“…So the fusions of a benzene or naphthalene on the one-sided benzene ring of CZ could expand the π-conjugation and keep the electron-donating ability of CZ . 44–48 The CZ -based donors could be diversified in the form of the structural isomers through the extended conjugation in different directions. Thus donor units of 11-phenyl-11 H -benzo[ a ]carbazole ( PB[ a ]CZ ), 5-phenyl-5 H -benzo[ b ]carbazole ( PB[ b ]CZ ), 7-phenyl-7 H -benzo[ c ]carbazole ( PB[ c ]CZ ), 13-phenyl-13 H -naphtho[ a ]carbazole ( PN[ a ]CZ ), 5-phenyl-5 H -naphtho[ b ]carbazole ( PN[ b ]CZ ), and 9-phenyl-9 H -naphtho[ c ]carbazole ( PN[ c ]CZ ) are the candidates to construct D–A type molecules with BN and BPN , as illustrated in Fig.…”