Introduction to N Annulated Perylene

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10.1021/jacs.1c09481

We report the design, synthesis, and characterization of four N-annulated perylene diimide (NPDI) functionalized rhenium bipyridine [Re(bpy)] supramolecular dyads.

Lowering Electrocatalytic CO2 Reduction Overpotential Using N-Annulated Perylene Diimide Rhenium Bipyridine Dyads with Variable Tether Length.

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10.1021/jacs.1c06125

The synthesis of two series of N-annulated perylene bisimides (PBIs), compounds 1 and 2, is reported, and their self-assembling features are thoroughly investigated by a complete set of spectroscopic measurements and theoretical calculations.

Distance Matters: Biasing Mechanism, Transfer of Asymmetry, and Stereomutation in N-Annulated Perylene Bisimide Supramolecular Polymers

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10.1039/d0ma00827c

We have designed and synthesized three N-annulated perylene diimide (PDI) compounds containing sterically bulky alkyl-substituted benzyl moieties (PDI-X, where X = 1, 2, 3) with photoluminescence quantum yield (PLQY) in the solid-state >20%.

Improved performance of solution processed OLEDs using N-annulated perylene diimide emitters with bulky side-chains

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10.1039/d1qo00837d

The chiroptical features of self-assembled N-annulated perylenetetracarboxamides 1–4 are investigated.

Unravelling the limits of the transfer of asymmetry in supramolecular polymers

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10.1021/ACS.JPCC.1C01964

N-Annulated perylene diimide (PDI) dimers offer added advantages over conventional (non-annulated) dimers or S/Se-annulated dimers due to the two extra positions of functionalization that they prov.

Impact of Ring-Fusion on the Excited State Decay Pathways of N-Annulated Perylene Diimides

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N Annulated Perylene
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What is/are N Annulated Perylene?

N Annulated Perylene - We report the design, synthesis, and characterization of four N-annulated perylene diimide (NPDI) functionalized rhenium bipyridine [Re(bpy)] supramolecular dyads. [1] The synthesis of two series of N-annulated perylene bisimides (PBIs), compounds 1 and 2, is reported, and their self-assembling features are thoroughly investigated by a complete set of spectroscopic measurements and theoretical calculations. [2] We have designed and synthesized three N-annulated perylene diimide (PDI) compounds containing sterically bulky alkyl-substituted benzyl moieties (PDI-X, where X = 1, 2, 3) with photoluminescence quantum yield (PLQY) in the solid-state >20%. [3] The chiroptical features of self-assembled N-annulated perylenetetracarboxamides 1–4 are investigated. [4] N-Annulated perylene diimide (PDI) dimers offer added advantages over conventional (non-annulated) dimers or S/Se-annulated dimers due to the two extra positions of functionalization that they prov. [5]