Forces to reckon with : Supramolecular complexes, such as the one shown, are normally based on a combination of different interactions such as ion pairing, hydrogen bonds, and stacking interactions. The not always simple characterization of the nature and strength of intermolecular forces provides assistance to the understanding of biomimetic systems, as well as for the design of synthetic receptors, drugs, and intelligent materials.
All ways lead to Rome? Computer modeling and kinetic measurements identified a distinct residue in Phe/Tyr ammonia lyases (PAL/TAL) which controls whether the Friedel–Crafts or an E1cB reaction mechanism takes place. Hence, Glu484 in pcPAL favors the Friedel–Crafts reaction (see picture, MIO=4‐methylidene imidazol‐5‐one) whereas an Asn in TAL gives an elimination reaction. These mechanistic investigations also reveal activity of a PAL mutant and a TAL towards an amino alcohol.
Easy come, easy go? Transport resistances on particle surfaces are important for mass transfer in nanoporous materials and bulk diffusion in crystals. Interference microscopy and IR micro‐imaging are shown to be excellent tools for determining such transport resistances. By studying short‐chain‐length alkane guest molecules in crystals of the metal–organic framework compound Zn(tbip) a data collection of surface permeabilities is established.
Last but not least : A simple molecular redox system is used to split water into hydrogen and oxygen photochemically. Two separate photolyses are combined to a cyclic process (see scheme). Osmocene ([Cp2OsII] with Cp?=C5H5?) serves as photocatalyst.
Tea time! Gold nanoparticles (GNPs) could be readily prepared by a general strategy involving the reduction of aqueous HAuCl4 in the presence of traditional Chinese medicines (TCMs). Spheroidal and triangular gold nanoparticles were observed depending on the TCM used. The strategy exemplified the universal application of plant bioresources for the synthesis of GNPs and catalytic purposes.
Pass the salt, please! State‐of‐the‐art computations indicate that the stacking complex of a guanine quartet and an adenine quartet (G4A4) can function as a potent ditopic receptor for NaCl in aqueous solution (see picture; Na+, Cl? yellow, O red, N blue, C black, H white).
Alkynes of reactions : Recent breakthroughs in metal‐catalyzed alkyne reactions, which expand the synthetic utility of alkynes, have been achieved. These approaches broaden the range of alkynes that are accessible by C? N and C? C bond‐forming reactions and demonstrate that the use of bifunctional heterobimetallic catalysts can lead to new reactivity and excellent enantioselectivity (see scheme).
Indoles are not indolent : Various indoles react with arylboronic acids chemodivergently. C? H arylation of free indole and N‐methylindole gives the corresponding C(2)‐arylated indoles A whereas N‐acylated, N‐benzoylated, and N‐Boc‐protected indoles provide the corresponding arylcarboaminoxylated products B with excellent diastereoselectivity in good to excellent yields.
Inorganic enzyme? Ceria nanoparticles exhibit unique oxidase‐like activity at acidic pH values. These redox catalysts can be used in immunoassays (ELISA) when modified with targeting ligands (see picture; light blue and yellow structures are nanoparticles with attached ligands). This modification allows both for binding and for detection by the catalytic oxidation of sensitive colorimetric dyes (e.g. TMB).
Y not? A unique, three‐coordinate Y‐shaped bis(silyl)platinum(II) complex was isolated and characterized (see structure; C light gray, N blue, Si pink, Pt dark gray). DFT studies on a model system shed light on the nature of this unusual coordination mode for platinum(II).
Funky discotics : Photoconductivity is measured in newly synthesized cyclopalladated metallomesogens exhibiting hexagonal columnar mesophases at room temperature. The tuning of the HOMO/LUMO energy levels by modification of the chain/core linkage (ester 1 vs ether 2 ) makes compound 2 photoconductive across the whole UV/Vis/NIR range.
A spin‐crossover cluster with the {FeII4O4} core structure is presented by D. Y. Wu, O. Sato et al. in their Communication on page 1475 ff. The cluster is synthesized by self‐assembly and shows an abrupt spin transition, giving two high‐spin and two low‐spin states. It exhibits complete light‐induced excited spin‐state trapping effects. Importantly, synergy effects between the magnetic interaction and spin transition operate in the cluster.