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.
The highest Hg‐ion adsorbance so far , namely up to 2063 mg g?1, has been achieved by poly(aniline‐co‐5‐sulfo‐2‐anisidine) nanosorbents. Sorption of Hg ions occurs mainly by redox and chelation mechanisms (see scheme), but also by ion exchange and physisorption.
The fibril structure formed by the amyloidogenic fragment SNNFGAILSS of the human islet amyloid polypeptide (hIAPP) is determined with 0.52 Å resolution. Symmetry information contained in the easily obtainable resonance assignments from solid‐state NMR spectra (see picture), along with long‐range constraints, can be applied to uniquely identify the supramolecular organization of fibrils.
Lighting up new platinum anticancer complexes : Photoactivation of a platinum(IV) diazido anticancer complex in the presence of a derivative of imidazole, an important constituent of biomolecules, gives surprising photoproducts, including a tetrakis imidazole platinum(II) adduct (see figure), together with free azide, dioxygen and ammonia.
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.
No hurdle is too high : The regioselectivity and stereoselectivity of the halohydroxylation of non‐activated allenes are controlled by a remote sulfinyl group through anchimeric assistance (see scheme). The resulting halohydrines are excellent chiral targets for the preparation of optically pure propargylic alcohols and Baylis–Hillman‐type products.
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.
Our Schiff has come in : A homochiral porous lamellar solid based on chiral unsymmetrical Schiff base metal complexes was assembled by using coordination and hydrogen bonds (see picture). The host features a flexible helical framework and chiral amphiphilic channel surfaces capable of multiple interactions with guest species.
Prominent donors : A pyridyl, an imidazolyl, and a pyrazolyl donor function are part of the novel tripodal ligand depicted, which thus combines three of the most prominent donors applied in ligands for bioinorganic chemistry within one coordination unit. To exploit its behaviour and potential, first investigations have been carried out in relation to catechol dioxygenase mimicry.
The center of it all : An antitumor‐active trinuclear platinum complex forms unprecedented interstrand cross‐linked triadducts with 18‐mer DNA duplexes (see figure; complex in yellow with the platinum centers in red) and behaves differently from its dinuclear analogue.
Ligand design by‐pam : A ruthenium‐catalyzed asymmetric arylation of aldehydes with arylboronic acids has been developed, giving chiral diarylmethanols in good yields. The use of a chiral bidentate phosphoramidite ligand ((R,R)‐Me‐bipam) led to excellent enantioselectivities.
Two‐step magnetic transitions : An azide‐bridged 1D MnIII coordination polymer with a unique single end‐on mode was prepared; it displayed atypical antiferromagnetic couplings and field‐induced two‐step magnetic transitions (see figure). The spin‐canted phenomenon in the antiferromagnetic chain complex plays a pivotal role in establishing the slow magnetic relaxation.
Oil and water : A new energy‐efficient and atom‐economical catalytic route for the production of alkanes and methanol by upgrading the phenolic fraction of bio‐oil has been developed. The one‐pot aqueous‐phase hydrodeoxygenation process is based on two catalysts facilitating consecutive hydrogenation, hydrolysis, and dehydration reactions.
