A general method for the synthesis of bench-stable bis(difluoromethyl)pentacoordinate phosphoranes has been developed.The reaction is rapid,operationally simple,and easily scalable.The pentacoordinate phosphoranes can...A general method for the synthesis of bench-stable bis(difluoromethyl)pentacoordinate phosphoranes has been developed.The reaction is rapid,operationally simple,and easily scalable.The pentacoordinate phosphoranes can generate both difluoromethyl radical(·CF_(2)H)and difluorocarbene(:CF_(2))intermediates.Thus,a variety of fluoroalkylation transformations havebeen achieved by·CF_(2)H,such asoxidativedifluoromethylation of electron-deficient heterocycles,nickel/photoredox dual-catalyzed difluoromethylation of aryl bromides,and photoredox difluoromethylation of alkenes,or by:CF_(2),such as gem-difluorocyclopropanation of alkenes,base-promoted difluoromethylation of heteroatom nucleophiles,Pd-catalyzed difluoromethylation of arylboronic acids,and Cu-mediated trifluoromethylation of aryl iodides(via:CF_(2) and recombined CF_(3)-).These fluoroalkylation methods have been successfully applied to late-stage fluoroalkylation of drugs and drug-like molecules.展开更多
In the presence of K2CO3, 2-hydroxyethyltripheny phosphonium bromide (1) reacts with substituted salicylaldehyde (2) and 2-hydroxy-1 naphthaldehyde (4) at 110 ℃ in a sealed tube. The title compounds were prepared in ...In the presence of K2CO3, 2-hydroxyethyltripheny phosphonium bromide (1) reacts with substituted salicylaldehyde (2) and 2-hydroxy-1 naphthaldehyde (4) at 110 ℃ in a sealed tube. The title compounds were prepared in medium yield. The ratio of bromide (1) to aldehyde derivatives was also discussed in this paper.展开更多
The title compounds 5a-5c were prepared via the reaction of methyl 2-perfluoroalkynoates (4) with methyl 5-oxo-4-(triphenylphosphoranylidene)hex-2-enoate (3), which was obtained from the reaction of methyl propynate (...The title compounds 5a-5c were prepared via the reaction of methyl 2-perfluoroalkynoates (4) with methyl 5-oxo-4-(triphenylphosphoranylidene)hex-2-enoate (3), which was obtained from the reaction of methyl propynate (2) with acetylmethylenetriphenylphosphorane (1) at -5-0 degrees C. Intramolecular elimination of Ph(3)PO took place when compound 5 was heated in aqueous methanol at 115-120 degrees C in sealed tube, yielding dimethyl 2-trifluoromethyl-4-methylisophthalate (6a) from 5a and methyl 5-acetyl-4-hydroxy-2-heptafluoropropanylbenzoate (6b) from 5b, respectively. The structures of compounds 5, 6a and 6b were confirmed by IR, MS, H-1 NMR, F-19 NMR and C-13 NMR spectroscopy and elemental analyses. Rection mechanisms for the formation of compounds 5, 6a and 6b were proposed.展开更多
Chemical modification and vertical stacking of two-dimensional materials are promising techniques for new nanoelectronic devices. We present Density Functional Tight Binding(DFTB) calculations of a field-effect device...Chemical modification and vertical stacking of two-dimensional materials are promising techniques for new nanoelectronic devices. We present Density Functional Tight Binding(DFTB) calculations of a field-effect device,based on lateral and vertical heterostructures of 2D materials. The device consists of a phosphorene channel protected by graphene sheets, which work as contacts and are divided into the source and drain by local hydrogenation of graphene, which gives insulating graphane. In this device composed of only 3 layers, single sheets of graphene-graphane can work as both leads and oxide gate, while also acting as protective layers for a phosphorene channel. We show how for perfect vd W heterostructures of graphane/phosphorene/graphane and graphene/phosphorene/graphene the Schottky barrier is deeply influenced by normal electric fields, and we characterize electronic transport of such a device. Finally, we characterize phosphorene channel doping and defects, which, at very high densities in the transport direction, enables transport inside the phosphorene bandgap.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
Q-Acyl phosphoranes can readily react with areneselenium canons,which can be obtained from diaryl diselenides by oxidative reaction, to give a-arylseleno-a-acyl phosphoranes in good yields. The a-arylseleno-a-acyl pho...Q-Acyl phosphoranes can readily react with areneselenium canons,which can be obtained from diaryl diselenides by oxidative reaction, to give a-arylseleno-a-acyl phosphoranes in good yields. The a-arylseleno-a-acyl phosphoranes can undergo intramolecular Wittig reaction to afforda convenient synthesis of arylselenoacetylenes.展开更多
Numerous round to oblate opaque assemblages (OAs) are found in chondrules and matrix of the Ningqiang carbonaceous chondrite. They are mainly composed of Ni-rich metal,magnetite,Fe,Ni-sulfides,with minor amounts of ph...Numerous round to oblate opaque assemblages (OAs) are found in chondrules and matrix of the Ningqiang carbonaceous chondrite. They are mainly composed of Ni-rich metal,magnetite,Fe,Ni-sulfides,with minor amounts of phosphate,phosphoran-olivine,pyroxene and trace amounts of nano-sized platinum-group metal alloys. The mineralogy of Ningqiang OAs is very similar to that of OAs previously reported in Ca,Al-rich inclusions of CV chondrites. Being a rare mineral phase in nature,phosphoran-olivine is thought to form by nonequilibrium reactions between P-bearing molten metal and olivine crystals during rapid cooling. Its occurrence in Ningqiang OAs indicates that the precursor of OAs was locally produced during chondrule formation,rather than directly condensed from the solar nebula as previously thought. The petrographic and mineralogical characteristics of Ningqiang OAs reveal that OAs formed by low temperature alterations of pre-existing homogeneous alloys within chondrules on a planetary body.展开更多
基金supported by National Natural Science Foundation of China(grant no.21901196)the Natural Science Basic Research Plan in Shaanxi Province of China(grant nos.2020JQ-016 and 2021GXLH-Z-096)+1 种基金the Fundamental Research Funds for the Central Universities(grant no.xhj032021007-01)Xi’an Jiaotong University(grant no.71211920000001).
文摘A general method for the synthesis of bench-stable bis(difluoromethyl)pentacoordinate phosphoranes has been developed.The reaction is rapid,operationally simple,and easily scalable.The pentacoordinate phosphoranes can generate both difluoromethyl radical(·CF_(2)H)and difluorocarbene(:CF_(2))intermediates.Thus,a variety of fluoroalkylation transformations havebeen achieved by·CF_(2)H,such asoxidativedifluoromethylation of electron-deficient heterocycles,nickel/photoredox dual-catalyzed difluoromethylation of aryl bromides,and photoredox difluoromethylation of alkenes,or by:CF_(2),such as gem-difluorocyclopropanation of alkenes,base-promoted difluoromethylation of heteroatom nucleophiles,Pd-catalyzed difluoromethylation of arylboronic acids,and Cu-mediated trifluoromethylation of aryl iodides(via:CF_(2) and recombined CF_(3)-).These fluoroalkylation methods have been successfully applied to late-stage fluoroalkylation of drugs and drug-like molecules.
文摘In the presence of K2CO3, 2-hydroxyethyltripheny phosphonium bromide (1) reacts with substituted salicylaldehyde (2) and 2-hydroxy-1 naphthaldehyde (4) at 110 ℃ in a sealed tube. The title compounds were prepared in medium yield. The ratio of bromide (1) to aldehyde derivatives was also discussed in this paper.
基金Project supported by the National Natural Science Foundation of China.
文摘The title compounds 5a-5c were prepared via the reaction of methyl 2-perfluoroalkynoates (4) with methyl 5-oxo-4-(triphenylphosphoranylidene)hex-2-enoate (3), which was obtained from the reaction of methyl propynate (2) with acetylmethylenetriphenylphosphorane (1) at -5-0 degrees C. Intramolecular elimination of Ph(3)PO took place when compound 5 was heated in aqueous methanol at 115-120 degrees C in sealed tube, yielding dimethyl 2-trifluoromethyl-4-methylisophthalate (6a) from 5a and methyl 5-acetyl-4-hydroxy-2-heptafluoropropanylbenzoate (6b) from 5b, respectively. The structures of compounds 5, 6a and 6b were confirmed by IR, MS, H-1 NMR, F-19 NMR and C-13 NMR spectroscopy and elemental analyses. Rection mechanisms for the formation of compounds 5, 6a and 6b were proposed.
基金supported through the German Research Foundation within the project “Straintronics of imperfect quasi-two-dimensional materials: coplanar vs lamellar heterostructures” (CU 44/43).
文摘Chemical modification and vertical stacking of two-dimensional materials are promising techniques for new nanoelectronic devices. We present Density Functional Tight Binding(DFTB) calculations of a field-effect device,based on lateral and vertical heterostructures of 2D materials. The device consists of a phosphorene channel protected by graphene sheets, which work as contacts and are divided into the source and drain by local hydrogenation of graphene, which gives insulating graphane. In this device composed of only 3 layers, single sheets of graphene-graphane can work as both leads and oxide gate, while also acting as protective layers for a phosphorene channel. We show how for perfect vd W heterostructures of graphane/phosphorene/graphane and graphene/phosphorene/graphene the Schottky barrier is deeply influenced by normal electric fields, and we characterize electronic transport of such a device. Finally, we characterize phosphorene channel doping and defects, which, at very high densities in the transport direction, enables transport inside the phosphorene bandgap.
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.
基金Project supported by the National Natural Science Foundation of China(Nos.21778042,41876072,21772163,41576081)the Xiamen Southern Oceanographic Center(No.17GYY002NF02)the Fundamental Research Funds for the Central Universities(No.20720170069)~~
文摘Q-Acyl phosphoranes can readily react with areneselenium canons,which can be obtained from diaryl diselenides by oxidative reaction, to give a-arylseleno-a-acyl phosphoranes in good yields. The a-arylseleno-a-acyl phosphoranes can undergo intramolecular Wittig reaction to afforda convenient synthesis of arylselenoacetylenes.
基金Supported by the Chinese National Natural Science Foundation for Distinguished Young Scholars (Grant No. 40325009)the One-Hundred-Talent Program of Chinese Academy of Sciencesthe Minor Planet Foundation of China
文摘Numerous round to oblate opaque assemblages (OAs) are found in chondrules and matrix of the Ningqiang carbonaceous chondrite. They are mainly composed of Ni-rich metal,magnetite,Fe,Ni-sulfides,with minor amounts of phosphate,phosphoran-olivine,pyroxene and trace amounts of nano-sized platinum-group metal alloys. The mineralogy of Ningqiang OAs is very similar to that of OAs previously reported in Ca,Al-rich inclusions of CV chondrites. Being a rare mineral phase in nature,phosphoran-olivine is thought to form by nonequilibrium reactions between P-bearing molten metal and olivine crystals during rapid cooling. Its occurrence in Ningqiang OAs indicates that the precursor of OAs was locally produced during chondrule formation,rather than directly condensed from the solar nebula as previously thought. The petrographic and mineralogical characteristics of Ningqiang OAs reveal that OAs formed by low temperature alterations of pre-existing homogeneous alloys within chondrules on a planetary body.
