1. Han, Y., Mayer, D., Offenhäusser, A., and Ingebrandt, S. Surface activation of thin silicon oxides by wet cleaning and silanization. Thin Solid Films, 2006, 510, 175–180.
doi:10.1016/j.tsf.2005.11.048

  2. Qin, M., Hou, S., Wang, L. K., Feng, X. Z., Wang, R., Yang, Y. L., Wang, C., Yu, L., Shao, B., and Qiao, M. Q. Two methods for glass surface modifica­tion and their application in protein immobilization. Colloids Surf., B, 2007, 60, 243–249.
doi:10.1016/j.colsurfb.2007.06.018

  3. Aziz, A., Patra, S., and Yang, H. A facile method of achieving low surface coverage of Au nanoparticles on an indium tin oxide electrode and its application to protein detection. Chem. Commun., 2008, 38, 4607–4609.
doi:10.1039/b808026g

  4. Kozma, P., Nagy, N., Kurunczi, S., Petrik, P., Hameri, A., Muskotal, A., Vondervizt, F., Frid, M., and Barsony, I. Ellipsometric characterization of flagellin films for biosensor applications. Phys. Stat. Sol. (c)., 2008, 5(5), 1427–1430.
doi:10.1002/pssc.200777845

  5. Oh, S., Kang, T., Kim, H., Moon, J., Hong, S., and Yi, J. Preparation of novel ceramic membranes modified by mesoporous silica with 3-aminopropyltriethoxysilane (APTES) and its application to Cu²⁺ separation in the aqueous phase. J. Membrane Sci., 2007, 301(1 + 2), 118–125.
doi:10.1016/j.memsci.2007.06.006

  6. Zhang, L., Yu, C., Zhao, W., Hua, Z., Chen, H., Li, L., and Shi, J. Preparation of multi-amine-grafted mesoporous silicas and their application to heavy metal ions adsorption. J. Non-Crys. Solids, 2007, 353, 4055–4061.

  7. Yang, H., Xu, R., Xue, X., Li, F., and Li, G. Hybrid surfactant-templated mesoporous silica formed in ethanol and its application for heavy metal removal. J. Hazard. Mater., 2008, 152(2), 690–698.
doi:10.1016/j.jhazmat.2007.07.060

  8. Mayani, V. J., Abdi, S. H. R., Kureshy, R. I., Khan, N. H., Agrawal, S., and Jasra, R. V. Synthesis and charac­teriza­tion of mesoporous silica modified with chiral auxiliaries for their potential application as chiral stationary phase. J. Chromatogr. A., 2008, 1191, 223–230.
doi:10.1016/j.chroma.2008.02.041

  9. Speier, J. L., Webster, J. A., and Barnes, G. H. The addidion of silicon hydrides to olefinic double bonds. Part II. The use of group VIII metal catalysts. J. Am. Chem. Soc., 1957, 79(4), 974–979.
doi:10.1021/ja01561a054

10. Takatsuna, K., Tachikawa, M., Shlozawa, K., Oka­moto, N., and Okumura, Y. Process for preparing aminopropyl alkoxy silanes. EP0302672, 1988.

11. Shizawa, K., Okamoto, N., Takai, H., Okumura, Y., Takatsuna, K., and Imai, C. Process for preparing aminopropyl alkoxy silanes. EP0284447, 1988.

12. Takatsuna, K., Nakajima, M., Tachikawa, M., Shino­hara, A., Shiozawa, K., and Okumura, Y. Process for preparing aminopropyl alkoxy silanes. EP0321174, 1988.

13. Kalia, J. and Raines, R. T. Hydrolytic stability of hydrazones and oximes. Angew. Chem. Int. Ed., 2008, 47(39), 7523–7526.
doi:10.1002/anie.200802651

14. Põhako, K., Mäeorg, U., Saal, K., Kisseljova, K., Bredih­hin, A., and Kink, I. A route towards a new hydrazino-ormosil. J. Phys.: Conf. Ser., 2007, 93.

15. Sabourault, N., Mignani, G., Wagner, A., and Mios­kowski, C. Platinum oxide (PtO₂): a potent hydro­silylation catalyst. Org. Lett., 2002, 4(13), 2117–2119.
doi:10.1021/ol025658r

16. Condon, F. E. The influence of hydration on base strength. III. Alkylhydrazines. J. Am. Chem. Soc., 1965, 87(20), 4491–4494.
doi:10.1021/ja00948a015

17. Schmidt, E. W. Hydrazine and Its Derivatives: Prepara­tion, Properties, Applications. John Wiley and Sons, New York, 2001.

18. Satyanarayana, S. V. and Bhattacharya, P. K. Pervapora­tion of hydrazine hydrate: separation characteristics of membranes with hydrophilic to hydrophobic behavior. J. Membrane Sci., 2004, 238, 103–115.
doi:10.1016/j.memsci.2004.03.025

19. Ioffe, B. V., Sergeeva, Z. I., and Kochetov, A. P. Synthesis and properties of allylhydrazines. Zh. Org. Khim., 1967, 3(6), 983–988 (in Russian).

20. Nakagawa, M., Sogawa, M., and Shimada, K. Preparation of monoallylhydrazine. JP 07112963 A2, 1995.

21. Mäeorg, U., Grehn, L., and Ragnarsson, U. Prototypical reagent for synthesis of substituted hydrazines. Angew. Chem. Int. Ed., 1996, 35(22), 2626–2627.
doi:10.1002/anie.199626261

22. Põhako, K., Saal, K., Kink, I., Bredihhin, A., and Mäe­org, U. Synthesis of allyl hydrazine: a comparative study of different methods. Arkivoc, 2008, IX, 116–125.

23. Penneman, R. A. and Audrieth, L. F. The ternary system: hydrazine-water-sodium hydroxide. J. Am .Chem. Soc., 1949, 71(5), 1644–1647.
doi:10.1021/ja01173a030

24. Hale, F. C. and Shetterly, F. F. Anhydrous hydrazine I. A convenient apparatus for the preparation of anhydrous hydrazine. J. Am. Chem. Soc., 1911, 33(7), 1071–1076.
doi:10.1021/ja02220a007

25. Burfield, D. R., Smithers, R. H., and Sui Chai Tan, A. Desiccant efficiency in solvent and reagent drying. 5. Amines. J. Org. Chem., 1981, 46(3), 629–631.
doi:10.1021/jo00316a030

26. Zhun, V. I., Zhun, A. B., Vlasenko, S. D., Belo­russ­kaya, L. A., Chernyshe, E. A., and Sheludyakov, V. D. Reactivity of silicon–hydrogen bonds in organo­silanes. Zh. Obsh. Khim., 1982, 52(11), 2565–2570 (in Russian).