Publications by authors named "D B Hayrapetyan"

Liquid crystals (LC) are widely used in various optical devices due to their birefringence, dielectric anisotropy, and responsive behavior to external fields. Enhancing the properties of existing LCs through doping with nanoparticles, including semiconductor quantum dots, offers a promising route for improving their performance. Among various nanoparticles, QDs stand out for their high charge mobility, sensitivity in the near-infrared spectral region, and cost-effectiveness.

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Aza-annulation of enamines derived from β-ketoesters with maleic and itaconic anhydrides proceeds with excellent diastereoselectivity to provide functionalized γ- and δ-lactams. Further hydrolysis of the aza-annulation products resulted in dicarboxylic acids that underwent spontaneous decarboxylation under ambient conditions. The decarboxylation of β-γ unsaturated carboxylic acids with an electron-rich enamide C═C bond proceeds with the migration of the C═C bond and serves as a practical synthetic entry into 3-pyrrolin-2-ones and 1,2,3,4-tetrahydropyridin-2-ones.

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The thermodynamic characteristics of a pair-interacting hole gas localized in a Ge/Si lens-shaped quantum dot are studied. The pair-interaction potential is modeled by the oscillator function, which depends on the distance between the particles. The analytical form of the spectra makes it possible to calculate the partition function in Boltzmann approximation.

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Article Synopsis
  • Quantum dots (QDs) are known for their light-emitting properties, but there are still limitations in controlling their characteristics that affect higher-level applications.
  • This study focuses on engineering the exciton and biexciton emission order in indium phosphide (InP) QDs embedded in a polymer matrix using size, dielectric confinement, and electric fields.
  • Results suggest that smaller QDs (1 nm, 1.5 nm) in materials with high dielectric constants and external electric fields could enable optical gain and photon entanglement, providing a new approach beyond traditional type II core-shell QDs.
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Simple and scalable electrochemical oxidation of the electron-rich benzene ring followed by intramolecular capture of reactive cation-radical intermediates opens access to spirocyclic morpholines and tetrahydrofurans. The obtained molecules can be readily modified to value-added building blocks.

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