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nuclear-magnetic resonance - translation to ρωσικά
общая лексика
ядерно-магнитный резонанс (ЯМР)
[nju:kliəmægnetik'rezənəns]
общая лексика
ядерный магнитный резонанс
ЯМР
медицина
магнитный резонанс
Ορισμός
Βικιπαίδεια
Nuclear magnetic resonance (NMR) in the geomagnetic field is conventionally referred to as Earth's field NMR (EFNMR). EFNMR is a special case of low field NMR.
When a sample is placed in a constant magnetic field and stimulated (perturbed) by a time-varying (e.g., pulsed or alternating) magnetic field, NMR active nuclei resonate at characteristic frequencies. Examples of such NMR active nuclei are the isotopes carbon-13 and hydrogen-1 (which in NMR is conventionally known as proton NMR). The resonant frequency of each isotope is directly proportional to the strength of the applied magnetic field, and the magnetogyric or gyromagnetic ratio of that isotope. The signal strength is proportional both to the stimulating magnetic field and the number of nuclei of that isotope in the sample. Thus in the 21 tesla magnetic field that may be found in high resolution laboratory NMR spectrometers, protons resonate at 900 MHz. However, in the Earth's magnetic field the same nuclei resonate at audio frequencies of around 2 kHz and generate very weak signals.
The location of a nucleus within a complex molecule affects the 'chemical environment' (i.e. the rotating magnetic fields generated by the other nuclei) experienced by the nucleus. Thus different hydrocarbon molecules containing NMR active nuclei in different positions within the molecules produce slightly different patterns of resonant frequencies.
EFNMR signals can be affected by both magnetically noisy laboratory environments and natural variations in the Earth's field, which originally compromised its usefulness. However this disadvantage has been overcome by the introduction of electronic equipment which compensates changes in ambient magnetic fields.
Whereas chemical shifts are important in NMR, they are insignificant in the Earth's field. The absence of chemical shifts causes features such as spin-spin multiplets (that are separated by high fields) to be superimposed in EFNMR. Instead, EFNMR spectra are dominated by spin-spin coupling (J-coupling) effects. Software optimised for analysing these spectra can provide useful information about the structure of the molecules in the sample.
