氫譜 的英文怎麼說

中文拼音 [qīng]
氫譜 英文
proton magnetic resonance spectrum pmr
  • : 名詞[化學] (氣體元素) hydrogen (h)
  • : Ⅰ名詞[書面語]1 (按類別或系統編成的書或冊子等) table; chart; register 2 (指導練習的格式或圖形)...
  1. In this paper, we reported the synthesis of three supramolecular complexes between - cyclodextrin and anisole, ethyl benzoate, m - cresol, respectively, which are identified by means of 1hnmr technique

    摘要以-環糊精與苯甲酸乙酯、苯甲醚和間甲酚在水相中通過范德華力發生包合反應形成了主客體超分子絡合物,並用核磁共振氫譜對絡合物進行了表徵。
  2. The changing tendencies of the relative contents of phosphorous contained substances have been detected by in - vivo " p magnetic resonance spectroscopy ( in - vivo " p mrs ) during the whole hatching process. in - vivo ] p mrs proved the catabolism of adenosine 5 ' - triphosphate ( atp ), phosphorous ester and phosphocreatine ( pcr ) when the embryo dead. the results could be used to deduce the conversion of phosphorous contained metabolites during the chicken embryo developed

    用活體核磁共振定域氫譜( in - vivohmagneticresonancespectroscopy , in - vivohmrs )對胚胎發育過程中羊水和蛋白、蛋黃的成分進行了分析;用活體磷( in - vivo 』 』 pmrs )的方法分析了在整個胚胎發育過程中含磷代謝物的相對含量隨時間的變化,表明了磷脂類物質及三磷酸腺苷( atp ) 、磷酸肌酸( pcr )在此過程中的變化及可能的相互轉化的趨勢,胚胎死亡后的磷也證明了磷脂類物質及三磷酸腺苷( atp ) 、磷酸肌酸( pcr )在死亡過程中降解為無機磷的現象。
  3. Abstract : several - aromaticamino ketones, which were designed according to some hypothetical models of the cyclooxygenase and 5 - lipoxygenase active sites, were synthesized by an amino exchange reaction. the structures of the eight new compounds were confirmed by ir, 1h - nmr and elemental analysis. the results of the pharmacological tests showed some of the investigated compounds had significant anti - inflammatory activity on croton oil - induced ear edema of mice

    文摘:根據環氧化酶、 5 -脂氧化酶活性中心結構模型設計了一組-芳胺酮類化合物,並用胺交換反應合成了這些化合物.經紅外光、核磁共振氫譜及元素分析證實了8個未見文獻報道的化合物的結構.藥理實驗結果顯示.部分受試化合物在巴豆油誘發小鼠足趾腫脹模型中表現出一定的抗炎活性
  4. The molecular structure of ethyl cellulose was characterized and confirmed by elementary analysis, ft - ir and 1h nmr, and the compound obtained was final objective product

    通過元素分析、紅外光和核磁共振氫譜對產物的分子結構進行表徵,確定所合成的化合物即為目標產物。
  5. Meso - tetra ( 4 - acyloxyphenyl ) pophyrin was prepared by usual procedure from acyl chloride and meso - tetra ( 4 - hydroxyphenyl ) porphyrin in benzene and obtained in 86. 4 % yield. treatment of the free base with zinc chloride in dimethyl formamide ( dmf ) - dichloromethane ( ch2cl2 ) yielded corresponding zinc porphyrin complex. the spectral data ( uv - visjr / h - nmr ) and elemental analysis are in agreement with the assigned structures

    在合成工作基礎上,採用紫外可見光( uv - vis ) 、紅外光聲光( ftir - pas ) 、核磁共振氫譜( ~ 1hnmr ) 、元素分析、摩爾電導等手段研究了卟啉及金屬卟啉材料的組成及結構。
  6. Conclusion the efficiency for finding of leading compounds could be improved if the isolation is based on metabonomics under the guidence of the new method of botanical mixture determination by 1h - nmr

    結論基於植物代謝組學混合物氫譜測定指導下的分離是一種高效發現先導化合物的新方法。
  7. Its stucture was investigated through ir, 1h nmr and mass spectrum

    用紅外光、核磁共振氫譜和質推測了產物的結構。
  8. Identification of lactic acid bacteria 32 by sequence analysis of 16s rdna and reca - gene

    呋喃的核磁共振氫譜分析
  9. The structures of the intermediates and product were characterized with 1h nmr and mass spectra

    中間體及產物用質和核磁氫譜進行了結構表徵。
  10. The structures of new compounds 7 and 8 were identified by 1h nmr, 13c nmr and hrms spectra

    新化合物7 , 8經核磁共振氫譜、碳和高解析度質予以證實。
  11. The structures of the target molecules and the key intermediates were confirmed by 1h nmr, 13c nmr and ir spectra in our experiments

    關鍵中間體及最終化合物的結構經核磁共振氫譜、碳及紅外光確證。
  12. 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

    關鍵中間體及最終化合物的結構經核磁共振氫譜及碳確證。
  13. Methods a mixture fraction was determined by 1h - nmr techniques to find any evidence, further isolation of the fraction guided with this evidence was carried out

    方法混合組分測定氫譜,用混合物氫譜測定獲得的線索指導進一步分離。
  14. 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

    分別用紅外光、核磁共振氫譜、碳、質以及元素分析對所得化合物進行了表徵。
  15. In this paper, three alkyl substituted dimethyl phosphonates have been synthesized by trimethyl phosphite with 1 - bromopentane, 1 - bromohexane and 1, 2 - dibromoethane. ir, 1h - nmr and 13c - nmr data of these compounds have been reported

    摘要以溴戊烷、溴己烷、 1 , 2 -二溴乙烷和亞磷酸三甲酯為原料,分別合成了戊基、己基、溴乙基取代的三種膦酸二甲酯化合物。並報道了所合成的化合物的紅外光、核磁共振氫譜及核磁共振碳的數據。
  16. In this paper we describe the synthesis of six derivitives of a - aminomethylphosphonic acids, three of which were synthesized for the first time, the structure of them were characterized by ir spectrum, 1h nmr and 31p nmr spectrum, the structure of proline - n - methylphosphorus acid was discussed

    本文報道合成了五種-氨基膦酸衍生物,用紅外光( ir ) ,核磁共振氫譜( ~ 1hnmr )和核磁共振磷( ~ ( 31 ) pnmr )表徵其結構,詳細討論了脯氨酸- n -甲基膦酸的結構。
  17. Five derivatives of metal phthalocyanines were synthesized. the structures of products were characterized by means of ir, hnmr spectra and elementary analysis. and then, the metal phthalocyanine / polymethy methacrylate ( pmma ) were prepared

    合成了五種金屬酞菁化合物,利用元素分析、紅外光、核磁共振氫譜等方法,驗證了化合物的分子結構。
  18. Three derivatives of alkoxy phthalocyanine pb were synthesized as optical limiting materials. the structures of products were characterized by means of ir, hnmr spectra and elementary analysis. and then, the phthalocyanine pb / polymethy methacrylate ( pmma ) were prepared

    合成了三種烷氧基取代的金屬酞菁鉛類光限幅材料,利用元素分析、紅外光、核磁共振氫譜等方法,驗證了化合物的分子結構。
  19. In order to research the application of nonlinear optical materials for optical limiting, four derivatives of alkoxy metal phthaloyanines were synthesized. the structures of the products were characterized by means of ir. 1hnmr spectra and elementary analysis

    為探索有機非線性光學材料在光限幅方面的應用,本論文合成了四種烷氧基取代的金屬酞菁化合物,並利用元素分析、紅外光、核磁共振氫譜等方法,驗證了化合物的分子結構。
  20. By choosing different solvents, concentrations and temperatures, and using nmr spectrum technique, to determine the hydroxyl of z / e isomers of perillartine, the concentration of which was 3. 125 mg / ml, present different chemical shifts in c6d6, solvent and carbon tetrachloride and in the 1h nmr, and accordingly, conduct qualitative and quantitative analysis of z / e isomers of perillartine

    摘要本文利用核磁共振波儀,通過對紫蘇葶溶液不同溶劑、不同濃度和不同測試溫度的選擇,使順式結構和反式結構的紫蘇葶羥基峰在核磁共振維氫譜中呈現出不同化學位移值,從而對其順式結構和反式結構進行了定性、定量分析。
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