Crystal Structures, Topological Analyses, and Magnetic Properties of Manganese-Dihydroxyterephthalate Complexes

2010 ◽  
Vol 63 (2) ◽  
pp. 286 ◽  
Author(s):  
Qiang Gao ◽  
Fei-Long Jiang ◽  
Ming-Yan Wu ◽  
You-Gui Huang ◽  
Wei Wei ◽  
...  

Two manganese(ii)-dihydroxyterephthalate complexes were obtained under solvothermal conditions: [Mn(H2dhtp)(H2O)2] n (1) and [Mn2(dhtp)(H2O)2] n (2) (H4dhtp = 2,5-dihydroxyterephthalate). The 3D framework of complex 1 is constructed by H2dhtp ligands joined to 1D carboxylate-bridged Mn(ii) chains, which features a (4,4)-connected PtS net. Complex 2 contains a novel inorganic honeycomb Mn(ii)–O layer, which is further connected into a 3D (4,8)-connected flu net by dhtp ligands. Magnetic measurements of 1 and 2 were performed in the range of 2–300 K and the results indicate that antiferromagnetic coupling exits in the manganese(ii) centres of both complexes.

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Jing Chen ◽  
You-Juan Zhang ◽  
Kun-Tao Huang ◽  
Qiang Huang ◽  
Jun-Jie Wang

Two new cobalt(II) complexes of formula [Co(hfac)2(NITphtrz) 1 and Co(hfac)2(IMphtrz) 2] have been prepared and characterized structurally [where NITphtrz = 4,4,5,5-tetramethyl-2-(2-phenyl-1,2,3-triazole-4-yl)imidazoline-1-oxyl-3-oxide and IMphtrz = 4,4,5,5-tetramethyl-2-(2-phenyl-1,2,3-triazole-4-yl)imidazoline-1-oxyl]. All of the complexes crystallize in an isomorphous triclinic space group P1- with the Co(II) ion octahedrally coordinated via the bidentate chelating mode. The magnetic measurements show that two complexes exhibit antiferromagnetic interactions between the metal ions and the nitroxide radicals.


2019 ◽  
Vol 5 (1) ◽  
pp. 14
Author(s):  
Yuki Suemitsu ◽  
Ryuji Matsunaga ◽  
Takashi Toyofuku ◽  
Yasunori Yamada ◽  
Masahiro Mikuriya ◽  
...  

Tetranuclear hetero-metal MnIII2NiII2 complexes, [Mn2Ni2(L)4(OAc)2] (1) and [Mn2Ni2(L)4(NO3)2] (2) [H2L = N-(2-hydroxymethylphenyl)-5,6-benzosalicylideneimine], have been synthesized and characterized by X-ray crystal structure analyses, infrared spectra, and elemental analyses. The structure analyses revealed that the complexes have a defective double-cubane metal core connected by μ3-alkoxo bridges. Complexes consist of two bis-μ-alkoxo bridged MnIIINiII heteronuclear units making a dimer-of-dimers structure. The double-cubane cores are significantly distorted due to an effect of syn–syn mode acetato or nitrato bridges. Magnetic measurements indicate that weak antiferromagnetic interactions (Mn-Ni = −0.66 ~ −4.19 cm–1) are dominant in the hetero-metal core.


2021 ◽  
Vol 7 (7) ◽  
pp. 105
Author(s):  
Min Zeng ◽  
Xi Chen ◽  
Hui-Zhong Kou

Two carboxylate-bridged one-dimensional chain complexes, {[MnII(MeOH)2][FeIII(L)2]2}n (1) and {[MnII(DMF)2][MnIII(L)2]2·DMF}n (2) [H2L = ((2-carboxyphenyl)azo)-benzaldoxime], containing a low-spin [FeIII(L)2]− or [MnIII(L)2]− unit were synthesized. Magnetic measurements show that the adjacent high-spin MnII and low-spin MIII ions display weak antiferromagnetic coupling via the syn–anti carboxyl bridges, with J = −0.066(2) cm−1 for complex 1 and J = −0.274(2) cm−1 for complex 2.


2020 ◽  
pp. 174751982092601
Author(s):  
Yong-Jun Bian ◽  
Yuan Tian ◽  
Ai-Hua Zhang ◽  
Yong-Qiang Chen

A new coordination framework {[Mn7(L)4(OH)2(H2O)4(DMA)4]·8H2O·6DMA}n (H3 L = 3,3′,3″-[1,3,5-benzenetriyltris(carbonylimino)]tris(benzoate); DMA = N,N-dimethylacetamide) is synthesized under mixed solvothermal conditions. Structural analysis reveals that this complex possesses a three-dimensional framework with (3,10)- c topology based on different [Mn6] clusters. Moreover, magnetic investigations suggest that intra-cluster Mn(II) ions exhibit antiferromagnetic coupling.


2020 ◽  
Vol 7 (1) ◽  
pp. 247-259 ◽  
Author(s):  
Monotosh Mondal ◽  
Soumavo Ghosh ◽  
Souvik Maity ◽  
Sanjib Giri ◽  
Ashutosh Ghosh

An N2O donor reduced Schiff base in presence of Ni(ClO4)2·6H2O and SCN− transforms into N2O2 donor ligand via deaminative coupling. Metal complexes 1 and 3 exhibit catecholase like activity and antiferromagnetic coupling between the Ni(ii) ions.


2005 ◽  
Vol 60 (11) ◽  
pp. 1113-1117 ◽  
Author(s):  
Dieter Fischer ◽  
Rudolf Hoppe ◽  
Kailash M. Mogare ◽  
Martin Jansen

Potassium and rubidium oxoruthenates, A2RuO4, were synthesized from the alkali peroxides/ hyperoxides and ruthenium dioxide. Both compounds crystallize in the orthorhombic space group Pnma (no. 62), (K2RuO4: a = 7.673(2), b = 6.153(2) and c = 10.564(3)Å , Z = 4, 796 unique reflections, R=3.5%; Rb2RuO4: a =8.106(2), b = 6.270(1) and c =11.039(2)Å , Z =4, 889 unique reflections, R = 3.6%). The crystal structures, as determined from single crystal data, are of the β - K2SO4 type. Magnetic measurements reveal that both compounds are paramagnetic down to temperatures of around 60 K and further exhibit antiferromagnetic transitions, at around TN = 9 K for Rb2RuO4, and two transitions with TN = 14 K and 4 K for K2RuO4. The magnetic moments as determined applying Curie-Weiss law for both compounds are 2.68 μB, thus confirming the oxidation state +6 of ruthenium.


CrystEngComm ◽  
2020 ◽  
Vol 22 (16) ◽  
pp. 2806-2816
Author(s):  
Xiaoyun Hao ◽  
Jingwen Shi ◽  
Yong Dou ◽  
Tong Cao ◽  
Zhen Zhou ◽  
...  

Six new cyanide-bridged complexes (0–3D) have been assembled by employing one copper compound and six cyano precursors. Investigation of the magnetic properties revealed the ferro- or antiferromagnetic coupling between FeIII/CrI ion and CuII ion.


2020 ◽  
Vol 49 (24) ◽  
pp. 8209-8225 ◽  
Author(s):  
Matthias Hämmer ◽  
Oliver Janka ◽  
Judith Bönnighausen ◽  
Steffen Klenner ◽  
Rainer Pöttgen ◽  
...  

An exploration of the crystal chemistry of exciting luminescent title compounds – possible phosphors – is discussed also employing magnetic measurements.


2014 ◽  
Vol 43 (3) ◽  
pp. 945-949 ◽  
Author(s):  
Daopeng Zhang ◽  
Yongzhong Bian ◽  
Jie Qin ◽  
Ping Wang ◽  
Xia Chen

Two cyanide-bridged enantiopure one-dimensional single chain complexes have been synthesized and structurally characterized. Systematically magnetic investigations show the antiferromagnetic coupling between the Mn(iii)–Fe(iii) centers and the metamagnetic behavior at about 5.0 K.


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