English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Isotopic orientational order in acetyl salicylic acid

MPS-Authors
/persons/resource/persons92644

Detken,  Andreas
Emeritus Group Bioorganic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons93258

Haeberlen,  Ulrich
Research Group Prof. Dr. Haeberlen, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons128263

Zimmermann,  Herbert
Emeritus Group Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Schiebel, P., Prandl, W., Papoular, R., Paulus, W., Detken, A., Haeberlen, U., et al. (2000). Isotopic orientational order in acetyl salicylic acid. Physica B-Condensed Matter, 276, 816-817. doi:10.1016/S0921-4526(99)01337-X.


Cite as: https://hdl.handle.net/21.11116/0000-0002-4795-6
Abstract
Isotopically mixed methyl groups CDxH3−x with zero averaged deuteron/hydrogen scattering length 0=〈a〉=xaD+(3−x)aH are expected to be invisible in a neutron diffraction experiment. We find, indeed, in the scattering length density of aspirin-CDxH3−x, reconstructed by maximum-entropy methods, at room temperature only three very week minima. At 10 K, however, one positive and two negative extrema are visible: unique evidence for orientational isotopic order. From a combination of 1-d-Fourier and algebraic methods we deconvolute 〈a〉 and derive the orientational distribution function f(φ) which has three equivalent maxima/minima at 300 K and loses this 3φ periodicity at 10 K. f(φ) is the basis for the determination of the hindrance potential with cos(φ) as the leading term.