• The success of the synthesis of the PEG TEFE silane was confirmed with (1)H NMR and Fourier transform infrared spectroscopy (FTIR).

    TEFE硅烷成功组装已经1H NMR傅里叶变换红外光谱(FTIR)分析中得到证实

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  • The condensations of 2-aminofluorene with a series of aldehyde gave the corresponding schiff bases(a~h), and their structures were confirmed by IR, 1H NMR, MS and elemental analysis.

    采用原料芴经硝化、还原反应得到2-氨基,再一系列的芳香醛缩合得到相应席夫碱类化合物。

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  • The structure and composition of the copolymer were identified and examined by infrared spectrogram and NMR-H spectrum.

    通过红外光谱核磁共振氢明确了聚合物组成结构

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  • The occurrence of SBR cyclization was confirmed by the primary analysis of ir and 1 H-NMR spectra.

    通过红外光谱1H - nmr初步解析证实了化反应发生

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  • The pyrazoles ramification containing dithioether is synthesized by one-step method and characterized by H-NMR, IR and UV-Vis spectra.

    采用核磁共振红外光谱紫外吸收光谱手段进行了表征

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  • The structures of Pamicogrel and its derivatives were confirmed by H-NMR, IR, MS.

    帕米格雷及其衍生物结构经过磁共振氢谱、红外光谱、谱等确证。

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  • When PVP or HCO-60 was added to a deuterated chloroform solution of nitrazepam, the 1H-NMR signals of N (1 )-H shifted to lower magnetic fields.

    PVP在氘氯仿中可使硝基安定1位氢核磁信号磁场方向位移。PVP与硝基安定的相互作用比HCO-60等要强。

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  • The structure of all compounds were confirmed by MS and 'H-NMR.

    所有化学结构经由质谱核磁共振氢谱得以确认。

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  • The results of IR and H-NMR spectrometry show that it possesses the structure of heparinoid, which accords with the preceding design.

    利用红外光谱磁共振对魔芋葡甘低聚糖醛酸丙酯硫酸酯钠结构进行了分析,表明合成 物结构试验设计吻合

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  • The structure of the product is identified with IR, H-NMR and C-NMR.

    利用红外光谱核磁共振产品结构进行了确定

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  • Sulfonated polymers 'structures are characterized by FT-IR and 'h-nmr, and the result show that ideal polymers are obtained.

    利用FT - IRH - NMR对所合成的磺化产物进行了结构表征表明得到了理想聚合物

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  • Sulfonated polymers 'structures are characterized by FT-IR and 'h-nmr, and the result show that ideal polymers are obtained.

    利用FT - IRH - NMR对所合成的磺化产物进行了结构表征表明得到了理想聚合物

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