Publications by authors named "Denis Ari"

A new host material for Single-Layer Phosphorescent Organic Light-Emitting Diodes (SL-PhOLED) is reported, namely SPA-2-FDMB, using the dimesitylborane (DMB) fragment as an acceptor unit. The molecular design is constructed on the general donor-spiro-acceptor architecture, which consists of connecting, via a spiro bridge, a donor and an acceptor units in order to avoid strong interaction between them. The DMB fragment is known for many electronic applications (notably Aggregation-Induced Emission) but has not been used yet for SL-PhOLED applications.

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Article Synopsis
  • Pure aromatic hydrocarbon materials (PHCs) are emerging as superior host materials for phosphorescent OLEDs (PhOLEDs) due to their simple synthesis, absence of heteroatoms, and potential for enhanced device robustness.
  • Their development is critical because heteroatoms can lead to degradation in operating OLEDs, making PHCs a crucial focus for advancing OLED technology.
  • The research introduces a series of new PHCs made from spirobifluorene fragments that show excellent triplet energy levels and other favorable properties, achieving a high external quantum efficiency (EQE) of 24% in blue-emitting PhOLEDs, thereby supporting the effectiveness of PHCs in creating efficient OLED devices.
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We report the synthesis and full characterization of a family of phosphorus-containing polymethine cyanines (phospha-cyanines). The compounds are easily prepared in two steps, starting from readily available phosphanes. The impact of the P-substituents and the counterions on the structural and optical properties is investigated through a joint experimental/theoretical approach.

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We report the synthesis and characterization of two new fluorophores, consisting of a [8]cyclo--phenylene core in which two phenylenes are bridged by either a nitrogen atom or a carbonyl group. The nitrogen bridge increases the HOMO-LUMO gap, whereas the carbonyl bridge decreases it. These results provide guidelines to control the electronic properties of nanohoops.

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We introduce a versatile Rh(i)-catalyzed cascade reaction, combining C(sp)-H bond functionalization and amidation between -arylphosphanamines and acrylates. This innovative approach enables the rapid synthesis of dihydroquinolinone scaffolds, a common heterocycle found in various pharmaceuticals. Notably, the presence of the phosphorus atom facilitates the aniline -C(sp)-H bond activation prior to N-P bond hydrolysis, streamlining one-pot intramolecular amidation.

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