Homopolymer and Random Copolymer of Polyhedral Oligomeric Silsesquioxane (POSS)-Based Side-Chain Polynorbornenes: Flexible Spacer Effect and Composition Dependence

A series of homopolymers and random copolymers of polyhedral oligomeric silsesquioxane (POSS)-based side-chain polynorbornenes were prepared using ring-opening metathesis polymerization. For the homopolymer P-<i>z</i>-POSS (<i>z</i> represents the spacer length, <i>z</i> = 5, 12, and 17), the POSS groups tethered to the side chain are linked to the polynorbornene backbone through the flexible spacer with different lengths. For the random copolymer P-6-<i>co</i>-17­(<i>X</i>/<i>Y</i>) (<i>X</i>/<i>Y</i> = 1/1, 3/1, 6/1, and 9/1), the composition was regulated by adjusting the molar feed ratio <i>X</i>/<i>Y</i> of the norbornene monomer with butyl ester side group (M-6) to the POSS containing monomer with the longest spacer (M-17-POSS). Using various techniques, we studied the spacer length effect on POSS crystallization of the homopolymers and the composition dependence of physical properties of the copolymers. It is found that P-5-POSS is amorphous. On the contrary, POSS crystallization is observed in P-12-POSS and P-17-POSS, and the longer the spacer is, the higher the POSS crystallization ability is. With the comonomer of M-17-POSS, all the P-6-<i>co</i>-17­(<i>X</i>/<i>Y</i>) samples can have the POSS group to crystallize, resulting in a nanosegregation similar to the lamellar morphology. The lamellar period is inversely proportional to the POSS volume fraction. The POSS crystallites are raft-like, containing two layers of POSS groups stacked together. Uniaxial stretching can well align the POSS crystallites in the copolymers to be parallel to the stretching direction, and the lamellar period is decreased with increasing the strain. Varying <i>X</i>/<i>Y</i> from 1/1 to 9/1 changes the copolymer from plastic to thermoplastic elastomer, wherein the latter takes the POSS crystallites as the physical cross-links

“Brill Transition” Shown by Green Material Poly(octamethylene carbonate)

Poly­(octamethylene carbonate) (POMC), as the eighth member of the newly developed biodegradable aliphatic polycarbonate family, demonstrates a reversible crystal–crystal transition, which is highly similar to Brill transition extensively studied in the nylon family. With the dipole–dipole interaction in POMC much weaker than the hydrogen bonding, POMC exhibits its “Brill transition” temperature at around 42 °C, much lower than nylons. The two crystalline structures of POMC at below and above the transition temperature can be identified. The transition of POMC is largely associated with the reversible conformation change of methylene sequences from trans-dominated at low temperatures to trans/gauche coexistence at high temperatures