Recently, direct kinetic experiments have shown that the oxidation of sulfur dioxide to sulfur trioxide by reaction with stabilized Criegee intermediates (CIs) is an important source of sulfuric acid in the atmosphere. So far, only small CIs, generated in photolysis experiments, have been directly detected. Herein, it is shown that large, stabilized CIs can be detected in the gas phase by FTIR spectroscopy during the ozonolysis of β-pinene. Their transient absorption bands between 930 and 830 cm(-1) appear only in the initial phase of the ozonolysis reaction when the scavenging of stabilized CIs by the reaction products is slow. The large CIs react with sulfur dioxide to give sulfur trioxide and nopinone with a yield exceeding 80%. Reactant consumption and product formation in time-resolved β-pinene ozonolysis experiments in the presence of sulfur dioxide have been kinetically modeled. The results suggest a fast reaction of sulfur dioxide with CIs arising from β-pinene ozonolysis.

Direct hydrogenation of CO2 to CO, the reverse water–gas shift reaction, is an attractive route to CO2 utilization. However, the use of molecular catalysts is impeded by the general reactivity of metal hydrides with CO2. Insertion into M–H bonds results in formates (MO(O)CH), whereas the abnormal insertion to the hydroxycarbonyl isomer (MC(O)OH), which is the key intermediate for CO-selective catalysis, has never been directly observed. We here report that the selectivity of CO2 insertion into a Ni–H bond can be inverted from normal to abnormal insertion upon switching from thermal to photochemical conditions. Mechanistic examination for abnormal insertion indicates photochemical N–H reductive elimination as the pivotal step that leads to an umpolung of the hydride ligand. This study conceptually introduces metal-ligand cooperation for selectivity control in photochemical transformations.

Photon-powered charge separation is achieved in a supramolecular architecture based on the dense packing of functional building blocks. Therefore, self-assembled dimers of interpenetrated coordination cages consisting of redoxactive chromophors were synthesized in a single assembly step starting from easily accessible ligands and Pd(II) cations. Two backbones consisting of electron rich phenothiazine (PTZ) and electron deficient anthraquinone (ANQ) were used to assemble either homo-octameric or mixed-ligand double cages. The electrochemical and spectroscopic properties of the pure cages, mixtures of donor and acceptor cages and the mixedligand cages were compared by steady-state UV−vis and transient absorption spectroscopy, supported by cyclic voltammetry and spectroelectrochemistry. Only the mixedligand cages, allowing close intra-assembly communication between the donors and acceptors, showed the evolution of characteristic PTZ radical cation and ANQ radical anion features upon excitation in the transient spectra. In contrast, excitation of the mixtures of the homo-octameric donor and acceptor cages in solution did not lead to any signs of electron transfer. Densely packed photo-and redox-functional self-assemblies promise molecular-level control over the morphology of the charge separation layer in future photovoltaic applications.

The synthesis of a centrally functionalized, ribbon-shaped [6]polynorbornane ligand L that self-assembles with Pd(II) cations into a {Pd2 L4 } coordination cage is reported. The shape-persistent {Pd2 L4 } cage contains two axial cationic centers and an array of four equatorial H-bond donors pointing directly towards the center of the cavity. This precisely defined supramolecular environment is complementary to the geometry of classic octahedral complexes [M(XY)6 ] with six diatomic ligands. Very strong binding of [Pt(CN)6 ](2-) to the cage was observed, with the structure of the host-guest complex {[Pt(CN)6 ]@Pd2 L4 } supported by NMR spectroscopy, MS, and X-ray data. The self-assembled shell imprints its geometry on the encapsulated guest, and desymmetrization of the octahedral platinum species by the influence of the D4h -symmetric second coordination sphere was evidenced by IR spectroscopy. [Fe(CN)6 ](3-) and square-planar [Pt(CN)4 ](2-) were strongly bound. Smaller octahedral anions such as [SiF6 ](2-) , neutral carbonyl complexes ([M(CO)6 ]; M=Cr, Mo, W) and the linear [Ag(CN)2 ](-) anion were only weakly bound, showing that both size and charge match are key factors for high-affinity binding.

Bitterfeld amber, sometimes referred to as Saxon or Saxonian amber, is a potentially significant but poorly known source of arthropod data for the Palaeogene of northern Europe. An important aspect is a long-standing controversy about the age of this amber: namely whether it is equivalent to, and perhaps merely a southerly extension of, the better-known Baltic amber, or whether it is a unique and geological younger deposit sampling a different fauna. Here, we briefly review the Bitterfeld arachnids with particular emphasis on how these data could be used to elucidate the age of this deposit. Five arachnid orders have been recorded from Bitterfeld amber: spiders (Araneae), acariform mites (Acariformes), parasitiform mites (Parasitiformes), harvestmen (Opiliones) and pseudoscorpions (Pseudoscorpiones). This is a lower diversity than Baltic amber, where scorpions (Scorpiones) and camel spiders (Solifugae) have also been recorded. Spiders are the most comprehensively studied group, with more than 75 described species. Other groups such as pseudoscorpions and mites appear to be very diverse, but are virtually undescribed. Morphological overlap is apparent in the arachnid fauna and 40 species are currently shared between Baltic and Bitterfeld amber whilst 50 species are unique to the Bitterfeld deposit. At the family level overlap is even higher, but in all groups Baltic amber appears more diverse than Bitterfeld. This overlap may be interpreted as evidence for temporal conspecifity of the Baltic and Bitterfeld ambers, albeit with the Bitterfeld and Baltic ambers possibly representing independent localities within a larger Eocene European amber area which also included the Rovno amber from the Ukraine. However, caution should be exercised because the taxonomic foundation for such assumptions is far from comprehensive, most of the material remains to be studied in detail using modern techniques of morphological reconstruction. There are further issues with date estimates because some arachnid groups show extraordinary morphological stasis over time, even at species level, which may bias the analyses available. Here, we review the available knowledge on Bitterfeld arachnids and discuss how a detailed assessment of this fauna, and other arthropod taxa, could be generated. Several natural history museums – including Hamburg and Berlin – as well as private collectors host major assemblages of Bitterfeld fossils which may help to clarify the debate about the age and provenance of the material, and the extent to which (morpho)-species were maintained both over geographical distances and potentially geological time.