4.8 Article

Self-Assembly-Directed Organization of a Fullerene-Bisporphyrin into Supramolecular Giant Donut Structures for Excited-State Charge Stabilization

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 143, 期 29, 页码 11199-11208

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c05133

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资金

  1. Spanish MICINN [PID2019-105049RB-I00, PGC2018-099568-B-I00, RED2018-102815-T]
  2. Unidad de Excelencia Maria de Maeztu [CEX2019-000919-M]
  3. Junta de Comunidades de Castilla-La Mancha
  4. European Social Fund [SBPLY/17/180501/000254]
  5. Generalitat Valenciana [PROMETEO/2020/077]
  6. European FEDER funds [PGC2018-099568-B-I00]
  7. US-National Science Foundation
  8. MICINN [RyC-2017-23500]
  9. ISCIII [CD18/00145]

向作者/读者索取更多资源

A new fullerene-bis-Zn-porphyrin e-bisadduct has been successfully synthesized in this study, demonstrating the potential application of these supramolecular oligomers in the field of solar energy photovoltaic devices. The structure and formation process of the complex were determined through experiments and theoretical calculations, highlighting its significance for light energy harvesting applications.
Functional materials composed of spontaneously self-assembled electron donor and acceptor entities capable of generating long-lived charge-separated states upon photoillumination are in great demand as they are key in building the next generation of light energy harvesting devices. However, creating such well-defined architectures is challenging due to the intricate molecular design, multistep synthesis, and issues associated in demonstrating long-lived electron transfer. In this study, we have accomplished these tasks and report the synthesis of a new fullerene-bis-Zn-porphyrin e-bisadduct by tether-directed functionalization of C-60 via a multistep synthetic protocol. Supramolecular oligomers were subsequently formed involving the two porphyrin-bearing arms embracing a fullerene cage of the vicinal molecule as confirmed by MALDI-TOF spectrometry and variable temperature NMR. In addition, the initially formed worm-like oligomers are shown to evolve to generate donut-like aggregates by AFM monitoring that was also supported by theoretical calculations. The final supramolecular donuts revealed an inner cavity size estimated as 23 nm, close to that observed in photosynthetic antenna systems. Upon systematic spectral, computational, and electrochemical studies, an energy level diagram was established to visualize the thermodynamic feasibility of electron transfer in these donor-acceptor constructs. Subsequently, transient pump-probe spectral studies covering the wide femtosecond-to-millisecond time scale were performed to confirm the formation of long-lived charge-separated states. The lifetime of the final charge-separated state was about 40 mu s, thus highlighting the significance of the current approach of building giant self-organized donor-acceptor assemblies for light energy harvesting applications.

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