J-coupling nuclear magnetic resonance spectroscopy of liquids in nT fields

被引:43
|
作者
Bernarding, J [1 ]
Buntkowsky, G
Macholl, S
Hartwig, S
Burghoff, M
Trahms, L
机构
[1] Otto Von Guericke Univ, Magdeburg, Germany
[2] Univ Jena, D-6900 Jena, Germany
[3] Phys Tech Bundesanstalt, Berlin, Germany
关键词
D O I
10.1021/ja055273e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In ultralow magnetic fields, liquid state nuclear magnetic resonance (NMR) spectra of homonuclear spin systems exhibit line widths dominated by their natural lifetime. Chemical shifts become negligible, and heteronuclear NMR spectra show predominantly the electron-mediated field-independent J-coupling. However, weak polarization and Larmor frequencies down to a few hertz require special detectors, such as Superconducting Quantum Interference Devices (SQUID), that also enable the simultaneous detection of broad band spectra of heteronuclear spin systems. We acquired spectra of 2,2,2-trifluoroethanol and trimethyl phosphate at detection fields varying from 444 nT to 3.34 μT after prepolarizing the sample in a field of 250 μT. Down to a 1H Larmor frequency of 40 Hz, the spectra of trifluoroethanol exhibited four clearly resolvable peaks. The numerical simulation agreed well with the measured spectra. Trimethyl phosphate exhibited two major groups of nonresolved proton lines. At 1H Larmor frequencies below 150 Hz, the separation of the two groups decreased, reflecting the transition from weakly to strongly coupled spin systems. Direct determination of 3J(H,P) from the peak separation is possible only at Larmor frequencies above 150 Hz. The experimental setup allowed an easy adjustment of the detection field over several octaves. This enabled us to adapt the detection field to the best-suited measurement window providing the maximum spectral information. Low-field NMR may open new applications, such as monitoring heteronuclear reactions, low-field imaging, simultaneous NMR/magnetoencephalography measurements, or quantum computing. Copyright © 2006 American Chemical Society.
引用
收藏
页码:714 / 715
页数:2
相关论文
共 50 条
  • [31] Nuclear magnetic resonance spectroscopy
    Susanta Das
    Resonance, 2004, 9 (1) : 34 - 49
  • [32] NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY
    MONIZ, WB
    PORANSKI, CF
    REPORT OF NRL PROGRESS, 1967, (JUN): : 19 - &
  • [33] Nuclear magnetic resonance signal dynamics of liquids in the presence of distant dipolar fields, revisited
    Barros, Wilson, Jr.
    Gochberg, Daniel F.
    Gore, John C.
    JOURNAL OF CHEMICAL PHYSICS, 2009, 130 (17):
  • [34] MEASUREMENT OF INDIRECT (J) COUPLING BETWEEN NUCLEI IN LIQUIDS IN MAGNETIC RESONANCE BY TRANSIENT METHOD
    POWLES, JG
    HARTLAND, A
    PROCEEDINGS OF THE PHYSICAL SOCIETY OF LONDON, 1961, 77 (494): : 273 - &
  • [35] Nuclear magnetic resonance in inhomogeneous magnetic fields
    Balibanu, F
    Hailu, K
    Eymael, R
    Demco, DE
    Blümich, B
    JOURNAL OF MAGNETIC RESONANCE, 2000, 145 (02) : 246 - 258
  • [36] Direct coupling of capillary electrophoresis and nuclear magnetic resonance spectroscopy for the identification of a dinucleotide
    Schewitz, J
    Pusecker, K
    Gfrörer, P
    Götz, U
    Tseng, LH
    Albert, K
    Bayer, E
    CHROMATOGRAPHIA, 1999, 50 (5-6) : 333 - 337
  • [37] Coupling Liquid Phase Electrochemistry with Nuclear Magnetic Resonance Spectroscopy and Its Applications
    Ni Zu-rong
    Cui Xiao-hong
    Sun Shi-gang
    Chen Zhong
    SPECTROSCOPY AND SPECTRAL ANALYSIS, 2011, 31 (01) : 1 - 6
  • [38] Using nuclear magnetic resonance spectroscopy to study molecular diffusion in liquids: The DOSY technique
    de Souza, AA
    Laverde, A
    QUIMICA NOVA, 2002, 25 (6A): : 1022 - 1026
  • [39] Direct coupling of capillary electrophoresis and nuclear magnetic resonance spectroscopy for the identification of a dinucleotide
    J. Schewitz
    K. Pusecker
    P. Gfrörer
    U. Götz
    L. -H. Tseng
    K. Albert
    E. Bayer
    Chromatographia, 1999, 50 : 333 - 337
  • [40] NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY . CARBON-CARBON COUPLING IN CYCLOPROPANE DERIVATIVES
    WEIGERT, FJ
    ROBERTS, JD
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1967, 89 (23) : 5962 - &