The effects of the chain length, active end group and concentration on the association of living polystyryllithium (PS(-)Li(+)) chains in benzene were examined by a combination of static and dynamic laser light scattering in a cuvette equipped with a high-vacuum stopcock. The results show that long PS(-)Li(+) chains (M(w) > 1 x 10(4)) usually form dimers in the solution. In contrast, shorter PS(-)Li(+) chains exhibit two relaxation modes, where the fast mode is related to the translational diffusion of the living chain dimers. The end capping of the living chain with bulky 1,1-diphenylethene (DPE) leads to an intensity increase of the slow mode, indicating that the slow mode is not due to the chain aggregates but to temporal aggregates or long-range density fluctuation induced by weak electrostatic dipole-dipole interaction between ionic pairs at the chain ends.
A high molecular weight (M_w=1.85×10~7) polystyrene (PS) with narrow distribution was prepared by high vacuum anionic polymerization in tetrahydrofuran.By use of dynamic light scattering,the dynamics of PS chains in cyclohexane was studied around theθtemperature.For the first time,we have observed the internal motion of polymer chains in solutions below theθtemperature by using dynamic light scattering at smaller angles (even qR_g<1).
