scholarly journals Near-Infrared Emissive Cyanido-Bridged {YbFe2} Molecular Nanomagnets Sensitive to the Nitrile Solvents of Crystallization

2021 ◽  
Vol 7 (6) ◽  
pp. 79
Author(s):  
Michal Liberka ◽  
Kseniia Boidachenko ◽  
Jakub J. Zakrzewski ◽  
Mikolaj Zychowicz ◽  
Junhao Wang ◽  
...  
Keyword(s):  
Single Molecule ◽  
Self Assembly ◽  
Near Infrared ◽  
Magnetic Data ◽  
Phonon Modes ◽  
Single Molecule Magnets ◽  
Molecular Nanomagnets ◽  
Dipole Interactions ◽  
Raman Process ◽  
Slow Magnetic Relaxation

One of the pathways toward luminescent single-molecule magnets (SMMs) is realized by the self-assembly of lanthanide(3+) ions with cyanido transition metal complexes. We report a novel family of emissive SMMs, {YbIII(4-pyridone)4[FeII(phen)2(CN)2]2}(CF3SO3)3·solv (solv = 2MeCN, 1·MeCN; 2AcrCN, 1·AcrCN; 2PrCN, 1·PrCN; 2MalCN·1MeOH; 1·MalCN; MeCN = acetonitrile, AcrCN = acrylonitrile, PrCN = propionitrile, MalCN = malononitrile). They are based on paramagnetic YbIII centers coordinating diamagnetic [FeII(phen)2(CN)2] metalloligands but differ in the nitrile solvents of crystallization. They exhibit a field-induced slow magnetic relaxation dominated by a Raman process, without an Orbach relaxation as indicated by AC magnetic data and the ab initio calculations. The Raman relaxation is solvent-dependent as represented by the power “n” of the BRamanTn contribution varying from 3.07(1), to 2.61(1), 2.37(1), and 1.68(4) for 1·MeCN, 1·PrCN, 1·AcrCN, and 1·MalCN, respectively, while the BRaman parameter adopts the opposite trend. This was correlated with the variation of phonon modes schemes, including the number of available vibrational modes and their energies, dependent on the increasing complexity of the applied nitrile. 1·MeCN and 1·MalCN show the additional T-independent relaxation assignable to dipole-dipole interactions as confirmed by its suppression in 1·AcrCN and 1·PrCN revealing longer Yb–Yb distances and the disappearance in the LuIII-diluted 1·MeCN@Lu. All compounds exhibit YbIII–centered near-infrared photoluminescence sensitized by organic ligands.

Near-infrared emissive Er(iii) and Yb(iii) molecular nanomagnets in metal–organic chains functionalized by octacyanidometallates(iv)

2019 ◽  
Vol 6 (9) ◽  
pp. 2423-2434 ◽  
Author(s):  
Robert Jankowski ◽  
Jakub J. Zakrzewski ◽  
Olga Surma ◽  
Shin-ichi Ohkoshi ◽  
Szymon Chorazy ◽  
...  
Keyword(s):  
Single Molecule ◽  
Crucial Role ◽  
Near Infrared ◽  
Single Molecule Magnets ◽  
Molecular Nanomagnets ◽  
Metal Organic ◽  
Nir Emission

Photoluminescent single-molecule magnets are formed in lanthanide(pyrazine N,N′-dioxide) chains with octacyanidometallate(iv) coordination branches playing a crucial role in sensitized NIR emission.

scholarly journals Organometallic Single-Ion Magnets

2014 ◽  
Vol 70 (a1) ◽  
pp. C274-C274
Author(s):  
Bing-Wu Wang ◽  
Zhe-Ming Wang ◽  
Song Gao
Keyword(s):  
Single Molecule ◽  
Basic Research ◽  
Information Storage ◽  
Tunneling Effect ◽  
Single Molecule Magnets ◽  
Magnetization Relaxation ◽  
Molecular Nanomagnets ◽  
Design And Synthesis ◽  
Potential Applications ◽  
Slow Magnetic Relaxation

The single-molecule magnets (SMMs) are attracting the increasing interesting due to their potential applications in high density information storage, quantum computing, molecular spintronics, and magnetic refrigeration. This field provides scientists a possible access into the crossover of the classical and quantum world, and a wonderful model to study the fascinating magnetic properties between microscopic and macroscopic materials, such as slow magnetization relaxation and quantum tunneling effect. After the milestone discovery of the first single-molecule magnets (SMMs) Mn12ac, many new SMMs were structurally and magnetically characterized. The most studied systems are mainly traditional coordination compounds with polynuclear structures. However, for the difficulties in the control of magnetic anisotropy and exchange coupling interactions of the cluster-type molecules, Mn12ac molecule is still one of the most important SMMs with the high relaxation barrier. From 2011 [1-3], we explored an organometallic sandwich molecule, Cp*ErCOT(Cp* = pentamethylcyclopenta-dienide; COT = cyclooctatetraenide), which behaves as a single-ion magnets, into the field of molecular nanomagnets. It opened a door of SMMs to the chemists in organometallic chemistry. Recently, we found some new sandwich or half-sandwich lanthanide organometallic molecules could also show the slow relaxation of magnetization. We hope these systems can provide new understandings of slow magnetic relaxation and new clues on the design and synthesis of molecular nanomagnets. This work was supported by NSFC, the National Basic Research Program of China.

scholarly journals Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad Ligand

Inorganics ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 50
Author(s):  
Bertrand Lefeuvre ◽  
Jessica Flores Gonzalez ◽  
Carlo Andrea Mattei ◽  
Vincent Dorcet ◽  
Olivier Cador ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Single Molecule ◽  
Applied Magnetic Field ◽  
Near Infrared ◽  
Dinuclear Complexes ◽  
Single Molecule Magnets ◽  
Single Molecule Magnet ◽  
X Ray ◽  
Redox Active ◽  
Raman Process

The reactions between the bis(1,10-phenantro[5,6-b])tetrathiafulvalene triad (L) and the metallo-precursors Yb(hfac)3(H2O)2 (hfac− = 1,1,1,5,5,5-hexafluoroacetylacetonato anion) and Dy(facam)3 (facam− = 3-trifluoro-acetyl-(+)-camphorato anion) lead to the formation of two dinuclear complexes of formula [Yb2(hfac)6(L)]·2(C7H16) ((1)·2(C7H16)) and [Dy2((+)facam)6(L)]·2(C6H14) ((2)·2(C6H14)). The X-ray structures reveal that the L triad bridges two terminal Yb(hfac)3 or Dy(facam)3 units. (1)·2(C7H16) behaved as a near infrared YbIII centered emitter and a field-induced Single-Molecule Magnet (SMM) while (2)·2(C6H14) displayed SMM behavior in both zero- and in-dc field. The magnetization mainly relaxes through a Raman process for both complexes under an optimal applied magnetic field.

Cu(ii)–Dy(iii) and Co(iii)–Dy(iii) based single molecule magnets with multiple slow magnetic relaxation processes in the Cu(ii)–Dy(iii) complex

2015 ◽  
Vol 44 (29) ◽  
pp. 13242-13249 ◽  
Author(s):  
Malay Dolai ◽  
Mahammad Ali ◽  
Ján Titiš ◽  
Roman Boča
Keyword(s):  
Schiff Base ◽  
Single Molecule ◽  
Schiff Base Ligand ◽  
Magnetic Relaxation ◽  
Magnetic Behaviour ◽  
Dinuclear Complexes ◽  
Relaxation Processes ◽  
Single Molecule Magnets ◽  
Slow Magnetic Relaxation

Two CuII–DyIII and CoIII–DyIII dinuclear complexes of a Schiff base ligand (H3L) exhibit single-molecule magnetic behaviour with multiple slow magnetic relaxation processes for the former.

Structural anisotropy of cyanido-bridged {CoII9WV6} single-molecule magnets induced by bidentate ligands: towards the rational enhancement of an energy barrier

2016 ◽  
Vol 52 (26) ◽  
pp. 4772-4775 ◽  
Author(s):  
Szymon Chorazy ◽  
Michał Rams ◽  
Anna Hoczek ◽  
Bernard Czarnecki ◽  
Barbara Sieklucka ◽  
...  
Keyword(s):  
Single Molecule ◽  
Energy Barrier ◽  
Magnetic Relaxation ◽  
Bidentate Ligands ◽  
Single Molecule Magnets ◽  
Structural Anisotropy ◽  
Slow Magnetic Relaxation

{CoII9[WV(CN)8]6} clusters capped by odd and even number of bidentate ligands reveal the improved slow magnetic relaxation due to the significant structural anisotropy.

Strictly linear trinuclear Dy–Ca/Mg–Dy single-molecule magnets: the impact of long-range f–f ferromagnetic interactions on suppressing quantum tunnelling of magnetization leading to slow magnetic relaxation

2017 ◽  
Vol 46 (25) ◽  
pp. 8259-8268 ◽  
Author(s):  
Wan-Ying Zhang ◽  
Yong-Mei Tian ◽  
Hong-Feng Li ◽  
Peng Chen ◽  
Yi-Quan Zhang ◽  
...  
Keyword(s):  
Long Range ◽  
Single Molecule ◽  
Magnetic Relaxation ◽  
Single Molecule Magnets ◽  
Quantum Tunnelling ◽  
Trinuclear Complexes ◽  
Slow Magnetic Relaxation ◽  
Ferromagnetic Interactions ◽  
The Impact

A series of linear trinuclear complexes Ln2M(OQ)8 [Ln(iii) = Dy and Er, M(ii) = Ca and Mg] were structurally and magnetically investigated.

Polyoxometalate-Supported Lanthanoid Single-Molecule Magnets

2014 ◽  
Vol 67 (11) ◽  
pp. 1542 ◽  
Author(s):  
Michele Vonci ◽  
Colette Boskovic
Keyword(s):  
Single Molecule ◽  
Energy Barrier ◽  
Magnetic Relaxation ◽  
Donor Ligands ◽  
Single Molecule Magnets ◽  
Single Molecule Magnet ◽  
Coordination Numbers ◽  
Oxygen Donor ◽  
Slow Magnetic Relaxation

Polyoxometalates are robust and versatile multidentate oxygen-donor ligands, eminently suitable for coordination to trivalent lanthanoid ions. To date, 10 very different structural families of such complexes have been found to exhibit slow magnetic relaxation due to single-molecule magnet (SMM) behaviour associated with the lanthanoid ions. These families encompass complexes with between one and four of the later lanthanoid ions: Tb, Dy, Ho, Er, and Yb. The lanthanoid coordination numbers vary between six and eleven and a range of coordination geometries are evident. The highest energy barrier to magnetisation reversal measured to date for a lanthanoid–polyoxometalate SMM is Ueff/kB = 73 K for the heterodinuclear Dy–Eu compound (Bu4N)8H4[DyEu(OH)2(γ-SiW10O36)2].

Magnetic field and dilution effects on the slow relaxation of {Er3} triangle-based arsenotungstate single-molecule magnets

2020 ◽  
Vol 49 (35) ◽  
pp. 12458-12465 ◽  
Author(s):  
Hanhan Chen ◽  
Lin Sun ◽  
Jinpeng Zhang ◽  
Zikang Xiao ◽  
Pengtao Ma ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Single Molecule ◽  
Magnetic Relaxation ◽  
Slow Relaxation ◽  
Relaxation Processes ◽  
Single Molecule Magnets ◽  
Thermally Activated ◽  
Slow Magnetic Relaxation ◽  
Dilution Effects

Triangular {Er3} cluster containing POM exhibits field-induced two thermally activated relaxation processes. Whereas, the diamagnetic dilution sample indicates slow magnetic relaxation with the QTM being partially suppressed.

Humidity driven molecular switch based on photoluminescent DyIIICoIII single-molecule magnets

2019 ◽  
Vol 7 (14) ◽  
pp. 4164-4172 ◽  
Author(s):  
Szymon Chorazy ◽  
Jakub J. Zakrzewski ◽  
Mateusz Reczyński ◽  
Koji Nakabayashi ◽  
Shin-ichi Ohkoshi ◽  
...  
Keyword(s):  
Single Molecule ◽  
Magnetic Relaxation ◽  
Room Temperature ◽  
Functional Materials ◽  
Molecular Switch ◽  
Dehydration Process ◽  
Single Molecule Magnets ◽  
Visible Photoluminescence ◽  
Slow Magnetic Relaxation

Functional materials incorporating cyanido-bridged DyIIICoIII molecules combine visible photoluminescence and slow magnetic relaxation, both switchable by the level of humidity within the reversible room temperature dehydration process.

Single-molecule magnets under dc field with an anion effect: self-assembly of pure dysprosium(iii) metallacycles

2021 ◽  
Vol 50 (1) ◽  
pp. 262-269
Author(s):  
Jianfeng Wu ◽  
Qianqian Yang ◽  
Haoyu Wang ◽  
Yan Ge ◽  
Jinkui Tang ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Single Molecule ◽  
Self Assembly ◽  
Structural Factors ◽  
Single Molecule Magnets ◽  
Anion Effect

The anion-adaptive self-assembly described here not only offers a facile approach to produce large single-molecule magnets but also provides an understanding of how structural factors affect the magnetic properties.

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