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Homolytic N–H Activation of Ammonia: Hydrogen Transfer of Parent Iridium Ammine, Amide, Imide, and Nitride Species

[Image: see text] The redox series [Ir(n)(NH(x))(PNP)] (n = II–IV, x = 3–0; PNP = N(CHCHPtBu(2))(2)) was examined with respect to electron, proton, and hydrogen atom transfer steps. The experimental and computational results suggest that the Ir(III) imido species [Ir(NH)(PNP)] is not stable but unde...

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Detalles Bibliográficos
Autores principales: Scheibel, Markus G., Abbenseth, Josh, Kinauer, Markus, Heinemann, Frank W., Würtele, Christian, de Bruin, Bas, Schneider, Sven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597254/
https://www.ncbi.nlm.nih.gov/pubmed/26192601
http://dx.doi.org/10.1021/acs.inorgchem.5b00829
Descripción
Sumario:[Image: see text] The redox series [Ir(n)(NH(x))(PNP)] (n = II–IV, x = 3–0; PNP = N(CHCHPtBu(2))(2)) was examined with respect to electron, proton, and hydrogen atom transfer steps. The experimental and computational results suggest that the Ir(III) imido species [Ir(NH)(PNP)] is not stable but undergoes disproportionation to the respective Ir(II) amido and Ir(IV) nitrido species. N–H bond strengths are estimated upon reaction with hydrogen atom transfer reagents to rationalize this observation and are used to discuss the reactivity of these compounds toward E–H bond activation.