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Engineering a high-barrier d-f single-molecule magnet centered with hexagonal bipyramidal Dy(Ⅲ)unit

Science China Chemistry 2024年第10期67卷 3291-3298页

作者： Wei Deng Chan-Ying Yao Yan-Cong Chen Ying-Qian Zhou Shan-Nan Du Jun-Liang Liu Ming-Liang Tong Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education School of ChemistryInstitute of Green Chemistry and Molecular EngineeringGuangdong Basic Research Center of Excellence for Functional Molecular EngineeringSun Yat-sen UniversityGuangzhou 510006China

In the pursuit of high-performance single-molecule magnets(SMMs),incorporating intramolecular magnetic coupling emerges as a pivotal *** these,d-f SMMs have garnered significant attention due to their remarkable versatility,which lies in their ability to tune coordination environments and facilely substitute metal ***,achieving performance-centric d-f SMMs through the synergistic interplay between highly anisotropic f ions and d-f magnetic interactions remains a formidable *** mononuclear hexagonal bipyramidal(D_(6h))Dy^(Ⅲ)SMMs have been successfully isolated,the exploration of d-f SMMs featuring D_(6h)-lanthanide metal centers remains uncharted *** this study,we employed planar bipodal ligands in conjunction with“staple-like”axial phenoxide ligands to synthesize the first hexagonal bipyramidal d-f ***,this compound exhibits alternating-current magnetic susceptibilities peaking up to 68 K with an energy barrier surpassing 1,200 K,thus establishing a new benchmark within the heterometallic d-f SMM landscape inclusive of complexes with diamagnetic d metals and paramagnetic f ***,the ferromagnetic interaction at the d-f sites engenders oscillating relaxation times contingent on the magnetic field—a characteristic distinct from mononuclear *** findings shed light on a deliberate design approach for d-f SMMs,emphasizing the cooperative utilization of high-barrier lanthanide modules alongside d ions through magnetic *** synergy significantly enhances and diversifies the magnetic dynamics of these intriguing molecular systems.

关键词： single-molecule magnets magnetic coupling crystal engineering hexagonal bipyramid energy barrier

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3D TEM study on hollow α-Fe2O3 nanostructures and nanorings

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Progress in Natural Science:Materials International 2019年第6期29卷 685-689页

作者： Ming Lin Enyi Ye Jia Zhang Institute of Materials Research and Engineering A*STAR (Agency for Science Technology and Research) Institute of High Performance Computing A*STAR (Agency for Science Technology and Research)

Controlled synthesis of hollow structures with non-spherical holes is significant in fabricating nanomaterials with well-defined geometries and specific catalytic and electrochemical properties. Here we report the synthesis of uniform hexagonal bipyramid hematite(α-Fe2O3) nanoparticles with hollow and faceted interior via directional etching process in solution. The delicate hollow structures were investigated by electron tomography and growth mechanism was revealed unambiguously. The three-dimensional visualization demonstrates the outside surfaces of hematite particles are enclosed by six {104} and twelve {113} planes, due to the stabilizing effect of the F-anions on the exposed surfaces. The concurrent etching process is a reverse process of crystal growth and leads to the dissolution occurring at the edges and tips of the hexagonal bipyramid particles, resulting in the perforated crystals with exposed {102} internal facets or overetched nanorings with hexagonal *** nanoscale growth and etching process still strictly follows the bulk crystal growth mechanism, thus shedding light on the synthesis of other nanoparticle with controlled morphologies and porous structures.

关键词： Tomography hexagonal bipyramid Dissolution Facet control Phase transformation

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