期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 61, 期 48, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202213499
关键词
Asymmetric Ligands; Lanthanide; Magnetic Anisotropy; Mixed Anions; Nonlinear Optical
资金
- Clemson University, College of Science, Department of Chemistry
- Gdansk University of Technology [2019/35/D/ST5/03769]
- Ministry of Science and Higher Education
By using mixed-ligand design, we have developed a new chemical pathway for creating lanthanide materials with noncentrosymmetric chiral properties and multiple functionalities, exhibiting excellent performance in terms of optical nonlinearity and magnetic anisotropy.
Bottom-up assembly of optically nonlinear and magnetically anisotropic lanthanide materials involving precisely placed spin carriers and optimized metal-ligand coordination offers a potential route to developing electronic architectures for coherent radiation generation and spin-based technologies, but the chemical design historically has been extremely hard to achieve. To address this, we developed a worthwhile avenue for creating new noncentrosymmetric chiral Ln(3+) materials Ln(2)(SeO3)(2)(SO4)(H2O)(2) (Ln=Sm, Dy, Yb) by mixed-ligand design. The materials exhibit phase-matching nonlinear optical responses, elucidating the feasibility of the heteroanionic strategy. Ln(2)(SeO3)(2)(SO4)(H2O)(2) displays paramagnetic property with strong magnetic anisotropy facilitated by large spin-orbit coupling. This study demonstrates a new chemical pathway for creating previously unknown polar chiral magnets with multiple functionalities.
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