Fig. 3.
a) Schematic of polyacene synthesis using the MOF. b) Solid-state 13C NMR spectra of BBMN, BBMA, PNTD, PATD, and polyacene. The asterisk (*) corresponds to spinning side bands. c) FT-IR spectra of tetracene, pentacene, hexacene, heptacene, and polyacene synthesized using the MOFs (left). The relative peak area of SOLO and QUATRO vibration modes (ASOLO:AQUATRO) plotted against the number of benzene rings for the acene series (right) (black, tetracene; purple, pentacene; sky blue, hexacene; green, heptacene; blue, polyacene from PNTD; red, polyacene from PATD). The mean number of benzene rings in polyacene was calculated using the correlation between ASOLO:AQUATRO and the number of benzene rings (dotted line). Reprinted with permission from Kitao et al.46 Copyright 2023 Macmillan Publishers Ltd.

a) Schematic of polyacene synthesis using the MOF. b) Solid-state 13C NMR spectra of BBMN, BBMA, PNTD, PATD, and polyacene. The asterisk (*) corresponds to spinning side bands. c) FT-IR spectra of tetracene, pentacene, hexacene, heptacene, and polyacene synthesized using the MOFs (left). The relative peak area of SOLO and QUATRO vibration modes (ASOLO:AQUATRO) plotted against the number of benzene rings for the acene series (right) (black, tetracene; purple, pentacene; sky blue, hexacene; green, heptacene; blue, polyacene from PNTD; red, polyacene from PATD). The mean number of benzene rings in polyacene was calculated using the correlation between ASOLO:AQUATRO and the number of benzene rings (dotted line). Reprinted with permission from Kitao et al.46 Copyright 2023 Macmillan Publishers Ltd.

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