中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
H-1 nmr study on the ring opening selectivity of aromatic dianhydrides towards methanol

文献类型:期刊论文

作者Huang WX ; Gao LX ; Yang ZH ; Zhang X ; Xu JP ; Ding MX
刊名polymer
出版日期1997
卷号38期号:9页码:2033-2039
关键词IMIDIZATION ACIDS
ISSN号0032-3861
中文摘要several isomeric aromatic diester-diacids may appear as a result of the opening selectivity of anhydride groups towards the alcohol. h-1 n.m.r. was thus used to characterize the isomeric structure and to quantify the isomer composition. it was found that the isomer ratios quantitatively correlate with electron affinity of bridged dianhydrides and is independent of the alcohol structure used. furthermore, the h-1 n.m.r chemical shift of bridged diester-diacids was found to be a very sensitive probe of chemical nature of bridged groups and can be used as indices of the opening selectivity. (c) 1997 elsevier science ltd.
收录类别SCI收录期刊论文
语种英语
公开日期2010-12-22
源URL[http://ir.ciac.jl.cn/handle/322003/24311]  
专题长春应用化学研究所_长春应用化学研究所知识产出_期刊论文
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GB/T 7714
Huang WX,Gao LX,Yang ZH,et al. H-1 nmr study on the ring opening selectivity of aromatic dianhydrides towards methanol[J]. polymer,1997,38(9):2033-2039.
APA Huang WX,Gao LX,Yang ZH,Zhang X,Xu JP,&Ding MX.(1997).H-1 nmr study on the ring opening selectivity of aromatic dianhydrides towards methanol.polymer,38(9),2033-2039.
MLA Huang WX,et al."H-1 nmr study on the ring opening selectivity of aromatic dianhydrides towards methanol".polymer 38.9(1997):2033-2039.

入库方式: OAI收割

来源:长春应用化学研究所

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