A novel 2D inorganic-organic hybrid compound constructed from{CuMo 2 O7}n bimetallic oxide chains bridged by N-containing ligand Xiang-Guang Guo, Wen-Bin Yang, Xiao-Yuan Wu, Qi-Kai Zhang, Lang Lin, Can-Zhong Lu PII: DOI: Reference:
S1387-7003(14)00204-4 doi: 10.1016/j.inoche.2014.04.033 INOCHE 5572
To appear in:
Inorganic Chemistry Communications
Received date: Revised date: Accepted date:
21 March 2014 21 April 2014 25 April 2014
Please cite this article as: Xiang-Guang Guo, Wen-Bin Yang, Xiao-Yuan Wu, Qi-Kai Zhang, Lang Lin, Can-Zhong Lu, A novel 2D inorganic-organic hybrid compound constructed from{CuMo2 O7 }n bimetallic oxide chains bridged by N-containing ligand, Inorganic Chemistry Communications (2014), doi: 10.1016/j.inoche.2014.04.033
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ACCEPTED MANUSCRIPT A novel 2D inorganic-organic hybrid compound constructed
N-containing ligand
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from {CuMo2O7}n bimetallic oxide chains bridged by
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Xiang-Guang Guoa,b, Wen-Bin Yanga,b, Xiao-Yuan Wua,b, Qi-Kai Zhanga,b, Lang Lina,b, Can-Zhong Lua,b*
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a. Key Laboratory of Design and Assembly of Functional Nanostructures, Chinese Academy of
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Sciences; b. State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian, 350002, China; *Corresponding author: Fax: +86-591-83714946. Telephone: +86-591-83705794. E-mail:
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[email protected].
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Abstract: A novel inorganic-organic hybrid compound [Cu(Mo2O7)(H2MDP)] (1) has been hydrothermally synthesized from the self-assembly of CuI, H2MoO4 and
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H2MDP ([Methylenebis(3,5-dimethylpyrazole)]). Compound 1 is constructed from
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one-dimensional {Cu(Mo2O7)}n bimetallic oxide chains bridged by H2MDP ligands into a novel two-dimensional hybrid compound. There exist left- and right-handed Cu-O-Mo helical chains in the bimetallic oxide chains. Key words: hybrid compound; hydrothermal synthesis; bimetallic oxide chain, helical chains
The exploration of molybdenum oxide based inorganic-organic hybrid materials is of great interest not only due to their fascinating architectures but also because of their potential applications in magnetic, optical fields and so on.[1-4] One attractive 1
ACCEPTED MANUSCRIPT approach for the preparation of new metal oxide hybrid materials is to exploit organic molecules to modify inorganic microstructures.[5-6] Zubieta and co-workers have
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introduced secondary metal-ligand coordination complex cations synthetic strategy to
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prepare various molybdenum oxides, which has been successfully used in the development of the chemistry of bimetallic oxides of the copper molybdate family
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Cu/Mo/O/ligand.[7-9] Some bidentate chelating organoamine ligands such as
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o-Phenanthroline, 2, 2’-bipyridine, 2, 3-bis(2-pyridyl)pyrazine have been used in the preparation of such hybrid materials. In this article, we choose the flexible H2MDP ([Methylenebis(3,5-dimethylpyrazole)]) ligand which has proven to be a good ditopic
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ligand in the construction of coordination polymers with diverse structures.[10-11]
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However, it is never involved in the self-assembly of polyoxometalate-based materials. Herein by introducing the H2MDP ligand we report the synthesis and characterization a
novel
two-dimensional
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of
bimetallic
inorganic-organic
framework,
chains.
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[Cu(H2MDP)(Mo2O7)] (1), which contains left- and right-handed Cu-O-Mo helical
Green crystals of 1 were hydrothermally synthesized by mixing CuI, H2MoO4 and H2MDP in distilled water at 180 °C for 3 days.[12] The structure of 1 was characterized by single-crystal X-ray diffraction, element analysis, IR.[13] The pure phase was confirmed by PXRD (Fig. S1).The asymmetric unit contains one Cu(H2MDP)2+ ion and one Mo2O72- anion. As shown in Fig. 1b, one dinuclear molybdenum oxide unit was assembled from two edge-sharing [Mo1O5] square pyramids with Mo-O bond lengths from 1.700(11) to 2.125(9) Å, while another 2
ACCEPTED MANUSCRIPT dinuclear molybdenum oxide unit from two edge-sharing [Mo2O6] distorted octahedra with Mo-O bond lengths from 1.663(10) to 2.504(10) Å (Fig. 1b). Each Cu
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center is coordinated by four oxygen atoms from three Mo2O72- anions and two
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nitrogen atoms from two H2MDP ligand, showing a distorted octahedral [CuN2O4] coordination geometry. The basal plane of the Cu octahedron is defined by two
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nitrogen atoms from two H2MDP ligands and two oxygen atoms from molybdate
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cluster (Cu1-N2 = 1.979(12) Å, Cu1-N4 = 1.986(12) Å, Cu1-O5 = 2.052 Å, Cu1-O2 = 1.994(10) Å), while the apical position is occupied by two oxygen atoms with longer Cu-O bond lengths (Cu1-O3 = 2.319(11), Cu1-O6 = 2.331(10) Å). The
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significantly longer Cu-O bond lengths in the apical position is caused by the
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polymers.[14]
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Jahn-Teller effect, which are comparable to those previously reported Cu
Figure 1. (a) View of the coordination environment of metal atoms (all hydrogen atoms are omitted for clarity); (b) View of molybdenum oxide cluster; (c) Representation of connection between structural unit [MoOx] and [CuN2O4]; (d) View of 1D bimetallic oxide chains {Cu(Mo2O7)}n; (e) View of 2D hybrid framework constructed from bimetallic oxide chains bridged by H2MDP ligands. 3
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Scheme 1. Representation of coordination between Cu(II) centers 1.
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The two-dimensional layer structure of 1 is constructed from copper-molybdenum bimetallic {Cu(Mo2O7)}n chains and tethered (H2MDP)n ligands occupying the
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interchain region (Fig. 1d, e). The identical bimetallic {Cu(Mo2O7)}n chains have been reported by Zubieta and co-workers in three compounds: [Cu(2,2’-bpy)Mo2O7],
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[Cu(pyrpyrz)Mo2O7], [Cu(tpa)Mo2O7].[15-17] However, the above compounds are all
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one-dimensional chains structure due to bidentate N-containing chelating ligands used, which block the formation high-dimensional networks. As reported previously, the
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H2MDP ligand has the tendency to form a M2L2-type metallocyclic motif. Furthermore each M2L2 motif can connect two molybdenum oxide chains to form high-dimensional networks. In the bimetallic oxide chain, pairs of different dinuclear molybdenum oxide units assemble together to form a tetranuclear molybdenum oxide cluster extended to an infinite molybdenum oxide chain [Mo2O7]n2n- (Fig. 1b). Each [CuN2O4] octahedra is connected to one [Mo1O5] square-pyramid and one pair of [Mo2O6] octahedra through corner- and edge-sharing, respectively (Fig. 1c). It is noted that there are closed loops constructed from two H2MDP ligands and two copper atoms, in which the Cu…Cu distance is 8.4527(19) Å (Fig. 1e). 4
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Figure 2. (a) A view of the left-handed and right-handed Cu-O-Mo helical chains in 1;
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(b) Polyhedral view of two kinds of helical chains; (c) Representation of connections between pairs of [Mo2O6] octahedra and helical chains. Compound
1
consists
of
helical
chains
constructed
from
[Mo1O5]
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square-pyramids and [CuN2O4] octahedra. As shown in Fig. 2a, b, the [Mo1O5]
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square-pyramids and [CuN2O4] octahedra are corner-shared to form left- and right-handed helical chains. The space between two helical chains is occupied by pairs
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of [Mo2O6] octahedra through edge-sharing (Fig. 2c).
Figure 3.Plots of χmT and χm−1 versus T for complexes 1. The temperature dependence of the magnetic susceptibility of 1 in the 2–300 K temperature range under an applied field of 1000 Oe, as is shown in Fig. 3. The χmT value at room temperature is 0.440 cm3 mol-1 K, slightly higher than the spin-only value expected for one isolated Cu2+ center (0.375 cm3 mol-1 K and S = 1/2).[18-20] 5
ACCEPTED MANUSCRIPT In complex 1, the χmT value decreases to 0.128 cm3 K mol-1 at 13.8 K, then increases sharply to 0.18 cm3 mol-1 K at about 11.4 K, and then finally drops until the lowest
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temperature 2 K. The best fit with the Curie-Weiss law gives C = 0.468 cm3 mol-1 K
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and θ = -16.1 K, indicating weak antiferromagnetic interactions among the isolated magnetic Cu2+ ions, through the long pathway of Cu-O-Mo-O-Cu. The
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antiferromagnetic coupling dominates in a higher temperature region above 50 K,
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whereas the abrupt increase in χmT value below 13 K suggests the weak ferromagnetism, which is probably related to spin-canting.[21-22] In summary, under hydrothermal condition we have isolated a new
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inorganic-organic hybrid framework constructed from copper-molybdenum bimetallic
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oxide {Cu(Mo2O7)}n chains, which contains left- and right-handed Cu-O-Mo helical chains.
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Acknowledgements
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This work was supported by the Chinese Academy of Sciences (KJCX2-YW-319, KJCX2-EW-H01), the 973 key program of the MOST (2010CB933501, 2012CB821705), the National Natural Science Foundation of China and the Natural Science
Foundation
of
Fujian
Province
(2007HZ0001-1,
2009HZ0004-1,
2009HZ0005-1, 2009HZ0006-1, 2006L2005). Appendix A. Supplementary data Supplementary data associated with this article can be found, in the online version, at doi: References 6
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ACCEPTED MANUSCRIPT [12] Synthesis of 1: A mixture of H2MoO4 (0.1 g, 0.62 mmol), CuI (0.1 g, 0.52 mmol), H2MDP (0.040 g, 0.2 mmol), H2O (10 mL) was heated in a 23 mL Teflon-lined
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reaction vessel at 180 °C for 3 days. Then the autoclave was cooled at 3 °C h -1 to
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room temperature. The green block crystals were isolated, washed with water and dried at room temperature. Yield: (58% based on Mo). Elemental analysis
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(%) calcd for C11H16CuMo2N4O7: H, 2.80; C, 23.08; N, 9.79. Found: H, 2.96; C,
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22.70; N, 9.54. IR spectrum (KBr pellets, ν/cm-1): 3412 (m), 3259 (m), 1580 (w), 1464 (w), 1278 (w), 1185 (m), 949 (m), 920 (m), 890 (m), 837 (m), 760 (m), 620 (m).
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[13] Crystal data: C11H16CuMo2N4O7, M = 571.70, monoclinic, P2/c, a =11.7088(6),
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b = 7.1445(3), c = 20.8780(12) Å, α = 90, β = 105.433(6), γ = 90°, V = 1688.93(12) Å3, Z = 4, T =293(2) K, 6188 reflections measured, 3323
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independent reflections (Rint = 0.0347). The final R1 value was 0.0675 (I > 2σ(I)).
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5,5’-dimethyl-2,2’-bipyridine, t-Bu2bpy
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Graphical Abstract
Here we present a novel 2D inorganic-organic hybrid compound constructed from
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{CuMo2O7}n bimetallic oxide chains, which contains left- and right-handed Cu-O-Mo
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helical chains.
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ACCEPTED MANUSCRIPT
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Highlights
A new inorganic-organic hybrid compound with {Cu(Mo2O7)}n bimetallic oxide
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chains
An unprecedented hybrid materials tuned by [Methylenebis(3,5-dimethylpyrazole)]
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The compound consists of left- and right-handed helical chains
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