Most nontraditional intrinsic luminescent (NTIL) polymers currently show blue fluorescence. Tuning the emission color of NTIL polymers is of fundamental importance for their applications, but it still remains a scientific challenge. Herein, we initially develop an efficient strategy for bathochromic shifting of NTIL polymers by through-space acceptor-donor charge transfer between the in chain and the side chain. A variety of functionalized polyketones (FPK-R; where R = H, Ph, Me, tBu, F, and Cl) with furan rings built into the polymer chain were prepared by the Paal-Knorr reaction. FPK-R polymers showed bright and bathochromic-shifted fluorescence compared with their counterparts. The emission color could be tuned by changing the postfunctionalization conversion and varying the styrenic monomer substituent. Experimental and theoretical investigations revealed that the color tunability originated from enhanced through-space charge transfer between the side chain phenyl and the in chain furan rings.
Keywords: bathochromic shift; nonconjugated polymer; photoluminescence; polyketone; postfunctionalization; through-space charge transfer.