2,2'-Bis (4H-3,1-benaoxazin-4-one) (BBON) has been proved to be an effective chain extender for poly (ethylene terephthalate) (PET). In order to study the reaction mechanism and kinetics of chain-extending reactio...2,2'-Bis (4H-3,1-benaoxazin-4-one) (BBON) has been proved to be an effective chain extender for poly (ethylene terephthalate) (PET). In order to study the reaction mechanism and kinetics of chain-extending reaction, beta-bishydroxyethylene terephthalate (BHET) was selected as model compound. The NMR data, IR spectra and number average molecular weight (<(M)over bar (n)>) of the products obtained from the reaction of BBON and BHET verify that BBON is a hydroxyl-reactive extender. The mechanism was discussed. Kinetics data indicate that extending reaction is a second order reaction, and BBON has high reactivity. The activation energy (E(a)) was measured.展开更多
An efficient,economical,and phosgene-free approach was developed for the preparation of l,4-dihydro-2H-3,l-benzoxazin-2-one from 2-aminobenzyl alcohol.In terms of its key features,this reaction uses the cheap and recy...An efficient,economical,and phosgene-free approach was developed for the preparation of l,4-dihydro-2H-3,l-benzoxazin-2-one from 2-aminobenzyl alcohol.In terms of its key features,this reaction uses the cheap and recyclable non-metal selenium as a catalyst instead of the noble metal palladium;carbon monoxide as a carbonylation agent instead of virulent phosgene or one of its derivatives;and oxygen as an oxidant.The selenium-catalyzed oxidative carbonylation reaction of2-aminobenzyl alcohol proceeded efficiently in a single pot in the presence of triethylamine to afford l,4-dihydro-2H-3,l-benzoxazin-2-one in 87%yield.Furthermore,the selenium catalyst was readily recovered and recycled,affording a product yield of 80%after five cycles.展开更多
文摘2,2'-Bis (4H-3,1-benaoxazin-4-one) (BBON) has been proved to be an effective chain extender for poly (ethylene terephthalate) (PET). In order to study the reaction mechanism and kinetics of chain-extending reaction, beta-bishydroxyethylene terephthalate (BHET) was selected as model compound. The NMR data, IR spectra and number average molecular weight (<(M)over bar (n)>) of the products obtained from the reaction of BBON and BHET verify that BBON is a hydroxyl-reactive extender. The mechanism was discussed. Kinetics data indicate that extending reaction is a second order reaction, and BBON has high reactivity. The activation energy (E(a)) was measured.
基金supported by the Program for Changjiang Scholars and Innovative Research Team in University(IRT1061)the Program for Innovative Research Team in Science and Technology in University of Henan Province(15IRTSTHN003)+1 种基金the Young Backbone Teachers Training Fund of the Education Department of Henan Province(2013GGJS-059)Henan Normal University(2011-8)
文摘An efficient,economical,and phosgene-free approach was developed for the preparation of l,4-dihydro-2H-3,l-benzoxazin-2-one from 2-aminobenzyl alcohol.In terms of its key features,this reaction uses the cheap and recyclable non-metal selenium as a catalyst instead of the noble metal palladium;carbon monoxide as a carbonylation agent instead of virulent phosgene or one of its derivatives;and oxygen as an oxidant.The selenium-catalyzed oxidative carbonylation reaction of2-aminobenzyl alcohol proceeded efficiently in a single pot in the presence of triethylamine to afford l,4-dihydro-2H-3,l-benzoxazin-2-one in 87%yield.Furthermore,the selenium catalyst was readily recovered and recycled,affording a product yield of 80%after five cycles.
