 1996 · 8 · 310.1021/cm950398b ↗
15. Recently · 2001
16. The · Eur. J. Inorg. Chem. · 1998 · 1998 · 85510.1002/(SICI)1099-0682(199806)1998:6<855::AID-EJIC855>3.0.CO;2-M ↗
17. For · Chem. Mater. · 1993 · 5 · 54710.1021/cm00028a024 ↗
18. Appl. Organomet. Chem. · 2000 · 14 · 67110.1002/1099-0739(200011)14:11<671::AID-AOC65>3.0.CO;2-I ↗
19. Cheng F. · J. Organomet. Chem. · 2002 · 657 · 7110.1016/S0022-328X(02)01566-8 ↗
20. Bai J. · Inorg. Chem. · 1991 · 30 · 463110.1021/ic00024a033 ↗
21. Blanchard C. · 1993
22. Wideman T. · Inorg. Synth. · 1998 · 32 · 23210.1002/9780470132630.ch39 ↗
23. Haberecht J. · Dalton Trans. · 2003 · 11 · 212610.1039/B302275G ↗
24. Nesper R. · 2003
25. Weinmann, M.Chemiedozentagung; Chemnitz, 2003.
26. Nöth H. · 1985 · 14
27. Rappoport Z. · 2001 · 310.1002/0470857269 ↗
28. Marsmann · 1987 · 17 · 65
29. Schrock R. · Z. Naturforsch. (B) · 1994 · 49 · 103610.1515/znb-1994-0805 ↗
30. Hassler, K.; Köll, W.; Pöschel, U. InOrganosilicon Chemistry III; Auner, N., Weiss, J., Eds.; Wiley-VCH: Weinheim, 1997; p 301.
31. Rudinger C. · Chem. Ber.-Recl. · 1992 · 125 · 140110.1002/cber.19921250616 ↗
32. Beach D. B. · Inorg. Chem. · 1992 · 31 · 417410.1021/ic00046a035 ↗
33. van Wüllen L. · Chem. Mater. · 2000 · 12 · 234710.1021/cm001016r ↗
34. Weinmann M. · Chem. Mater. · 2000 · 12 · 62310.1021/cm9910299 ↗
35. Weinmann M. · Chem. Mater. · 2000 · 12 · 211210.1021/cm001031w ↗
36. Krummland, A. Ph.D. Thesis, ETH Zurich, No. 14179, 2001.
37. Müller U. Ph.D. · 2002
38. van Wüllen L. · Angew. Chem., Int. Ed. · 2000 · 39 · 251910.1002/1521-3773(20000717)39:14<2519::AID-ANIE2519>3.0.CO;2-G ↗
39. Jansen M. · Z. Anorg. Allg. Chem. · 2000 · 626 · 163410.1002/1521-3749(200007)626:7<1634::AID-ZAAC1634>3.0.CO;2-1 ↗
40. Schuhmacher J. Ph.D. · 2000
41. Günther D. · Fresenius' J. Anal. Chem. · 2000 · 368 · 410.1007/s002160000495 ↗
42. Günther D. · J. Anal. At. Spectrom. · 1997 · 12 · 93910.1039/A701423F ↗
43. Lide D. R. · 2002