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New palladium(II) wheel-and-axle diols are synthesized and structurally characterized after which they are converted into the crystalline solvates both by recrystallization and by exposure to guest vapors and recovered upon removal of the guest. It is proposed that the solvation/desolvation process is based on a concerted rotation of the complex molecules in the layer plane.

Research has been conducted on photoactivatable Ca (super)2+ compounds. The authors describe the synthesis of these compounds carried out in an effort to afford calcium ions' fast concentration jump in solution.

Photocatalysis provides a sustainable pathway to produce the consumer chemical H 2 O 2 from atmospheric O 2 via an oxygen reduction reaction (ORR). Such an alternative is attractive to replace the cumbersome traditional anthraquinone method for H 2 O 2 synthesis on a large scale. Carbon nitrides have shown very interesting results as heterogeneous photocatalysts in ORR because their covalent two-dimensional (2D) structure is believed to increase selectivity toward the two-electron process. However, an efficient and scalable application of carbon nitrides for this reaction is far from being achieved. Poly(heptazine imides) (PHIs) are a more powerful subgroup of carbon nitrides whose structure provides high crystallinity and a scaffold to host transition-metal single atoms. Herein, we show that PHIs functionalized with sodium and the recently reported fully protonated PHI exhibit high activity in two-electron ORR under visible light. The latter converted O 2 to up to 1556 mmol L -1 h -1 g -1 H 2 O 2 under 410 nm irradiation using inexpensive but otherwise chemically demanding glycerin as a sacrificial electron donor. We also prove that functionalization with transition metals is not beneficial for H 2 O 2 synthesis, as the metal also catalyzes its decomposition. Transient photoluminescence spectroscopy suggests that H-PHIs exhibit higher activity due to their longer excited-state lifetime. Overall, this work highlights the high photocatalytic activity of the rarely examined fully protonated PHI and represents a step forward in the application of inexpensive covalent materials for photocatalytic H 2 O 2 synthesis.

Plasmonic catalysis in the colloidal phase requires robust surface ligands that prevent particles from aggregation in adverse chemical environments and allow carrier flow from reagents to nanoparticles. This work describes the use of a water-soluble conjugated polymer comprising a thiophene moiety as a surface ligand for gold nanoparticles to create a hybrid system that, under the action of visible light, drives the conversion of the biorelevant NAD + to its highly energetic reduced form NADH. A combination of advanced microscopy techniques and numerical simulations revealed that the robust metal-polymer heterojunction, rich in sulfonate functional groups, directs the interaction of electron-donor molecules with the plasmonic photocatalyst. The tight binding of polymer to the gold surface precludes the need for conventional transition-metal surface cocatalysts, which were previously shown to be essential for photocatalytic NAD + reduction but are known to hinder the optical properties of plasmonic nanocrystals. Moreover, computational studies indicated that the coating polymer fosters a closer interaction between the sacrificial electron-donor triethanolamine and the nanoparticles, thus enhancing the reactivity.