Copy the page URI to the clipboard
Bassindale, Alan Richard; Parker; Taylor, Peter Geoffrey and Watt, Alison Claire
(2003).
DOI: https://doi.org/10.1139/V03-138
URL: http://search.ebscohost.com/login.aspx?direct=true...
Abstract
The products from the reaction of octahydrosilsesquioxane (T-8-H) with different molar ratios of phenol and undec-1-ene or methyl 3,3-dimethylpent-4-enoate (MDP) in the presence of chloroplatinic acid have been analysed by Si-29 NMR spectroscopy. The distribution of the two different pendant groups leads to tetrad patterns where the relative chemical peak intensities reflect the selectivity for particular patterns of substitution. As well as analysing the cause of these tetrad patterns we also discuss how the regioselectivity of hydrosilylation can be determined.