Barbituric acid derivative modified molybdenum disulfide two-dimensional nano material and application thereof
A two-dimensional nanomaterial, molybdenum disulfide technology, applied in the direction of molybdenum sulfide, medical preparations with non-active ingredients, medical preparations containing active ingredients, etc.
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Embodiment 1
[0054] Embodiment 1 Ligand 2-thiobarbituric acid, molybdenum disulfide nanomaterial (MoS 2 -1) Synthesis
[0055] Two-dimensional molybdenum disulfide nanomaterials (MoS) modified with 2-thiobarbituric acid, benzoic acid (Ligand1) 2 -1) As an example, the synthesis of the two-dimensional molybdenum disulfide nanomaterial modified by barbituric acid derivatives described in the present invention is described.
[0056] The reaction formula involved in the specific reaction pathway is as follows:
[0057]
[0058] (1) Molybdenum disulfide (4.8 g, 0.03 mol) was mixed with 30 mL of N,N-dimethylformamide (DMF) in an ice bath, and stirred evenly. Under vigorous stirring, 2-thiobarbituric acid (7.0 g, 0.06 mol) was thus added to the above reaction system. React under ice bath for 4-6 hours, heat and reflux for 4-6 hours, after the reaction, sonicate at 290K for 120 hours to obtain a suspension of the intermediate product (1).
[0059] (2) Under ice bath, mix and dissolve benzoi...
Embodiment 2
[0061] Example 2 For 2-thiobarbituric acid, the two-dimensional molybdenum disulfide nanomaterial (MoS) modified by cyclohexyl formic acid (Ligand2) 2 -2) Synthesis
[0062] The preparation method is similar to that of MoS in Example 1 2 -1 preparation, the difference is that the 6.1g benzoic acid used in step b is replaced by 6.4g cyclohexyl formic acid to finally obtain the DMF solution of cyclohexyl formic acid-N-hydroxysuccinimide active ester; The benzoic acid-N-hydroxysuccinimide active ester was replaced by the cyclohexylcarboxylic acid-N-hydroxysuccinimide active ester.
Embodiment 3
[0063] Example 3 For 2-thiobarbituric acid, n-heptanoic acid (Ligand3) modified two-dimensional molybdenum disulfide nanomaterials (MoS 2 -3) Synthesis
[0064] The preparation method is similar to that of MoS in Example 1 2-1, the difference is that the 6.1g benzoic acid used in step b is replaced by 6.5g n-heptanoic acid to finally obtain the DMF solution of n-heptanoic acid-N-hydroxysuccinimide active ester; The benzoic acid-N-hydroxysuccinimide active ester was replaced by n-heptanoic acid-N-hydroxysuccinimide active ester.
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