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Journal ArticleDOI

Mononuclear lanthanide single-molecule magnets based on polyoxometalates.

TLDR
This single lanthanide ion polyoxometalate is the inorganic analogue of the bis(phthalocyaninato)lanthanide SMMs, both exhibiting very similar ligand field symmetries around the lanthanides ion (idealized D4d).
Abstract
[ErW10O36]9− is the first polyoxometalate behaving as a single-molecule magnet (SMM). It shows frequency-dependent out-of-phase magnetization and a thermally activated single relaxation process with an effective barrier of 55.8 K. This single lanthanide ion polyoxometalate is the inorganic analogue of the bis(phthalocyaninato)lanthanide SMMs, both exhibiting very similar ligand field symmetries around the lanthanide ion (idealized D4d). It is chemically stable and offers new avenues for organization and processing of single-molecule magnets. Furthermore, it can be made free from nuclear spins and opens the possibility to be used for studies of decoherence on unimolecular qubits.

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Citations
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Polyoxometalates: Building Blocks for Functional Nanoscale Systems

TL;DR: The possibilities of creating highly sophisticated functional hierarchical systems with multiple, interdependent, functionalities along with a critical analysis that allows the non-specialist to learn the salient features of POMs are discussed.
Journal ArticleDOI

Strategies towards single molecule magnets based on lanthanide ions

TL;DR: In this article, the authors reviewed the synthetic strategies employed in a concerted effort to obtain new single molecule magnets based on lanthanide ions in the framework of the research program on Molecular Magnetism funded by the Deutsche Forschungsgemeinschaft.
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Photocatalytic organic pollutants degradation in metal–organic frameworks

TL;DR: In this paper, a review of the application of metal-organic frameworks (MOFs) in photocatalytic degradation of organic pollutants is presented, where the reported examples are collected and analyzed; and the reaction mechanism, the influence of various factors on the catalytic performance, involved challenges, and the prospect are discussed and estimated.
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Lanthanides in molecular magnetism: old tools in a new field

TL;DR: This tutorial review discusses some basic aspects concerning the magnetic properties of rare-earth ions, and focuses on Dy(III) derivatives of the relation of the crystal field parameters, which determine the anisotropy of these systems and consequently their interesting magnetic properties.
References
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Journal ArticleDOI

Dispersion and Absorption in Dielectrics I. Alternating Current Characteristics

TL;DR: In this paper, the locus of the dielectric constant in the complex plane was defined to be a circular arc with end points on the axis of reals and center below this axis.
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Molecular spintronics using single-molecule magnets

TL;DR: This work reviews the first progress in the resulting field, molecular spintronics, which will enable the manipulation of spin and charges in electronic devices containing one or more molecules, and discusses the advantages over more conventional materials, and the potential applications in information storage and processing.
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Quantum Tunneling of Magnetization and Related Phenomena in Molecular Materials

TL;DR: The fundamental concepts needed to understand quantum size effects in molecular magnets are reviewed and critically report what has been done in the field to date are critically reported.
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Quantum computing in molecular magnets

TL;DR: In this article, an implementation of Grover's algorithm that uses molecular magnets was proposed, which can be used to build dense and efficient memory devices based on the Grover algorithm, in which one single crystal can serve as a storage unit of a dynamic random access memory device.
Journal ArticleDOI

Lanthanide Double-Decker Complexes Functioning as Magnets at the Single-Molecular Level

TL;DR: Double-decker phthalocyanine complexes with Tb3+ or Dy3+ showed slow magnetization relaxation as a single-molecular property and a significant temperature rise results from a mechanism in the relaxation process different from that in the transition-metal-cluster SMMs.
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