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- W2891827610 abstract "Both heteroleptic (phthalocyaninato)(hemiporphyrazinato) and homoleptic bis(hemiporphyrazinato) dysprosium double-decker complexes, Dy[H(Hp)2] (1) and Dy[H(Pc)(Hp)] (2) (H2Pc = metal-free phthalocyanine; H2Hp = metal-free hemiporphyrazine), were designed, synthesized, and structurally characterized. The dysprosium center in both double-deckers are octa-coordinated with a nearly ideal square-antiprismatic coordination geometry, which provides an increased molecular anisotropy for the dysprosium ion and ensures the strengthened magnetic properties of both single-ion magnets (SIMs) in terms of coordination geometry. Magnetic studies reveal that both double-deckers exhibit typical SIM behavior with a spin reversal energy barrier of 80.1 ± 6.3 K for 1 and 57.3 ± 3.8 K for 2 as well as the hysteresis loops emerging at 3 K. In particular, introduction of two Hp ligands with four pyridine nitrogen atoms coordinated with the dysprosium spin center endows Dy[H(Hp)2] (1) with the thus far highest energy barrier among the sandwich-type dysprosium SIMs with N4-macrocyclic ligands, revealing the potential applications of sandwich-type lanthanide complexes with Hp ligands in molecular-based information storage." @default.
- W2891827610 created "2018-09-27" @default.
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- W2891827610 date "2018-09-19" @default.
- W2891827610 modified "2023-10-13" @default.
- W2891827610 title "Hemiporphyrazine-Involved Sandwich Dysprosium Double-Decker Single-Ion Magnets" @default.
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- W2891827610 doi "https://doi.org/10.1021/acs.inorgchem.8b02068" @default.
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- W2891827610 hasPublicationYear "2018" @default.
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