Publications by authors named "A Barbon"

In the field of RNA therapy, innovative approaches based on adenosine deaminases acting on RNA (ADAR)-mediated site-directed RNA editing (SDRE) have been established, providing an exciting opportunity for RNA therapeutics. ADAR1 and ADAR2 enzymes are accountable for the predominant form of RNA editing in humans, which involves the hydrolytic deamination of adenosine (A) to inosine (I). This inosine is subsequently interpreted as guanosine (G) by the translational and splicing machinery because of their structural similarity.

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Malaysian fire snails , face threats to their environment, including habitat destruction and the illegal wildlife trade. Captive breeding projects are likely to play a role in the survival of this species; however, mortality in captive populations potentially presents a significant challenge. This paper presents the results of histopathologic examination of tissues from 10 casualties in a captive population at Chester Zoo.

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A borazine derivative functionalized by nitroxide free radicals, ,',″-(tris(4-Bromophenyl))-,',″-tris((2,6-dimethyl-4-(--butyl--oxyamino)phenyl) borazine (), was synthesized as a milestone of open-shell inorganic benzene. The crystal structure determined from X-ray diffraction on a single crystal ascertains the grafting of three nitroxide radicals. The temperature dependence of the magnetic susceptibility evidences weak intramolecular antiferromagnetic interactions between the radicals with strong intermolecular antiferromagnetic interactions between two nitroxide moieties of two neighboring molecules.

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Article Synopsis
  • TADF molecules are important for applications like OLEDs and require a small singlet-triplet energy gap (ΔE) and high radiative rate constants (k) for efficient usage.
  • A new method for adjusting ΔE is introduced by extending the π-conjugation of a triplet constrainer, which allows for reduced ΔE while maintaining high k values across varying molecular structures.
  • This research demonstrates a novel TADF molecule design that improves fluorescence efficiency and lowers ΔE significantly, which is important for advancing photophysics and material science.
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Electron paramagnetic resonance (EPR) pulsed dipolar spectroscopy (PDS) using triplet states of organic molecules is a growing area of research due to the favourable properties that these transient states may afford over stable spin centers, such as switchability, increased signal intensity when the triplet is formed in a non-Boltzmann distribution and the triplet signal is used for detection, and high orientation selection, when the triplet signal is probed by microwave pulses. This arises due to the large spectral width at low fields, a result of the large zero field splitting, and limited bandwidth of microwave pulses used. Here we propose the triplet state of a substituted BODIPY moiety as a spin label in light induced PDS, coupled to a nitroxide, in a model peptide with a rigid structure.

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