• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在线表面诱导解离装置在四极杆质谱仪中的设计与性能。

Design and performance of an in-line surface-induced dissociation device in a four-sector mass spectrometer.

机构信息

Department of Cell and Molecular Pharmacology, Medical University of South Carolina, 171 Ashley Avenue, 29425, Charleston, SC.

出版信息

J Am Soc Mass Spectrom. 1995 Apr;6(4):257-63. doi: 10.1016/1044-0305(95)00025-9.

DOI:10.1016/1044-0305(95)00025-9
PMID:24214171
Abstract

A new in-line surface-induced dissociation device has been designed and characterized in a high performance four-sector tandem mass spectrometer. The design incorporates a target electrode parallel to the ion beam axis and an angled deflector plate (45° relative to the ion beam) to provide large collision angles. In addition, an extraction electrode (parallel to the target electrode) is employed to efficiently extract product ions from the target surface. Results obtained with this device indicate high internal energy deposition (up to 16. 3 eV) as measured with the thermometer ions W(CO) 6 (+·) and Si(C2H5)4/+·, as evidenced by extensive dissociation of the refractory pyrene molecular ion, and as indicated by the b 3/y 2 ratio in the product ion spectrum of leucine enkephalin. High resolution provided by the four-sector instrument for both precursor ions and product ions allows the observation of previously unobserved dissociation products in the surface-induced dissociation spectra of Si(C2H5)4/+· and novel ion-surface reaction products in spectra of W(CO)6/+· ions after collisions with hydrocarbon-covered surfaces. Both hydrogen atom and hydrocarbon abstraction products are observed. The dissociation efficiencies measured with the in-line device are approximately 1% when hydrocarbon-coated surfaces are used and increase fivefold with a fluorinated surface.

摘要

一种新的在线表面诱导解离装置已被设计并在高性能四极串联质谱仪中进行了表征。该设计采用了一个与离子束轴平行的靶电极和一个倾斜的偏转板(相对于离子束成 45°角),以提供较大的碰撞角度。此外,还采用了一个萃取电极(与靶电极平行),以有效地从靶表面提取产物离子。该装置的结果表明,内部能量沉积很高(高达 16.3 eV),这可以通过温度计离子 W(CO)6 (+·)和 Si(C2H5)4/+·来测量,其证据是难熔的苝分子离子的广泛解离,以及亮氨酸脑啡肽产物离子谱中的 b 3/y 2 比值所表明的。四极仪器为前体离子和产物离子提供的高分辨率允许观察到 Si(C2H5)4/+·的表面诱导解离谱中以前未观察到的解离产物,以及 W(CO)6/+·离子与烃覆盖表面碰撞后的新型离子-表面反应产物。观察到了氢原子和碳氢化合物的抽取产物。当使用烃涂覆表面时,在线装置测量的解离效率约为 1%,而使用氟化表面时则增加了五倍。

相似文献

1
Design and performance of an in-line surface-induced dissociation device in a four-sector mass spectrometer.在线表面诱导解离装置在四极杆质谱仪中的设计与性能。
J Am Soc Mass Spectrom. 1995 Apr;6(4):257-63. doi: 10.1016/1044-0305(95)00025-9.
2
Collisions of slow polyatomic ions with surfaces: dissociation and chemical reactions of C2H2+*, C2H3+, C2H4+*, C2H5+, and their deuterated variants C2D2+* and C2D4+* on room-temperature and heated carbon surfaces.慢速多原子离子与表面的碰撞:C2H2+*、C2H3+、C2H4+*、C2H5+及其氘代变体C2D2+*和C2D4+*在室温及加热的碳表面上的解离和化学反应。
J Phys Chem A. 2005 Nov 17;109(45):10208-15. doi: 10.1021/jp053064a.
3
Silylation of an OH-terminated self-assembled monolayer surface through low-energy collisions of ions: a novel route to synthesis and patterning of surfaces.通过离子的低能碰撞对羟基封端的自组装单分子层表面进行硅烷化:一种合成和图案化表面的新途径。
J Mass Spectrom. 2002 Jun;37(6):591-602. doi: 10.1002/jms.317.
4
Dissociative scattering of hyperthermal energy CF3+ ions from modified surfaces.来自改性表面的超热能CF3+离子的离解散射。
J Chem Phys. 2007 Feb 28;126(8):084701. doi: 10.1063/1.2484290.
5
Surface-induced dissociation and chemical reactions of C2D4(+) on stainless steel, carbon (HOPG), and two different diamond surfaces.C2D4(+)在不锈钢、碳(高定向热解石墨)和两种不同金刚石表面上的表面诱导解离及化学反应
J Am Soc Mass Spectrom. 2009 Jun;20(6):927-38. doi: 10.1016/j.jasms.2009.01.016. Epub 2009 Jan 31.
6
Translational to vibrational energy conversion during surface-induced dissociation of n-butylbenzene molecular ions colliding at self-assembled monolayer surfaces.在自组装单分子层表面碰撞的正丁基苯分子离子的表面诱导解离过程中,从平动能到振动能的转换
Eur J Mass Spectrom (Chichester). 2003;9(4):237-4. doi: 10.1255/ejms.554.
7
Reactions of BBr(n)(+) (n = 0--2) at fluorinated and hydrocarbon self-assembled monolayer surfaces: observations of chemical selectivity in ion--surface scattering.BBr(n)(+)(n = 0--2)在氟化和烃类自组装单分子层表面的反应:离子-表面散射中化学选择性的观测
J Mass Spectrom. 2001 Jul;36(7):717-25. doi: 10.1002/jms.177.
8
Collisions of slow polyatomic ions with surfaces: the scattering method and results.慢速多原子离子与表面的碰撞:散射方法及结果。
J Am Soc Mass Spectrom. 2003 Dec;14(12):1360-72. doi: 10.1016/j.jasms.2003.09.002.
9
Surface-Induced dissociation from a liquid surface.从液体表面引发的离解。
J Am Soc Mass Spectrom. 1993 Oct;4(10):769-73. doi: 10.1016/1044-0305(93)80033-U.
10
Relative dissociation energies of protonated peptides by electrospray ionization/surface-induced dissociation.电喷雾电离/表面引发解吸中质子化肽的相对离解能。
Anal Chem. 1999 Jul 1;71(13):2307-17. doi: 10.1021/ac981411p.

引用本文的文献

1
Evaluation of Surface-Induced Dissociation Ion Mobility-Mass Spectrometry for Lipid Structural Characterization.表面诱导解吸离子淌度-质谱法用于脂质结构表征的评估。
J Am Soc Mass Spectrom. 2024 Feb 7;35(2):214-223. doi: 10.1021/jasms.3c00319. Epub 2024 Jan 12.
2
Surface-induced Dissociation Mass Spectrometry as a Structural Biology Tool.表面诱导解吸质谱法作为结构生物学工具。
Chem Rev. 2022 Apr 27;122(8):7442-7487. doi: 10.1021/acs.chemrev.1c00309. Epub 2021 Nov 2.
3
Design and Performance of a Second-Generation Surface-Induced Dissociation Cell for Fourier Transform Ion Cyclotron Resonance Mass Spectrometry of Native Protein Complexes.

本文引用的文献

1
Surface-induced dissociation of peptide ions in Fourier-transform mass spectrometry.傅里叶变换质谱中肽离子的表面诱导解离。
J Am Soc Mass Spectrom. 1990 Sep;1(5):413-6. doi: 10.1016/1044-0305(90)85022-E.
2
Surface-induced dissociation in tandem quadrupole mass spectrometers: A comparison of three designs.串联四极杆质谱仪中的表面诱导解离:三种设计的比较。
J Am Soc Mass Spectrom. 1992 Jan;3(1):27-32. doi: 10.1016/1044-0305(92)85015-C.
3
Surface-induced dissociation of molecular ions in a quadrupole ion trap mass spectrometer.
第二代用于傅里叶变换离子回旋共振质谱分析天然蛋白复合物的表面诱导解吸池的设计与性能。
Anal Chem. 2019 Nov 5;91(21):14049-14057. doi: 10.1021/acs.analchem.9b03746. Epub 2019 Oct 22.
4
Fragmentation of molecules sliding along surfaces in the speed range above thermal and below Bohr velocity.分子在热速度和玻尔速度以下的速度范围内沿着表面滑动时的碎片化。
J Am Soc Mass Spectrom. 1999 Jun;10(6):471-82. doi: 10.1016/S1044-0305(99)00018-5.
5
A new approach for effecting surface-induced dissociation in an ion cyclotron resonance mass spectrometer: a modeling study.离子回旋共振质谱仪中实现表面诱导解离的一种新方法:建模研究。
J Am Soc Mass Spectrom. 2000 Dec;11(12):1107-17. doi: 10.1016/S1044-0305(00)00188-4.
在四极离子阱质谱仪中分子离子的表面诱导解离。
J Am Soc Mass Spectrom. 1991 Dec;2(6):487-91. doi: 10.1016/1044-0305(91)80036-7.
4
A new tandem mass spectrometer for the study of molecular dissociations.一种用于研究分子离解的新型串联质谱仪。
J Am Soc Mass Spectrom. 1992 Jul;3(5):487-92. doi: 10.1016/1044-0305(92)85025-F.
5
XeF(+), IF (+), and other unusual ions generated by reactions of hyperthermal ion beams at self-assembled monolayer surfaces.由自组装单分子层表面的超热离子束反应产生的 XeF(+)、IF (+) 和其他不寻常离子。
J Am Soc Mass Spectrom. 1993 Dec;4(12):938-42. doi: 10.1016/1044-0305(93)80019-U.
6
Surface-Induced dissociation from a liquid surface.从液体表面引发的离解。
J Am Soc Mass Spectrom. 1993 Oct;4(10):769-73. doi: 10.1016/1044-0305(93)80033-U.
7
Enhancement of ion transmission at low collision energies via modifications to the interface region of a spectrometer.通过对谱仪界面区域的修改来增强在低碰撞能下的离子传输。
J Am Soc Mass Spectrom. 1994 May;5(5):460-9. doi: 10.1016/1044-0305(94)85062-3.
8
Fragmentation of protonated peptides: surface-induced dissociation in conjunction with a quantum mechanical approach.质子化肽段的碎片化:结合量子力学方法的表面诱导解离
Anal Chem. 1993 Oct 15;65(20):2859-72. doi: 10.1021/ac00068a024.
9
Contributions of mass spectrometry to peptide and protein structure.质谱对肽和蛋白质结构的贡献。
Biomed Environ Mass Spectrom. 1988 Oct;16(1-12):99-111. doi: 10.1002/bms.1200160119.
10
Surface-induced dissociation by Fourier transform mass spectrometry.傅里叶变换质谱法中的表面诱导解离
Anal Chem. 1990 Jul 1;62(13):1295-9. doi: 10.1021/ac00212a017.