The synthesis,H-1 NMR and IR study of [(n-Bu)(4)N](2) MO2O5(OC10H6O)(2)] and [(n-Bu)(4)N](2) [Mo4O10H6O)(2) (OCH3)(2)]
文献类型:期刊论文
作者 | Lu, XM; Zhu, HJ; Yuan, HZ; Mao, XA |
刊名 | SPECTROSCOPY AND SPECTRAL ANALYSIS
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出版日期 | 2002-02-01 |
卷号 | 22期号:1页码:36-38 |
关键词 | 2 organo-molybdate derivative IR H-1 NMR 3-dihydroxynaphthalene |
英文摘要 | The title organo-molybdate derivatives are synthesized and their IR, H-1 NMR spectra have been determined and the relations between the structures and the I H NMR and IR parameters have been studied. The results indicate that the red shift of the IR frequency of Mo-O-Mo in [(n-Bu)(4)N](2)[MO2O5(OC10H6O)(2)] (complex I) takes place to compare with that in [(n-Bu)(4)N](2)[MO4O10(OC10H6O2(OCH3)(2)] (complex II) and lower filed shift of H-1 NMR of the aromatic H atoms in complex U occurs as contrasted to that in the complex I. It is found also the organo-molybdate derivatives are very sensitive to the acidity of the chemical system. |
WOS标题词 | Science & Technology ; Technology |
类目[WOS] | Spectroscopy |
研究领域[WOS] | Spectroscopy |
关键词[WOS] | CRYSTAL |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000174255200010 |
公开日期 | 2015-12-08 |
源URL | [http://ir.wipm.ac.cn/handle/112942/8755] ![]() |
专题 | 武汉物理与数学研究所_2011年以前论文发表(包括2011年) |
作者单位 | 1.Chinese Acad Sci, Wuhan Inst Phys & Math, Wuhan 430071, Peoples R China 2.Capital Normal Univ, Dept Chem, Beijing 100037, Peoples R China |
推荐引用方式 GB/T 7714 | Lu, XM,Zhu, HJ,Yuan, HZ,et al. The synthesis,H-1 NMR and IR study of [(n-Bu)(4)N](2) MO2O5(OC10H6O)(2)] and [(n-Bu)(4)N](2) [Mo4O10H6O)(2) (OCH3)(2)][J]. SPECTROSCOPY AND SPECTRAL ANALYSIS,2002,22(1):36-38. |
APA | Lu, XM,Zhu, HJ,Yuan, HZ,&Mao, XA.(2002).The synthesis,H-1 NMR and IR study of [(n-Bu)(4)N](2) MO2O5(OC10H6O)(2)] and [(n-Bu)(4)N](2) [Mo4O10H6O)(2) (OCH3)(2)].SPECTROSCOPY AND SPECTRAL ANALYSIS,22(1),36-38. |
MLA | Lu, XM,et al."The synthesis,H-1 NMR and IR study of [(n-Bu)(4)N](2) MO2O5(OC10H6O)(2)] and [(n-Bu)(4)N](2) [Mo4O10H6O)(2) (OCH3)(2)]".SPECTROSCOPY AND SPECTRAL ANALYSIS 22.1(2002):36-38. |
入库方式: OAI收割
来源:武汉物理与数学研究所
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