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In this study, sulfur‐enriched microporous organic polymer (MOP) was prepared using one‐pot Shiff‐base type polycondensation reaction of thiophendicarboxaldehyde with melamine. With 195.731 m2 g−1 surface area and 0.047 cm3 g−1 pore volume, the as‐synthesized MOP has a cotton‐like morphology and a micropore‐dominated pore size distribution. After loading MOP with nickel as a co‐catalyst, we demonstrated that the obtained framework could be used as an efficient and robust electrocatalyst for hydrogen evolution reaction (HER) in an alkaline medium with the optimum composite (Ni2@MOP) exhibiting a low onset potential of −66 mV. Furthermore, the optimum electrocatalyst showed good stability, delivering 91% faradaic efficiency (FE) after a 3.5 h chronoamperometry experiment. [ABSTRACT FROM AUTHOR]

We report here the synthesis and characterization of a water dispersible conjugated polymer nanoparticle‐based photosensitizer and its application in the antibacterial and anticancer phototherapies. Nanoparticles (CPPN) were synthesized in one‐pot by nanoprecipitation method, in which a hydrophobic azide functionalized, red‐emitting thiophene‐benzothiodiazole based conjugated polymer (CP‐AZ) was cross‐linked with a hydrophilic, propargylamine functionalized porphyrin (TPP‐4AL) through cucurbit[6]uril (CB6) catalyzed azide‐alkyne cycloaddition (CB6‐AAC) reaction. CPPN demonstrated high stability in aqueous medium for more than a month without any visible aggregation and appeared to be a good photosensitizer with high light‐triggered reactive oxygen species (ROS) generation ability. Consequently, CPPN displayed photo‐induced biocidal activity against Gram‐negative (Escherichia coli, E. coli) and Gram‐positive (Bacillus subtilis, B. subtilis and Staphylococcus aureus, S. aureus) bacteria. When bacteria suspension was incubated with CPPN (20 μg ml−1) and irradiated with white light (22 mW cm−2) for 10 min, more than 3.5‐log reduction in colony‐forming units (CFUs) was recorded for the three model bacteria. CPPN demonstrated minimal dark cytotoxicity against the bacteria. Moreover, the cytotoxicity of CPPN on mammalian cell was studied using MCF‐7 breast cancer cell line. The results demonstrated that CPPN is non‐toxic to mammalian cells in the dark even at a high concentration of 112.5 μg ml−1 and this feature makes CPPN an ideal photosensitizer. [ABSTRACT FROM AUTHOR]

Visible‐light triggerable, stable, organic material‐based photocatalysts that can function in alkaline media without the necessity of sacrificial agent for hydrogen production are highly sought after. Here, we report a novel supramolecular photocatalyst that confers the aforementioned features. This supramolecular photocatalyst (TPP‐4CB7) is synthesized through the conjugation of monohydroxylated cucurbit(7)uril (CB7) hosts to a suitably substituted tetraphenyl porphyrin. Although TPP‐4CB7 by its own preforms as an efficient visible light triggered photocatalyst, the hydrogen production efficiency is significantly enhanced upon mixing with TiO2. The resulting nanocomposite (TPP‐CB‐TiO2@Pt) is observed to exhibit remarkable electrophotocatalytic activity under visible light and produces hydrogen (onset potential −10 mV, turn over frequency (TOF) 0.202 s−1, 24.5 mmol h−1 g−1) from water splitting without any significant degradation during four runs (5 h each) in alkaline media and in the absence of sacrificial agent. [ABSTRACT FROM AUTHOR]

Front Cover: Novel Supramolecular Photocatalyst Based on Conjugation of Cucurbit[7]uril to Non-Metallated Porphyrin for Electrophotocatalytic Hydrogen Generation from Water Splitting (ChemCatChem 13/2019) B The Front Cover b shows solar energy promoted photoelectrocatalytic water splitting for hydrogen generation using a supramolecular photocatalyst. In their Communication, Dönüs Tuncel and co-workers synthesize a novel, visible light triggerable, stable supramolecular photocatalyst based on conjugation of cucurbit[7]uril to non-metallated porphyrin. [Extracted from the article]