Axially-chiral boramidine for detailed (chir)optical studies.

The inclusion of boron atoms into chiral π-conjugated systems is an effective strategy to unlock unique chiroptical properties. Herein, the preparation and characterization of a configurationally stable axially-chiral boramidine are reported, showcasing absorption in the UV domain, deep-blue fluorescence (Φ up to 94%), and ca. |10-3| gabs and glum values. Detailed photophysical studies and quantum-chemical calculations clearly elucidate the deactivation pathways of the emissive state to triplet excited states, involving increased spin-orbit coupling between the lowest singlet excited state and an upper triplet state.

Dissecting conjugation and electronic effects on the linear and non-linear optical properties of rhenium(I) carbonyl complexes.

Herein, we report a theoretical and experimental analysis of the conjugation and electronic effects on the one-photon (1PA) and two-photon absorption (2PA) properties of a series of Re(I) carbonyl complexes with terpyridine-based ligands. An excellent agreement was obtained between the calculated and experimental 2PA spectra of the κ2N-terpyridine tricarbonyl complexes (1a-b), with 2PA cross sections reaching up to ca. 40 GM in DMF. By stepwise lowering the conjugation length in the terpy ligand and changing the local symmetry around the metal centre, we show that conjugation and delocalisation play a major role in increasing 2PA cross sections, and that the character of the excited states does not directly enhance the non-linear properties of these complexes-contrary to the results observed in 1PA. Altogether, these results give valuable guidelines towards more efficient two-photon-absorbing coordination complexes of Re(I), with potential applications in photodynamic therapy and two-photon imaging.

Ultrasensitive Visual Detection of Glucose in Urine Based on the Iodide-Promoted Etching of Gold Bipyramids.

Blood glucose monitoring is an essential but painful component of diabetes management, so it is urgent to develop simple, convenient, and noninvasive glucose monitoring methods as alternatives. Because the glucose level in urine is directly related to the blood glucose, urine can be an alternative for blood glucose monitoring. Herein, we report the development of a new and highly sensitive noninvasive colorimetric assay to detect the glucose content in urine samples using gold bipyramids (GBPs). The principle of this method is to utilize hydrogen peroxide (H2O2), the oxidation product of glucose, to etch GBPs, where the urine glucose will be quantified based on the displacement of the absorption peak of GBPs. The unique morphology (sharp tips) and etching mechanism (from tips) of GBPs determine the high sensitivity of this assay. Under optimal conditions, this colorimetric assay shows a dynamic range of 0.5-250 µM and a detection limit of 0.34 µM for artificial urine samples. This detection capability is ideal when sample dilution is necessary. Another advantage is that the color change of the GBP solution in this assay is convenient for the visual readout of the urine glucose semiquantitatively by the naked eye. Furthermore, it has been demonstrated here that the iodide ion has the horseradish peroxidase (HRP) activity and can be used alone to promote the reduction reaction of H2O2, which eliminates the use of HRP enzymes, simplifies the reaction, and reduces costs. The role of iodide ions has been studied and mainly attributed as a catalyst with I2 as the reaction intermediate, which reduced the activation energy for the reduction of H2O2.