Photoinduced Electron Transfer within a Zinc Porphyrin-Cyclobis(paraquat-p-phenylene) Donor-Acceptor Dyad

被引:18
作者
Fathalla, Maher [1 ]
Barnes, Jonathan C. [1 ]
Young, Ryan M. [1 ,2 ]
Hartlieb, Karel J. [1 ]
Dyar, Scott M. [1 ]
Eaton, Samuel W. [1 ,2 ]
Sarjeant, Amy A. [1 ]
Co, Dick T. [1 ,2 ]
Wasielewski, Michael R. [1 ,2 ]
Stoddart, J. Fraser [1 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Argonne Northwestern Solar Energy Res ANSER Ctr, Evanston, IL 60208 USA
基金
美国国家科学基金会;
关键词
donor-acceptor systems; electron transfer; porphyrinoids; transient absorption spectroscopy; OXIDATION-REDUCTION; CHARGE SEPARATION; SPIN-RESONANCE; PORPHYRIN; ENERGY; SYSTEMS; STATE; VIOLOGEN; PAIR; RECOMBINATION;
D O I
10.1002/chem.201403744
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Understanding the mechanism of efficient photoinduced electron-transfer processes is essential for developing molecular systems for artificial photosynthesis. Towards this goal, we describe the synthesis of a donor-acceptor dyad comprising a zinc porphyrin donor and a tetracationic cyclobis(paraquat-p-phenylene) (CBPQT(4+)) acceptor. The X-ray crystal structure of the dyad reveals the formation of a dimeric motif through the intermolecular coordination between the triazole nitrogen and the central Zn metal of two adjacent units of the dyad. Photoinduced electron transfer within the dyad in MeCN was investigated by femtosecond and nanosecond transient absorption spectroscopy, as well as by transient EPR spectroscopy. Photoexcitation of the dyad produced a weakly coupled ZnP+.-CBPQT(3+.) spin-correlated radical-ion pair having a =146ns lifetime and a spin-spin exchange interaction of only 0.23mT. The long radical-ion-pair lifetime results from weak donor-acceptor electronic coupling as a consequence of having nine bonds between the donor and the acceptor, and the reduction in reorganization energy for electron transfer caused by charge dispersal over both paraquat units within CBPQT(3+.).
引用
收藏
页码:14690 / 14697
页数:8
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