Format:
1 Online-Ressource (7 Seiten)
ISSN:
1477-9234
,
1477-9234
Content:
Two new heterobimetallic [LNiO2Cu(RPY2)]+ (RPY2 = N-substituted bis 2-pyridyl(ethylamine) ligands with R = indane, 3a or R = Me, 3b) complexes have been spectroscopically trapped at low temperatures. They were prepared by reacting the mononuclear side-on LNiII superoxo precursor bearing a β-diketiminate ligand (L = [HC-(CMeNC6H3(iPr)2)2]) with the Cu(I) complexes. In contrast to the oxo groups in known high-valent [M2(μ-O)2]n+ (M = Fe, Co, Ni, Cu) cores that display electrophilic reactivities, 3a and 3b display rather nucleophilic oxo cores active in aldehyde deformylation reactions. However, the spectroscopic and reactivity properties of 3a/3b are found to be distinct relative to that of the previously reported [LNiO2Cu(MeAN)]+ complex containing a more basic (nucleophilic) N,N,N′,N′,N′-pentamethyl-dipropylenetriamine (MeAN) ligand at the copper centre. The geometry and electronic properties of the copper ligands affect the electron density of the oxygen atoms of the heterodinuclear {Ni(μ-O)2} core and 3a/3b undergo slower nucleophilic and faster electrophilic reactions than the previously reported [LNiO2Cu(MeAN)]+ intermediate. The present study therefore demonstrates the tuning of the electrophilicity/nucleophilicity of the oxygen atoms of the heterobimetallic [Ni(μ-O)2Cu]2+ cores by controlling the electron donation from the ancillary ligands, and underlines the significance of subtle electronic changes in the physical and chemical properties of the biologically relevant heterobimetallic metal–dioxygen intermediates.
Content:
Peer Reviewed
Note:
Available open access thanks to the RSC Gold for Gold initiative. Shared according to the terms set out in the CC licence.
In:
: The Royal Society of Chemistry, 45,40, Seiten 15994-16000, 1477-9234
Language:
English
URN:
urn:nbn:de:kobv:11-110-18452/19292-7
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