Yu-De Huang †, Peng Huo †, Ming-Yan Shao †, Jing-Xue Yin †, Wei-Chun Shen †, Qin-Yu Zhu *†‡（朱琴玉）, and Jie Dai *†‡ （戴洁）
† College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, People’s Republic of China
‡ State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing 210093, People’s Republic of China
Inorg. Chem. 2014, 53, 3480–3487
Although charge-transfer compounds based on tetrathiafulvalene (TTF) derivatives have been intensively studied, {[cation]n+·[TTFs]n–} ion pair charge-transfer (IPCT) salts have not been reported. The aim of this research is to introduce functional organic cations, such as photoactive methyl viologen (MV2+), into the negatively charged TTF–metal coordination framework to obtain this new type of IPCT complex. X-ray structural analysis of the four compounds (MV)2[Li4(L)2(H2O)6] (1), {(MV)(L)[Na2(H2O)8]·4H2O}n (2), {(MV)[Mn(L)(H2O)2]·2H2O}n (3), and {(MV)[Mn(L)(H2O)2]}n (4), reveals that the electron donor (D) TTF moiety and the electron acceptor (A) MV2+ form a regular mixed-stack arrangement in alternating DADA fashion. The TTF moiety and the MV2+ cation are essentially parallel stacked to form the column structures. The strong electrostatic interaction is a main force to shorten the distance between the cation and anion planes. Optical diffuse-reflection spectra indicate that charge transfer occurs in these complexes. The ESR and magnetic measurements confirm that there is strong charge-transfer-induced partial electron transfer. Compounds 2, 3, and 4 show an effective and repeatable photocurrent response. The current intensities of 3 and 4 are higher than that of 2, which reflects that the coordination center of the Mn(II) ion has a great effect on the increasing photocurrent response.
链接：
http://pubs.acs.org/doi/abs/10.1021/ic402926n
