Tuning the Electron Acceptor in Phthalocyanine-Based Electron Donor-Acceptor Conjugates

Chemistry. 2015 Dec 21;21(52):19028-40. doi: 10.1002/chem.201503237. Epub 2015 Nov 23.

Abstract

Zinc phthalocyanines (ZnPc) have been attached to the peri-position of a perylenemonoimide (PMI) and a perylenemonoanhydride (PMA), affording electron donor-acceptor conjugates 1 and 2, respectively. In addition, a perylene-monoimide-monoanhydride (PMIMA) has been connected to a ZnPc through its imido position to yield the ZnPc-PMIMA conjugate 10. The three conjugates have been studied for photoinduced electron transfer. For ZnPc-PMIMA 10, electron transfer occurs upon both ZnPc and PMIMA excitation, giving rise to a long-lived (340 ps) charge-separated state. For ZnPc-PMI 1 and ZnPc-PMA 2, stabilization of the radical ion pair states by using polar media is necessary. In THF, photoexcitation of either ZnPc or PMI/PMA produces charge-separated states with lifetimes of 375 and 163 ps, respectively.

Keywords: anhydrides; electron transfer; imides; perylene; phthalocyanine.

Publication types

  • Research Support, Non-U.S. Gov't