Go for the gold! The structural evolution of peptide binding and assembly on a Au(111) surface is dynamic and involves surface diffusion and multiple stages of molecular thin‐film topology development (see schematic depiction and corresponding AFM images). The new fundamental observations may form the basis of peptide‐based novel hybrid molecular technologies of the future.
Don′t tell azole : The first metal‐catalyzed direct coupling of metal sulfides with aryl halides and subsequent intramolecular condensation provided substituted benzothiazoles (see scheme). A wide range of functional groups are tolerated under the reaction conditions.
The novel Yb succinate metal–organic framework exhibits a reversible single‐crystal to single‐crystal polymorphic transformation (see figure) when it is heated above 130 °C, returning to its initial form when back at room temperature. This transformation produces a change in the coordination sphere of the Yb atoms, which influences the catalytic activity of the material.
Making ends meet : The L ‐gulopyranosyl trichloroacetimidate and 1,6‐anhydro‐2,3‐di‐O‐benzyl‐β‐L ‐gulopyranose, efficiently derived from L ‐ascorbic acid, were individually used as a starting unit and an elongation unit to prepare L ‐guluronic acid linked alginate oligosaccharides in excellent α selectivity and in good yields.
Hide and seek : The composition of a dynamic covalent equilibrium reaction is determined by measuring the ‘left‐over’ concentration of a reference compound (blue object, see picture). Reaction of the reference compound with a scavenger generates a characteristic UV/Vis signal that is independent of the molecular structure of the target.
Looks matter: Generally, the morphology of titania thin films is crucial for their performance, hence much effort is spent to tailor the desired morphology. X‐ray scattering enables the monitoring of the crystalline titania layer morphology during build‐up of the functional multilayer stack (see Figure). Herein evidence is provided that the morphology is preserved throughout the fabrication process.
The next generation : The grafting of titanocene complexes on the surfaces of MCM‐41 and SBA‐15 led to a new generation of anticancer drugs, which are very active against human cancer cells.
Wheels of steel : Two enantiomerically pure chiral {Fe28} wheel‐like aggregates have been synthesized from the acetate buffer solution containing ferric ions and chiral tartrate ligands (see picture). These compounds are the largest chiral ferric aggregates isolated to date.
Solid‐state route to a cyclobutenone : Ruthenium perchlorocyclobutenonyl complex 2 is obtained by solid‐state photoisomerization of ruthenium trichloroacetyl acetylide complex 1 . The four‐membered ring is sufficiently robust that transfer of the intact ligand could be readily achieved in a reaction of 2 with an enyne. Cyclobutenedionyl complex 3 was obtained by hydrolysis of 2 in H2O/THF.
MOF on MOF: Core–shell porous coordination polymer (PCP) crystals are fabricated at the single‐crystal level by epitaxial growth in solution. Synchrotron X‐ray diffraction measurements unveiled the structural relationship between the shell crystal and the core crystal, where in‐plane rotational epitaxial growth compensates the difference in lattice constant.
Seeing is sensing : Calsequestrin (CSQ) functionalized gold nanoparticles undergo calcium‐dependent CSQ polymerization, which results in a clear color change (see picture) together with precipitation. The sensing system is specific for Ca2+ ions and the differences between normal and disease‐associated abnormal (hypercalcemia) Ca2+ ion levels in serum can be distinguished with the naked eye.
Highly active, selective, and stable : Highly ordered mesoporous carbon without deposition of metal particles catalyzes the oxidative dehydrogenation of ethyl benzene to styrene. A high activity and selectivity as well as long catalytic stability when compared with activated carbon, is observed from this catalyst.
