193Ir nuclear forward scattering of an iridium(I) complex

  • Synchrotron based nuclear forward scattering (NFS) experiments using the 193Ir nucleus have been performed for the first time on a dinuclear iridium(I) complex, [IrCl(COD)]2 with COD being cycloocta-1,5-diene. This complex serves as a catalyst for hydrogenation and other chemical reactions. Both, the obtained absolute values of the isomer shift \(\delta =0.87 \ {\text{mm s}}^{-1}\) and the quadrupole splitting \(\varDelta {E}_{Q}=3.82 \ {\text{mm s}}^{-1}\) agree within the experimental error with values obtained via conventional 193Ir Mössbauer spectroscopy reported earlier (Gál M. et al. J. Radioanal. Nucl. Chem., 260 (1) 2004, 133). In addition, we present density functional theory (DFT) calculations of the complex yielding its electronic structure and related Mössbauer parameters.

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Metadaten
Author:Maren H. Hoock, Olaf Leupold, Alexander Haag, Andreas Omlor, Rene Steinbrügge, Ilya Sergueev, Ralf Röhlsberger, Hans-Jörg Krüger, Juliusz A. Wolny, Volker Schünemann
URN:urn:nbn:de:hbz:386-kluedo-89558
DOI:https://doi.org/10.1007/s10751-023-01836-3
ISSN:3005-0731
Parent Title (English):Hyperfine Interactions
Publisher:Springer Nature
Editor:John G. Weisend II
Document Type:Conference Proceeding
Language of publication:English
Date of Publication (online):2025/04/14
Year of first Publication:2023
Publishing Institution:Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau
Date of the Publication (Server):2025/04/24
Issue:(2023) Vol.244
Page Number:12
Source:https://link.springer.com/article/10.1007/s10751-023-01836-3
Faculties / Organisational entities:Kaiserslautern - Fachbereich Physik
DDC-Cassification:5 Naturwissenschaften und Mathematik / 530 Physik
Collections:Open-Access-Publikationsfonds
Licence (German):Creative Commons 4.0 - Namensnennung (CC BY 4.0)