CN109942604A - A kind of big ring pentacoordinate copper (II) complex and its in-situ synthetic method of sulfur-bearing-sulfide linkage - Google Patents

A kind of big ring pentacoordinate copper (II) complex and its in-situ synthetic method of sulfur-bearing-sulfide linkage Download PDF

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CN109942604A
CN109942604A CN201910324828.5A CN201910324828A CN109942604A CN 109942604 A CN109942604 A CN 109942604A CN 201910324828 A CN201910324828 A CN 201910324828A CN 109942604 A CN109942604 A CN 109942604A
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complex
sulfur
sulfide linkage
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CN109942604B (en
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蒋毅民
王慧
许小陵
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Guangxi Normal University
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Abstract

The invention discloses big ring pentacoordinate copper (II) complex and its in-situ synthetic method of a kind of sulfur-bearing-sulfide linkage, the chemical formulas of big ring pentacoordinate copper (II) complex are as follows: [Cu (H4L1)Cl]Cl·H2O, wherein H4L1The macrocyclic ligand formed for two 3,3 '-two (5- sulfydryl -1,2,4- triazole) by sulphur-sulfide linkage.The in-situ synthetic method of complex includes the following steps: that (1) weighs 0.04-0.05g 3,3 '-two (5- sulfydryl -1,2,4- triazole) and 0.03-0.04g Copper dichloride dihydrate CuCl2·2H2O is mixed in 7-9mL dimethylformamide, mixed solution is placed in and is stirred to react 6-7h at room temperature;(2) above-mentioned mixed liquor is filtered, obtains green solution, filtrate is placed in a beaker, volatilized naturally at room temperature, obtain monocrystalline grade green platelet-type crystal.Big ring pentacoordinate copper (II) complex of sulfur-bearing-sulfide linkage of the present invention antibacterial, it is antitumor and as drug targeting release in terms of have potential application, this method has wide application prospects in terms of the fabricated in situ of sulfur-bearing-sulfide linkage Macrocyclic metal complex.

Description

A kind of big ring pentacoordinate copper (II) complex and its fabricated in situ of sulfur-bearing-sulfide linkage Method
Technical field
The present invention relates to copper complex, big ring pentacoordinate copper (II) complex and its original of specifically a kind of sulfur-bearing-sulfide linkage Position synthetic method.
Background technique
Reaction in-situ is one of the hot spot of Coordinative Chemistry research.Though there are much document reports about reaction in-situ at present, But it there are no 3,3 '-two (5- sulfydryl -1,2,4- triazoles) and be oxidized the big cyclodimerization ligand of generation sulfur-bearing-sulfide linkage and then shape At the report of pentacoordinate Cu (II) complex.
Sulfur-bearing triazole is widely used in the fields such as medicine, pesticide as intermediate, the cooperation formed with metal ion Object also has preferable antibacterial and anticancer activity.It, can be because in cell when due to reaching tumour cell containing sulphur-sulfide linkage compound A large amount of existing glutathione and the reaction of sulphur-sulfide linkage scission of link occurs, therefore, by 3,3 '-two (5- sulfydryl -1,2,4- triazoles) It is oxidized the carrier that can be used as potential drug targeting release containing sulphur-sulfide linkage macrocyclic complex of generation.
Summary of the invention
In order to obtain new sulfur-bearing-sulfide linkage macrocyclic complex, one aspect of the present invention is to provide a kind of sulfur-bearing-sulfide linkage Big ring pentacoordinate copper (II) complex, on the other hand also provides with 3,3 '-two (5- sulfydryl -1,2,4- triazole) (H4It L is) original The in-situ synthetic method of the complex of material.
A kind of chemical formula of big ring pentacoordinate copper (II) complex of sulfur-bearing-sulfide linkage of the present invention are as follows: [Cu (H4L1)Cl] Cl·H2O, wherein H4L1The macrocyclic ligand formed for two 3,3 '-two (5- sulfydryl -1,2,4- triazole) by sulphur-sulfide linkage, H4L1Structural formula is as follows:
Big ring pentacoordinate copper (II) complex of sulfur-bearing-sulfide linkage of the present invention, crystal belong to monoclinic system,P21/cSpace Group, Z=4, cell parameter are as follows:a=11.679 (4),b=12.052 (4),c = 14.887(4)Å,α= 90.00 °,β =118.28(2) °,γ= 90.00 °,V =1845.3(11)Å3
The in-situ synthetic method of big ring pentacoordinate copper (II) complex of sulfur-bearing-sulfide linkage of the present invention, includes the following steps:
(1) 0.04-0.05g 3,3 '-two (5- sulfydryl -1,2,4- triazole) (H is weighed4L) and 0.03-0.04g bis- is hydrated chlorine Change copper CuCl2·2H2O, mixing, mixed solution is placed in and is stirred to react 6- at room temperature in 7-9mL dimethylformamide (DMF) 7h;
(2) above-mentioned mixed liquor is filtered, obtains green solution, filtrate is placed in a beaker, volatilized naturally at room temperature, obtain monocrystalline Grade green platelet-type crystal.
In the reaction process of big ring pentacoordinate copper (II) complex of sulfur-bearing-sulfide linkage of the present invention, first wife's body 3,3 '-two (5- sulfydryl -1,2,4- triazole) (H4L the sulfydryl in) is aoxidized by the oxygen in air, by joining end to end, generates two pairs Sulphur-sulfide linkage connects into macrocyclic ligand (H for two 3,3 '-two (5- sulfydryl -1,2,4- triazole)4L1), and then it is anti-with copper ion Big ring pentacoordinate Cu (II) complex should be generated.
Big ring pentacoordinate copper (II) complex of sulfur-bearing-sulfide linkage of the present invention is in antibacterial, antitumor and as drug targeting Carrier of release etc. has potential application, and this method is closed in the original position of sulfur-bearing-sulfide linkage Macrocyclic metal complex Have wide application prospects at aspect.
Detailed description of the invention
Fig. 1 is the schematic arrangement of big ring pentacoordinate copper (II) complex of embodiment sulfur-bearing-sulfide linkage.
Specific embodiment
The content of present invention is further described below with reference to embodiment, but is not limitation of the invention.
Embodiment
A kind of in-situ synthetic method of big ring pentacoordinate copper (II) complex of sulfur-bearing-sulfide linkage, includes the following steps:
(1) 0.0400g 3,3 '-two (5- sulfydryl -1,2,4- triazole) (H is weighed4) and 0.0342g Copper dichloride dihydrate L CuCl2·2H2O, mixing, mixed solution is placed in and is stirred to react 6h at room temperature in 8mL dimethylformamide (DMF);
(2) above-mentioned mixed liquor is filtered, obtains green solution, filtrate is placed in a beaker, volatilized naturally at room temperature, obtain monocrystalline Grade green platelet-type crystal.
Referring to Fig. 1, the schematic arrangement of big ring pentacoordinate copper (II) complex of embodiment sulfur-bearing-sulfide linkage, in order to Convenient for observation, extraneous chloride ion Cl is deleted-And crystalline water molecules.From figure it will be evident that the interior boundary of the complex is by one A copper ion Cu2+, a chloride ion Cl-With a macrocyclic ligand (H4L1) composition.Cu2+Four N originals of ion and macrocyclic ligand Sub (N1, N4, N7, N10) and chloride ion (Cl1) coordination, forms the CuN of a deformation4Tetra- jiaos of wimble structures of Cl, Cl are in The top of quadrangular pyramid.
The crystal structure determination of big ring pentacoordinate copper (II) complex of embodiment sulfur-bearing-sulfide linkage:
The all proper cluster compound monocrystalline of size and shape is selected, is placed on SuperNova single crystal diffractometer, using graphite list Color Mo-Radiation (λ= 0.71073 Å).Respectively certain under the conditions of 298 (2) KθIn range withφ-ωScanning side Formula collects point diffraction and is used for structure elucidation and amendment.Non-hydrogen atom is solved with direct method, and to their coordinate and its respectively to different Property thermal parameter corrected with complete matrix least square method.Mixed hydrogenation, hydrogen atom use isotropism thermal parameter;Non-hydrogen atom Using anisotropy thermal parameter.The parsing of crystal structure and structural modifications respectively by SHELX-97 (Sheldrick, 1990) and SHELXL-97 (Sheldrick, 1997) program bag is completed.1 is shown in Table in relation to crystallography and structural modifications data.
The crystallography and structural modifications data of big ring Cu (II) complex of table 1, pentacoordinate

Claims (3)

1. big ring pentacoordinate copper (II) complex of a kind of sulfur-bearing-sulfide linkage, it is characterized in that: big ring pentacoordinate copper (II) complex Chemical formula are as follows: [Cu (H4L1)Cl]Cl·H2O, wherein H4L1Pass through for two 3,3 '-two (5- sulfydryl -1,2,4- triazole) The macrocyclic ligand that sulphur-sulfide linkage is formed.
2. big ring pentacoordinate copper (II) complex of sulfur-bearing-sulfide linkage according to claim 1, it is characterized in that: described is big Ring pentacoordinate copper (II) complex, crystal belong to monoclinic system,P21/cSpace group, Z=4, cell parameter are as follows:a = 11.679 (4),b=12.052 (4),c = 14.887(4)Å,α = 90.00 °,β =118.28(2) °,γ = 90.00 °,V =1845.3(11)Å3
3. the in-situ synthetic method of big ring pentacoordinate copper (II) complex of sulfur-bearing-sulfide linkage according to claim 1, special Sign is to include the following steps:
(1) 0.04-0.05g 3,3 '-two (5- sulfydryl -1,2,4- triazole) and 0.03-0.04g Copper dichloride dihydrate are weighed CuCl2·2H2O is mixed in 7-9mL dimethylformamide, mixed solution is placed in and is stirred to react 6-7h at room temperature;
(2) above-mentioned mixed liquor is filtered, obtains green solution, filtrate is placed in a beaker, volatilized naturally at room temperature, obtain monocrystalline Grade green platelet-type crystal.
CN201910324828.5A 2019-04-22 2019-04-22 Macrocyclic pentacoordinate copper (II) complex containing sulfur-sulfur bond and in-situ synthesis method thereof Expired - Fee Related CN109942604B (en)

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WO2022052391A1 (en) * 2020-09-10 2022-03-17 苏州富德兆丰生化科技有限公司 Method for synthesizing vortioxetine

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