“…Herein, we designed and synthesized two groups of isomers (BP-DPA and BP-DMAc) based on biphenyl (BP) through changing the positions of diphenylamine (DPA) and 9,9-dimethyl-9,10-dihydroacridine (DMAc), which were named as N 2 ,N 2 ,N 2' ,N 2' -tetraphenyl-[1,1'-biphenyl]-2,2'-diamine (o-DDPA), N 3 ,N 3 ,N 3' ,N 3' -tetraphenyl-[1,1'-biphenyl]-3,3'-diamine (m-DDPA), N 4 ,N 4 ,N 4' ,N 4' -tetraphenyl-[1,1'-biphenyl]-4,4'-diamine (p-DDPA), 2,2'-bis(9,9-dimethylacridin-10(9H)-yl)-1,1'-biphenyl (o-DDMAc), 3,3'-bis(9,9-dimethylacridin-10(9H)-yl)-1,1'-biphenyl (m-DDMAc), and 4,4'-bis(9,9-dimethylacridin-10(9H)-yl)-1,1'-biphenyl (p-DDMAc), respectively. DPA and DMAc were donors widely used in luminescent materials [17,19,25,26] and biphenyl was utilized due to its simple structure. Expectably, the steady state conformations and luminescent efficiencies of the isomers were distinctly different.…”