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Reversible Hyperpolarization of Ketoisocaproate Using Sulfoxide‐containing Polarization Transfer Catalysts

The substrate scope of sulfoxide‐containing magnetisation transfer catalysts is extended to hyperpolarize α‐ketoisocaproate and α‐ketoisocaproate‐1‐[(13)C]. This is achieved by forming [Ir(H)(2)(κ (2)‐ketoisocaproate)(N‐heterocyclic carbene)(sulfoxide)] which transfers latent magnetism from p‐H(2) v...

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Detalles Bibliográficos
Autores principales: Tickner, Ben. J., Ahwal, Fadi, Whitwood, Adrian C., Duckett, Simon B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839500/
https://www.ncbi.nlm.nih.gov/pubmed/33196137
http://dx.doi.org/10.1002/cphc.202000825
Descripción
Sumario:The substrate scope of sulfoxide‐containing magnetisation transfer catalysts is extended to hyperpolarize α‐ketoisocaproate and α‐ketoisocaproate‐1‐[(13)C]. This is achieved by forming [Ir(H)(2)(κ (2)‐ketoisocaproate)(N‐heterocyclic carbene)(sulfoxide)] which transfers latent magnetism from p‐H(2) via the signal amplification by reversible exchange (SABRE) process. The effect of polarization transfer field on the formation of enhanced (13)C magnetization is evaluated. Consequently, performing SABRE in a 0.5 μT field enabled most efficient magnetisation transfer. (13)C NMR signals for α‐ketoisocaproate‐1‐[(13)C] in methanol‐d (4) are up to 985‐fold more intense than their traditional Boltzmann derived signal intensity (0.8 % (13)C polarisation). Single crystal X‐ray diffraction reveals the formation of the novel catalyst decomposition products [Ir(μ‐H)(H)(2)(IMes)(SO(Ph)(Me)(2))](2) and [(Ir(H)(2)(IMes)(SO(Me)(2)))(2)(μ‐S)] when the sulfoxides methylphenylsulfoxide and dimethylsulfoxide are used respectively.