No Switching Cooperativity between Coordinated Azo Ligands on Complexes Having $M^{II}(phosphane-k^2P)\}^{2+}\ ( M = Pd, Pt)$ Scaffolds

A series of square-planar palladium and platinum compounds with cis-blocking phosphanes and terminal azobenzene ligands ${[M(dppp)-(azo)_{2}] (OTf)_{2} (azo = CN(C_{6}H_{4})-N = N-(C_{6}H_{4})CN (iso-cyano), CN(C_{6}H_{4})-N = N-(C_{6}H_{5}) (iso-Ph)) and [{M_{2}(tpbz)}(azo)_{4}](OTf)_{4}(azo = CN(C...

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Detalles Bibliográficos
Autores: Raïch Panisello, Ot, Jover Modrego, Jesús, Puigjaner Vallet, Ma. Cristina, Ferrer García, Montserrat, Martínez López, Manuel, 1957-
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:dnet:ubarcelona__::0b6e1a6fc7caab9764274b6492122186
Acceso en línea:https://hdl.handle.net/2445/228570
Access Level:acceso abierto
Palabra clave:Lligands
Pal·ladi (Element químic)
Dissolvents
Platí
Ligands
Palladium
Solvents
Platinum
Descripción
Sumario:A series of square-planar palladium and platinum compounds with cis-blocking phosphanes and terminal azobenzene ligands ${[M(dppp)-(azo)_{2}] (OTf)_{2} (azo = CN(C_{6}H_{4})-N = N-(C_{6}H_{4})CN (iso-cyano), CN(C_{6}H_{4})-N = N-(C_{6}H_{5}) (iso-Ph)) and [{M_{2}(tpbz)}(azo)_{4}](OTf)_{4}(azo = CN(C_{6}H_{4})-N = N-(C_{6}H_{5})}$ have been synthesized and fully characterised. Similarly to the uncoordinated ligands, the new coordination compounds have shown to be photochemically active with respect to their trans-to-cis isomerization process. Their cis-to-trans back spontaneous reaction have been studied as a function of solvent, temperature and pressure and the corresponding activation parameters determined in order to investigate the mechanism of these transformations. The results obtained are indicative of the operation of a rotational mechanism with no cooperativity between the azo ligands attached to the same metal. DFT calculations have been carried out in order to estimate the relative energies of the different photoisomers for the theoretical interpretation of the experimental data.