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Phenolate Hydroxylation in a Bis(μ-oxo)dicopper(III) Complex: Lessons from the Guanidine/Amine Series

Open access
Herres-Pawlis, Sonja, Verma, Pratik, Haase, Roxana, Kang, Peng, Lyons, Christopher T., Wasinger, Erik C., Flörke, Ulrich, Henkel, Gerald, Stack, T. Daniel P.·2009·Journal of the American Chemical Society

Abstract

A new hybrid permethylated-amine-guanidine ligand based on a 1,3-propanediamine backbone (2L) and its Cu-O2 chemistry is reported. [(2L)CuI(MeCN)]1+ complex readily oxygenates at low temperatures in polar aprotic solvents to form a bis(mu-oxo)dicopper(III) (O) species (2b), similar to the parent bis-guanidine ligand complex (1b) and permethylated-diamine ligand complex (3b). UV-vis and X-ray absorption spectroscopy experiments confirm this assignment of 2b as an O species, and full formation of the 2:1 Cu-O2 complex is demonstrated by an optical titration with ferrocene-monocarboxylic acid (FcCOOH). The UV-vis spectra of 1b and 2b with guanidine ligation show low-intensity visible features assigned as guanidine pi --> Cu2O2 core transitions by time-dependent density functional theory (TD-DFT) calculations. Comparison of the reactivity among the three related complexes (1b-3b) with phenolate at 195 K is particularly insightful as only 2b hydroxylates 2,4-di-tert-butylphenolate to yield 3,5-di-tert-butylcatecholate (>95% yield) with the oxygen atom derived from O2, reminiscent of tyrosinase reactivity. 1b is unreactive, while 3b yields the C-C radical-coupled bis-phenol product. Attenuated outer-sphere oxidative strength of the O complexes and increased phenolate accessibility to the Cu2O2 core are attributes that correlate with phenolate hydroxylation reactivity observed in 2b. The comparative low-temperature reactivity of 1b-3b with FcCOOH (O-H BDE 71 kcal mol(-1)) to form the two-electron, two-proton reduced bis(mu-hydroxo)dicopper(II,II) complex is quantitative and presumably precedes through two sequential proton-coupled electron transfer (PCET) steps. Optical titrations along with DFT calculations support that the reduced complexes formed in the first step are more powerful oxidants than the parent O complexes. These mechanistic insights aid in understanding the phenol to bis-phenol reactivity exhibited by 2b and 3b.

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Metadata

Authors
Herres-Pawlis, S., Verma, P., Haase, R., Kang, P., Lyons, C. T., Wasinger, E. C., Flörke, U., Henkel, G., & Stack, T. D. P.
Venue
Journal of the American Chemical Society
Published
2009-01-02
Volume
131
Issue
3
Pages
1154-1169
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2079607301
Cited by
163
References
2
FWCI
9.99
Type
journal article
Language
en
Open access
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Herres-Pawlis, S., Verma, P., Haase, R., Kang, P., Lyons, C. T., Wasinger, E. C., Flörke, U., Henkel, G., & Stack, T. D. P. (2009). Phenolate Hydroxylation in a Bis(μ-oxo)dicopper(III) Complex: Lessons from the Guanidine/Amine Series. Journal of the American Chemical Society. https://doi.org/10.1021/ja807809x

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