Publications by authors named "R Streubel"

Compared to aziridines, azaphosphiridines, which formally result from the replacement of a carbon atom by phosphorus, have been much less studied. In this work, accurate values for one of the most prominent properties, the ring strain energy (RSE), have been theoretically examined for a wide range of azaphosphiridine derivatives. Strongly related aspects of interest for developing the use of azaphosphiridines in heteroatom and polymer chemistry are ring opening reactions and polymerisations, the latter facilitated by their significantly high RSE.

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The transition from planar to three-dimensional (3D) magnetic nanostructures represents a significant advancement in both fundamental research and practical applications, offering vast potential for next-generation technologies like ultrahigh-density storage, memory, logic, and neuromorphic computing. Despite being a relatively new field, the emergence of 3D nanomagnetism presents numerous opportunities for innovation, prompting the creation of a comprehensive roadmap by leading international researchers. This roadmap aims to facilitate collaboration and interdisciplinary dialogue to address challenges in materials science, physics, engineering, and computing.

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Combining different heteroatoms in an epoxide-type ring having Lewis basic and acidic characteristics is challenging as it creates an increasing number of polar bonds and high ring strain energy. The first examples of isolable oxaphosphiranes, , epoxide rings with a phosphorus atom, have been synthesized using a facile and effective protocol starting from [pentacarbonyl{dichloro(trityl)phosphane}molybdenum(0)] (trityl = CPh), -butyllithium and commercially available fluorinated benzaldehydes. Reactions with various acids and bases will be described.

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We study the effect of strain on the magnetic properties and magnetization configurations in nanogranular FeGe1-xfilms (x=0.53±0.05) with and without B20 FeGe nanocrystals surrounded by an amorphous structure.

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Planar P- or P-bridged bis(NHCs), which have only been employed in transition metal complex chemistry so far, were subjected to BCl-containing solutions targeting the corresponding bis(NHC) BCl adducts. While the P(O)NEt-bridged bis(NHC) showed the expected adduct formation, the PNEt-bridged bis(NHC) reacted not only at the carbene moiety but also at the P-NEt functional group. The latter enabled access to the first 1,4-diphosphinine bis(NHC) main group adduct; its formation and properties were investigated by DFT calculations.

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