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Carbonyl complexes of copper(i) stabilized by bridging fluorinated pyrazolates and halide ions

dc.contributor.authorParasar D.
dc.contributor.authorJayaratna N.B.
dc.contributor.authorMuñoz-Castro A.
dc.contributor.authorConway A.E.
dc.contributor.authorMykhailiuk P.K.
dc.contributor.authorDias H.V.R.
dc.date.accessioned2020-09-02T22:25:20Z
dc.date.available2020-09-02T22:25:20Z
dc.date.issued2019
dc.identifier10.1039/c9dt00486f
dc.identifier.citation48, 19, 6358-6371
dc.identifier.issn14779226
dc.identifier.urihttps://hdl.handle.net/20.500.12728/5745
dc.descriptionSyntheses of neutral and anionic, di- and tetra-nuclear copper carbon monoxide complexes using binary copper(i) pyrazolate precursors are reported. The reaction of {[3,5-(CF3)2Pz]Cu}3 (2), {[4-Cl-3,5-(CF3)2Pz]Cu}3 (3) or {[3,4,5-(CF3)3Pz]Cu}3 (4) with CO in CH2Cl2 led to copper carbonyl complexes. They however, lose CO quite easily if not kept under a CO atmosphere. Compounds {[3,5-(CF3)2Pz]Cu(CO)}2 (5) and {[3,4,5-(CF3)3Pz]Cu(CO)}2 (7) were characterized by X-ray crystallography. They are dinuclear species with a Cu2N4 core. The reaction of {[3,5-(CF3)2Pz]Cu}3 with CO in the presence of [NEt4]Br or [NEt4][3,5-(CF3)2Pz] affords relatively more stable [NEt4][{[3,5-(CF3)2Pz]Cu(CO)}4(μ4-Br)] (8) and [NEt4]{[3,5-(CF3)2Pz]3Cu2(CO)2} (9). The related [NEt4][{[4-Cl-3,5-(CF3)2Pz]Cu(CO)}4(μ4-Br)] (10) and [NEt4][{[4-Cl-3,5-(CF3)2Pz]Cu(CO)}4(μ4-Cl)] (11) can be synthesized using {[4-Cl-3,5-(CF3)2Pz]Cu}3, CO and [NEt4]Br or [NEt4]Cl. The X-ray structures show that 8, 10 and 11 are tetranuclear species with terminal Cu-CO groups and quadruply bridging Cl- and Br- ions. Compound 9 features an anionic cage of nearly D3h symmetry formed by three bridging [3,5-(CF3)2Pz]- ions and two terminal Cu-CO moieties. Theoretical calculations show that bonding in these 16- and 18-electron copper complexes follows Dewar-Chatt-Duncanson (DCD) model, where the CO stretching frequencies correlate well to the orbital interaction energy ΔEorb. The major Cu-CO interaction however is electrostatic in nature. Further theoretical exploration of the role of the substituent at pyrazolyl ring 4-position between -H, -Cl, and -CF3, shows a slight decrease in covalent character of the Cu-CO interaction and diminished π-back bonding as pyrazolate groups become more weakly donating with added electron withdrawing substituents. © 2019 The Royal Society of Chemistry.
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.titleCarbonyl complexes of copper(i) stabilized by bridging fluorinated pyrazolates and halide ions
dc.typeArticle


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