“…As can be seen from Fig. 2 (a), the IR spectra of the starting precursors of HKH and BPTA are distinct from that of C 4 N. The carbonyl group (C = O) at 1637 cm −1 for HKH disappears while the characteristic band at 1612 cm −1 assigned to C = N stretching in pyrazine rings appears, confirming the formation of the C 4 N chemical structure [26] . In the solid -state 13 C NMR spectra, C 4 N exhibited two NMR signals located at 129 and 141 ppm attributed to the C = C carbons of benzene rings and the C = N carbons in pyrazine rings of C 4 N, respectively, and no residual carbonyl signal around 190 ppm of the starting monomer HKH was observed [27] , which further verify the successful generation of the C 4 N structure ( Fig.…”