Copolycondensation mechanisms for the terpolyester system from m-methoxy-p-acetoxybenzoic acid,p-acetoxybenzoic acid and poly(ethylene terephthalate)are first investigatedby high resolution proton NMR spectroscopy at ...Copolycondensation mechanisms for the terpolyester system from m-methoxy-p-acetoxybenzoic acid,p-acetoxybenzoic acid and poly(ethylene terephthalate)are first investigatedby high resolution proton NMR spectroscopy at 400 MHz.A series of reactivity ratios of thecopolycondensation reactions are given.The results shown that the m-methoxy-p-acetoxybenzoicacid tends to homopolymerize,while the p-acetoxybenzoic acid,and the ethylene terephthalate unitespecially,tend to copolymerize with the m-methoxy-p-acetoxybenzoic acid.展开更多
1 Introduction A particularly efficient and elegant route to chiral mesophases is based on the addition of small amounts of an enantiomerically pure dopant to a nematic phase so that the latter is converted into a cho...1 Introduction A particularly efficient and elegant route to chiral mesophases is based on the addition of small amounts of an enantiomerically pure dopant to a nematic phase so that the latter is converted into a cholesteric phase(See Fig.1).Fig.1 A nematic phase is converted into a cholesteric phase Fig.2 Bis-chelated imine-alkoxy-titanium complexes2 ExperimetalBis-chelated imine-alkoxy-titanium complexes like 1 and 2 (Fig.2) have been synthesizedstarting from triphenyl-substituted aminoethanols, T...展开更多
文摘Copolycondensation mechanisms for the terpolyester system from m-methoxy-p-acetoxybenzoic acid,p-acetoxybenzoic acid and poly(ethylene terephthalate)are first investigatedby high resolution proton NMR spectroscopy at 400 MHz.A series of reactivity ratios of thecopolycondensation reactions are given.The results shown that the m-methoxy-p-acetoxybenzoicacid tends to homopolymerize,while the p-acetoxybenzoic acid,and the ethylene terephthalate unitespecially,tend to copolymerize with the m-methoxy-p-acetoxybenzoic acid.
文摘1 Introduction A particularly efficient and elegant route to chiral mesophases is based on the addition of small amounts of an enantiomerically pure dopant to a nematic phase so that the latter is converted into a cholesteric phase(See Fig.1).Fig.1 A nematic phase is converted into a cholesteric phase Fig.2 Bis-chelated imine-alkoxy-titanium complexes2 ExperimetalBis-chelated imine-alkoxy-titanium complexes like 1 and 2 (Fig.2) have been synthesizedstarting from triphenyl-substituted aminoethanols, T...
