372 research outputs found

    Report on the role of extra-institutional actors in the democratic system (lobbying)

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    Sequential localization of a complex electron fluid

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    Complex and correlated quantum systems with promise for new functionality often involve entwined electronic degrees of freedom. In such materials, highly unusual properties emerge and could be the result of electron localization. Here, a cubic heavy fermion metal governed by spins and orbitals is chosen as a model system for this physics. Its properties are found to originate from surprisingly simple low-energy behavior, with two distinct localization transitions driven by a single degree of freedom at a time. This result is unexpected, but we are able to understand it by advancing the notion of sequential destruction of an SU(4) spin-orbital-coupled Kondo entanglement. Our results implicate electron localization as a unified framework for strongly correlated materials and suggest ways to exploit multiple degrees of freedom for quantum engineering.Comment: 21 pages, 4 figures (preprint format

    Transanular interaction in [2.2]phanes: [2.2](4,4')diphenylophane and [2.2](2,7) fluorenophane

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    The emission spectra and the zero field splitting parameters D and E of the first excited triplet states of [2.2](4,4′) diphenylophane 3 and of the two stereoisomeric syn- and anti [2.2] (2,7) fluorenophanes 4a and 4b are investigated and compared with those of the corresponding monomers

    Transannular interactions in [2.2] phanes as studied by luminescence and optical detection of magnetic resonance

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    Emission spectra of different types of [2.2] naphthalenophanes were measured at 1.25 K in glasses as well as in small single crystals. In addition, the D and E values of the excited triplet states were studied by optical detection of magnetic resonance in zero field and the results compared with the corresponding monomeres
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