Nitrogen-containing two-dimensional conjugated carbon material, preparation method and application thereof
A two-dimensional conjugated, carbon material technology, applied in the field of electrochemical materials, can solve the problems of low energy density of supercapacitors and hinder the application of supercapacitors, and achieve excellent thermal stability, excellent cycle stability, and broad commercial application prospects Effect
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Embodiment 1
[0070] In this embodiment, the nitrogen-containing two-dimensional conjugated carbon material HATP-COF was prepared by the following steps:
[0071] Step (1): Synthesis of hexaaminotriphenylene monomer (HATP): Combine triphenylene compound 1 with liquid bromine, iron, nitrobenzene (PhNO 2 ) Perform bromination reaction at 205°C for 2 hours to obtain the hexabromo compound, compound 2. Combine compound 2 with 1,1'-binaphthyl-2,2'-bisdiphenylphosphine (rac-BINAP) and benzophenone Imine (Ph 2 C=NH), three (dibenzylideneacetone) two palladium (Pd 2 (dba) 3 ) React overnight at 110°C in toluene to produce imine compound 3; finally, acidolysis in tetrahydrofuran (THF) to obtain hexaaminotriphenylene monomer, compound 4 (HATP), the synthesis route is as follows:
[0072]
[0073] Step (2): Synthesis of HATP-COF precursor compound: 40.00 mg monomer HATP, 23.5 mg hexaketocyclohexane octahydrate and 0.1 mL 98% concentrated sulfuric acid were added to 2 mL of NMP. The mixed solution is placed...
Embodiment 2
[0080] In this embodiment, the nitrogen-containing two-dimensional conjugated carbon material HATP-COF was prepared by the following steps:
[0081] Step (1): Synthesis of hexaaminotriphenylene monomer (HATP): Combine triphenylene compound 1 with liquid bromine, iron, nitrobenzene (PhNO 2 ) Perform bromination reaction at 205°C for 2 hours to obtain the hexabromo compound, compound 2. Combine compound 2 with 1,1'-binaphthyl-2,2'-bisdiphenylphosphine (rac-BINAP) and benzophenone Imine (Ph 2 C=NH), three (dibenzylideneacetone) two palladium (Pd 2 (dba) 3 ) Reacted overnight at 110°C in toluene to produce imine compound 3; finally, acidolysis in tetrahydrofuran (THF) to obtain hexaaminotriphenylene monomer, compound 4 (HATP), its synthesis route is as follows:
[0082]
[0083] Step (2): Synthesis of HATP-COF precursor compound: 40.00 mg monomer HATP, 70.5 mg hexaketocyclohexane octahydrate and 0.2 mL 98% concentrated sulfuric acid were added to 3 mL of NMP. The mixed solution is plac...
Embodiment 3
[0087] In this embodiment, the nitrogen-containing two-dimensional conjugated carbon material HATP-COF was prepared by the following steps:
[0088] Step (1): Synthesis of hexaaminotriphenylene monomer (HATP): Combine triphenylene compound 1 with liquid bromine, iron, nitrobenzene (PhNO 2 ) Perform bromination reaction at 205°C for 2 hours to obtain the hexabromo compound, compound 2. Combine compound 2 with 1,1'-binaphthyl-2,2'-bisdiphenylphosphine (rac-BINAP) and benzophenone Imine (Ph 2 C=NH), three (dibenzylideneacetone) two palladium (Pd 2 (dba) 3 ) Reacted overnight at 110°C in toluene to produce imine compound 3; finally, acidolysis in tetrahydrofuran (THF) to obtain hexaaminotriphenylene monomer, compound 4 (HATP), its synthesis route is as follows:
[0089]
[0090] Step (2): Synthesis of HATP-COF precursor compound: 120.00 mg monomer HATP, 23.5 mg hexaketocyclohexane octahydrate and 0.15 mL 98% concentrated sulfuric acid were added to 2.5 mL of NMP. The mixed solution was...
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