Potassium Poly(Heptazine Imide): Transition Metal‐Free Solid‐State Triplet Sensitizer in Cascade Energy Transfer and [3+2]‐cycloadditions

Aleksandr Savateev(Max Planck Institute of Colloids and Interfaces), Nadezda V. Tarakina(Max Planck Institute of Colloids and Interfaces), Volker Strauß(Max Planck Institute of Colloids and Interfaces), Tanveer Hussain(The University of Western Australia), Katharina ten Brummelhuis(Max Planck Institute of Colloids and Interfaces), José Manuel Sánchez Vadillo, Yevheniia Markushyna(Max Planck Institute of Colloids and Interfaces), Stefano Mazzanti(Max Planck Institute of Colloids and Interfaces), А. P. Tyutyunnik(Institute of Solid State Chemistry), Ralf Walczak(Max Planck Institute of Colloids and Interfaces), Martin Oschatz(Max Planck Institute of Colloids and Interfaces), Dirk M. Guldi(Friedrich-Alexander-Universität Erlangen-Nürnberg), Amir Karton(The University of Western Australia), Markus Antonietti(Max Planck Institute of Colloids and Interfaces)
Angewandte Chemie International Edition
May 16, 2020
Cited by 159Open Access
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Abstract

Abstract Polymeric carbon nitride materials have been used in numerous light‐to‐energy conversion applications ranging from photocatalysis to optoelectronics. For a new application and modelling, we first refined the crystal structure of potassium poly(heptazine imide) (K‐PHI)—a benchmark carbon nitride material in photocatalysis—by means of X‐ray powder diffraction and transmission electron microscopy. Using the crystal structure of K‐PHI, periodic DFT calculations were performed to calculate the density‐of‐states (DOS) and localize intra band states (IBS). IBS were found to be responsible for the enhanced K‐PHI absorption in the near IR region, to serve as electron traps, and to be useful in energy transfer reactions. Once excited with visible light, carbon nitrides, in addition to the direct recombination, can also undergo singlet–triplet intersystem crossing. We utilized the K‐PHI centered triplet excited states to trigger a cascade of energy transfer reactions and, in turn, to sensitize, for example, singlet oxygen ( 1 O 2 ) as a starting point to synthesis up to 25 different N‐rich heterocycles.


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