Influence of the spacer and molecular weight on the phase behavior of side-chain liquid crystalline polymers containing triphenylene discotic mesogen units as side groups

Two series of side chain liquid crystalline polymers (SCLCPs), poly{[3,6,7,10,11-pentakis(hexyloxy)-2-oxy-triphenylene]methacrylate} (PMTS with no flexible spacer) and poly{6-[3,6,7,10,11-pentakis(hexyloxy)-2-oxytriphenylene]hexyl methacrylate} (PMT6S with 6 methylene units as a flexible spacer), with different molecular weights (M-n) and low molecular weight distributions have been successfully synthesized via atom transfer radical polymerization (ATRP). The phase behavior of the polymers has been investigated by a combination of techniques, including differential scanning calorimetry (DSC), polarized optical microscopy (POM), and 1D and 2D wide-angle X-ray diffraction (1D and 2D WXRD). The experimental results revealed that the LC phase structures of PMTS were found to be strongly M-n dependent. The PMTS polymers were amorphous when the Mn was lower than a critical Mn of approximately 2.03 x 10(4) g mol(-1). When the Mn was higher than this critical value, the PMTS polymers displayed a rectangular (Phi(R)) columnar phase. On the contrary, the PMT6S polymers displayed a higher symmetry hexagonal (Phi(H)) columnar phase, which was independent of M-n. A comparison between PMTS and PMT6S suggested that the spacer plays an important role in the construction of liquid crystalline (LC) ordered structures. For the former, PMTS polymers without the spacer formed rectangular Phi(R) phases caused by the Tp moieties and the main chain as a whole, due to the strong coupling effect between the Tp moieties and the main chain. For the latter, PMT6S polymers with 6 methylene units as a flexible spacer gave a higher symmetry FH phase owing to the decoupling and self-organization of the Tp moieties.