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http://dx.doi.org/10.18419/opus-13976
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DC Element | Wert | Sprache |
---|---|---|
dc.contributor.author | Jordan, Rose | - |
dc.contributor.author | Niazi, Maryam | - |
dc.contributor.author | Schäfer, Sascha | - |
dc.contributor.author | Kaim, Wolfgang | - |
dc.contributor.author | Klein, Axel | - |
dc.date.accessioned | 2024-02-29T10:26:28Z | - |
dc.date.available | 2024-02-29T10:26:28Z | - |
dc.date.issued | 2022 | de |
dc.identifier.issn | 1420-3049 | - |
dc.identifier.other | 188233454X | - |
dc.identifier.uri | http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-139954 | de |
dc.identifier.uri | http://elib.uni-stuttgart.de/handle/11682/13995 | - |
dc.identifier.uri | http://dx.doi.org/10.18419/opus-13976 | - |
dc.description.abstract | The excellent π-accepting azodicarboxylic esters adcOR (R = Et, iPr, tBu, Bn (CH2-C6H5) and Ph) and the piperidinyl amide derivative adcpip were used as bridging chelate ligands in dinuclear Re(CO)3 complexes [{Re(CO)3Cl}2(µ-adcOR)] and [{Re(CO)3Cl}2(µ-adcpip)]. From the adcpip ligand the mononuclear derivatives [Re(CO)3Cl(adcpip)] and [Re(CO)3(PPh3)(µ-adcpip)]Cl were also obtained. Optimised geometries from density functional theory (DFT) calculations show syn and anti isomers for the dinuclear fac-Re(CO)3 complexes at slightly different energies but they were not distinguishable from experimental IR or UV–Vis absorption spectroscopy. The electrochemistry of the adc complexes showed reduction potentials slightly below 0.0 V vs. the ferrocene/ferrocenium couple. Attempts to generate the radicals [{Re(CO)3Cl}2(µ-adcOR)]•− failed as they are inherently unstable, losing very probably first the Cl− coligand and then rapidly cleaving one [Re(CO)3] fragment. Consequently, we found signals in EPR very probably due to mononuclear radical complexes [Re(CO)3(solv)(adc)]•. The underlying Cl−→solvent exchange was modelled for the mononuclear [Re(CO)3Cl(adcpip)] using DFT calculations and showed a markedly enhanced Re-Cl labilisation for the reduced compared with the neutral complex. Both the easy reduction with potentials ranging roughly from −0.2 to −0.1 V for the adc ligands and the low-energy NIR absorptions in the 700 to 850 nm range place the adc ligands with their lowest-lying π* orbital being localised on the azo function, amongst comparable bridging chelate N^N coordinating ligands with low-lying π* orbitals of central azo, tetrazine or pyrazine functions. Comparative (TD)DFT-calculations on the Re(CO)3Cl complexes of the adcpip ligand using the quite established basis set and functionals M06-2X/def2TZVP/LANL2DZ/CPCM(THF) and the more advanced TPSSh/def2-TZVP(+def2-ECP for Re)/CPCMC(THF) for single-point calculations with BP86/def2-TZVP(+def2-ECP for Re)/CPCMC(THF) optimised geometries showed a markedly better agreement of the latter with the experimental XRD, IR and UV–Vis absorption data. | en |
dc.description.sponsorship | University of Cologne, Faculty of Mathematics and Natural Sciences | de |
dc.language.iso | en | de |
dc.relation.uri | doi:10.3390/molecules27238159 | de |
dc.rights | info:eu-repo/semantics/openAccess | de |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | de |
dc.subject.ddc | 540 | de |
dc.title | Rhenium tricarbonyl complexes of azodicarboxylate ligands | en |
dc.type | article | de |
dc.date.updated | 2023-11-14T00:09:08Z | - |
ubs.fakultaet | Chemie | de |
ubs.fakultaet | Fakultätsübergreifend / Sonstige Einrichtung | de |
ubs.institut | Institut für Anorganische Chemie | de |
ubs.institut | Fakultätsübergreifend / Sonstige Einrichtung | de |
ubs.publikation.seiten | 19 | de |
ubs.publikation.source | Molecules 27 (2022), No. 8159 | de |
ubs.publikation.typ | Zeitschriftenartikel | de |
Enthalten in den Sammlungen: | 03 Fakultät Chemie |
Dateien zu dieser Ressource:
Datei | Beschreibung | Größe | Format | |
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molecules-27-08159-v2.pdf | Artikel | 4,44 MB | Unknown | Öffnen/Anzeigen |
molecules-27-08159-s001.zip | Supplement | 4,5 MB | Unknown | Öffnen/Anzeigen |
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