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Qubits are the basic unit of quantum information and computation. To realize quantum computing and information processing, the decoherence times of qubits must be long enough. Among the studies of molecule-based electron spin qubits, most of the work focused on the ions with the spin S=1/2, where only single-bit gates can be constructed. However, quantum operations require the qubits to interact with each other, so people gradually carry out relevant research in ions or systems with S>1/2 and multilevel states. In this work, a two-dimensional (2D) oxygen-coordinated Gd Na -based oxamato supramolecular coordination framework, Na[Gd(4-HOpa) (H O)] ⋅ 2H O (1, 4-HOpa=N-4-hydroxyphenyloxamate), was selected as a possible carrier of qubit. The field-induced slow magnetic relaxation shows this system has phonon bottleneck (PB) effect at low temperatures with a very weak magnetic anisotropy. The pulse electron paramagnetic resonance studies show the spin-lattice and spin-spin relaxation times are T =1.66 ms at 4 K and T =4.25 μs at 8 K for its diamagnetically diluted sample (1Gd0.12 %). It suggested that the relatively long decoherence time is mainly ascribed to its near isotropic and the PB effect from resonance phonon trapped for pure sample, while the dilution further improves its qubit performance.
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http://dx.doi.org/10.1002/chem.202301771 | DOI Listing |
Chemistry
November 2023
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, 210023, Nanjing, P. R. China.
Qubits are the basic unit of quantum information and computation. To realize quantum computing and information processing, the decoherence times of qubits must be long enough. Among the studies of molecule-based electron spin qubits, most of the work focused on the ions with the spin S=1/2, where only single-bit gates can be constructed.
View Article and Find Full Text PDFChem Commun (Camb)
January 2023
Instituto de Ciencia Molecular (ICMol), Universidad de Valencia, 46980, Paterna, Valencia, Spain.
Since the emergence of metal-organic frameworks (MOFs), a myriad of thrilling properties and applications, in a wide range of fields, have been reported for these materials, which mainly arise from their porous nature and rich host-guest chemistry. However, other important features of MOFs that offer great potential rewards have been only barely explored. For instance, despite the fact that MOFs are suitable candidates to be used as chemical nanoreactors for the preparation, stabilization and characterization of unique functional species, that would be hardly accessible outside the functional constrained space offered by MOF channels, only very few examples have been reported so far.
View Article and Find Full Text PDFInorg Chem
May 2021
Instituto de Química, Universidade Federal de Goiás, Goiânia, Goiás, Brazil, 74690-900.
Dalton Trans
January 2021
Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, IPCM, F-75252, Paris, France.
The use of solvothermal conditions has succesfully led to the preparation of heterometallic 1D coordination polymers from a co-bidentate-tridentate phenolato-oxamato ligand. The reaction of the N-(2-hydoxyphenyl)oxamic acid (ohpma) with acetate salts of transition metal ions at 80 °C has yielded the heterobimetallic [Cu(ohpma)M(OAc)(DMF)2] (M = Co (1); Mn (2)) and the heterotrimetallic [Cu(ohpma)Co0.57Mn0.
View Article and Find Full Text PDFInorg Chem
November 2019
Departament de Química Inorgànica, Instituto de Ciencia Molecular , Universitat de València, 46980 Paterna , València , Spain.
Achieving fine control on the structure of metal-organic frameworks (MOFs) is mandatory to obtain target physical properties. Herein, we present how the combination of a metalloligand approach and a postsynthetic method is a suitable and highly useful synthetic strategy to success on this extremely difficult task. First, a novel oxamato-based tetranuclear cobalt(III) compound with a tetrahedron-shaped geometry is used, for the first time, as the metalloligand toward calcium(II) metal ions to lead to a diamagnetic Ca-Co three-dimensional (3D) MOF ().
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