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40 years of Fourier transform ion cyclotron resonance mass spectrometry

机译:傅立叶变换离子回旋共振质谱技术40年

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This article reviews the development of Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) in several respects: (a) a strong static magnetic field serves to convert ion mass-to-charge ratio into cyclotron frequency. Because frequency is the most accurately measurable property, ICR MS inherently offers higher mass resolution and mass accuracy than any other mass analyzer. (b) Coherent excitation followed by induced charge detection yields a time-domain signal whose discrete Fourier transform produces a mass spectrum of ions spanning a wide m/z range simultaneously. By simple analogy to weighing objects with a mechanical balance, that "multiplex" advantage can be shown to be equivalent to "multichannel" detection by an array of individual single-channel detectors. (c) FT-ICR MS performance benefits from near-elimination of magnetic field inhomogeneity by inherent ion cyclotron rotation and ion axial oscillation; inherent nearly quadrupolar electrostatic trapping potential and nearly uniform rf electric field homogeneity near the center of the ICR ion trap (both improved even further by recent ICR cell designs); and theoretically optimal excitation and mass selection produced by stored-aveform inverse Fourier transformation (SWIFT). (d) External ion accumulation allows efficient coupling of atmospheric pressure continuous ionization sources (notably electrospray ionization) with pulsed high-vacuum FT-ICR MS excitation/detection, and injection of externally trapped ions through the "magnetic mirror" into the ICR ion trap has been optimized based on ion trajectory simulations. (e) MS/MS can be performed either inside (e.g., electron capture dissociation, infrared multiphoton dissociation) or outside (e.g., collision-induced dissociation, electron transfer dissociation) the ICR ion trap. (f) Finally, FT-ICR MS instrumentation and experimental event sequences have benefited from striking parallels to prior nuclear magnetic resonance spectroscopy developments. Similarly, non-ICR FT MS development (notably the orbitrap) has benefited from FT-ICR precedents. (C) 2014 Elsevier B.V. All rights reserved.
机译:本文从几个方面回顾了傅立叶变换离子回旋共振质谱(FT-ICR MS)的发展:(a)强静磁场用于将离子质荷比转换为回旋频率。因为频率是最准确的可测量属性,所以ICR MS固有地提供了比任何其他质量分析仪更高的质量分辨率和质量精度。 (b)相干激发后进行感应电荷检测,产生一个时域信号,其离散傅里叶变换会同时产生跨越m / z宽范围的离子质谱。通过简单地类比称量具有机械天平的物体,可以证明“多重”优势等同于通过单个单通道检测器阵列进行的“多通道”检测。 (c)FT-ICR MS的性能得益于固有的离子回旋加速器旋转和离子轴向振荡,从而几乎消除了磁场的不均匀性;在ICR离子阱中心附近固有的接近四极的静电俘获势和接近均匀的rf电场均匀性(最近的ICR电池设计进一步改善了两者);以及通过存储波形逆傅立叶变换(SWIFT)产生的理论上最佳的激励和质量选择。 (d)外部离子积累使大气压连续电离源(尤其是电喷雾电离)与脉冲高真空FT-ICR MS激发/检测有效耦合,并通过“磁镜”将外部捕获的离子注入ICR离子阱已基于离子轨迹模拟进行了优化。 (e)MS / MS可以在ICR离子阱的内部(例如电子捕获解离,红外多光子解离)或外部(例如碰撞诱导解离,电子转移解离)进行。 (f)最后,FT-ICR MS仪器和实验事件序列得益于与先前的核磁共振波谱学发展的相似之处。同样,非ICR FT MS的开发(尤其是轨道飞行器)也受益于FT-ICR的先例。 (C)2014 Elsevier B.V.保留所有权利。

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