Literature DB >> 14558790

Distinguishing rate-limiting electron versus H-atom transfers in Cu2O2-mediated oxidative N-dealkylations: application of inter- versus intramolecular kinetic isotope effects.

Jason Shearer1, Christiana Xin Zhang, Lanying Q Hatcher, Kenneth D Karlin.   

Abstract

Copper-dioxygen adducts are important biological oxidants. To gain a better understanding of the underlying chemistries of such species, we report on a series of Cu2II-O2 complexes, [{CuII(MePY2)R'}2(O2)](B(C6F5)4)2 (1R') (where (MePY2)R' is a 4-pyridyl substituted bis[2-(2-(4-R'-pyridyl)ethyl]methylamine; R' = H, MeO, Me2N; Zhang, C. X.; et al. J. Am. Chem. Soc. 2003, 125, 634-635), which readily oxidize exogenous substrates. In this study, we explore the mechanism by which 1R' facilitates the oxidative N-dealkylation of para-substituted N,N-dimethylanilines (R-DMA; R = MeO, Me, H, CN). In the case of 1H, the linear free-energy correlation plot (rho = -2.1) and intramolecular deuterium kinetic isotope effect (KIEintra, using p-R-(C6H4)-N(CH3)(CD3)) profile suggest that R-DMA oxidation occurs through rate-limiting electron transfer (ET). This mechanism was further enforced by comparison of KIEintra versus the intermolecular KIE (KIEinter, using p-R-(C6H4)-N(CH3)2 versus p-R-(C6H4)-N(CD3)2). It was found that KIEinter < KIEintra, suggesting an ET process. In the case of both 1MeO and 1Me2N, the KIEintra profile and linear free-energy correlation plots (rho = -0.49 and -0.99 for 1Me2N and 1MeO with especially poor fitting for the latter) are inconclusive in distinguishing between a rate-limiting ET or hydrogen atom transfer (HAT) pathway. Comparisons of KIEinter versus KIEintra demonstrate a switch in mechanism from ET to HAT for 1Me2N and 1MeO oxidation of R-DMA as R-DMA is made less reducing. In the case of 1Me2N, MeO-DMA and Me-DMA are oxidized via a rate-limiting ET (KIEinter < KIEintra), while H-DMA and CN-DMA are oxidized through a HAT pathway (KIEinter approximately KIEintra). For 1MeO, oxidation occurs through an ET pathway for MeO-, Me-, and H-DMA (KIEinter < KIEintra), while CN-DMA is oxidized though a HAT process (KIEinter approximately KIEintra). Copper complex attributes, which may contribute to the mechanistic observations, are suggested.

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Year:  2003        PMID: 14558790     DOI: 10.1021/ja0359409

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  12 in total

1.  Mechanistic Analysis of Oxidative C-H Cleavages Using Inter- and Intramolecular Kinetic Isotope Effects.

Authors:  Hyung Hoon Jung; Paul E Floreancig
Journal:  Tetrahedron       Date:  2009-12-26       Impact factor: 2.457

2.  Toluene and ethylbenzene aliphatic C-H bond oxidations initiated by a dicopper(II)-mu-1,2-peroxo complex.

Authors:  Heather R Lucas; Lei Li; Amy A Narducci Sarjeant; Michael A Vance; Edward I Solomon; Kenneth D Karlin
Journal:  J Am Chem Soc       Date:  2009-03-11       Impact factor: 15.419

3.  Mechanistic studies of the oxidative N-dealkylation of a substrate tethered to carboxylate-bridged diiron(II) complexes, [Fe2(mu-O2CAr(Tol))2(O2CAr(Tol))2(N,N-Bn2en)2].

Authors:  Sungho Yoon; Stephen J Lippard
Journal:  Inorg Chem       Date:  2006-07-10       Impact factor: 5.165

4.  Anilinic N-oxides support cytochrome P450-mediated N-dealkylation through hydrogen-atom transfer.

Authors:  Kenneth M Roberts; Jeffery P Jones
Journal:  Chemistry       Date:  2010-07-19       Impact factor: 5.236

5.  Mechanism-Guided Design and Discovery of Efficient Cytochrome P450-Derived C-H Amination Biocatalysts.

Authors:  Viktoria Steck; Joshua N Kolev; Xinkun Ren; Rudi Fasan
Journal:  J Am Chem Soc       Date:  2020-06-01       Impact factor: 15.419

6.  Selective DNA strand scission with binuclear copper complexes: implications for an active Cu2-O2 species.

Authors:  Sunita Thyagarajan; Narasimha N Murthy; Amy A Narducci Sarjeant; Kenneth D Karlin; Steve E Rokita
Journal:  J Am Chem Soc       Date:  2006-05-31       Impact factor: 15.419

Review 7.  Oxidant types in copper-dioxygen chemistry: the ligand coordination defines the Cu(n)-O2 structure and subsequent reactivity.

Authors:  Lanying Q Hatcher; Kenneth D Karlin
Journal:  J Biol Inorg Chem       Date:  2004-08-10       Impact factor: 3.358

8.  Dimethylanilinic N-Oxides and Their Oxygen Surrogacy Role in the Formation of a Putative High-Valent Copper-Oxygen Species.

Authors:  Daniel E Diaz; Mayukh Bhadra; Kenneth D Karlin
Journal:  Inorg Chem       Date:  2019-10-03       Impact factor: 5.165

9.  Access to a Cu(II)-O-Cu(II) motif: spectroscopic properties, solution structure, and reactivity.

Authors:  Peter Haack; Anne Kärgel; Claudio Greco; Jadranka Dokic; Beatrice Braun; Florian F Pfaff; Stefan Mebs; Kallol Ray; Christian Limberg
Journal:  J Am Chem Soc       Date:  2013-10-17       Impact factor: 15.419

10.  Enzymatic C(sp3)-H Amination: P450-Catalyzed Conversion of Carbonazidates into Oxazolidinones.

Authors:  Ritesh Singh; Joshua N Kolev; Philip A Sutera; Rudi Fasan
Journal:  ACS Catal       Date:  2015-01-29       Impact factor: 13.084

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