Diffusion of interstitial carbon atoms in iron is the rate-limiting phenomenon of a number of phase transitions in body-centered (bec) and body-centered tetragonal (bct) phases such as ferrite and martensite. These phases being rarely stress-free and undeformed, the influence of stress/strain on the diffusivity of carbon is essential, although scarcely documented. We developed a model of carbon elastodiffusion in bct-iron. We combined anisotropie linear elasticity theory of point defects, the dilute approximation of regular solutions and the multisite model of random walk into a coherent mean-field theory. The model allows predicting the effects of composition, temperature and mechanical loading on the anisotropy of carbon diffusion. Density functional theory calculations have provided most of the materials parameters. The predictions were successfully tested against kinetic Monte Carlo simulations. Our results show that compression of the crystal increases carbon diffusivity, while tension has the opposite effect. Axial straining is accompanied by a large anisotropy of diffusion. This effect could be exploited to produce stress-controlled diffusion channeling for the engineering of anisotropie micro structures during thermal ageing of martensitic Fe-C alloys.

An expedient synthesis of a new family of configurationally stable dioxa[6]helicenes was established using a sequential helicoselective organocatalyzed heteroannulation/eliminative aromatization via enantioenriched fused 2-nitro dihydrofurans featuring both central and helical chiralities. Starting from simple achiral precursors, a broad range of these previously unknown chiral heterocyclic scaffolds were obtained with good efficiency, and their aromatization proceeded with very high enantiopurity retention in most cases.

Porphyrin cage-compounds are used as biomimetic models and substrate-selective catalysts in supramolecular chemistry. In this work we present the resolution of planar-chiral porphyrin cages and the determination of their absolute configuration by vibrational circular dichroism in combination with density functional theory calculations. The chiral porphyrin-cages form complexes with achiral and chiral viologen-guests and upon binding one of the axial enantiomorphs of the guest is bound selectively, as is indicated by induced-electronic-dichroism-spectra in combination with calculations. This host-guest binding also leads to unusual enhanced vibrational circular dichroism, which is the result of a combination of phenomena, such as rigidification of the host and guest structures, charge transfer, and coupling of specific vibration modes of the host and guest. The results offer insights in how the porphyrin cage-compounds may be used to construct a future molecular Turing machine that can write chiral information onto polymer chains.