dc.contributor.author | Poole, Ethan W. | |
dc.contributor.author | Bustos Rosas, Itxaso | |
dc.contributor.author | Hood, Thomas M. | |
dc.contributor.author | Smart, Jennifer E. | |
dc.contributor.author | Chaplin, Adrian B. | |
dc.date.accessioned | 2023-01-30T18:34:46Z | |
dc.date.available | 2023-01-30T18:34:46Z | |
dc.date.issued | 2023 | |
dc.identifier.citation | Dalton Transactions 52(4) : 1096-1104 (2022) | es_ES |
dc.identifier.issn | 1477-9226 | |
dc.identifier.issn | 1477-9234 | |
dc.identifier.uri | http://hdl.handle.net/10810/59570 | |
dc.description.abstract | The synthesis and iridium coordination chemistry of a new pyridine-based phosphinito pincer ligand 2,6-
(ArF2PO)2 C5H 3N (PONOP-ArF ; ArF = 2-(CF3)C 6 H4 ) are described, where the P-donors have ortho-
trifluoromethylphenyl substituents. The iridium(III) 2,2’-biphenyl (biph) derivative [Ir(PONOP-ArF )(biph)Cl]
was obtained by reaction with [Ir(biph)(COD)Cl] 2 (COD = 1,5-cyclooctadiene) and subsequent halide ion
abstraction enabled isolation of [Ir(PONOP-ArF )(biph)]+ which features an Ir ← F–C bonding interaction in
the solid state. Hydrogenolysis of the biphenyl ligand and formation of [Ir(PONOP-Ar F )(H)2 ]+ was achieved
by prolonged reaction of [Ir(PONOP-ArF )(biph)]+ with dihydrogen. This transformation paved the way for
isolation and crystallographic characterisation of low valent iridium derivatives through treatment of the
dihydride with tert-butylethylene (TBE). The iridium(I ) π-complex [Ir(PONOP-ArF )(TBE)]+ is thermally stable
but substitution of TBE can be achieved by reaction with carbon monoxide. The solid-state structure of
the mono-carbonyl product [Ir(PONOP-ArF )(CO)]+ is notable for an intermolecular anagostic interaction
between the metal centre and a pentane molecule which co-crystallises within a cleft defined by two aryl
phosphine substituents. | es_ES |
dc.description.sponsorship | We thank the Spanish Ministry of Universities and the
European Union (Margarita Salas grant funded by the
European Union-NextGenerationEU, I. B.), the European
Research Council (ERC; grant agreement 637313, T. M. H. and
A. B. C.), and Royal Society (RGF\EA\180128, J. E. S.; UF100592
and UF150675; A. B. C.) for financial support. High-resolution
mass-spectrometry data were collected using instruments pur-
chased through support from Advantage West Midlands and the
European Regional Development Fund. Crystallographic data
were collected using an instrument that received funding from
the ERC under the European Union’s Horizon 2020 research
and innovation programme (grant agreement No 637313). | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Royal Society of Chemistry | es_ES |
dc.relation | info:eu-repo/grantAgreement/EC/ERC/637313 | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/3.0/es/ | * |
dc.title | Iridium complexes of an ortho-trifluoromethylphenyl substituted PONOP pincer ligand | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.rights.holder | © The Royal Society of Chemistry 2023. This article is licensed under a Creative Commons Atribution-Non Commercial 3.0 unported licence. | es_ES |
dc.rights.holder | Atribución-NoComercial 3.0 España | * |
dc.relation.publisherversion | https://pubs.rsc.org/en/content/articlelanding/2023/DT/D2DT03608H | es_ES |
dc.identifier.doi | 10.1039/d2dt03608h | |
dc.contributor.funder | European Commission | |
dc.departamentoes | Química aplicada | es_ES |
dc.departamentoeu | Kimika aplikatua | es_ES |