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Pentacene appended to a TEMPO stable free radical: the effect of magnetic exchange coupling on photoexcited pentacene.

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TLDR
Time-resolved electron paramagnetic resonance experiments confirm that triplet quenching is accompanied by electron spin polarization transfer from the pentacene excited state to the TEMPO doublet state in the weak coupling regime.
Abstract
Understanding the fundamental spin dynamics of photoexcited pentacene derivatives is important in order to maximize their potential for optoelectronic applications. Herein, we report on the synthesis of two pentacene derivatives that are functionalized with the [(2,2,6,6-tetramethylpiperidin-1-yl)oxy] (TEMPO) stable free radical. The presence of TEMPO does not quench the pentacene singlet excited state, but does quench the photoexcited triplet excited state as a function of TEMPO-to-pentacene distance. Time-resolved electron paramagnetic resonance experiments confirm that triplet quenching is accompanied by electron spin polarization transfer from the pentacene excited state to the TEMPO doublet state in the weak coupling regime.

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Citations
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Strongly exchange-coupled triplet pairs in an organic semiconductor

TL;DR: Gates-Cambridge Trust, Winton Programme for the Physics of Sustainability, Freie Universitat Berlin within the Excellence Initiative of the German Research Foundation, Engineering and Physical Sciences Research Council (Grant ID: EP/G060738/1) as discussed by the authors
Journal ArticleDOI

Azaacenes as active elements for sensing and bio applications

TL;DR: It is believed that a rapid development in the research of sensors and bio applications based on azaacenes will be witnessed in the coming years due to their tuneable structures, optical properties and binding abilities.
Journal ArticleDOI

A Derivative of the Blatter Radical as a Potential Metal-Free Magnet for Stable Thin Films and Interfaces

TL;DR: This work has investigated the thin films of a derivative of the Blatter radical that was synthesized bearing in mind the thermodynamic factors that govern thin film stability, and proved the concept by investigating the electronic structure, the paramagnetic character, and stability of the obtained films under UHV and ambient conditions by in situ X-ray photoelectron spectroscopy, ex situ atomic force microscopy, and electron paramagnetic resonanceSpectroscopy.
Journal ArticleDOI

Strategies for the Synthesis of Higher Acenes

TL;DR: The outstanding performance of pentacene‐based molecules in molecular electronics, as well as the predicted enhanced semiconducting properties of extended acenes, have stimulated the development of new synthetic methods and functionalization strategies for the preparation of stable and soluble acenes larger than tetracene with the aim of obtaining improved functional materials.
References
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Journal ArticleDOI

The larger acenes: versatile organic semiconductors.

TL;DR: New approaches to add functionality were developed to improve the processability of these materials in solution, allowing the synthesis of acenes larger than pentacene, which have hitherto been largely unavailable and poorly studied.
Journal ArticleDOI

Functionalized Pentacene: Improved Electronic Properties from Control of Solid-State Order

TL;DR: The preparation of two functionalized pentacene derivatives, and the effect of this functionalization on both the solid-state ordering and the electronic properties of the resulting crystals is reported.
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