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005     20250731122414.0
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|a 1661-6596
024 7 _ |2 ISSN
|a 1422-0067
024 7 _ |2 WOS
|a WOS:000272191200008
024 7 _ |2 doi
|a 10.3390/ijms10114754
024 7 _ |a openalex:W2077259506
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037 _ _ |a PHPPUBDB-17381
041 _ _ |a eng
082 _ _ |a 570
100 1 _ |0 P:(DE-H253)PIP1010871
|a Quevedo, W.
|b 0
110 1 _ |a DESY
|b Experiments with synchrotron radiation
245 _ _ |a Time-resolved soft x-ray diffraction reveals transient structural distortions of ternary liquid crystals
260 _ _ |a Basel
|b Molecular Diversity Preservation International
|c 2009
300 _ _ |a 4754-4771
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440 _ 0 |0 PERI:(DE-600)2019364-6
|a Int. J. Mol. Sci.
|v 10
|x 1422-0067
500 _ _ |3 Converted on 2013-05-30 14:04
500 _ _ |3 Converted on 2013-06-21 19:20
520 _ _ |a Home-based soft X-ray time-resolved scattering experiments with nanosecond time resolution (10 ns) and nanometer spatial resolution were carried out at a table top soft X-ray plasma source (2.2-5.2 nm). The investigated system was the lyotropic liquid crystal C(16)E(7)/paraffin/glycerol/formamide/IR 5. Usually, major changes in physical, chemical, and/or optical properties of the sample occur as a result of structural changes and shrinking morphology. Here, these effects occur as a consequence of the energy absorption in the sample upon optical laser excitation in the IR regime. The liquid crystal shows changes in the structural response within few hundred nanoseconds showing a time decay of 182 ns. A decrease of the Bragg peak diffracted intensity of 30% and a coherent macroscopic movement of the Bragg reflection are found as a response to the optical pump. The Bragg reflection movement is established to be isotropic and diffusion controlled (1 micros). Structural processes are analyzed in the Patterson analysis framework of the time-varying diffraction peaks revealing that the inter-lamellar distance increases by 2.7 A resulting in an elongation of the coherently expanding lamella crystallite. The present studies emphasize the possibility of applying TR-SXRD techniques for studying the mechanical dynamics of nanosystems.
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700 1 _ |a Peth, C.
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700 1 _ |a Busse, G.
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700 1 _ |0 P:(DE-H253)PIP1021265
|a Scholz, M.
|b 3
700 1 _ |0 P:(DE-H253)PIP1010368
|a Mann, K.
|b 4
700 1 _ |0 P:(DE-H253)PIP1008775
|a Techert, S.
|b 5
773 _ _ |0 PERI:(DE-600)2019364-6
|a 10.3390/ijms10114754
|g Vol. 10, p. 4754-4771
|p 4754-4771
|q 10<4754-4771
|t International journal of molecular sciences
|v 10
|x 1422-0067
|y 2009
856 4 _ |y OpenAccess
856 7 _ |2 Pubmed Central
|u http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2808009
856 4 _ |u https://bib-pubdb1.desy.de/record/90874/files/ijms-10-04754.pdf
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|b Programmorientierte Förderung I
|l Struktur der Materie
|v Großgeräte für die Forschung mit Photonen, Neutronen, Ionen
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