1.
The structures of the intermediates and product were characterized with 1H NMR and Mass spectra.
中间体及产物用质谱和核磁氢谱进行了结构表徵。
2.
Proton Nuclear Magnetic Resonance Analysis of Two Ru(Ⅱ ) Complexes
两种钌(Ⅱ)络合物的核磁共振氢谱分析
3.
The structures of new compounds 7 and 8 were identified by 1H NMR, 13C NMR and HRMS spectra.
新化合物7,8经核磁共振氢谱、碳谱和高分辨率质谱予以证实。
4.
Its stucture was investigated through IR,1H NMR and mass spectrum.
用红外光谱、核磁共振氢谱和质谱推测了产物的结构。
5.
Acute Toxicity of Lu(NO 3) 3 Studies by Proton Nuclear Magnetic Resonance Spectroscopy of Biofluids
硝酸镥急性毒性的体液核磁共振氢谱研究
6.
The Study Based on ～1H-NMR-MSA on the Plants of Hippophae Linn.;
沙棘的氢核磁共振图谱—多元统计分析研究
7.
The H-NMR Study of Licorice and Compound Liquorice Tablets;
甘草及复方甘草片核磁共振氢谱的研究
8.
Application of ~1H NMR Method in the Organic Chemical Comprehensive Experiment
核磁共振氢谱在有机综合实验中的应用
9.
Quantitive determination of berberine hydrochloride by proton nuclear magnetic resonance spectroscopy with internal standard method
核磁共振氢谱内标法测定盐酸小檗碱的含量
10.
~1H NMR Investigations of Supramolecular Complex between β-cyclodextrin and Tetrahydrofuran;
超分子络合物β-环糊精——四氢呋喃的核磁共振氢谱分析
11.
The structures of the intermediates and the target molecule were confirmed by (superscript 1)H NMR and (superscript 13)C NMR spectra in our experiments.
关键中间体及最终化合物的结构经核磁共振氢谱及碳谱确证。
12.
The structure of the resulting pyrylium salts was confirmed by FT/IR, (superscript 1)H NMR, (superscript 13)C NMR, MS spectroscopies and elemental analyses.
分别用红外光谱、核磁共振氢谱、碳谱、质谱以及元素分析对所得化合物进行了表征。
13.
STRUCTURE ELUCIDATION AND NMR CHARACTERIZATION OF 5,10-DIHYDROPHENOPHOSPHAZINE DERIVATIVES
5,10-二氢磷杂吖嗪衍生物结构的核磁共振波谱表征
14.
Proton Magnetic Resonance Spectroscopy of Normal Human Brain and Glioma: The In-vivo and In-vitro Quantitive Studies;
人脑组织和胶质瘤的活体和离体定量核磁共振氢谱研究
15.
Application of ～1Hydrogen Proton Magnetic Resonance Spectroscopy in Temporal Lobe Epilepsy;
氢质子核磁共振波谱分析在颞叶癫痫中的应用价值
16.
Application of ~1H NMR on Structural Elucidation of β-Cyclodextrin and β-Cyclodextrin Complexes
核磁共振氢谱在β-环糊精及其包合物研究中的应用
17.
Their structures havebeen characterized by elemental analysis, MS, IR and1 HNMR spectra.
通过元素分析、谱、外光谱和核磁共振氢谱对两种化合物的结构进行了表征。
18.
The structures of the target molecules and the key intermediates were confirmed by 1H NMR, 13C NMR and IR spectra in our experiments.
关键中间体及最终化合物的结构经核磁共振氢谱、碳谱及红外光谱确证。