Field-induced slow magnetic relaxation in two-dimensional and three-dimensional Co(ii) coordination polymers

2019 ◽  
Vol 48 (41) ◽  
pp. 15529-15536 ◽  
Author(s):  
Deyun Ma ◽  
Guo Peng ◽  
Ying-Ying Zhang ◽  
Bo Li
Keyword(s):  
Coordination Polymers ◽  
Magnetic Relaxation ◽  
Three Dimensional ◽  
High Dimensional ◽  
Two Dimensional ◽  
The Family ◽  
Slow Magnetic Relaxation

Two two-dimensional and three-dimensional Co(ii) coordination polymers with slow magnetic relaxation are reported, which enlarge the family of high-dimensional coordination polymers exhibiting single ion magnet behavior.

Two-dimensional heterometallic CuIILnIII (Ln = Tb and Dy) coordination polymers bridged by dicyanamides showing slow magnetic relaxation behavior

CrystEngComm ◽  
2019 ◽  
Vol 21 (34) ◽  
pp. 5145-5151 ◽  
Author(s):  
Jiao-Jiao Kong ◽  
Jia-Chen Zhang ◽  
Yu-Xuan Jiang ◽  
Jin-Xia Tao ◽  
Wen-Yan Wang ◽  
...  
Keyword(s):  
Hysteresis Loop ◽  
Coordination Polymers ◽  
Magnetic Relaxation ◽  
Magnetic Hysteresis ◽  
Magnetic Hysteresis Loop ◽  
Relaxation Behavior ◽  
Relaxation Behaviour ◽  
Two Dimensional ◽  
Slow Magnetic Relaxation

Two-dimensional heterometallic CuIILnIII (Ln = Gd, Tb and Dy) coordination polymers bridged by dicyanamides showed slow magnetic relaxation behaviour and a magnetic hysteresis loop at 1.8 K was observed for the CuTb compound.

Non-traditional thermal behavior of Co(II) coordination networks showing slow magnetic relaxation

2021 ◽  
Author(s):  
Anna Switlicka ◽  
Barbara Machura ◽  
Alina Bieńko ◽  
Dariusz Bieńko ◽  
Cyril Rajnák ◽  
...  
Keyword(s):  
Thermal Behavior ◽  
Coordination Polymers ◽  
Spin System ◽  
Magnetic Relaxation ◽  
Magnetic Data ◽  
Zero Field ◽  
Two Dimensional ◽  
Coordination Networks ◽  
One Dimensional ◽  
Slow Magnetic Relaxation

Three new coordination polymers, one-dimensional ones [Co(5,6-(Me)2–bzim)2(dca)2] (1), [Co(5-Mebzim)2(dca)2]n (2) and two-dimensional polymer [Co(2-Mebzim)(dca)2]n (3), show DC magnetic data consistent with the S = 3/2 spin system with large zero-field...

scholarly journals Crystal structures of {[Cu(Lpn)2][Fe(CN)5(NO)]·H2O}nand {[Cu(Lpn)2]3[Cr(CN)6]2·5H2O}n[where Lpn = (R)-propane-1,2-diamine]: two heterometallic chiral cyanide-bridged coordination polymers

2015 ◽  
Vol 71 (4) ◽  
pp. 392-397
Author(s):  
Olha Sereda ◽  
Helen Stoeckli-Evans
Keyword(s):  
Hydrogen Bonds ◽  
Coordination Polymers ◽  
Three Dimensional ◽  
Water Molecules ◽  
Two Dimensional ◽  
Asymmetric Unit ◽  
Compound I ◽  
Distorted Octahedral ◽  
Coordination Spheres ◽  
Compound Ii

The title compounds,catena-poly[[[bis[(R)-propane-1,2-diamine-κ2N,N′]copper(II)]-μ-cyanido-κ2N:C-[tris(cyanido-κC)(nitroso-κN)iron(III)]-μ-cyanido-κ2C:N] monohydrate], {[Cu(Lpn)2][Fe(CN)5(NO)]·H2O}n, (I), and poly[[hexa-μ-cyanido-κ12C:N-hexacyanido-κ6C-hexakis[(R)-propane-1,2-diamine-κ2N,N′]dichromium(III)tricopper(II)] pentahydrate], {[Cu(Lpn)2]3[Cr(CN)6]2·5H2O}n, (II) [where Lpn = (R)-propane-1,2-diamine, C3H10N2], are new chiral cyanide-bridged bimetallic coordination polymers. The asymmetric unit of compound (I) is composed of two independent cation–anion units of {[Cu(Lpn)2][Fe(CN)5)(NO)]} and two water molecules. The FeIIIatoms have distorted octahedral geometries, while the CuIIatoms can be considered to be pentacoordinate. In the crystal, however, the units align to form zigzag cyanide-bridged chains propagating along [101]. Hence, the CuIIatoms have distorted octahedral coordination spheres with extremely long semicoordination Cu—N(cyanido) bridging bonds. The chains are linked by O—H...N and N—H...N hydrogen bonds, forming two-dimensional networks parallel to (010), and the networks are linkedviaN—H...O and N—H...N hydrogen bonds, forming a three-dimensional framework. Compound (II) is a two-dimensional cyanide-bridged coordination polymer. The asymmetric unit is composed of two chiral {[Cu(Lpn)2][Cr(CN)6]}−anions bridged by a chiral [Cu(Lpn)2]2+cation and five water molecules of crystallization. Both the CrIIIatoms and the central CuIIatom have distorted octahedral geometries. The coordination spheres of the outer CuIIatoms of the asymmetric unit can be considered to be pentacoordinate. In the crystal, these units are bridged by long semicoordination Cu—N(cyanide) bridging bonds forming a two-dimensional network, hence these CuIIatoms now have distorted octahedral geometries. The networks, which lie parallel to (10-1), are linkedviaO—H...O, O—H...N, N—H...O and N—H...N hydrogen bonds involving all five non-coordinating water molecules, the cyanide N atoms and the NH2groups of the Lpn ligands, forming a three-dimensional framework.

scholarly journals Different Benzendicarboxylate-Directed Structural Variations and Properties of Four New Porous Cd(II)-Pyridyl-Triazole Coordination Polymers

2020 ◽  
Vol 8 ◽  
Author(s):  
Ying Zhao ◽  
Jin Jing ◽  
Ning Yan ◽  
Min-Le Han ◽  
Guo-Ping Yang ◽  
...  
Keyword(s):  
Solid State ◽  
Coordination Polymers ◽  
Three Dimensional ◽  
Two Dimensional ◽  
Gas Sorption ◽  
Structural Variations ◽  
Benzenedicarboxylic Acid ◽  
Topological Framework ◽  
The Stability

Four new different porous crystalline Cd(II)-based coordination polymers (CPs), i. e., [Cd(mdpt)2]·2H2O (1), [Cd2(mdpt)2(m-bdc)(H2O)2] (2), [Cd(Hmdpt)(p-bdc)]·2H2O (3), and [Cd3(mdpt)2(bpdc)2]·2.5NMP (4), were obtained successfully by the assembly of Cd(II) ions and bitopic 3-(3-methyl-2-pyridyl)-5-(4-pyridyl)-1,2,4-triazole (Hmdpt) in the presence of various benzendicarboxylate ligands, i.e., 1,3/1,4-benzenedicarboxylic acid (m-H2bdc, p-H2bdc) and biphenyl-4,4′-bicarboxylate (H2bpdc). Herein, complex 1 is a porous 2-fold interpenetrated four-connected 3D NbO topological framework based on the mdpt− ligand; 2 reveals a two-dimensional (2D) hcb network. Interestingly, 3 presents a three-dimensional (3D) rare interpenetrated double-insertion supramolecular net via 2D ···ABAB··· layers and can be viewed as an fsh topological net, while complex 4 displays a 3D sqc117 framework. Then, the different gas sorption performances were carried out carefully for complexes 1 and 4, the results of which showed 4 has preferable sorption than that of 1 and can be the potential CO2 storage and separation material. Furthermore, the stability and luminescence of four complexes were performed carefully in the solid state.

Effect of the distant substituent on the slow magnetic relaxation of the mononuclear Co(ii) complex with pincer-type ligands

2020 ◽  
Vol 49 (14) ◽  
pp. 4206-4210
Author(s):  
Cyril Rajnák ◽  
Ján Titiš ◽  
Ján Moncol' ◽  
Roman Boča
Keyword(s):  
Magnetic Relaxation ◽  
Pincer Complexes ◽  
The Family ◽  
Slow Magnetic Relaxation

A hexacoordinated complex [Co(pydm)2](mdnbz)2 from the family of pincer complexes was prepared and structurally characterized.

Substituent effects of two isophthalate derivatives on the construction of cadmium coordination polymers incorporating a dipyridyl ligand

2018 ◽  
Vol 74 (8) ◽  
pp. 894-900 ◽  
Author(s):  
Lin Wang ◽  
Qian-Kun Zhou ◽  
Yun Xu ◽  
Ni-Ya Li
Keyword(s):  
Coordination Polymers ◽  
Self Assembly ◽  
Three Dimensional ◽  
Substituent Effects ◽  
Dicarboxylic Acids ◽  
Two Dimensional ◽  
Reaction Conditions ◽  
Thermal Stabilities ◽  
Coordination Network ◽  
Potential Applications

In recent years, the design and construction of crystalline coordination complexes by the assembly of metal ions with multitopic ligands have attracted considerable attention because of the unique architectures and potential applications of these compounds. Two new coordination polymers, namely poly[[μ-trans-1-(2-aminopyridin-3-yl)-2-(pyridin-4-yl)ethene-κ2 N:N′](μ3-5-methylisophthalato-κ4 O 1,O 1′:O 3:O 3′)cadmium(II)], [Cd(C9H6O4)(C12H11N3)] n or [Cd(5-Me-ip)(2-NH2-3,4-bpe)] n , (I), and poly[[μ-trans-1-(2-aminopyridin-3-yl)-2-(pyridin-4-yl)ethene-κ2 N:N′](μ2-5-hydroxyisophthalato-κ4 O 1,O 1′:O 3:O 5)cadmium(II)], [Cd(C8H4O5)(C12H11N3)] n or [Cd(5-HO-ip)(2-NH2-3,4-bpe)] n , (II), have been prepared hydrothermally by the self-assembly of Cd(NO3)2·4H2O and trans-1-(2-aminopyridin-3-yl)-2-(pyridin-4-yl)ethene (2-NH2-3,4-bpe) with two similar dicarboxylic acids, i.e. 5-methylisophthalic acid (5-Me-H2ip) and 5-hydroxyisophthalic acid (5-HO-H2ip). The coordination network of (I) is a two-dimensional sql net parallel to (101). Adjacent sql nets are further linked to form a three-dimensional supramolecular framework via hydrogen-bonding interactions. Compound (II) is a two-dimensional (3,5)-connected coordination network parallel to (010) with the point symbol (63)(55647). As the other reactants and reaction conditions are the same, the structural differences between (I) and (II) are undoubtedly determined by the different substituent groups in the 5-position of isophthalic acid. Both (I) and (II) exhibit good thermal stabilities and photoluminescence properties.

The effect of the coordination orientation of N atoms on polymeric structures: synthesis and characterization of one- and two-dimensional CuII coordination polymers based on 4-amino-3-(pyridin-2-yl)-5-[(pyridin-3-ylmethyl)sulfanyl]-1,2,4-triazole

2019 ◽  
Vol 75 (4) ◽  
pp. 443-450
Author(s):  
Guiying Zhu ◽  
Yang Lu ◽  
Guoxia Jin ◽  
Xuan Ji ◽  
Jianping Ma
Keyword(s):  
Hydrogen Bonding ◽  
Coordination Polymers ◽  
3D Structure ◽  
Three Dimensional ◽  
Great Influence ◽  
Two Dimensional ◽  
3D Network ◽  
Solvent Molecules ◽  
Bonding Systems ◽  
Polymeric Structures

Three new one- (1D) and two-dimensional (2D) CuII coordination polymers, namely poly[[bis{μ2-4-amino-3-(pyridin-2-yl)-5-[(pyridin-3-ylmethyl)sulfanyl]-1,2,4-triazole}copper(II)] bis(methanesulfonate) tetrahydrate], {[Cu(C13H12N5S)2](CH3SO3)2·4H2O} n (1), catena-poly[[copper(II)-bis{μ2-4-amino-3-(pyridin-2-yl)-5-[(pyridin-4-ylmethyl)sulfanyl]-1,2,4-triazole}] dinitrate methanol disolvate], {[Cu(C13H12N5S)2](NO3)2·2CH3OH} n (2), and catena-poly[[copper(II)-bis{μ2-4-amino-3-(pyridin-2-yl)-5-[(pyridin-4-ylmethyl)sulfanyl]-1,2,4-triazole}] bis(perchlorate) monohydrate], {[Cu(C13H12N5S)2](ClO4)2·H2O} n (3), were obtained from 4-amino-3-(pyridin-2-yl)-5-[(pyridin-3-ylmethyl)sulfanyl]-1,2,4-triazole with pyridin-3-yl terminal groups and from 4-amino-3-(pyridin-2-yl)-5-[(pyridin-4-ylmethyl)sulfanyl]-1,2,4-triazole with pyridin-4-yl terminal groups. Compound 1 displays a 2D net-like structure. The 2D layers are further linked through hydrogen bonds between methanesulfonate anions and amino groups on the framework and guest H2O molecules in the lattice to form a three-dimensional (3D) structure. Compound 2 and 3 exhibit 1D chain structures, in which the complicated hydrogen-bonding interactions play an important role in the formation of the 3D network. These experimental results indicate that the coordination orientation of the heteroatoms on the ligands has a great influence on the polymeric structures. Moreover, the selection of different counter-anions, together with the inclusion of different guest solvent molecules, would also have a great effect on the hydrogen-bonding systems in the crystal structures.

Magnetocaloric Effect and Slow Magnetic Relaxation on Two-Dimensional Layered 3d-4f Cluster-Based Metal–Organic Frameworks

2020 ◽  
Vol 20 (6) ◽  
pp. 4005-4012 ◽  
Author(s):  
Jia-Jia Yin ◽  
Tian-Qi Lu ◽  
Cheng Chen ◽  
Gui-Lin Zhuang ◽  
Jun Zheng ◽  
...  
Keyword(s):  
Magnetocaloric Effect ◽  
Magnetic Relaxation ◽  
Metal Organic Frameworks ◽  
Two Dimensional ◽  
Slow Magnetic Relaxation ◽  
Metal Organic

3D isomorphous lanthanide coordination polymers displaying magnetic refrigeration, slow magnetic relaxation and tunable proton conduction

2018 ◽  
Vol 47 (43) ◽  
pp. 15405-15415 ◽  
Author(s):  
Siba Prasad Bera ◽  
Arpan Mondal ◽  
Subhadip Roy ◽  
Bijoy Dey ◽  
Atanu Santra ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Coordination Polymers ◽  
Magnetic Relaxation ◽  
Magnetic Refrigeration ◽  
Proton Conduction ◽  
Lanthanide Coordination Polymers ◽  
Slow Magnetic Relaxation ◽  
Coordination Frameworks

Four lanthanide 3D coordination frameworks with 1D hydrophilic channels along the crystallographic c direction have been investigated for their proton conduction and magnetic properties.

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