Expanding a fluorescent RNA alphabet: synthesis, photophysics and utility of isothiazole-derived purine nucleoside surrogates.

A series of emissive ribonucleoside purine mimics, all comprised of an isothiazolo[4,3-d]pyrimidine core, was prepared using a divergent pathway involving a key Thorpe-Ziegler cyclization. In addition to an adenosine and a guanosine mimic, analogues of the noncanonical xanthosine, isoguanosine, and 2-aminoadenosine were also synthesized and found to be emissive. Isothiazolo 2-aminoadenosine, an adenosine surrogate, was found to be particularly emissive and effectively deaminated by adenosine deaminase. Competitive studies with adenosine deaminase with each analogue in combination with native adenosine showed preference for the native substrate while still deaminating the isothiazolo analogues

Effect of sodium hydroxide pretreatment of NiOx cathodes on the performance of squaraine-sensitized p-type dye-sensitized solar cells

Squaraines are full-organic dyes employed as sensitizers in ptype dye-sensitized solar cells (p-DSSC). Their absorption spectrum shows a wide tunability that ranges from visible to NIR. Sensitization in the NIR region is crucial for exploiting a particularly intense portion of the solar spectrum. In this work three squaraines will be presented and tested as sensitizers in NiO-based p-type DSSC O4_C2, O4_C4 and O4_C12). The structures of the dyes differ for the length of the alkyl side chain (C2, C4 and C12). Alkyl side chains improve the solubility of the dye, influence the extent of dye loading on the electrode and affect the overall efficiency of devices. The generally low stability of squaraines represents a critical issue in view of their employment as sensitizers of p-DSSC. Such a problem becomes even more evident when this class of molecules is bound onto an acidic surface like the one of the photocathode here employed: non-stoichiometric nickel oxide (NiOx). NiOx possesses a quite acidic character because of the high surface concentration of Ni(III) sites. To buffer the surface acidity of NiOx due to the presence of high-valence states of nickel, we considered the electrode pretreatment with sodium hydroxide (NaOH) prior to sensitization. This assures a major stability of the solar cell. At the same time the chemisorbed hydroxyl moieties act as passivating agents of the Ni(III) sites thus diminishing the surface concentration of sites for dye anchoring. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Behavior of Ternary Mixtures of Hydrogen Bond Acceptors and Donors in Terms of Band Gap Energies

Three ternary mixtures composed by choline chloride (ChCl), ethylene glycol (EG), and a second hydrogen bond donor (HBD) as ethanol (A), 2-propanol (B), and glycerol (C) were studied in terms of composition related to the band gap energy (BGE). A Design of Experiments (DoE) approach, and in particular a Simple Lattice three-components design, was employed for determining the variation of the BGE upon the composition of each system. UV-VIS analysis and subsequent Tauc plot methodology provided the data requested from the DoE, and multivariate statistical analysis revealed a drop of the BGE in correspondence to specific binary compositions for systems A and B. In particular, a BGE of 3.85 eV was registered for the mixtures ChCl/EtOH (1:1) and ChCl/2-propanol (1:1), which represents one of the lowest values ever observed for these systems