A chloride-responsive molecular switch: driving ion transport and empowering antibacterial properties.

A molecular switch was developed to recognize and transport Cl- across lipid bilayers. The XRD-crystal structure and NOESY NMR spectra of a potent 4-aminoquinazoline analogue confirmed Cl--induced conformation changes. Systematic biophysical studies revealed that the quinazoline moiety forms cooperative interactions of H+ and Cl- ions with the thiourea moiety, resulting in the transport of H+/Cl- across the membranes. A pH-dependent analysis revealed that the transport of Cl- by the potent compound increased in an acidic environment. The potent compound could also transport H+/Cl- across Gram-positive bacteria, leading to antibacterial activities.

Guanidine-Functionalized Fluorescent sp2 Carbon-Conjugated Covalent Organic Framework for Sensing and Capture of Pd(II) and Cr(VI) Ions.

Palladium is a key element in fuel cells, electronic industries, and organic catalysis. At the same time, chromium is essential in leather, electroplating, and metallurgical industries. However, their unpremeditated leakage into aquatic systems has caused human health and environmental apprehensions. Herein, we reported the development of an sp2 carbon-conjugated fluorescent covalent organic framework with a guanidine moiety (sp2 c-gCOF) that showed excellent thermal and chemical stability. The sp2 c-gCOF showed effective sensing, capture, and recovery/removal of Pd(II) and Cr(VI) ions, which could be due to the highly accessible pore walls decorated with guanidine moieties. The fluorescent sp2 c-gCOF showed higher selectivity for Pd(II) and Cr(VI) ions, with an ultra-low detection limit of 2.7 and 3.2 nM, respectively. The analysis of the adsorption properties with a pseudo-second-order kinetic model showed that sp2 c-gCOF could successfully and selectively remove both Pd(II) and Cr(VI) ions from aqueous solutions. The polymer also showed excellent capture efficacy even after seven consecutive adsorption-desorption cycles. Hence, this study reveals the potential of fluorescent sp2 c-gCOF for detecting, removing, and recovering valuable metals and hazardous ions from wastewater, which would be useful for economic benefit, environmental safety, human health, and sustainability. The post-synthetic modification of sp2 c-COF with suitable functionalities could also be useful for sensing and extracting other water pollutants and valuable materials from an aqueous system.

Multi-stimuli controlled release of a transmembrane chloride ion carrier from a sulfonium-linked procarrier.

In recent times, anion transporters have received substantial consideration due to their ability to disrupt the ionic equilibrium across membrane bilayers. While numerous Cl- ion transporters were developed for channelopathies, unfortunately, poor aqueous solubility precluded their bioapplicability. Herein, we demonstrate the development of a multi-stimuli activatable anion transport approach to induce regulated transport of Cl- ions across membranes under specific conditions. The sulfonium-based procarrier was initially inactive, but the transmembrane transport of Cl- ions was activated in the presence of stimuli such as glutathione (GSH), reactive oxygen species (ROS) and light. The release of the hydrophobic anionophore from the aqueous-soluble procarrier under specific conditions leads to the successful transport of Cl- ions. Under physiological conditions, these anion carriers follow an antiport exchange mechanism to transport Cl- ions across lipid bilayers. Such multi-stimuli activatable procarriers have great potential to combat various types of channelopathies, including cancer, cystic fibrosis, kidney stones, myotonia, and others.