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Phenolate Hydroxylation in a Bis(μ-oxo)dicopper(III) Complex: Lessons from the Guanidine/Amine Series
Open accessAbstract
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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Cites
Multicopper oxidases and oxygenases
Solomon, E. I., Sundaram, U. M., & Machonkin, T. E. (1996) · Chemical Reviews · doi:10.1021/cr950046o · Cited by 3,664
Proton-coupled electron transfer
Huynh, M. H. V., & Meyer, T. J. (2007) · Chemical Reviews · doi:10.1021/cr0500030 · Cited by 1,659
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Bioinspired Metal–Organic Framework Catalysts for Selective Methane Oxidation to Methanol
Baek, J., Rungtaweevoranit, B., Pei, X., Park, M., Fakra, S. C., Liu, Y.-S., Matheu, R., Alshmimri, S. A., Alshehri, S., Trickett, C. A., et al. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b11525 · Cited by 417
Oxidation Reactions with Bioinspired Mononuclear Non‐Heme Metal–Oxo Complexes
Engelmann, X., Monte‐Pérez, I., & Ray, K. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201600507 · Cited by 300
Synthetic Fe/Cu Complexes: Toward Understanding Heme-Copper Oxidase Structure and Function
Adam, S. M., Wijeratne, G. B., Rogler, P. J., Diaz, D. E., Quist, D. A., Liu, J. J., & Karlin, K. D. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00074 · Cited by 264
Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactide
Schäfer, P. M., McKeown, P., Fuchs, M., Rittinghaus, R. D., Hermann, A., Henkel, J., Seidel, S., Roitzheim, C., Ksiazkiewicz, A. N., Hoffmann, A., et al. (2019) · Dalton Transactions · doi:10.1039/c8dt04938f · Cited by 52
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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
- Publisher
- American Chemical Society (ACS)
- 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
- green
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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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