“…The strong emission peak could be assigned to metal chain centered emission, which originates from the Cd II −O−Cd II charge transfer (O → Cd II ) excited state. 63 The weak shoulder peak at 557 nm can be attributed to the ligand-centered π → π* and or n → π* transition with a red shift (41 nm) with respect to free H 3 PTB, and the weaker emission on FJU-35 may be caused by more sensitive Cd II −O−Cd II chains. 64,65 Such interesting fluorescent features stimulate us to further explore their photoluminescent properties in different solvents, such as, N,N-dimethylformamide (DMF), acetonitrile, dichloromethane, 1,4-dioxane, methanol (CH 3 OH), ether, acetone, N, N-dimethylacetamide (DMA), ethyl acetate (EAC), chloroform (CHCl 3 ), and nitrobenzene (NB).…”