The twist and bend viscosities of dilute nematic solutions in 4'-(pentyloxy)-4-cyanobiphenyl (50CB) and in 4'-pentyl-4-cyanobiphenyl (5CB) of the main-chain liquid crystal polymers, TPB10 and TPB13, which have a mesogenic group, l-(4-hydroxy-4'-biphenyl)-2-(4-hydroxyphenyl)butane, separated, respectively, by flexible decamethylene and tridecamethylene spacers, were determined via dynamic light scattering analysis. A theoretical expression for the increment of twist viscosity, 71, derived by Brochard can be applied to interpret the experimental results in terms of changes in the mean square end-to-end distances parallel (R¡2) and perpendicular (R±2) to the nematic director. We find that the hydrodynamic behavior ofTPBlO oligomers moves closer to that predicted for a rigid rod as the temperature decreases. By modeling the oligomers as a mixture of configurational isomers, the hairpin probability per repeat unit and the associated activation energy can be found. The latter is approximately twice the energy barrier of a trans to gauche transformation. As the molecular weight is increased from oligomers to polymers a decrease in the exponent characterizing the contour length dependence of the intrinsic twist and bend viscosities, [71] and [m»nd], is found, emblematic of a crossover from rigid rod to biased random walk behavior. The effect of absolute temperature on the viscometric properties of TPB13 polymer (GPC determined Mw = 79100 g/mol) was studied by comparing the viscosity in high and low temperature nematic solvents at equal order parameters, viz. TPB13/5CB at T = 27.3 °C and TPB13/50CB at T = 62.0 °C. A large increase in [71] but negligible change in [tjbendl was found on decreasing temperature.