The molecular carbon nanoring, cycloparaphenylene (CPP), is fascinating as a new class of carbonaceous porous solids with the uniform structure of an all-benzene surface. We explored the feasibility of [12]CPP as a carbon-based porous material and uncovered its unique adsorption properties due to its shape and highly nonpolar surface. Unlike other porous carbon solids, [12]CPP shows stepwise adsorption behaviors sensitive to the functionalities of the guest molecules. In situ powder X-ray diffraction and infrared spectra provided insights into how [12]CPP accommodates the guest molecules with structural deformation retaining its structural periodicity during the whole adsorption process, which exemplifies that this molecular nanoring represents an unprecedented carbon-based soft porous solid.

A novel thermotropic liquid-crystalline (LC) biocopolymer, poly{trans-3-methoxyl-4-hydroxycinnamic acid (MHCA: ferulic acid)-co-trans-3,4-dihydroxycinnamic acid (DHCA: caffeic acid)}, was synthesized by a thermal acidolysis-polycondensation of MHCA and DHCA, efficiently catalyzed by Na₂HPO₄. When the MHCA composition of poly(MHCA-co-DHCA) was 60, 75, and 90 mol %, the copolymers showed a nematic LC phase although individual homopolymers such as polyMHCA and polyDHCA did not exhibit LC phase. Poly(MHCA-co-DHCA)s showed high molecular weight (M _w) ranged between M _n 2.6 × 10⁴ to 3.7 × 10⁴ and M _w 8.2 × 10⁴ to 13.1 × 10⁴, respectively, high glass-transition temperature (T _g) with the range of 115 to 140 °C and high degradation temperature T ₁₀, from 315 to 356 °C. In the adhesive test of copolymers against the surface of carbon substrate, the copolymers showed high shear strength at fracture.