Alkoxysilane functionalized isocyanurates were prepared from hexamethylene
diisocyanate (HDI) isocyanurate and 3-aminopropyltriethoxysilane. The react
ants and functionalized isocyanurate were characterized by H-1, C-13 and Si
-29 NMR, IR and electrospray ionization-mass spectrometry. Two-dimensional
NMR was necessary to accurately assign the proton and carbon spectra for bo
th the reactants and functionalized products. The composition of the HDI is
ocyanurate was a mixture of oligomers ranging from two to three HDI monomer
s. The functionalization reaction was performed neat, and as a function of
dilution. As expected, substitution on the isocyanurate becomes more unifor
m with increasing solvent content. (C) 1999 Elsevier Science Ltd. All right
s reserved.