The factors that affect the kinetics of the aza-Bergman cyclization of aza-enediynes (C,N-dialkynyl imines) have not previously been elucidated. Here we report our kinetic studies of the aza-Bergman reactions of a series of 6-triisopropylsilyl and 6-unsubstituted 1-phenyl-4-aryl-3-aza-3-ene-1,4-diynes in which the aryl group is phenyl, o-(methoxy)phenyl, or p-(methoxy)phenyl. These aza-enediynes are prepared as single isomers in modest yield from the corresponding 1-aryl-3-(triisopropylsilyl)propynone oximes. These aza-enediynes undergo aza-Bergman reaction followed by a rapid retro-aza-Bergman cyclization to afford beta-alkynyl acrylonitrile products. In no case are products corresponding to trapping the intermediate 2,5-didehydropyridine diradical isolated. While the rate of aza-Bergman cyclization is not greatly affected by the nature of the 4-aryl substituent, the rate is very dependent on the nature of the 6-substituent. 1-Phenyl-4-aryl-3-aza-3-ene-1,5-diynes that lack a 6-substituent undergo aza-Bergman cyclization spontaneously at 20 degrees C with first-order half-lives of 36-78 min. The effect of solvent on the kinetics of aza-Bergman cyclization of 1,4-diphenyl-3-aza-3-ene-1,5-diyne was investigated. The rate of this cyclization is solvent dependent, proceeding more rapidly in less polar solvents.
This article reports a novel method for three‐dimensional (3D) printing of continuous fibers into ceramics to improve the mechanical properties of printed ceramics, which is difficult in other 3D printing technologies. The ceramics were derived by pyrolysis of thermoplastic ceramic precursor feedstocks, which were prepared by two methods. One is homogeneously mixing thermoplastic resins and ceramic precursors. The feedstocks prepared by this method exhibit good thermoplastic properties and can be extruded into filaments. Ceramics were obtained by heating the feedstocks to 1100°C in argon atmosphere. The ceramics were amorphous and remained stable during 1100‐1300°C; at 1400°C they decomposed into β–SiC with simultaneous volatile gas generation. Above 1400°C, their quality decreased significantly due to cracking of ceramic skeletons. The other method is directly heating, extruding and printing the ceramic precursor. The precursors showed good printability and complex ceramic structures were printed with continuous carbon fibers inside. The continuous carbon fibers improved the flexural strength of pyrolytic ceramics, which is about 7.6 times better than that of the ceramics without fibers. The novel method unravels the potential of 3D printing of continuous fibers into ceramics with complex lightweight structures to improve the strength.
[reaction: see text] On the basis of density functional calculations, the isomerization of skipped azaenediynes (C-alkynyl-N-propargylimines) to azaenyne allenes and subsequent rapid aza-Myers-Saito cyclization to alpha,5-didehydro-3-picoline were predicted. We prepared the N-propargylimine of 1-phenyl-3-tri(isopropyl)silylprop-2-yn-1-one, which undergoes proto-desilylation and isomerization to an azaenyne allene when treated with tetrabutylammonium fluoride. In the presence of 1,4-cyclohexadiene, this azaenyne allene affords 6-phenyl-3-picoline and other products corresponding to the trapping of an alpha,5-didehydro-3-picoline diradical.
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