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New theory for analysing interacting nuclear spins in solvents

Date:
September 24, 2013
Source:
Ruhr-Universitaet-Bochum
Summary:
Hardly a spectroscopic method boasts so many different applications as nuclear magnetic resonance spectroscopy, better known as "NMR." The approach of NMR spectroscopy is based on monitoring the so-called nuclear spin, namely the angular momentum of atoms, or, more precisely: the magnetic moment associated with them. The atom thus becomes a bar magnet, whose axis is aligned within a magnetic field but is otherwise arbitrarily oriented within its environment.

The image shows a computer simulation of a frequently-used ionic solvent. NOE experiments at low frequencies capture the structure of the entire area. Experiments at high frequencies provide information regarding the local structure of two neighbouring particles, highlighted by the magnifying glass.
Credit: © AG Physikalische Chemie der Flüssigkeiten

Hardly a spectroscopic method boasts so many different applications as nuclear magnetic resonance spectroscopy, better known as "NMR." The approach of NMR spectroscopy is based on monitoring the so-called nuclear spin, namely the angular momentum of atoms, or, more precisely: the magnetic moment associated with them. The atom thus becomes a bar magnet, whose axis is aligned within a magnetic field but is otherwise arbitrarily oriented within its environment.

The alignment can be altered by applying electromagnetic radiation in the radio wavelength, typically at several 100 Megahertz. The result is an NMR spectrum that is determined by the atom's environment and provides a detailed insight into the structures and motions of molecules. NMR spectroscopy applications range from identifying molecules in chemical analysis to characterising large molecular clusters.

Physicians, too, make use of NMR to look into the body, with CAT scan technology being the result of an NMR experiment. Among the various available methods, it is the Nuclear Overhauser Effect (NOE) analysis that is of particular importance.

Anticipated by Albert Overhauser in 1953, this effect predicts a coupling of nuclear spins through interaction of their magnetic moments. Within the very same molecule this effect is extremely short-range and should apply only to neighbouring nuclear spins. On the basis of these postulations, a group of scientists headed by the Swiss chemist Kurt Wüthrich had developed methods for the identification of protein structures in solvents, for which he was awarded the Nobel Prize in Chemistry in 2002.

Interactions between the molecules

In proteins, the interacting nuclear spins belong to the same molecule; the fact that their relative distance does not vary in the course of the experiment facilitates their theoretical description. If the approach is extended to include monitoring of the interactions between molecules, it has the potential for various applications, for example the identification of the water structures and water dynamics on the surface of proteins or of local structures in novel "designer solvents" (so-called ionic fluids) -both of which are central issues for RESOLV. In these cases, the nuclear spins belong to different molecules and can move relatively to each other; the distance between them does not remain constant.

This fact has made theoretical research difficult, and only partial solutions have been achieved to date. "A new theory regarding this effect has given this field of study a boost," says Prof Dr Hermann Weingärtner, head of the RUB task force "Physical Chemistry of Fluids."

He has developed the theory in collaboration with Prof Dr Othmar Steinhauser (Institute for Computational Biological Chemistry at the University of Vienna). The team has succeeded in developing a realistic model in which all crucial factors are taken into consideration and which is manageable on a mathematical level. The results are surprising, because it turns out that the range of the Nuclear Overhauser Effect with spins in different molecules is determined by the frequency of the deployed electromagnetic radiation. Under typical experimental conditions, the effect is a long-range one.

This, in turn, means that the experiments describe the structure of the entire fluid rather than just -- as previously assumed -- a molecule's closest environment.

The new theory thus constitutes the first step towards clarifying questions that have remained unanswered for a long time as well as conflicting interpretations of such experiments. Weingärtner and Steinhauser's research has been financed by the "Cluster of Excellence RESOLV" (EXC 1069) of the German Research Foundation (DFG).


Story Source:

The above story is based on materials provided by Ruhr-Universitaet-Bochum. Note: Materials may be edited for content and length.


Journal Reference:

  1. Sonja Gabl, Othmar Steinhauser, Hermann Weingärtner. From Short-Range to Long-Range Intermolecular NOEs in Ionic Liquids: Frequency Does Matter. Angewandte Chemie International Edition, 2013; 52 (35): 9242 DOI: 10.1002/anie.201302712

Cite This Page:

Ruhr-Universitaet-Bochum. "New theory for analysing interacting nuclear spins in solvents." ScienceDaily. ScienceDaily, 24 September 2013. <www.sciencedaily.com/releases/2013/09/130924091532.htm>.
Ruhr-Universitaet-Bochum. (2013, September 24). New theory for analysing interacting nuclear spins in solvents. ScienceDaily. Retrieved September 20, 2014 from www.sciencedaily.com/releases/2013/09/130924091532.htm
Ruhr-Universitaet-Bochum. "New theory for analysing interacting nuclear spins in solvents." ScienceDaily. www.sciencedaily.com/releases/2013/09/130924091532.htm (accessed September 20, 2014).

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