Quantum magnetism of spin qubits in S = 1/2 Cu(II) systems in discrete complexes, chains, and metal-organic frameworks

被引:0
作者
Wakizaka, Masanori [1 ]
Yamashita, Masahiro [2 ,3 ]
机构
[1] Chitose Inst Sci & Technol, Fac Sci & Technol, Dept Appl Chem & Biosci, 758-65 Bibi, Chitose 0668655, Japan
[2] Tongji Univ, Sch Chem Sci & Engn, Siping Rd 1239, Shanghai 200092, Peoples R China
[3] Tohoku Univ, Grad Sch Sci, Dept Chem, 6-3 Aramaki Aza Aoba,Aoba Ku, Sendai 9808578, Japan
来源
CHEMICAL PHYSICS REVIEWS | 2025年 / 6卷 / 01期
关键词
LATTICE-RELAXATION; MOLECULAR QUBITS; DYNAMICS; DESIGN; CU;
D O I
10.1063/5.0226942
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In the last decade, S = 1/2 systems of Cu(II) complexes and Cu(II) ions in the solid state have been found to exhibit slow magnetic relaxations. The mechanism driving this magnetic behavior is different from that of high spin single-molecule magnets and that of bulk/nanoparticle magnets. This behavior is related to spin qubits and is considered to be a new type of quantum magnetism. This review focuses on the magnetic relaxation (tau), spin-lattice relaxation (T-1), and spin-spin relaxation (T-2 or T-m) of isolated Cu(II) complexes, Cu(II) 1D-chains, and Cu(II)-doped metal-organic frameworks. Although these properties have been well studied in isolated Cu(II) systems, studies on systems that exhibit magnetic interactions are still elusive. With the aim of progressing toward the entanglement of spin states and quantum computing using spin qubits, a greater number of studies on molecule-based spin qubits that exhibit magnetic interactions will be conducted and will be of increasing importance from now on.
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页数:8
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