Chain Packing and Dynamics in Polycarbonate Block Copolymers

Dynamic mechanical-loss spectra at 1 Hz, and dipolar rotational spin-echo 13 C NMR spectra at 15.1 MHz, have been obtained for a series of copolymers of polycarbonate made from monodisperse oligomers of Bisphenol A polycarbonate (B X ), alternating ( via connecting carbonate linkages) with single units of 3,3‘,5,5‘-tetramethylbisphenol A (T). The mechanical-loss relaxation of B X T suggests cooperative motions in the copolymer glass at T = −100 and −20 °C. The NMR results indicate that no phenylene rings undergo π flips in T units and that most but not all of the B rings flip faster than 10 kHz at 300 K. A necessary but not sufficient condition to constrain a B ring from flipping in B X T is the presence of both interchain and intrachain T-unit nearest neighbors. These results are interpreted in terms of a packing model for polycarbonate-like systems that emphasizes the importance for chain dynamics of the proximity and cooperative motion of nearest-neighbor chains having similar local orientational order.