1402162-64-4Relevant academic research and scientific papers
Dihydrogen-catalyzed reversible carbon-hydrogen and nitrogen-hydrogen bond formation in organometallic iridium complexes
Valpuesta, Jose E. V.,Rendon, Nuria,Lopez-Serrano, Joaquin,Poveda, Manuel L.,Sanchez, Luis,Alvarez, Eleuterio,Carmona, Ernesto
, p. 7555 - 7557 (2012)
Dihydrogen at work! H2 catalyzes with high efficiency a prototropic rearrangement of aminopyridinate ligands bound to a {(η5-C5Me5)IrIII} unit. The catalytic isomerization implies reversible formation and cleavage of H-H, C-H, and N-H bonds. Copyright
