An official website of the United States government
Abstract We have developed a reductive carbonylation method by which unactivated alkyl iodides can be hydroxymethylated to provide one‐carbon‐extended alcohol products under Cu‐catalyzed conditions. The method is tolerant of alkyl β‐hydrogen atoms, is robust towards a wide variety of functional groups, and was applied to primary, secondary, and tertiary alkyl iodide substrates. Mechanistic experiments indicate that the transformation proceeds by atom‐transfer carbonylation (ATC) of the alkyl iodide followed in tandem by two CuH‐mediated reductions in rapid succession. This radical mechanism renders the Cu‐catalyzed system complementary to precious‐metal‐catalyzed reductive carbonylation reactions.
more »
« less
Metal-catalysed radical carbonylation reactions
A review of metal-catalysed carbonylation reactions involving single-electron transfer mechanisms and organic radical intermediates is presented, emphasizing new avenues to carbonyl compounds that are enabled by this approach. Catalyst-induced, oxidant-induced, and photo-induced radical carbonylations are discussed, as are atom-transfer carbonylation chain processes. Collectively, this body of carbonylative coupling chemistry complements more traditional precious metal-based catalytic systems that engage in substrate carbonylation by two-electron pathways.
more »
« less
- Award ID(s):
- 1664632
- PAR ID:
- 10142365
- Date Published:
- Journal Name:
- Catalysis Science & Technology
- Volume:
- 9
- Issue:
- 14
- ISSN:
- 2044-4753
- Page Range / eLocation ID:
- 3603 to 3613
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Time-resolved electron paramagnetic resonance (TREPR) spectroscopy has been used to study the proton coupled electron transfer (PCET) reaction between a ruthenium complex (Ru(bpz)(bpy) 2 ) and several substituted hydroquinones (HQ). After excitation at 355 nm, the HQ moiety forms a strong hydrogen bond to the exposed N atoms in the bpz heterocycle. At some point afterwards, a PCET reaction takes place in which an electron from the O atom of the hydrogen bond transfers to the metal center, and the proton forming the hydrogen bond remains on the bpz ligand N atom. The result is a semiquinone radical (HQ˙), whose TREPR spectrum is strongly polarized by the triplet mechanism (TM) of chemically induced dynamic electron spin polarization (CIDEP). Closer examination of the CIDEP pattern reveals, in some cases, a small amount of radical pair mechanism (RPM) polarization. We hypothesize that when the HQ moiety has electron donating groups (EDGs) substituted on the ring, S–T − RPM polarization is observed in HQ˙. These anomalous intensities are accounted for by spectral simulation using polarization from S–T − mixing. The generation of S–T − RPM is attributed to slow radical separation after PCET due to stabilization of the positive charge on the ring by EDGs. Results from a temperature dependence support the hypothesis.more » « less
-
Abstract Palladium catalysis induced by visible light is an emerging field of catalysis. In contrast to classical reactions catalyzed by Pd complexes in the ground state, which mostly proceed through two‐electron redox processes, the mechanisms of these new methods based on photoexcited Pd complexes usually operate through transfer of a single electron. Such processes lead to putative hybrid Pd/radical species, which exhibit both radical and classical Pd‐type reactivity. This Minireview highlights the recent progress in this rapidly growing area.more » « less
-
The utilization of visible light to mediate chemical reactions in fluid solutions has applications that range from solar fuel production to medicine and organic synthesis. These reactions are typically initiated by electron transfer between a photoexcited dye molecule (a photosensitizer) and a redox-active quencher to yield radical pairs that are intimately associated within a solvent cage. Many of these radicals undergo rapid thermodynamically favored “geminate” recombination and do not diffuse out of the solvent cage that surrounds them. Those that do escape the cage are useful reagents that may undergo subsequent reactions important to the above-mentioned applications. The cage escape process and the factors that determine the yields remain poorly understood despite decades of research motivated by their practical and fundamental importance. Herein, state-of-the-art research on light-induced electron transfer and cage escape that has appeared since the seminal 1972 review by J. P. Lorand entitled “The Cage Effect” is reviewed. This review also provides some background for those new to the field and discusses the cage escape process of both homolytic bond photodissociation and bimolecular light induced electron transfer reactions. The review concludes with some key goals and directions for future research that promise to elevate this very vibrant field to even greater heights.more » « less
-
Significance Metabolic engineering benefits from the tunable and tightly controlled transformations afforded by biological systems. However, these reactions have generally been limited to naturally occurring pathways and products. In this work, we coopt metabolic electron transfer fromShewanella oneidensisto control the activity of an exogenous metal catalyst in an abiotic reaction scheme: atom-transfer radical polymerization. In the presence ofS. oneidensis, polymerizations exhibited well-defined kinetics and yielded polymers with controlled molecular weights and low polydispersities. Additionally, polymerization activity was dependent on electroactive metabolism and specific electron transport proteins, both of which provide handles to control material synthesis. This work serves as a proof-of-principle toward expanding the scope of reactions available to metabolic engineers to include previously discovered transition-metal–catalyzed reactions.more » « less
- Free Publicly Accessible Full Text
-
Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/C9CY00938H
