Abstract
In this paper we discuss and interpret the results of shear bond strengths achieved after the use of two silane coupling agents with isocyanato functionality, viz. 3-isocyanatopropyltrimethoxysilane and 3-isocyanatopropyltriethoxysilane. The silanes were used alone and also blended with a non-functional cross-linking silane on silicatized zirconia before light-curing of resin stubs on the surface, as described elsewhere in the first part of our study (see “Part I: Experimental”). A series of reaction mechanisms and conceptual diagrams are also presented. The reaction mechanisms illustrating the effect of adding a cross-linking silane into a silane blend, the silane hydrolysis and the behavior of two organofunctional groups (isocyanate and alkene) of silanes upon reaction with Rely X Unicem Aplicap resin-composite cement are discussed in detail.
Original language | English |
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Pages (from-to) | 163–169 |
Number of pages | 7 |
Journal | Silicon |
Volume | 2 |
Issue number | 3 |
Early online date | 5 Jun 2010 |
DOIs | |
Publication status | Published - Jul 2010 |
Keywords
- bimolecular nucleophilic substitution (SN2) reaction
- transition state
- siloxane network
- free radical reaction
- 3-isocyanatopropyltriethoxysilane
- 3-isocyanatopropyltrimethoxysilane
- cycloaddition