Dihydrogen Adduct (Co-H₂) Complexes Displaying H-atom and Hydride Transfer

The prototypical reactivity profiles of transition metal dihydrogen complexes (M‐H₂) are well‐characterized with respect to oxidative addition (to afford dihydrides, M(H)₂) and as acids, heterolytically delivering H⁺ to a base and H⁻ to the metal. In the course of this study we explored plausible alternative pathways for H₂ activation, namely direct activation through H‐atom or hydride transfer from the σ‐H₂ adducts. To this end, we describe herein the reactivity of an isostructural pair of a neutral S = ½ and an anionic S = 0 Co‐H₂ adduct, both supported by a trisphosphine borane ligand (P₃^B). The thermally stable metalloradical, (P₃^B)Co(H₂), serves as a competent precursor for hydrogen atom transfer to ᵗBu₃ArO·. What is more, its anionic derivative, the dihydrogen complex [(P₃^B)Co(H₂)]¹⁻, is a competent precursor for hydride transfer to BEt₃, establishing its remarkable hydricity. The latter finding is essentially without precedent among the vast number of M‐H₂ complexes known

Dihydrogen Adduct (Co-H₂) Complexes Displaying H-atom and Hydride Transfer

The prototypical reactivity profiles of transition metal dihydrogen complexes (M‐H₂) are well‐characterized with respect to oxidative addition (to afford dihydrides, M(H)₂) and as acids, heterolytically delivering H⁺ to a base and H⁻ to the metal. In the course of this study we explored plausible alternative pathways for H₂ activation, namely direct activation through H‐atom or hydride transfer from the σ‐H₂ adducts. To this end, we describe herein the reactivity of an isostructural pair of a neutral S = ½ and an anionic S = 0 Co‐H₂ adduct, both supported by a trisphosphine borane ligand (P₃^B). The thermally stable metalloradical, (P₃^B)Co(H₂), serves as a competent precursor for hydrogen atom transfer to ᵗBu₃ArO·. What is more, its anionic derivative, the dihydrogen complex [(P₃^B)Co(H₂)]¹⁻, is a competent precursor for hydride transfer to BEt₃, establishing its remarkable hydricity. The latter finding is essentially without precedent among the vast number of M‐H₂ complexes known

A mechanistic investigation of the photoinduced, copper-mediated cross-coupling of an aryl thiol with an aryl halide

Photoinduced, copper-catalyzed cross-coupling can offer a complementary approach to thermal (non-photoinduced) methods for generating C–X (X = C, N, O, S, etc.) bonds. In this report, we describe the first detailed mechanistic investigation of one of the processes that we have developed, specifically, the (stoichiometric) coupling of a copper–thiolate with an aryl iodide. In particular, we focus on the chemistry of a discrete [Cu^I(SAr)_2]− complex (Ar = 2,6-dimethylphenyl), applying a range of techniques, including ESI-MS, cyclic voltammetry, transient luminescence spectroscopy, optical spectroscopy, DFT calculations, Stern–Volmer analysis, EPR spectroscopy, actinometry, and reactivity studies. The available data are consistent with the viability of a pathway in which photoexcited [Cu^I(SAr)_2]−* serves as an electron donor to an aryl iodide to afford an aryl radical, which then reacts in cage with the newly generated copper(II)–thiolate to furnish the cross-coupling product in a non-chain process

Photoinduced, Copper-Catalyzed Alkylation of Amines: A Mechanistic Study of the Cross-Coupling of Carbazole with Alkyl Bromides

We have recently reported that a variety of couplings of nitrogen, sulfur, oxygen, and carbon nucleophiles with organic halides can be achieved under mild conditions (−40 to 30 °C) through the use of light and a copper catalyst. Insight into the various mechanisms by which these reactions proceed may enhance our understanding of chemical reactivity and facilitate the development of new methods. In this report, we apply an array of tools (EPR, NMR, transient absorption, and UV–vis spectroscopy; ESI–MS; X-ray crystallography; DFT calculations; reactivity, stereochemical, and product studies) to investigate the photoinduced, copper-catalyzed coupling of carbazole with alkyl bromides. Our observations are consistent with pathways wherein both an excited state of the copper(I) carbazolide complex ([Cu^I(carb)_2]^−) and an excited state of the nucleophile (Li(carb)) can serve as photoreductants of the alkyl bromide. The catalytically dominant pathway proceeds from the excited state of Li(carb), generating a carbazyl radical and an alkyl radical. The cross-coupling of these radicals is catalyzed by copper via an out-of-cage mechanism in which [Cu^I(carb)_2]^− and [Cu^(II)(carb)_3]^− (carb = carbazolide), both of which have been identified under coupling conditions, are key intermediates, and [Cu^(II)(carb)_3]^− serves as the persistent radical that is responsible for predominant cross-coupling. This study underscores the versatility of copper(II) complexes in engaging with radical intermediates that are generated by disparate pathways, en route to targeted bond constructions