A rapid and efficient method for the synthesis of isoxazolo[5,4-d]pyrimidin-4（5H）-ones has been developed through cyclocondensation of 5-aminoisoxazole-4-carboxamides with orthoesters under conventional heating and ...A rapid and efficient method for the synthesis of isoxazolo[5,4-d]pyrimidin-4（5H）-ones has been developed through cyclocondensation of 5-aminoisoxazole-4-carboxamides with orthoesters under conventional heating and solvent-free microwave irradiation with solid acid catalysis. In comparison, the reactions are faster and the yields are higher under microwave irradiation.展开更多
2, 7-Diaminothieno[2, 3-d：5, 4-d]dipyrimidine-4, 5（3H, 6H）diones 4 were synthesized by a facile synthetic method, which includes bis-aza-Wittig reaction of bis-iminophosphorane 1 with aromatic isocyanate to give bi...2, 7-Diaminothieno[2, 3-d：5, 4-d]dipyrimidine-4, 5（3H, 6H）diones 4 were synthesized by a facile synthetic method, which includes bis-aza-Wittig reaction of bis-iminophosphorane 1 with aromatic isocyanate to give bis-carbodiimide 2 and subsequent reaction of 2 with various dialkylamine in the presence of solid K2CO3 or EtONa.展开更多
A novel method to synthesize 2,6-bis(p-aminophenyl)benzo\[1,2-d;5,4-d'\]bisoxazole using 1,2,3-trichlorobenzene as the starting material through nitration, substitution, hydrogenation, and condensation was reporte...A novel method to synthesize 2,6-bis(p-aminophenyl)benzo\[1,2-d;5,4-d'\]bisoxazole using 1,2,3-trichlorobenzene as the starting material through nitration, substitution, hydrogenation, and condensation was reported. During the condensation, the influence of the amount of SnCl_2 on the yield of the product was studied. The electron spectra of the compound were discussed, the results showed that it is a fluorescence material with large Stokes shift.展开更多
Twenty-seven oxadiazolino[5,4-d][1,5]benzodiheteropine derivatives have been synthesized by the 1,3-dipolar cycloaddition of benzodiheteropines with nitrile oxide 1,3-dipoles,their conformations and the characteristic...Twenty-seven oxadiazolino[5,4-d][1,5]benzodiheteropine derivatives have been synthesized by the 1,3-dipolar cycloaddition of benzodiheteropines with nitrile oxide 1,3-dipoles,their conformations and the characteristics of the newly formed oxadiazoline fused on them have been studied.It has also been found that the mass spectra show characteristic fragmentation patterns.展开更多
Donor-Acceptor(D-A)alignment is considered a productive strategy to improve the charge separation efficiency of covalent organic frameworks(COFs)and enhance the charge-transfer yield(CTY)of COFs.Moreover,organic molec...Donor-Acceptor(D-A)alignment is considered a productive strategy to improve the charge separation efficiency of covalent organic frameworks(COFs)and enhance the charge-transfer yield(CTY)of COFs.Moreover,organic molecules containing heteroatoms can produce coordination interaction with PbI2 of perovskite precursor to affect the crystallization process,thereby impeding the decomposition and improving the stability of perovskite materials.Herein,a thiazolo[5,4-d]thiazole(TZ)-based D-A type COF_(TPDA-TZDA) was designed and synthesized from N,N,N′,N′-tetrakis(4-aminophenyl)-1,4-benzenediamine(TPDA)and 4,4′-(thiazolo[5,4-d]thiazole-2,5-diyl)dibenzaldehyde(TZDA).Upon incorporation into the FAPbI3 layer,COF_(TPDA-TZDA) not only restrained the perovskite defects and enhanced the grain size of perovskite films through the coordination effect of the N atoms of TZDA but also ameliorated the charge transport within the perovskite film,which was the benefit of the D-A structure of COF_(TPDA-TZDA).As a result,incorporation of COF_(TPDA-TZDA) into the perovskite solar cells(PSCs)led to a remarkable power conversion efficiency(PCE)of up to 23.51%.Furthermore,even after being stored in high relative humidity(RH≈60%)for 480 h,these PSCs maintained over 90.55%of their original PCE.This work sets the foundation for the development of highly efficient and stable PSCs by utilizing TZ-based D-A type COFs.展开更多
A facile and efficient approach was developed to access 5, 7-disubstitued thiazolo[5,4-d]pyrimidine-4, 6（5H, 7H）-diones through condensation of N-substituted 5-amino-4-carbethoxythiazole with structurally diverse is...A facile and efficient approach was developed to access 5, 7-disubstitued thiazolo[5,4-d]pyrimidine-4, 6（5H, 7H）-diones through condensation of N-substituted 5-amino-4-carbethoxythiazole with structurally diverse isocyanates in the presence of sodium hydride. The easy availability of substrates and tolerance of structural diversity in this reaction make it attractive to be used for construction of libraries in drug discovery process.展开更多
文摘A rapid and efficient method for the synthesis of isoxazolo[5,4-d]pyrimidin-4（5H）-ones has been developed through cyclocondensation of 5-aminoisoxazole-4-carboxamides with orthoesters under conventional heating and solvent-free microwave irradiation with solid acid catalysis. In comparison, the reactions are faster and the yields are higher under microwave irradiation.
基金We gratefully acknowledge financial support of this work by the National Key Project for Basic Research(2003CB114400,2003CB114406)the National Natural Science Foundation of China(Project No.20372023 and 20102001).
文摘2, 7-Diaminothieno[2, 3-d：5, 4-d]dipyrimidine-4, 5（3H, 6H）diones 4 were synthesized by a facile synthetic method, which includes bis-aza-Wittig reaction of bis-iminophosphorane 1 with aromatic isocyanate to give bis-carbodiimide 2 and subsequent reaction of 2 with various dialkylamine in the presence of solid K2CO3 or EtONa.
文摘A novel method to synthesize 2,6-bis(p-aminophenyl)benzo\[1,2-d;5,4-d'\]bisoxazole using 1,2,3-trichlorobenzene as the starting material through nitration, substitution, hydrogenation, and condensation was reported. During the condensation, the influence of the amount of SnCl_2 on the yield of the product was studied. The electron spectra of the compound were discussed, the results showed that it is a fluorescence material with large Stokes shift.
文摘Twenty-seven oxadiazolino[5,4-d][1,5]benzodiheteropine derivatives have been synthesized by the 1,3-dipolar cycloaddition of benzodiheteropines with nitrile oxide 1,3-dipoles,their conformations and the characteristics of the newly formed oxadiazoline fused on them have been studied.It has also been found that the mass spectra show characteristic fragmentation patterns.
基金supported by the National Natural Science Foundation of China (grant nos.22375070 and 22288101)the Jilin Province Science and Technology Development Plan (grant nos.20220101048JC and 20210101112JC)the 111 Project the Ministry of Education of China (grant no.B17020).
文摘Donor-Acceptor(D-A)alignment is considered a productive strategy to improve the charge separation efficiency of covalent organic frameworks(COFs)and enhance the charge-transfer yield(CTY)of COFs.Moreover,organic molecules containing heteroatoms can produce coordination interaction with PbI2 of perovskite precursor to affect the crystallization process,thereby impeding the decomposition and improving the stability of perovskite materials.Herein,a thiazolo[5,4-d]thiazole(TZ)-based D-A type COF_(TPDA-TZDA) was designed and synthesized from N,N,N′,N′-tetrakis(4-aminophenyl)-1,4-benzenediamine(TPDA)and 4,4′-(thiazolo[5,4-d]thiazole-2,5-diyl)dibenzaldehyde(TZDA).Upon incorporation into the FAPbI3 layer,COF_(TPDA-TZDA) not only restrained the perovskite defects and enhanced the grain size of perovskite films through the coordination effect of the N atoms of TZDA but also ameliorated the charge transport within the perovskite film,which was the benefit of the D-A structure of COF_(TPDA-TZDA).As a result,incorporation of COF_(TPDA-TZDA) into the perovskite solar cells(PSCs)led to a remarkable power conversion efficiency(PCE)of up to 23.51%.Furthermore,even after being stored in high relative humidity(RH≈60%)for 480 h,these PSCs maintained over 90.55%of their original PCE.This work sets the foundation for the development of highly efficient and stable PSCs by utilizing TZ-based D-A type COFs.
基金supported by the National Natural Science Foundation of China(No.30500634) and NSF of Beijing (No.7102112)
文摘A facile and efficient approach was developed to access 5, 7-disubstitued thiazolo[5,4-d]pyrimidine-4, 6（5H, 7H）-diones through condensation of N-substituted 5-amino-4-carbethoxythiazole with structurally diverse isocyanates in the presence of sodium hydride. The easy availability of substrates and tolerance of structural diversity in this reaction make it attractive to be used for construction of libraries in drug discovery process.
