Slow magnetic relaxation behaviors and diamagnetic dilution studies of a carboxyl bridged dinuclear dysprosium(III) complex
By using a rigid bulky carboxylic ligand α-cyanocinnamic acid (CCA), a dinuclear dysprosium (III) complex [Dy2(CCA)6 (MeOH)4] (1) was synthesized. Single crystal X-ray crystallography reveals that the two eight-coordinate dysprosium ions are bridged by four deprotonated carboxyl groups, forming a ce...
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Published in | Journal of rare earths Vol. 42; no. 11; pp. 2088 - 2096 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.11.2024
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Abstract | By using a rigid bulky carboxylic ligand α-cyanocinnamic acid (CCA), a dinuclear dysprosium (III) complex [Dy2(CCA)6 (MeOH)4] (1) was synthesized. Single crystal X-ray crystallography reveals that the two eight-coordinate dysprosium ions are bridged by four deprotonated carboxyl groups, forming a centrosymmetric paddle-wheel-like structure. Dynamic magnetic property measurements indicate that complex 1 displays field-induced slow magnetic relaxation. The temperature-dependent relaxation times can be fitted using Orbach and Raman processes with parameters of n = 2.8 (2), C = 27 (8) s−1/Kn, τ0 = 5 (2) × 10−10 s and Ueff = 40 (3) cm−1. Magnetic studies on the diamagnetic YIII-diluted analogue [Dy0.206Y1.794(CCA)6 (MeOH)4] (2) reveal its slow magnetic relaxation behavior without external dc field and the antiferromagnetic coupling between the DyIII ions in 1. Fits on the obtained relaxation times of 2 lead to the parameters of n = 4.5 (3), C = 0.7 (2) s−1/Kn, τ0 = 2.8 (2) × 10−9 s and Ueff = 38 (2) cm−1. The results suggest that slow magnetic relaxation originates from the single-ion relaxation of DyIII ions. Moreover, the diamagnetic dilution can suppress other fast relaxation pathways at low temperature, on account of the elimination of magnetic coupling and dipolar interaction. Ab initio calculations were then performed on the single DyIII ion species {YDy} and indicate that the first excited Kramers doublets (KDs) lie at ca. 76 cm−1, which is slightly higher than the experimental Ueff value. The intramolecular magnetic interactions were also calculated and indicate a weak ferromagnetic dipole-diploe magnetic interaction and an antiferromagnetic exchange coupling.
A dinuclear dysprosium (III) complex exhibiting field-induced slow magnetic relaxation was furtherly studied by ab initio calculations and diamagnetic dilution. [Display omitted] |
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AbstractList | By using a rigid bulky carboxylic ligand α-cyanocinnamic acid (CCA), a dinuclear dysprosium (III) complex [Dy2(CCA)6 (MeOH)4] (1) was synthesized. Single crystal X-ray crystallography reveals that the two eight-coordinate dysprosium ions are bridged by four deprotonated carboxyl groups, forming a centrosymmetric paddle-wheel-like structure. Dynamic magnetic property measurements indicate that complex 1 displays field-induced slow magnetic relaxation. The temperature-dependent relaxation times can be fitted using Orbach and Raman processes with parameters of n = 2.8 (2), C = 27 (8) s−1/Kn, τ0 = 5 (2) × 10−10 s and Ueff = 40 (3) cm−1. Magnetic studies on the diamagnetic YIII-diluted analogue [Dy0.206Y1.794(CCA)6 (MeOH)4] (2) reveal its slow magnetic relaxation behavior without external dc field and the antiferromagnetic coupling between the DyIII ions in 1. Fits on the obtained relaxation times of 2 lead to the parameters of n = 4.5 (3), C = 0.7 (2) s−1/Kn, τ0 = 2.8 (2) × 10−9 s and Ueff = 38 (2) cm−1. The results suggest that slow magnetic relaxation originates from the single-ion relaxation of DyIII ions. Moreover, the diamagnetic dilution can suppress other fast relaxation pathways at low temperature, on account of the elimination of magnetic coupling and dipolar interaction. Ab initio calculations were then performed on the single DyIII ion species {YDy} and indicate that the first excited Kramers doublets (KDs) lie at ca. 76 cm−1, which is slightly higher than the experimental Ueff value. The intramolecular magnetic interactions were also calculated and indicate a weak ferromagnetic dipole-diploe magnetic interaction and an antiferromagnetic exchange coupling.
A dinuclear dysprosium (III) complex exhibiting field-induced slow magnetic relaxation was furtherly studied by ab initio calculations and diamagnetic dilution. [Display omitted] |
Author | Lin, Weiquan Qiu, Yibo Cao, Manli Xu, Weiqin Liu, Wenting Deng, Xin |
Author_xml | – sequence: 1 givenname: Wenting orcidid: 0000-0002-6826-8594 surname: Liu fullname: Liu, Wenting email: wen-ting.liu@foxmail.com organization: School of Chemistry and Materials Science, Guangdong University of Education, Guangzhou, 510303, China – sequence: 2 givenname: Yibo surname: Qiu fullname: Qiu, Yibo organization: School of Chemistry and Chemical Engineering/Institute of Clean Energy and Materials, Guangzhou University, Guangzhou, 510006, China – sequence: 3 givenname: Weiqin surname: Xu fullname: Xu, Weiqin organization: School of Chemistry and Materials Science, Guangdong University of Education, Guangzhou, 510303, China – sequence: 4 givenname: Manli surname: Cao fullname: Cao, Manli organization: School of Chemistry and Materials Science, Guangdong University of Education, Guangzhou, 510303, China – sequence: 5 givenname: Xin surname: Deng fullname: Deng, Xin organization: School of Chemistry and Materials Science, Guangdong University of Education, Guangzhou, 510303, China – sequence: 6 givenname: Weiquan orcidid: 0000-0003-0698-0719 surname: Lin fullname: Lin, Weiquan email: linwquan@gzhu.edu.cn organization: School of Chemistry and Chemical Engineering/Institute of Clean Energy and Materials, Guangzhou University, Guangzhou, 510006, China |
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Snippet | By using a rigid bulky carboxylic ligand α-cyanocinnamic acid (CCA), a dinuclear dysprosium (III) complex [Dy2(CCA)6 (MeOH)4] (1) was synthesized. Single... |
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SubjectTerms | Diamagnetic dilution Dilanthanide complexes Rare earths Single-molecule magnets |
Title | Slow magnetic relaxation behaviors and diamagnetic dilution studies of a carboxyl bridged dinuclear dysprosium(III) complex |
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