2015
DOI: 10.1039/c5ce01378j
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A chiral coordination polymer with double coaxially nested helical chains exhibiting spin-canting antiferromagnetism

Abstract: A chiral coordination polymer, fabricated by the rare alternate arrangement of two types of double coaxially nested helical chains, which spiral towards the parallel and inverse directions, exhibits spin-canting antiferromagnetism.Chiral coordination polymers have been paid remarkable attention in recent years, not only because of their fascinating architectures, but also for their tremendous value in enantioselective separations, nonlinear optics, asymmetric catalysis and magnetism, etc. 1 Many of the synthes… Show more

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Cited by 13 publications
(6 citation statements)
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“…The χ m T value of compound 2 is 1.96 cm 3 ·mol –1 ·K at 300 K, slightly exceeding the expected value (1.20 cm 3 ·mol –1 ·K) for one Ni II ion ( S = 1, g = 2.19) (Figure ). With cooling, χ m T declines linearly with a minimum value of 1.49 cm 3 ·mol –1 ·K at 25 K, then increases to a maximum of 1.52 cm 3 ·mol –1 ·K at 7.50 K; afterward, it follows a rapid decrease with further cooling to 2.0 K. The spontaneous magnetization at low temperature may be ascribed to long-range magnetic order triggered by spin-canting behavior, similar to those in the literatures, which can be further testified by the field dependence of χ m T (Figure , inset), The AC susceptibility data show that no frequency dependence and no peaks appear above 2 K in the χ′ vs T and the χ″ vs T plots (Figure S4). Besides, the field dependence of the isothermal magnetization M ( H ) was measured at 2 K (Figure S5).…”
Section: Resultssupporting
confidence: 81%
“…The χ m T value of compound 2 is 1.96 cm 3 ·mol –1 ·K at 300 K, slightly exceeding the expected value (1.20 cm 3 ·mol –1 ·K) for one Ni II ion ( S = 1, g = 2.19) (Figure ). With cooling, χ m T declines linearly with a minimum value of 1.49 cm 3 ·mol –1 ·K at 25 K, then increases to a maximum of 1.52 cm 3 ·mol –1 ·K at 7.50 K; afterward, it follows a rapid decrease with further cooling to 2.0 K. The spontaneous magnetization at low temperature may be ascribed to long-range magnetic order triggered by spin-canting behavior, similar to those in the literatures, which can be further testified by the field dependence of χ m T (Figure , inset), The AC susceptibility data show that no frequency dependence and no peaks appear above 2 K in the χ′ vs T and the χ″ vs T plots (Figure S4). Besides, the field dependence of the isothermal magnetization M ( H ) was measured at 2 K (Figure S5).…”
Section: Resultssupporting
confidence: 81%
“…The above magnetic features are very similar to those of the reported [Ni 3 (OH) 2 ­(tp) 2 (H 2 O) 4 ] in terms of metamagnetic behavior, which drove us to further explore the magnetic phenomena of compound 1 . As expected, the plot of the isothermal magnetization M ( H ) to the field ( H = 0–8 T) at 2 K shows a sigmoidal shape (Figure b).…”
Section: Resultssupporting
confidence: 86%
“…Most synthetic strategies for fabricating these materials involve choosing the optimal bridging ligand, which enables magnetic interaction in addition to binding multiple paramagnetic metals with unusual coordination modes. Multifunctional carboxylic acids are often used as ligands for the generation of ferromagnetic, antiferromagnetic, and metamagnetic compounds. For example, 1,4-naphthalenedicarboxylic acid (1,4-H 2 ndc) is a commonly used linear rigid carboxylic acid ligand due to its strong coordination ability and flexible coordination modes (Scheme ), which provide different magnetic exchange pathways. Previous studies of both antiferromagnetic and ferromagnetic exchange interactions through the syn-syn and trans-syn conformations have been reported. Furthermore, aromatic groups can also help facilitate the exchange of spins between the metals of two different paramagnetic centers. , The choice of paramagnetic transition metal is also an essential parameter as the main spin barrier influences the difficulty of both experimental and theoretical analysis. For this, the 3d metal ions are easier to study when compared with the 4d and 5d metal ions.…”
Section: Introductionmentioning
confidence: 99%
“…The glassy carbon electrodes (GCEs) become an optimal choice for studying the electrochemical properties of compounds 1-3, because of their good electrical conductivities and high chemical stabilities. [36][37][38] In order to investigate the electrochemical behaviors of compounds 1-3, the three compounds have been used as modiers to fabricate chemically modied electrodes (1-GCE, 2-GCE and 3-GCE). The cyclic voltammetric behaviors for 1-GCE, 2-GCE and 3-GCE in 0.5 mol L À1 Na 2 SO 4 + 0.01 mol L À1 H 2 SO 4 aqueous solution at different scan rates were recorded with the scan rate varying from 80 to 200 mV s À1 for 2-GCE, from 50 to 200 mV s À1 for 1-GCE and 3-GCE.…”
Section: Electrochemical Properties Of Compounds 1-3mentioning
confidence: 99%