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Clicking in zeolites : Copper(I)‐exchanged zeolites proved to be practical and efficient catalysts for the cycloaddition of azomethine imines with alkynes, providing a convenient access to N,N‐bicyclic pyrazolidinone derivatives (see scheme). With high regioselectivity, 100 % atom economy, and convenient product isolation, this heterogeneously catalyzed version of the Dorn cycloaddition corresponds to click‐chemistry criteria.

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Borenes and boranes : Silylaminoiminoborenes, such as depicted, were isolated after treatment of halogen triels with silylaminofluoroboranes. In addition, novel aryl‐ and silyl‐substituted diaminofluoroboranes were also prepared in order to substantiate this reaction route.

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Self‐assembly line : In the presence of a DNA analyte or low‐molecular‐weight substrates, multicomponent nucleic acids self‐assemble into cooperatively stabilized functional nanostructures (see scheme) that activate DNAzyme cascades.

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Positive discrimination : Chemo‐ and regioselective palladium‐catalyzed cycloetherification of allendiols, namely β,γ‐ and γ,δ‐allendiols, may occur by judicious choice of palladium‐catalyzed conditions owing to their potential ability to discriminate between both nucleophilic sites (see scheme).

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Supramolecular chirality and liquid crystalline OFET : Achiral end‐capped oligothiophenes can be tuned to exhibit supramolecular chirality with unique striped textures showing distinct circular dichroism signals as well as a highly ordered SmE phase that leads to high hole carrier mobility.

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Fast detection of cellular thiols in aqueous medium was achieved using a newly developed fluorescence probe (see picture). Based on this probe, a high‐throughput fluorescence assay for glutathione reductase was developed.

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Picky ferryl : The complex [Fe(Tp)(BF)] (Tp=hydrotris(3,5‐diphenylpyrazolyl)borate; BF=benzoylformate) reacts with O2 to generate an oxidant (see picture; O red, pink; Fe yellow; N blue; C gray; H white) that oxidizes added hydrocarbons shape‐selectively. Discrimination derives from a cleft formed by two phenyl groups of the Tp ligand, favoring oblate spheroidal substrates.

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Donor1+donor2→acceptor : The second‐order NLO molecular properties of a class of dipolar chromophores that incorporate the following design elements are investigated: 1) a substituted hydrazono moiety as a strong donor; 2) a pyrrole ring as an auxiliary donor; 3) strong acceptor groups (see figure). Their first hyperpolarisabilities show good promise for use in electro‐optical devices.

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Stack them helically : A self‐assembled helically stacked array of up to 11 porphyrin (Po)‐modified uridines (red and blue in the double strand shown) is based on the supramolecular scaffold of duplex DNA and shows promising optical properties. Such architectures could find application as functional molecules for photoactive nanomaterials and photonic nanostructures.

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Radical assembly : Halogen bonding has been observed for the first time between an isoindoline nitroxide and an iodoperfluorocarbon (see figure), which cocrystallize to form a discrete 2:1 supramolecular compound in which N? O.???I halogen bonding is the dominant intermolecular interaction. This illustrates the potential use of halogen bonding and isoindoline nitroxide tectons for the assembly of organic spin systems.

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