A Cationic Coordination Polymer and Its Orange II Anion-Exchanged Products: Isolation, Structural Characterization, Photocurrent Responses, and Dielectric Properties.

Solvothermal reactions of AgNO with N,N-bis(5-fluoropyridin-3-yl)succinamide (bfps) in MeCN afforded the one-dimensional cationic coordination polymer {[Ag(bfps)]NO} (1). Upon treatment of 1 with the anionic azo dye orange II (NaOII) in aqueous solution, the NO anions of 1 could be gradually exchanged by the OII anions via an anion-exchange process. The resulting OII anion-exchanged products {Ag(bfps)(OII)} (2) and {Ag(bfps)(OII)} (3) were formed by different molar ratios of 1 and the newly formed phase "{Ag(bfps)}" (4), confirmed by PXRD patterns. Relative to those of the precursors 1 and NaOII, complexes 2 and 3 demonstrated enlarged photocurrent responses and reduced dielectric constants and dielectric losses, which could be correlated with the OII contents in their structures. Complex 3 acquired a stable anodic photocurrent of 12.06 μA, which was 4.9 times higher than that of 1. The dielectric constant (ε = 4.2) and dielectric loss (0.002) of 3 were nearly frequency independent in the range from 1 to 10 Hz. The results provide an interesting insight into the rational assembly of CP-dye complexes and their tunable optoelectronic applications.