Application of a simple copper(II) complex compound as an epinephrine selective voltammetric sensor in the presence of uric acid under aqueous conditions.

Developing sensors with high sensitivity and selectivity for detecting neurotransmitters under near-physiological conditions is a major challenge and is crucial for preventing diseases of the nervous, cardiovascular, and endocrine systems. Most existing systems that meet these requirements involve either complicated synthesis processes, require sulfur groups, or are not functional under aqueous conditions. Herein, we report that the self-organisation of a simple imine ligand L with copper(II) tetrafluoroborate leads to the formation of a [CuL](BF) complex (CuL) with a 2 : 1 ligand-to-metal ratio, as confirmed by high-resolution electrospray ionization mass spectrometry (HR ESI-MS), Fourier-transform infrared (FT-IR) spectroscopy and single-crystal X-ray analysis.

Optimizing photovoltaic performance of squaraine derivative dyes: a DFT study on different anchoring groups.

In this study, we designed squaraine-based dyes with a 2-amino pyrrole donor unit and acene groups like anthracene and pentacene. These dyes incorporate three different electron-withdrawing groups - cyanoacrylate (A1), phosphonate (A2) and boronic acid (A3) - as linkers to the TiO semiconductor. The spectroscopic, electronic and photochemical properties of these compounds were investigated using density functional theory (DFT) and time-dependent density functional theory (TDDFT) simulations.

The effect of ionic covalent functionalization of polyoxometalate hybrid materials with coordinating subunits on their stability and interaction with DNA.

Inorganic-organic hybrid materials that combine both Polyoxometalates (POMs) and metal ion coordinating subunits (CSUs) represent promising multifunctional materials. Though their individual components are often biologically active, utilization of hybrid materials in bioassays significantly depends on the functionalization method and thus resulting stability of the system. Quite intriguingly, these aspects were very scarcely studied in hybrid materials based on the Wells-Dawson POM (WD POM) scaffold and remain unknown.

Transfer Hydrogenation of Vinyl Arenes and Aryl Acetylenes with Ammonia Borane Catalyzed by Schiff Base Cobalt(II) Complexes.

A series of bench-stable Co(II) complexes containing hydrazone Schiff base ligands were evaluated in terms of their activity and selectivity in carbon-carbon multiple bond transfer hydrogenation. These cobalt complexes, especially a Co(II) precatalyst bearing pyridine-2-yl-N(Me)N=C-(1-methyl)imidazole-2-yl ligand, activated by LiHBEt, were successfully used in the transfer hydrogenation of substituted styrenes and phenylacetylenes with ammonia borane as a hydrogen source. Key advantages of the reported catalytic system include mild reaction conditions, high selectivity and tolerance to functional groups of substrates.