Deuteron NMR resolved mesogen vs. crosslinker molecular order and reorientational exchange in liquid single crystal elastomers

Differences in the temperature behaviour of orientational ordering of structurally equivalent side-chain liquid single crystal elastomers (LSCEs) with ²H-labelled crosslinker and mesogen have been studied by deuteron quadrupole-perturbed NMR. The impact of nematic director reorientations on the deuteron NMR spectral shapes was analyzed in terms of a discrete reorientational exchange model. This provided for the determination of the degree of nematic director alignment and for the quantification of the influence of the reorientational exchange on the ²H NMR spectra in terms of two parameters, the nematic director orientational dispersion parameter σ_θ and the motional effectiveness parameter α. A comparative analysis of model simulations and experimental spectra reveals that mesogenic molecules in LSCEs exhibit faster reorientational dynamics as compared to crosslinker molecules and that mesogens and crosslinkers exhibit a similar and rather substantial static director orientational disorder.