Spectroscopic analysis of methacrylate groups introduced on silica particle surfaces by the aza-Michael addition reaction
- 75 Downloads
- 2 Citations
Abstract
We modified silica nanoparticles with a N′-(3-trimethoxysilylpropyl)diethylenetriamine (TPDT) silane coupling agent, which has one primary and two secondary amino groups in each molecule, to introduce amino groups on silica surfaces. After surface modification of silica, we used an acrylate group containing 3-(acryloyloxy)-2-hydroxypropyl methacrylate (AHM) to introduce free radical polymerizable methacrylate groups by the aza-Michael addition reaction. Fourier transform infrared spectroscopy (FTIR), elemental analysis (EA), liquid state 1H and 13C nuclear magnetic resonance spectroscopy (NMR) and solid state cross polarization magic angle spinning (CP/MAS) 29Si NMR were used to investigate the effects of various reaction conditions on the degree of reaction between the N-H groups of the TPDT-modified silica surface and the acrylate groups of AHM. We found that approximately 48% of the N-H groups of the TPDT-modified silica surface reacted with the acrylate groups of AHM, compared with approximately 83% of the N-H groups of pure TPDT reacting with the acrylate groups of AHM at the same reaction conditions. This lower degree of the aza-Michael addition reaction between the N-H groups of the TPDT grafted on the solid silica particle versus the N-H groups of pure TPDT, both with acrylate groups of liquid AHM, may be caused by the lower mobility of the N-H groups of the grafted TPDT on the solid silica particle and the higher steric hindrance caused by the solid silica particle.
Keywords
Silica Silane Coupling Agent Hydrolysis Michael Addition Reaction Methacrylate GroupsPreview
Unable to display preview. Download preview PDF.
References
- 1.N. Rakhshan and M. Pakizeh, Korean J. Chem. Eng., 32, 2524 (2015).CrossRefGoogle Scholar
- 2.S.W. Kim, Korean J. Chem. Eng., 28, 298 (2011).CrossRefGoogle Scholar
- 3.S. M. Senani, C. Bonhomme, F. Ribot and F. Babonneau, J. Sol-Gel Sci. Technol., 50, 152 (2009).CrossRefGoogle Scholar
- 4.E. F. Vansant, P. Van der Voot and V. C. Vrancjen, in Characterization and Chemical Modification of the Silica Surface, Elsevier, Amsterdam (1995).Google Scholar
- 5.R.H. Halvorson, R. L. Erickson and C. L. Davidson, Dent. Mater., 19, 327 (2003).CrossRefGoogle Scholar
- 6.S. Lee and K. Ha, Polymer (Korea), 38, 257 (2014).CrossRefGoogle Scholar
- 7.H. N. Jeon and K. Ha, Polymer (Korea), 36, 668 (2012).CrossRefGoogle Scholar
- 8.T. Ishii, S. Fujioka, Y. Sekiguchi and H. Kotsuki, J. Am. Chem. Soc., 126, 9558 (2004).CrossRefGoogle Scholar
- 9.B.D. Mather, K. Viswanathan, K. M. Miller and T. E. Long, Prog. Polym. Sci., 31, 487 (2006).CrossRefGoogle Scholar
- 10.Gelest, Inc., Silane Coupling Agents, Mossisville, PA, USA, 3 (2006).Google Scholar
- 11.E. Satu, I. L. Eero and N. Lauri, J. Phys. Chem. B, 108, 9650 (2004).CrossRefGoogle Scholar
- 12.G.K. Dirk and B. Thomas, Langmuir, 11, 3061 (1995).CrossRefGoogle Scholar
- 13.T. Hooshmand, R.V. Noort and A. Keshvad, Dent. Mater., 20, 635 (2004).CrossRefGoogle Scholar
- 14.S.H. Yoo, H. J. Song and C. K. Kim, Polymer (Korea), 36, 721 (2012).CrossRefGoogle Scholar
- 15.J. P. Matinlinna, S. Areva, V. J. Lassila and P. K. Vallittu, Surf. Interface Anal,, 36, 1314 (2004).CrossRefGoogle Scholar
- 16.M. Michell, M. Tania, B. Guido, C. Lucia, C. Giovanna, C. Maila and T. Antonio, J. Phys. Chem. B, 108, 3563 (2004).CrossRefGoogle Scholar
- 17.M.-C. B. Salon, M Abdelmouleh, S. Boufi, M. N. Belgacem and A. Gandini, J. Colloid Interface Sci., 289, 249 (2005).CrossRefGoogle Scholar
- 18.M.-C. B. Salon, G. Gerbaud, M. Abdelmouleh, C. Bruzzese, S. Boufi and M.N. Belgacem, Magn. Reson. Chem., 45, 473 (2007).CrossRefGoogle Scholar
- 19.J. Kamer, A. Scholten, W. L. Driessen and J. Reedijk, Eur. J. Inorg. Chem., 6, 1488 (2002).CrossRefGoogle Scholar
- 20.D.W. Mayo, F. A. Miller and R.W. Hannah, Course Notes on the Interpretation of Infrared and Raman Spectra, Wiley, Hoboken, New Jersey, Chap. 7 (2004).CrossRefGoogle Scholar
- 21.L. Martin, J.O. Osso, S. Ricart, A. Roig, O. Garcia and R. Sastre, J. Mater. Chem., 18, 207 (2008).CrossRefGoogle Scholar
- 22.W. Decheng, L. Ye, H. Chaobin, C. Taishung and G. Suathong, Macromolecules, 37, 6763 (2004).CrossRefGoogle Scholar
- 23.S.B. Zeynep, D.O. Oznur, I. Mehtap and A. Duygu, J. Polym. Sci. Part A: Polym. Chem., 49, 5042 (2011).CrossRefGoogle Scholar