Abstract
Mononuclear [Ir{ArNC(NR(2))NAr}(C(8)H(12))] complexes (where R = Me or Et; Ar = Ph, 4-MeC(6)H(4), or 2,6-Me(2)C(6)H(3); and C(8)H(12) = 1,5-cyclooctadiene) were synthesized from the neutral N,N-dialkyl-N',N''-diarylguanidines via deprotonation and transmetalation. As confirmed by single-crystal structure determinations, the guanidinato(1-) ligands coordinate the low-valent d(8) Ir(I) center in an N,N'-chelating binding mode, and the (13)C NMR chemical shifts of the alkene carbon atoms establish that these ligands function as stronger donors than related monoanionic, bidentate nitrogen-based ligands. In the reactions of the complexes with O(2), the observed reactivity trends correlate with the electronic and steric influences of the substituents of the guanidinato ligands.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
