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电喷雾电离质谱

电喷雾电离质谱的相关文献在1994年到2022年内共计111篇,主要集中在化学、化学工业、轻工业、手工业 等领域,其中期刊论文88篇、会议论文13篇、专利文献127198篇;相关期刊52种,包括许昌学院学报、质谱学报、含能材料等; 相关会议11种,包括中国质谱学会第32届年会、2010全国有机质谱学术会议、第三届中国中西部地区色谱学术交流会等;电喷雾电离质谱的相关文献由354位作者贡献,包括丁传凡、陈焕文、魏先文等。

电喷雾电离质谱—发文量

期刊论文>

论文:88 占比:0.07%

会议论文>

论文:13 占比:0.01%

专利文献>

论文:127198 占比:99.92%

总计:127299篇

电喷雾电离质谱—发文趋势图

电喷雾电离质谱

-研究学者

  • 丁传凡
  • 陈焕文
  • 魏先文
  • 储艳秋
  • 周克瑜
  • 徐正
  • 戴军
  • 王仲孚
  • 黄琳娟
  • 徐远金
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 马洪悦; 杨敏莉; 张峰; 杨丙成; 章飞芳
    • 摘要: 基于分子印迹聚合物修饰铁片(molecularly imprinted polymer modified iron sheet,MIPIS)制备了一种选择性的敞开式质谱离子源,结合电喷雾电离质谱,构建一种快速检测食品基质中莠灭净和莠去津痕量残留的方法。分子印迹聚合物以氰草津为模板,使用甲基丙烯酸和苯胺在水溶液中聚合而成。将MIPIS作为萃取尖端对豆奶粉、小麦和牛奶中的莠灭净和莠去津进行富集,随后作为敞开式质谱离子源结合电喷雾电离质谱直接进行检测。结果显示,在0.2~200μg/L范围内线性良好,相关系数R^(2)为0.9982和0.9997,检出限和定量限分别为0.2~0.5μg/kg和0.6~1.5μg/kg,在3个加标水平下回收率在81.05%~109.66%。该方法操作简单,灵敏度高,省时高效,无需长时间的色谱分离,适用于食品中痕量三嗪类农药残留的快速检测。
    • 杜超; 林荣坤; 杭纬
    • 摘要: 多库酯钠(docusate sodium,DSS)广泛应用于生化研究中,探究其与人血清蛋白(human serum albumin,HSA)之间的非共价相互作用对于阐明其在人体内的结合、转运以及代谢有着重要作用.运用质谱法和光谱法,详细阐释了DSS与HSA之间的相互作用机理.电喷雾电离质谱实验结果表明1个HSA分子可以结合3个DSS分子.荧光光谱结果显示DSS与HSA之间可以通过疏水作用和静电作用相互结合,并且两者之间具有很强的亲和力(结合常数K大于105 L/mol).紫外-可见吸收光谱和圆二色谱结果进一步表明DSS与HSA之间形成了稳定的复合物,并且由于DSS的疏水链可以为HSA提供疏水性较强的环境,增强了两者之间的疏水作用,使HSA中α-螺旋含量从49.9% 上升到55.5%.
    • 吴海媚; 张荣楷; 徐伟
    • 摘要: 电喷雾电离质谱已经成为研究蛋白结构信息的一个重要工具,可以帮助弥补结构生物学和相互作用组学技术之间的差距.电喷雾电离过程中的电荷态分布主要受蛋白质转移到气相时所保持的构象的影响,通过电荷态分布确定的溶液可及表面积可以表征蛋白构象.本篇综述了目前电荷态分布对折叠蛋白和非折叠蛋白构象进行表征的研究,并对电荷态分布分析的未来发展进行展望.
    • 张华蓉; 陈奕伊; 聂长虹; 蒋可志
    • 摘要: 采用高分辨电喷雾质谱和量化计算研究了二甲基硅氧烷环体、线性体的ESI电离效率.实验发现,线性体比相应的环体更容易在ESI-MS中检测到;而环体中六甲基环三硅氧烷(D3)和八甲基环四硅氧烷(D4)在ESI-MS中几乎没有检测到.量化计算结果表明,线性体具有柔性结构,使得其[M+H]+结构中存在分子内氢键,其[M+Na]+结构中多个位点氧原子与Na+相作用,从而增加缔合物的稳定性.环体D3和D4具有刚性结构,其质子亲和能和Na+亲和能都比较小;十甲基环五硅氧烷(D5)和十二甲基环六硅氧烷(D6)结构具有一定柔软性,在准分子离子中存在氢键或与Na+多位点作用.计算结果比较合理地解释了ESI-MS实验结果.
    • 吴若菲; 黄彦东; 储艳秋; 刘智攀; 丁传凡
    • 摘要: 利用电喷雾电离质谱研究了在气相条件下18-冠醚-6与20余种天然氨基酸及其异构体间的非共价相互作用.定性结果表明,在气相中18-冠-6可以与氨基酸形成化学计量比为1:1的非共价复合物.配制一系列不同浓度的18-冠-6分别与固定浓度的氨基酸反应,利用质谱测得反应物和产物的质谱峰,计算冠醚分别与L-苯丙氨酸、L-酪氨酸、L-赖氨酸和L-天冬氨酸反应的复合物结合常数lgKa分别为3.90、3.75、4.06和3.64,基于此建立了校准曲线.通过竞争反应实验,以上述4种氨基酸与冠醚复合物的结合常数为参考值,可推算得到其余氨基酸与冠醚的结合常数.实验结果表明,冠醚-氨基酸复合物的稳定性与氨基酸的种类相关,节碱性氨基酸以及侧链是烷基(或氢原子)的氨基酸对冠醚的亲和性更好,而酸性氨基酸(如L-丝氨酸)以及侧链上有酰胺键的氨基酸,对冠醚的亲和性较低.研究了18-冠-6对L型氨基酸及其D型异构体的手性选择性,结果表明,18-冠-6只能识别部分中性氨基酸.%The non-covalent interactions between 18-crown-6 (18c6) and 20 common types of protonated amino acids were explored by electrospray ionization mass spectrometry (ESI-MS).The mass spectra showed the formation of 1:1 stoichiometric non-covalent complexes between 18c6 and amino acids.The calibration curves and linear equations for the complexes of L-Phe,L-Tyr,L-Lys and L-Asp with 18c6 were established by mass spectrometric titration and used as reference values for competitive ESI-MS.Through competitive equilibrium,the binding constants for the complexes of 18c6 with other L-amino acids and their D-isomers were derived.It was found,as a general trend,lgKa for the complexes of 18c6 with the basic amino acid and the amino acid with alkyl side chain were larger than other complexes,and among the amino acids with alkyl side chain,Gly and Ala exhibited greater 18c6 binding affinities.As for Ser and Thr,the intramolecular hydrogen bond between the nitrogen atom from terminal NH2and the oxygen atom from carboxyl may impede their protonated amino-group to attack the 18c6.Furthermore,Gln and Asn exhibited lower 18c6 binding affinities probably due to effects of electron-withdrawing group of acylamide.Finally,the chiral selectivity of 18c6 for 19 L-,or D-amino acids was measured by ESI-MS,indicating 18c6 could only recognize some neutral amino acid isomers.
    • 王立强; 王凤玲; 周玥莹; 李赞; 高源; 吴振; 方美娟
    • 摘要: The fragmentation pathways of three tyrosine kinase inhibitors with anilinoquinazoline moiety in-cluding gefitinib,erlotinib and icotinibwere analyzed by electrospray ionization tandem mass spectrometry in positive ion mode.The[M+H]+ions peaks were generated by electrospray ionization tandem mass spectrom-etry,and the subsequent product ions of[M+H]+ions information were obtained by using the higher energy collision induced dissociation and the collision induced dissociation.The results indicate that the fragmentation behavior mainly results from the cleavage of the C4,C6and C7substituent of the quinazoline ring,with intra-molecular rearrangement and migration rearrangement of H+,and the high-abundance characteristic ions for gefitinib is m/z=128.1,for erlotinib are m/z=278.1 and m/z=336.1,and for icotinib are m/z=278.1 and m/z=304.1 in the secondary mass spectrum.%研究吉非替尼、厄洛替尼和艾克替尼3种苯胺基喹唑啉类酪氨酸激酶抑制剂,在电喷雾质谱正离子模式下的裂解规律.通过电喷雾质谱产生各化合物稳定的[M+H]+准分子离子峰,进而对[M+H]+离子进行高能诱导裂解和碰撞诱导裂解,获得相应化合物的质谱图.结果表明:在电喷雾电离(ESI)多级质谱中,3种药物的裂解主要发生在喹唑啉环C4,C6和C7位取代基上,并伴随分子内重排和 H+的迁移重排;在二级质谱图中,吉非替尼的高丰度特征离子质荷比(m/z)为128.1,厄洛替尼的m/z值为278.1和336.1,埃克替尼的m/z值为278.1,304.1.
    • 王辉; 李吏详; 刘斯宁; 杜官本
    • 摘要: Urea-formaldehyde resin modified with melamine is a common method adopted widely in the industry. Melamine can effectively modify the water resistance and weather durability of urea-formaldehyde resin, and reduce the content of free formaldehyde. However, during the resin application, it is very important for melamine to take part in urea-formaldehyde resin reaction and form effective co-condensation composition or not. Based on above, a series of MUF resins are synthesized with different melamine and urea mass ratio under the same final F ∶( M+U) and the first stage F ∶( M1+U1 ) molar ratio condition. And the molecular distribution of different resins are represented by using electrospray ionization mass spectrometry ( ESI-MS) . By comparing figures of different samples, the results showed that different reaction material content has a great influence on the composition, molecular distribution and co-condensation content of co-condensation resin. And when the mass amount of melamine added to 40%, the molecular distribution of MUF resin changed qualitatively and co-condensation composition content also had significant increase. Therefore, under this experiment conditions, adding melamine content can effectively promote the co-condensation reaction, meanwhile, the formation of co-condensation resin requires melamine content at least about 40%.%三聚氰胺改性脲醛树脂,是业界普遍采用的脲醛树脂改性方法之一。三聚氰胺的加入可以有效改善脲醛树脂的耐水、耐候性,降低游离甲醛含量等。然而,三聚氰胺能否有效参与到脲醛树脂反应体系当中,形成有效的共缩聚成分,对树脂的应用性能更为关键。基于此,文中设置了在终反应摩尔比以及第1阶段摩尔比保持不变的条件下,通过改变反应原料用量,即三聚氰胺与尿素的用量,合成了一系列三聚氰胺-尿素-甲醛( MUF )共缩聚树脂,利用电喷雾电离质谱仪( ESI-MS)对合成的不同MUF共缩聚树脂的分子量分布情况进行了表征。比较不同样品所测图谱,结果表明,在合成反应过程中,通过改变三聚氰胺( M)与尿素( U)的用量对MUF共缩聚树脂分子量的形成、分布及共缩聚成分有较大影响,当M用量占M与U总质量比例增加至40%时, MUF共缩聚树脂分子量的分布发生了质的改变,同时,共缩聚成分的比例也有明显增加。因此,可以认为,在该试验条件下,增加M的用量可以有效促进共缩聚反应的进程,同时,真正意义上的共缩聚树脂的形成,要求M的加入量至少应控制在40%。
    • 梁坚坤; 丁跃; 吴志刚; 杜官本; 李涛洪; 雷洪; 王辉
    • 摘要: The related reactions and their mechanism of model compounds of urea formaldehyde resin in alkaline environment were studied by electrospray ionization mass spectrometry (ESI-MS).The results indicate that the process of urea hydroxymethylation is reversible,and the formation of tetrahydroxymethyl-urea probably appeares under the alkaline condition.The formations of ether bond (-NRCH2OCH2NR) and bridge bond (-NRCH2NP-) are competitive reactions,and the mass charge ratio peaks of 215,245 and 275 on the ESI-MS spectra mainly belong to the ether bonds,and the peaks of 227 and 257 correspond to the bridge bonds structure.The temperature has little effect on the distribution of the final structures.%以模型化合物为思维方式,采用电喷雾电离质谱仪(ESI-MS)来研究脲醛树脂(UF)在碱性环境下的相关反应进程和相关机理.研究结果表明,尿素羟甲基化过程是可逆的;碱性条件下羟甲基化可能会形成四羟甲基脲,其中有醚键(-NRCH2OCH2NR-)和桥键(-NRCH2NR-).ESI-MS中21 5、245、275质荷比峰值对应的是醚键结构,227、257质荷比的峰对应的是桥键结构.桥醚键结构的形成具有竞争关系.增加温度对最终UF结构的分布影响不大,但起始反应物摩尔浓度的提高有利于缩聚反应.
    • 曹明; 雷洪; 李涛洪; 郭东亮; 梁坚坤; 杜官本
    • 摘要: The effect of glyceryl triacetate on curing behavior of phenolic resin under alkaline conditions at room tem-perature was investigated by the differential scanning calorimetry ( DSC ) , 13 C nuclear magnetic resonance ( 13 C NMR) and electrospray ionization mass spectrometry ( ESI-MS) methods. The results showed that:after the addition of glyceryl triacetate, the exothermic peak of phenolic resin was divided into two parts, which showed that the curing of phenolic resin was promoted to a certain degree. The first exothermic peak was between 150°C and 160°C, which moved forward and the exothermic capacity increased with the increase in glyceryl triacetate. The temperature of the second exothermic peak was higher than that of the exothermic peak of the pure phenolic resin. With the increase a-mount of glyceryl triacetate, the second exothermic peak moved forward gradually, proving the etherification reaction of phenolic hydroxyl group. It was confirmed that the quinone methide structure existed, and the quinone methide was a reaction product rather than an active intermediate. It was indicated that the possible reaction mechanisms of quinone methide in phenolic resin were proposed, and the glyceryl triacetate was only involved in the process of the quinone methide structure formation rather than the condensation reactions of the phenolic resin.%通过差示扫描量热法(DSC)、13 C核磁共振(13 C NMR)和电喷雾电离质谱(ESI-MS)方法,研究了常温碱性条件下三乙酸甘油酯对酚醛(PF)树脂固化行为的影响.结果表明:三乙酸甘油酯的加入,增加了PF树脂固化反应放热峰的数量,在一定程度上促进了树脂的固化;第1个放热峰出现在150~160°C,且随着三乙酸甘油酯添加量的增加,放热峰逐渐提前,放热量增大;第2个放热峰的温度高于纯PF树脂的放热峰,且随着三乙酸甘油酯添加量的增加,第2个放热峰逐渐提前;证明了酚羟基醚化反应的存在.试验证明了亚甲基醌结构的真实存在,并认为亚甲基醌是一种反应产物而非活性中间体;推测亚甲基醌在酚醛树脂中可能的反应机理,并指出三乙酸甘油酯仅参与了亚甲基醌结构生成的过程,并不参与酚醛树脂的缩聚反应.
    • 王辉; 李吏详; 刘斯宁; 杜官本
    • 摘要: 三聚氰胺改性脲醛树脂,是业界普遍采用的脲醛树脂改性方法之一。三聚氰胺的加入可以有效改善脲醛树脂的耐水、耐候性,降低游离甲醛含量等。然而,三聚氰胺能否有效参与到脲醛树脂反应体系当中,形成有效的共缩聚成分,对树脂的应用性能更为关键。基于此,文中设置了在终反应摩尔比以及第1阶段摩尔比保持不变的条件下,通过改变反应原料用量,即三聚氰胺与尿素的用量,合成了一系列三聚氰胺-尿素-甲醛(MUF)共缩聚树脂,利用电喷雾电离质谱仪(ESI-MS)对合成的不同MUF共缩聚树脂的分子量分布情况进行了表征。比较不同样品所测图谱,结果表明,在合成反应过程中,通过改变三聚氰胺(M)与尿素(U)的用量对MUF共缩聚树脂分子量的形成、分布及共缩聚成分有较大影响,当M用量占M与U总质量比例增加至40%时,MUF共缩聚树脂分子量的分布发生了质的改变,同时,共缩聚成分的比例也有明显增加。因此,可以认为,在该试验条件下,增加M的用量可以有效促进共缩聚反应的进程,同时,真正意义上的共缩聚树脂的形成,要求M的加入量至少应控制在40%。
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