Resolution Resonance

Brown, J.K. and W.R. Ladner Jr (1960), Distribution in coallike materials by high-resolution nuclear magnetic resonance spectroscopy . Fuel, Vol. 39, p. 87. 

Ahn C B and Cho Z H 1989 A generalized formulation of diffusion effects in pm resolution nuclear magnetic-resonance imaging Med. Rhys. 16 22-8... 

Maudsley A A, Filial S K, Perman W FI and Simon FI E 1983 Spatially resolved high-resolution spectroscopy by 4-dimensional NMR J. Magn. Reson. 51 147-52... 

This corresponds to the physician s stethoscope case mentioned above, and has been realized [208] by bringing one leg of a resonatmg 33 kHz quartz tiinmg fork close to the surface of a sample, which is being rastered in the x-y plane. As the fork-leg nears the sample, the fork s resonant frequency and therefore its amplitude is changed by interaction with the surface. Since the behaviour of the system appears to be dependent on the gas pressure, it may be assumed that the coupling is due to hydrodynamic mteractions within the fork-air-sample gap. Since the fork tip-sample distance is approximately 200 pm -1.120), tire teclmique is sensitive to the near-field component of the scattered acoustic signal. 1 pm lateral and 10 mn vertical resolutions have been obtained by the SNAM. 

The main cost of this enlianced time resolution compared to fluorescence upconversion, however, is the aforementioned problem of time ordering of the photons that arrive from the pump and probe pulses. Wlien the probe pulse either precedes or trails the arrival of the pump pulse by a time interval that is significantly longer than the pulse duration, the action of the probe and pump pulses on the populations resident in the various resonant states is nnambiguous. When the pump and probe pulses temporally overlap in tlie sample, however, all possible time orderings of field-molecule interactions contribute to the response and complicate the interpretation. Double-sided Feymuan diagrams, which provide a pictorial view of the density matrix s time evolution under the action of the laser pulses, can be used to detenuine the various contributions to the sample response [125]. 

Banwell C N and Primas H 1963 On the analysis of high-resolution nuclear magnetic resonance spectra. I. Methods of calculating NMR spectra Mol. Phys. 6 225-56... 

The reactivity of size-selected transition-metal cluster ions has been studied witli various types of mass spectrometric teclmiques [1 ]. Fourier-transfonn ion cyclotron resonance (FT-ICR) is a particularly powerful teclmique in which a cluster ion can be stored and cooled before experimentation. Thus, multiple reaction steps can be followed in FT-ICR, in addition to its high sensitivity and mass resolution. Many chemical reaction studies of transition-metal clusters witli simple reactants and hydrocarbons have been carried out using FT-ICR [49, 58]. 

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