Preparation, characterization and application of a nanostructured composite: Octakis(cyanopropyldimethylsiloxy)octasilsesquioxane
Source abstract
Abstract
Abstract Octakis(cyanopropyldimethylsiloxy)octasilsesquioxane was prepared and characterized by 13C, 29Si NMR (MAS), SEM, FT-IR, XRD and thermogravimetric techniques. The four groups α, β, γ, κ (to the terminal silicon atom), associated with an acrylonitrile, were clearly seen in the 13C NMR (α-CH2 at 17.9; β-CH2 at 31.3; γ-CH2 at 50.4; κ-C N at 59.0 ppm). The 29Si NMR spectrum of the final product, exhibits only Q type silicon signal, ascribed to Q4 (−118.0 ppm). The presence of acrylonitrile substituted for octameric cube confers a relative change phase and thermal stability to the material. With regard to the applications for this new material, it was intended, in this case, to react with Na2[Fe(CN)5NH3] by chemical substitution. This composite was incorporated into a carbon paste electrode and the electrochemical studies were performed by cyclic voltammetry. The cyclic voltammogram of the modified graphite paste electrode, showed one redox couples with formal potential ( E 1 / 2 ox ) = 0.24 V versus SCE.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Silicone and Siloxane Chemistry · Synthesis and characterization of novel inorganic/organometallic compounds · Muon and positron interactions and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (27)
Show source-provided references
1. International Union of Pure and Applied Chemistry (IUPAC) 67 (1995).
2. Baney · Chem. Rev. · 1995 · 95 · 140910.1021/cr00037a012 ↗
3. Voronkov · Top. Curr. Chem. · 1982 · 102 · 19910.1007/3-540-11345-2_12 ↗
4. Zhang · J. Organomet. Chem. · 1996 · 521 · 19910.1016/0022-328X(96)06364-4 ↗
5. Provatas · Trends Polym. Sci. · 1997 · 5 · 327
6. Feher · J. Am. Chem. Soc. · 1989 · 111 · 174110.1021/ja00187a028 ↗
7. K. Kadama, M. Sugimura, H. Yuda, Japanese Patent 06 271 771.
8. Harrison · J. Organomet. Chem. · 1997 · 542 · 14110.1016/S0022-328X(96)06821-0 ↗
9. Feher · Polyhedron · 1995 · 14 · 323910.1016/0277-5387(95)85009-0 ↗
10. Moran · Organometallics · 1993 · 12 · 432710.1021/om00035a018 ↗
11. Jaffres · J. Chem. Soc. Dalton Trans. · 1998 · 16 · 276710.1039/a801510d ↗
12. Hong · Inorg. Chem. · 1997 · 36 · 614610.1021/ic971034j ↗
13. Feher · J. Am. Chem. Soc. · 1994 · 116 · 214510.1021/ja00084a065 ↗
14. Abbenhuis · Chem. Eur. J. · 2000 · 6 · 2510.1002/(SICI)1521-3765(20000103)6:1<25::AID-CHEM25>3.0.CO;2-Y ↗
15. Lucke · Appl. Surf. Sci. · 1999 · 145 · 71310.1016/S0169-4332(98)00912-X ↗
16. Hasegawa · J. Organomet. Chem. · 1992 · 441 · 37310.1016/0022-328X(92)80168-W ↗
17. Hasegawa · Trends Organomet. Chem. · 1994 · 1 · 131
18. Do Carmo · Mater. Res. · 2004 · 7 · 49910.1590/S1516-14392004000300020 ↗
19. Organic/inorganic hybrid materials
20. Gol’tsov · Russ. J. Electrochem. · 1995 · 31 · 19
21. Denq · J. Appl. Polym. Sci. · 1999 · 74 · 22910.1002/(SICI)1097-4628(19991003)74:1<229::AID-APP28>3.0.CO;2-C ↗
22. Bassindale · J. Organomet. Chem. · 1996 · 521 · 39110.1016/0022-328X(96)06322-X ↗
23. Provatas · J. Organomet. Chem. · 1998 · 565 · 15910.1016/S0022-328X(98)00450-1 ↗
24. Dittimar · J. Organomet. Chem. · 1995 · 489 · 18510.1016/0022-328X(94)05100-P ↗
25. Wang · Thermochim. Acta · 2002 · 381 · 8310.1016/S0040-6031(01)00644-X ↗
26. Ford · Coord. Chem. Rev. · 1970 · 5 · 7510.1016/S0010-8545(00)80075-2 ↗
27. Bard · 1980