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A Supramolecular [10]CPP Junction Enables Efficient Electron Transfer in Modular Porphyrin–[10]CPP⊃Fullerene Complexes

Youzhi XuInstitute of Organic Chemistry and Advanced Materials University of Ulm Albert-Einstein-Allee 11 89081 Ulm GermanyBingzhe WangDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials Friedrich-Alexander University Erlangen-Nürnberg Egerlandstrasse 3 91058 Erlangen GermanyRamandeep KaurDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials Friedrich-Alexander University Erlangen-Nürnberg Egerlandstrasse 3 91058 Erlangen GermanyMartin B. MinameyerDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials Friedrich-Alexander University Erlangen-Nürnberg Egerlandstrasse 3 91058 Erlangen GermanyMichael BotheInstitute of Organic Chemistry and Advanced Materials University of Ulm Albert-Einstein-Allee 11 89081 Ulm GermanyThomas DrewelloDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials Friedrich-Alexander University Erlangen-Nürnberg Egerlandstrasse 3 91058 Erlangen GermanyDirk M. GuldiDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials Friedrich-Alexander University Erlangen-Nürnberg Egerlandstrasse 3 91058 Erlangen GermanyMax von DeliusInstitute of Organic Chemistry and Advanced Materials University of Ulm Albert-Einstein-Allee 11 89081 Ulm Germany
2018en
ABI

Abstract

Abstract Efficient photoinduced electron transfer was observed across a [10]cycloparaphenylene ([10]CPP) moiety that serves as a rigid non‐covalent bridge between a zinc porphyrin and a range of fullerenes. The preparation of iodo‐[10]CPP is the key to the synthesis of a porphyrin–[10]CPP conjugate, which binds C 60 , C 70 , (C 60 ) 2 , and other fullerenes ( K A >10 5 m −1 ). Fluorescence and pump–probe spectroscopy revealed intramolecular energy transfer between CPP and porphyrin and also efficient charge separation between porphyrin and fullerenes, affording up to 0.5 μs lifetime charge‐separated states. The advantage of this approach towards electron donor–acceptor dyads is evident in the case of dumbbell‐shaped (C 60 ) 2 , which gave intricate charge‐transfer behavior in 1:1 and 2:1 complexes. These results suggest that [10]CPP and its cross‐coupled derivatives could act as supramolecular mediators of charge transport in organic electronic devices.

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