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Multicompartmental microcylinders can be produced by a combination of electrohydrodynamic co‐spinning and microsectioning, as described by J. Lahann et al. in their Communication on page 4589 ff. The number of individual compartments, relative compartment orientation, chemical composition and functionality, and aspect ratio can be precisely tuned. Each color in the longitudinal and cross‐sectional micrograph images depicts an individual compartment.

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Organic circularly polarized (CP) lasers have received increasing attention due to their future photoelectric applications. Here, we demonstrate a CP laser from a pure organic crystal-filled microcavity without any chiral molecules or chiral structures. Benefited from the giant anisotropy and excellent laser gain of organic crystals, optical Rashba-Dresselhaus spin-orbit coupling effect can be induced and is conductive to the CP laser in such microcavities. The maximum dissymmetry factor of the CP lasing with opposite helicities reachs 1.2. Our strategy may provide a new idea for the design of CP lasers towards future 3D laser displays, information storage and other fields.  相似文献   

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Perfluoroaryl boranes are an important class of organometallic Lewis acids. The synthesis of perfluorinated compounds brings special challenges to tried‐and‐true synthetic methodologies. In their Communication on page 2955 ff., W. E. Piers and co‐workers present the synthesis of a new, fully fluorinated heterocyclic borane that is also a member of the rare antiaromatic borole class of compounds. The route relies on normally facile transmetallation reactions made more difficult by the electron‐withdrawing C6F5 groups of the target product.

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Continuous switching between high‐spin and low‐spin magnetic states can be accomplished by irradiation with red and green laser light, respectively. In their Communication on page 2549 ff., S. R. Batten and co‐workers report a metallo‐supramolecule that undergoes spin crossover (SCO) switching induced by temperature change or light irradiation. The SCO behavior is also dependent on the presence and nature of intercalated solvent molecules within the porous crystal structure.

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