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Titel:Bonding in Low-Coordinated Organoarsenic and Organoantimony Compounds: A Threshold Photoelectron Spectroscopic Investigation
Autor:Karaev, Emil
Weitere Verfasser:Gerlach, Marius; Faschingbauer, Lukas; Ramler, Jacqueline; Krummenacher, Ivo; Lichtenberg, Crispin; Hemberger, Patrick; Fischer, Ingo
Veröffentlicht:2023
URI:https://archiv.ub.uni-marburg.de/es/2023/0070
URN: urn:nbn:de:hebis:04-es2023-00703
DOI: https://doi.org/10.1002/chem.202300637
DDC:540 Chemie
Publikationsdatum:2023-07-10
Lizenz:https://creativecommons.org/licenses/by-nc-nd/4.0/

Dokument

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Summary:
Methyl and methylene compounds of arsenic and antimony have been studied by photoelectron photoion coincidence spectroscopy to investigate their relative stability. While for As both HAs=CH2, As−CH3 and the methylene compound As=CH2 are identified in the spectrum, the only Sb compound observed is Sb−CH3. Thus, there is a step in the main group 15 between As and Sb, regarding the relative stability of the methyl compounds. Ionisation energies, vibrational frequencies and spin-orbit splittings were determined for the methyl compound from photoion mass-selected photoelectron spectra. Although the spectroscopic results for organoantimony resemble those for the previously investigated bismuth compounds, EPR spectroscopic experiments indicate a far lower tendency for methyl transfer for Sb(CH3)3 compared to Bi(CH3)3. This study concludes investigations on low-valent organopnictogen compounds.


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