Journal Article PUBDB-2016-05086

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First investigations of the kinetics of the topochemical reaction of p-formyl-trans-cinnamic acid by time-resolved X-ray diffraction.

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2003
Soc. Cambridge [u.a.]

Faraday discussions 122, 105-117 () [10.1039/b202831j]
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Abstract: Under UV irradiation p-formyl-trans-cinnamic acid (p-FCA) crystals in the β-phase dimerise irreversibly to solid 4,4′-diformyl-β-truxinic acid. The experimental conditions were chosen in such a way (non-aqueous environment and room temperature) that the product formed is amorphous. The kinetics of this bimolecular reaction, which has not yet been characterised, was investigated by picosecond time-resolved X-ray diffraction. From the experimental results a mechanism for this topochemical reaction is proposed including two observed time constants, one less than 100 ps and another of several seconds. The feasibility of investigating this class of substances by time-resolved X-ray diffraction from third generation synchrotron sources and future free-electron lasers is discussed.

Classification:

Contributing Institute(s):
  1. Strukturdynamik Chemischer Systeme (FS-SCS)
Research Program(s):
  1. 633 - Life Sciences – Building Blocks of Life: Structure and Function (POF4-633) (POF4-633)
Experiment(s):
  1. Measurement at external facility

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Medline ; Medline ; Allianz-Lizenz / DFG ; Allianz-Lizenz / DFG ; Clarivate Analytics Master Journal List ; Current Contents - Physical, Chemical and Earth Sciences ; Current Contents - Physical, Chemical and Earth Sciences ; Essential Science Indicators ; IF < 5 ; IF < 5 ; JCR ; JCR ; NCBI Molecular Biology Database ; National-Konsortium ; NationallizenzNationallizenz ; NationallizenzNationallizenz ; SCOPUS ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection ; Web of Science Core Collection
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 Record created 2016-11-13, last modified 2025-08-04


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