CN108727608B - A kind of zinc metal organic complex and preparation method thereof - Google Patents

A kind of zinc metal organic complex and preparation method thereof Download PDF

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CN108727608B
CN108727608B CN201810516037.8A CN201810516037A CN108727608B CN 108727608 B CN108727608 B CN 108727608B CN 201810516037 A CN201810516037 A CN 201810516037A CN 108727608 B CN108727608 B CN 108727608B
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organic complex
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CN108727608A (en
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胡劲松
董圣菊
吕超南
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Anhui University of Science and Technology
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Abstract

The invention discloses a kind of zinc metal organic complex, chemical formula is [Zn3(PIDPE)(OH)(chdc)2.5], PIDPE is 4- pyridyl group -4 '-imidazoles yl diphenyl ether, and chdc is Isosorbide-5-Nitrae-cyclohexane diacid of deprotonation, belongs to monoclinic system, space group P21/ c, cell parameter areα=90.00 °, β=109.402 (2) °, γ=90.00 °.The preparation method of zinc metal organic complex proposed by the present invention, it include: by 4- pyridyl group -4 '-imidazoles yl diphenyl ether, 1, N is added in 4- cyclohexane diacid and zinc salt, in the mixed solution of N '-dimethyl formamide and water, solvent thermal reaction 36-60h at 80-100 DEG C, cools down, is filtered, washed, dries.

Description

A kind of zinc metal organic complex and preparation method thereof
Technical field
The present invention relates to complex technology fields more particularly to a kind of zinc metal organic complex and preparation method thereof.
Background technique
Coordination polymer refer to central metallic ions and organic ligand by the effect of coordinate bond formed one kind it is inorganic- Organic hybrid functional material, because having novel structure, being widely applied, design, synthesis have become materials chemistry research A hot spot.Currently, coordination polymer be widely used in senser element, gas storage, dyestuff and pollutant absorption, from The fields such as son exchange, catalysis.In the preparation process of coordination polymer, the configuration of ligand to the final structure of complex play to Important role is closed, the arm of V-type ligand can occur fraction of torsion around central point to meet the needs of coordination, be likely to be obtained It is different from the complex of rigidity and flexible ligand, is had been a concern in recent years.
4- pyridyl group -4 '-imidazoles yl diphenyl ether has the V-structure of two kinds of co-ordinating functionalities, and Isosorbide-5-Nitrae-cyclohexane diacid is A kind of fats Carboxylic acid ligand cheap and easy to get assembles the coordination polymer network knot formed during the two mixture Structure is rich and varied, is difficult to control and prediction, the condition for being difficult control reaction synthesize target coordination polymer.Currently, using this two The coordination polymer that kind ligand is synthesized with zinc ion has not been reported.
Summary of the invention
Technical problems based on background technology, the invention proposes a kind of zinc metal organic complex and its preparation sides Method, zinc metal organic complex stable structure at room temperature, and there is excellent fluorescence property, the preparation method operation Simply, yield is high, and reproducibility is good.
A kind of zinc metal organic complex proposed by the present invention, chemical formula are [Zn3(PIDPE)(OH)(chdc)2.5], Wherein, PIDPE be 4- pyridyl group -4 '-imidazoles yl diphenyl ether, chdc be deprotonation Isosorbide-5-Nitrae-cyclohexane diacid, and PIDPE and H2The structural formula of chdc is as follows:
The zinc metal organic complex belongs to monoclinic system, space group P21/ c, cell parameter areα=90.00 °, β=109.402 (2) °, γ=90.00 °,
Preferably, the ir data of the zinc metal organic complex is as follows: 3408 (m), 3196 (w), 2931 (w), 2852 (w), 2364 (w), 1671 (m), 1603 (s), 1520 (s), 1486 (s), 1387 (s), 1239 (s), 1167 (m) 1129 (w), 1061 (m), 964 (w), 821 (m), 735 (w), 653 (w), 608 (w), 526 (w).
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: by 4- pyrrole In the mixed solution of piperidinyl -4 '-imidazoles yl diphenyl ether, Isosorbide-5-Nitrae-cyclohexane diacid and zinc salt addition N, N '-dimethyl formamide and water, It stirs evenly and is placed in the stainless steel cauldron of polytetrafluoroethylliner liner, 36-60h is reacted at 80-100 DEG C, reaction terminates By cooling, it is filtered, washed, is dried to obtain the zinc metal organic complex.
Preferably, the zinc salt is one or more of zinc nitrate, zinc sulfate, zinc chloride, zinc acetate, zinc perchlorate Mixture.
Preferably, 4- pyridyl group -4 '-imidazoles yl diphenyl ether, Isosorbide-5-Nitrae-cyclohexane diacid, zinc salt molar ratio be 1:1:2-3.
Preferably, 4- pyridyl group -4 '-imidazoles yl diphenyl ether, Isosorbide-5-Nitrae-cyclohexane diacid, zinc salt molar ratio be 1:1:2.
Preferably, in the mixed solution of the N, N '-dimethyl formamide and water, N, N '-dimethyl formamide and water Volume ratio is 1:2-3.
Preferably, the preparation method of the zinc metal organic complex, comprising the following steps: by 0.0313g 4- pyridine Base -4 '-imidazoles yl diphenyl ether, 0.0172g 1,4- cyclohexane diacid and 0.0595-0.0892g zinc nitrate are dissolved in 5-15g N, N ' - In the mixed solution of dimethylformamide and water, wherein in the mixed solution of N, N '-dimethyl formamide and water, N, N '-diformazan The volume ratio of base formamide and water is 1:2-3, stirs evenly and is placed in the stainless steel cauldron of polytetrafluoroethylliner liner, 36-60h is reacted at 80-100 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain the zinc metal organic complex.
Preferably, the preparation method of the zinc metal organic complex, comprising the following steps: by 0.0313g 4- pyridine Base -4 '-imidazoles yl diphenyl ether, 0.0172g 1,4- cyclohexane diacid and 0.0595g zinc nitrate are dissolved in 10g N, N '-dimethyl formyl In the mixed solution of amine and water, and N, in the mixed solution of N '-dimethyl formamide and water, N, N '-dimethyl formamide and water Volume ratio be 1:3, stir evenly be placed in the stainless steel cauldron of polytetrafluoroethylliner liner at room temperature, reacted at 90 DEG C 48h, after reaction through cooling, be filtered, washed, be dried to obtain the zinc metal organic complex.
The present invention provides a kind of new zinc metal organic complex and preparation method thereof, which, which has, stablizes Solid fluorescence property, can be used as potential light-emitting function material;It is placed to it at room temperature to stablize the several months, then knows it Stability is good, to provide the foundation as potential light-emitting function material;The preparation method is easy to operate, and yield is high, can weigh Existing property is good.
Detailed description of the invention
Fig. 1 is the minimum asymmetric cell figure of zinc metal organic complex proposed by the present invention;
Fig. 2 is ligand 1 in zinc metal organic complex proposed by the present invention, the three-dimensional that 4- cyclohexane diacid and zinc ion are formed Structure chart;
Fig. 3 is the final tomograph of zinc metal organic complex proposed by the present invention;
Fig. 4 is the infrared spectrogram of zinc metal organic complex prepared by the embodiment of the present invention 5;
Fig. 5 is the thermogravimetric curve of zinc metal organic complex prepared by the embodiment of the present invention 5;
Fig. 6 is the powder xrd pattern of zinc metal organic complex prepared by the embodiment of the present invention 5;
Fig. 7 is zinc metal organic complex prepared by the embodiment of the present invention 5 and the Solid fluorescene spectrum of PIDPE.
Specific embodiment
In the following, technical solution of the present invention is described in detail by specific embodiment.
The chemical formula of zinc metal organic complex of the present invention is [Zn3(PIDPE)(OH)(chdc)2.5], wherein PIDPE is 4- pyridyl group -4 '-imidazoles yl diphenyl ether, and chdc is Isosorbide-5-Nitrae-cyclohexane diacid of deprotonation, which belongs to Monoclinic system, space group P21/ c, cell parameter are α=90.00 °, β=109.402 (2) °, γ=90.00 °,Institute of the present invention In the zinc metal organic complex stated, Zn2+Coordination mode there are three types of form, Zn1 using pentacoordinate form, respectively with Four oxygen atoms and a nitrogen-atoms connect to form tetragonous Based On The Conic Model, and Zn1 is in the center of rectangular pyramid, wherein four oxygen atoms Four different Isosorbide-5-Nitraes-cyclohexane diacid ions are respectively from, a nitrogen-atoms is from PIDPE ligand;And Zn2 matches using four Bit pattern connect the tetrahedral configuration to form distortion with three oxygen atoms and a nitrogen-atoms, wherein Zn2 is in the tetrahedron Heart position, two oxygen atoms are respectively from the Isosorbide-5-Nitrae-cyclohexane diacid ion of two different coordinations, another oxygen atom comes from In O2-Ion, nitrogen-atoms is from ligand PIDPE;Equally, Zn3 is also to be connected finally using four-coordination mode with four oxygen atoms The tetrahedral configuration of distortion is formed, Zn3 is in the tetrahedron center, wherein three oxygen atoms are respectively from three not Isosorbide-5-Nitrae-cyclohexane diacid ion of same coordination, another oxygen atom is from O2-Ion.For the Carboxylic acid ligand 1 in complex, There are two types of coordination modes for carboxylic acid group in 4- cyclohexane diacid ion, are monodentate chelating and bidentate bridging, Zn1 and Isosorbide-5-Nitrae-hexamethylene respectively Two acid ions form the cluster unit of a double-core, Zn2 and Zn3 and Isosorbide-5-Nitrae-cyclohexane diacid ion and O2-Ion connects to form zigzag One-dimensional chain, final ligand 1,4- cyclohexane diacid and zinc ion form a three-dimensional structure, the rectangle duct quilt in three-dimensional structure Occupied by ligand PIDPE, duct is divided into many small ducts.
Embodiment 1
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: will 0.0313g 4- pyridyl group -4 '-imidazoles yl diphenyl ether, 0.0172g 1,4- cyclohexane diacid and 0.0595g zinc nitrate are dissolved in 10g In the mixed solution of N, N '-dimethyl formamide and water, and N, in the mixed solution of N '-dimethyl formamide and water, N, N '-two Methylformamide and the volume ratio of water are 1:3, stir evenly the stainless steel for being placed on the polytetrafluoroethylliner liner of 25mL at room temperature In reaction kettle, 36h is reacted at 80 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain that the zinc metal is organic to match Close object.
Embodiment 2
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: will 0.0313g 4- pyridyl group -4 '-imidazoles yl diphenyl ether, 0.0172g 1,4- cyclohexane diacid and 0.0892g zinc nitrate are dissolved in 10g In the mixed solution of N, N '-dimethyl formamide and water, and N, in the mixed solution of N '-dimethyl formamide and water, N, N '-two Methylformamide and the volume ratio of water are 1:2, stir evenly the stainless steel for being placed on the polytetrafluoroethylliner liner of 25mL at room temperature In reaction kettle, 60h is reacted at 100 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain that the zinc metal is organic to match Close object.
Embodiment 3
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: will 0.0313g 4- pyridyl group -4 '-imidazoles yl diphenyl ether, 0.0172g 1,4- cyclohexane diacid and 0.0892g zinc nitrate are dissolved in 10g In the mixed solution of N, N '-dimethyl formamide and water, and N, in the mixed solution of N '-dimethyl formamide and water, N, N '-two Methylformamide and the volume ratio of water are 1:3, stir evenly the stainless steel for being placed on the polytetrafluoroethylliner liner of 25mL at room temperature In reaction kettle, 55h is reacted at 85 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain that the zinc metal is organic to match Close object.
Embodiment 4
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: will 0.0313g 4- pyridyl group -4 '-imidazoles yl diphenyl ether, 0.0172g 1,4- cyclohexane diacid and 0.0892g zinc nitrate are dissolved in 5g N, In the mixed solution of N '-dimethyl formamide and water, and N, in the mixed solution of N '-dimethyl formamide and water, N, N '-diformazan The volume ratio of base formamide and water is 1:3, and the stainless steel for stirring evenly the polytetrafluoroethylliner liner for being placed on 25mL at room temperature is anti- Answer in kettle, 48h reacted at 100 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain the zinc metal organic complexes Object.
Embodiment 5
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: will 0.0313g 4- pyridyl group -4 '-imidazoles yl diphenyl ether, 0.0172g 1,4- cyclohexane diacid and 0.0595g zinc nitrate are dissolved in 10g In the mixed solution of N, N '-dimethyl formamide and water, and N, in the mixed solution of N '-dimethyl formamide and water, N, N '-two Methylformamide and the volume ratio of water are 1:3, stir evenly the stainless steel cauldron for being placed on polytetrafluoroethylliner liner at room temperature In, 48h is reacted at 90 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain the zinc metal organic complex.
Embodiment 6
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: will 0.0313g 4- pyridyl group -4 '-imidazoles yl diphenyl ether, 0.0172g 1,4- cyclohexane diacid and 0.0595g zinc nitrate are dissolved in 15g In the mixed solution of N, N '-dimethyl formamide and water, wherein in the mixed solution of N, N '-dimethyl formamide and water, N, The volume ratio of N '-dimethyl formamide and water is 1:2, stirs evenly the stainless steel cauldron for being placed on polytetrafluoroethylliner liner In, 36h is reacted at 100 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain the zinc metal organic complex.
Embodiment 7
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: will 0.0313g 4- pyridyl group -4 '-imidazoles yl diphenyl ether, 0.0172g 1,4- cyclohexane diacid and 0.0892g zinc nitrate are dissolved in 5g N, In the mixed solution of N '-dimethyl formamide and water, wherein in the mixed solution of N, N '-dimethyl formamide and water, N, N '- The volume ratio of dimethylformamide and water is 1:3, stirs evenly and is placed in the stainless steel cauldron of polytetrafluoroethylliner liner, 60h is reacted at 80 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain the zinc metal organic complex.
Embodiment 8
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: by 4- pyrrole N, the mixed solution of N '-dimethyl formamide and water is added in piperidinyl -4 '-imidazoles yl diphenyl ether, 1,4- cyclohexane diacid and zinc sulfate In, it stirs evenly and is placed in the stainless steel cauldron of polytetrafluoroethylliner liner, 60h is reacted at 80 DEG C, is passed through after reaction It cools down, be filtered, washed, being dried to obtain the zinc metal organic complex;
Wherein, 4- pyridyl group -4 '-imidazoles yl diphenyl ether, Isosorbide-5-Nitrae-cyclohexane diacid, zinc sulfate molar ratio be 1:1:3;
In the mixed solution of N, N '-dimethyl formamide and water, N, the volume ratio of N '-dimethyl formamide and water is 1:3.
Embodiment 9
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: by 4- pyrrole In the mixed solution of piperidinyl -4 '-imidazoles yl diphenyl ether, Isosorbide-5-Nitrae-cyclohexane diacid, zinc salt addition N, N '-dimethyl formamide and water, It stirs evenly and is placed in the stainless steel cauldron of polytetrafluoroethylliner liner, 36h is reacted at 100 DEG C, after reaction through cold But, it is filtered, washed, is dried to obtain the zinc metal organic complex;
Wherein, 4- pyridyl group -4 '-imidazoles yl diphenyl ether, Isosorbide-5-Nitrae-cyclohexane diacid, zinc salt molar ratio be 1:1:2;
The zinc salt is the mixture of zinc chloride and zinc acetate, and the weight ratio of zinc chloride and zinc acetate is 4:5;
In the mixed solution of N, N '-dimethyl formamide and water, N, the volume ratio of N '-dimethyl formamide and water is 1:2.
Embodiment 10
The preparation method for a kind of zinc metal organic complex that the present invention also proposes, comprising the following steps: by 4- pyrrole In the mixed solution of piperidinyl -4 '-imidazoles yl diphenyl ether, Isosorbide-5-Nitrae-cyclohexane diacid and zinc salt addition N, N '-dimethyl formamide and water, It stirs evenly and is placed in the stainless steel cauldron of polytetrafluoroethylliner liner, 40h is reacted at 95 DEG C, after reaction through cold But, it is filtered, washed, is dried to obtain the zinc metal organic complex;
Wherein, 4- pyridyl group -4 '-imidazoles yl diphenyl ether, Isosorbide-5-Nitrae-cyclohexane diacid, zinc salt molar ratio be 1:1:2.5;
The zinc salt is the mixture of zinc nitrate, zinc chloride, zinc perchlorate, and the weight of zinc nitrate, zinc chloride, zinc perchlorate Amount is than being 3:5:1;
In the mixed solution of N, N '-dimethyl formamide and water, the volume ratio of N, N '-dimethyl formamide and water are 1: 2.5。
The zinc metal organic complex prepared in Example 5 carries out crystal structure determination, predominant crystal data such as table 1 It is shown:
The predominant crystal data of the zinc metal organic complex prepared in 1 embodiment 5 of table
The chemical formula of zinc metal organic complex of the present invention is [Zn3(PIDPE)(O)(chdc)2.5], wherein PIDPE is 4- pyridyl group -4 '-imidazoles yl diphenyl ether, and chdc is Isosorbide-5-Nitrae-cyclohexane diacid of deprotonation, which belongs to Monoclinic system, space group P21/ c, cell parameter are α=90.00 °, β=109.402 (2) °, γ=90.00 °,Fig. 1 is this The minimum asymmetric cell figure of the zinc metal organic complex is invented, as shown in Figure 1, zinc metal of the present invention is organic to match It closes in object, Zn2+Coordination mode there are three types of form, Zn1 using pentacoordinate form, respectively with four oxygen atoms and one Nitrogen-atoms connects to form tetragonous Based On The Conic Model, and Zn1 is in the center of rectangular pyramid, wherein four oxygen atoms (O8, O11, O12 and O7# 1) four different Isosorbide-5-Nitraes-cyclohexane diacid ions are respectively from, a nitrogen-atoms (N3) is from PIDPE ligand;And Zn2 is adopted The tetrahedral configuration to form distortion is connect with three oxygen atoms and a nitrogen-atoms with four-coordination mode, wherein Zn2 be in this four Face body center, two oxygen atoms (O5#4 and O10#5) be respectively from the Isosorbide-5-Nitrae-cyclohexane diacid of two different coordinations from Son, another oxygen atom (O6) is from O2-Ion, nitrogen-atoms is from ligand PIDPE;Equally, Zn3 is also using four-coordination Mode is connected with four oxygen atoms ultimately forms the tetrahedral configuration of distortion, and Zn3 is in the tetrahedron center, wherein three Oxygen atom (O3, O4#6 and O9#5) is respectively from the Isosorbide-5-Nitrae-cyclohexane diacid ion of three different coordinations, another oxygen atom (O6) from O2-Ion.Coordination mode there are two types of carboxylic acid groups in Isosorbide-5-Nitrae-cyclohexane diacid ion is monodentate chelating respectively and double Bridge work connects, Zn1 and Isosorbide-5-Nitrae-cyclohexane diacid ion formed the cluster unit of a double-core, Zn2 and Zn3 and Isosorbide-5-Nitrae-cyclohexane diacid ion and O2-Ion connects the one-dimensional chain to form zigzag, final ligand 1, and 4- cyclohexane diacid and zinc ion form a three-dimensional structure, such as scheme Shown in 2, the rectangle duct in three-dimensional structure is divided into many small ducts occupied by ligand PIDPE, by duct, such as Fig. 3 institute Show.
Fig. 4 is the infrared spectrogram of zinc metal organic complex prepared by the embodiment of the present invention 5;The cooperation as shown in Figure 4 The major absorbance peak of object are as follows: 3408 (m), 3196 (w), 2931 (w), 2852 (w), 2364 (w), 1671 (m), 1603 (s), 1520 (s), 1486 (s), 1387 (s), 1239 (s), 1167 (m), 1129 (w), 1061 (m), 964 (w), 821 (m), 735 (w), 653 (w), 608 (w), 526 (w).
Fig. 5 is the thermogravimetric curve of zinc metal organic complex prepared by the embodiment of the present invention 5;As shown in Figure 5, when temperature reaches The zinc metal organic complex skeleton starts to collapse when to 300 DEG C, thus illustrates, which has good thermal stability.
Fig. 6 is the powder xrd pattern of zinc metal organic complex prepared by the embodiment of the present invention 5;It will be appreciated from fig. 6 that practical institute The curve of survey can be good at coincideing with the curve that single crystal data is simulated, and illustrate that the purity of sample is very high.
Fig. 7 is the Solid fluorescene spectrum of zinc metal organic complex prepared by the embodiment of the present invention 5;As shown in Figure 7, cooperate Object fluorescence emission peak (λ=375nm, λex=335nm) compared with ligand PIDPE (λ=345nm, λex=330nm) red shift 30nm is compared, This may be that energy transfer (LMCT) is caused between ligand → metal under excited state due to complex.
The foregoing is only a preferred embodiment of the present invention, but scope of protection of the present invention is not limited thereto, Anyone skilled in the art in the technical scope disclosed by the present invention, according to the technique and scheme of the present invention and its Inventive concept is subject to equivalent substitution or change, should be covered by the protection scope of the present invention.

Claims (8)

1. a kind of zinc metal organic complex, which is characterized in that its chemical formula is [Zn3(PIDPE)(OH)(chdc)2.5], wherein PIDPE is 4- pyridyl group -4 '-imidazoles yl diphenyl ether, and chdc is Isosorbide-5-Nitrae-cyclohexane diacid of deprotonation, and PIDPE and chdc Structural formula is as follows:
The zinc metal organic complex belongs to monoclinic system, space group P21/ c, cell parameter areα=90.00 °, β=109.402 (2) °, γ=90.00 °,
2. zinc metal organic complex according to claim 1, which is characterized in that the zinc metal organic complex it is infrared Spectroscopic data is as follows: 3408 (m), 3196 (w), 2931 (w), 2852 (w), 2364 (w), 1671 (m), 1603 (s), 1520 (s), 1486 (s), 1387 (s), 1239 (s), 1167 (m), 1129 (w), 1061 (m), 964 (w), 821 (m), 735 (w), 653 (w) 608 (w), 526 (w).
3. a kind of preparation method of zinc metal organic complex as claimed in claim 1 or 2, which is characterized in that including following step It is rapid: 4- pyridyl group -4 '-imidazoles yl diphenyl ether, 1,4- cyclohexane diacid and zinc salt are added N, N '-dimethyl formamide and water it is mixed It closes in solution, stirs evenly and be placed in the stainless steel cauldron of polytetrafluoroethylliner liner, react 36-60h at 80-100 DEG C, After reaction through cooling, be filtered, washed, be dried to obtain the zinc metal organic complex;4- pyridyl group -4 '-imidazole radicals two Phenylate, 1,4- cyclohexane diacid, zinc salt molar ratio be 1:1:2-3.
4. the preparation method of zinc metal organic complex according to claim 3, which is characterized in that the zinc salt is nitric acid The mixture of one or more of zinc, zinc sulfate, zinc chloride, zinc acetate, zinc perchlorate.
5. according to the preparation method of the zinc metal organic complex of claim 3 or 4, which is characterized in that 4- pyridyl group -4 ' - Imidazoles yl diphenyl ether, 1,4- cyclohexane diacid, zinc salt molar ratio be 1:1:2.
6. according to the preparation method of the zinc metal organic complex of claim 3 or 4, which is characterized in that the N, N '-diformazan In the mixed solution of base formamide and water, N, the volume ratio of N '-dimethyl formamide and water is 1:2-3.
7. according to the preparation method of the zinc metal organic complex of claim 3 or 4, which comprises the following steps: 0.0313g4- pyridyl group -4 '-imidazoles yl diphenyl ether, 0.0172g1,4- cyclohexane diacid and 0.0595-0.0892g zinc nitrate is molten In 5-15g N, in the mixed solution of N '-dimethyl formamide and water, wherein the mixing of N, N '-dimethyl formamide and water are molten In liquid, the volume ratio of N, N '-dimethyl formamide and water are 1:2-3, stir evenly and are placed on the stainless of polytetrafluoroethylliner liner In steel reaction kettle, 36-60h is reacted at 80-100 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain zinc gold Belong to organic coordination compound.
8. according to the preparation method of the zinc metal organic complex of claim 3 or 4, which comprises the following steps: 0.0313g4- pyridyl group -4 '-imidazoles yl diphenyl ether, 0.0172g1,4- cyclohexane diacid and 0.0595g zinc nitrate are dissolved in 10g In the mixed solution of N, N '-dimethyl formamide and water, and N, in the mixed solution of N '-dimethyl formamide and water, N, N '-two Methylformamide and the volume ratio of water are 1:3, stir evenly the stainless steel cauldron for being placed on polytetrafluoroethylliner liner at room temperature In, 48h is reacted at 90 DEG C, after reaction through cooling, be filtered, washed, be dried to obtain the zinc metal organic complex.
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104370952A (en) * 2014-10-22 2015-02-25 渤海大学 Organic-ligand-based multifunctional zinc complexes and application thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104370952A (en) * 2014-10-22 2015-02-25 渤海大学 Organic-ligand-based multifunctional zinc complexes and application thereof

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
Structural Diversity and Sensing Properties of Metal-Organic Frameworks with Multicarboxylate and 1H-4-yl-Containing Ligands;Zhi-Qiang Liu 等;《Cryst. Growth Des.》;20171228;第18卷;第1136-1146页 *
Three New Coordination Polymers Constructed by Adjusting the Angles of Pyridyl or Imidazolyl-based Synthons: Structures and Solid UV-vis Properties;ZHOU Chun-Hui等;《Chinese J. Struct. Chem.》;20160831;第35卷(第8期);第1245-1252页 *
四重穿插金刚石型三维锌(II)配位聚合物的水热合成晶体结构及荧光性质;陶兆林等;《人工晶体学报》;20130228;第42卷(第2期);第371-376页 *
基于双咪唑基配体的两个镉(II)配位聚合物合成晶体结构和表征;张卫国等;《无机化学学报》;20121130;第28卷(第11期);第2494-2500页 *
基于环己二酸和双苯并咪唑配体的一维钴(II)配位聚合物的合成结构和催化性能研究;王君文等;《无机化学学报》;20130630;第29卷(第6期);第1263-1268页 *
模拟含双锌核的甲烷单加氧酶催化甲烷和乙烷羟基化理论研究;徐建等;《化学研究与应用》;20090630;第21卷(第6期);第877-882页 *

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