Integrating hydrogen production with anodic selective oxidation of sulfides over a CoFe layered double hydroxide electrode

Replacing the sluggish oxygen evolution reaction (OER) with oxidation reactions for the synthesis of complex pharmaceutical molecules coupled with enhanced hydrogen evolution reaction (HER) is highly attractive, but it is rarely explored. Here, we report an electrochemical protocol for selective oxidation of sulfides to sulfoxides over a CoFe layered double hydroxide (CoFe-LDH) anode in an aqueous-MeCN electrolyte, coupled with 2-fold promoted cathodic H₂ productivity. This protocol displays high activity (85–96% yields), catalyst stability (10 cycles), and generality (12 examples) in selective sulfide oxidation. We demonstrate its applicability in the synthesis of four important pharmaceutical related sulfoxide compounds with scalability (up to 1.79 g). X-ray spectroscopy investigations reveal that the CoFe-LDH material evolved into amorphous CoFe-oxyhydroxide under catalytic conditions. This work may pave the way towards sustainable organic synthesis of valuable pharmaceuticals coupled with H₂ production.

Replacing anodic OER with selective sulfide oxidation produces sulfoxide-related pharmaceutical compounds over a CoFe-LDH catalyst with enhanced HER, providing a sustainable protocol for valuable pharmaceuticals synthesis without external oxidants.     

Regulating the Spin State of FeIII by Atomically Anchoring on Ultrathin Titanium Dioxide for Efficient Oxygen Evolution Electrocatalysis

Ferric oxides and (oxy)hydroxides, although plentiful and low‐cost, are rarely considered for oxygen evolution reaction (OER) owing to the too high spin state (e_g filling ca. 2.0) suppressing the bonding strength with reaction intermediates. Now, a facile adsorption–oxidation strategy is used to anchor Fe^III atomically on an ultrathin TiO₂ nanobelt to synergistically lower the spin state (e_g filling ca. 1.08) to enhance the adsorption with oxygen‐containing intermediates and improve the electro‐conductibility for lower ohmic loss. The electronic structure of the catalyst is predicted by DFT calculation and perfectly confirmed by experimental results. The catalyst exhibits superior performance for OER with overpotential 270 mV @10 mA cm^?2 and 376 mV @100 mA cm^?2 in alkaline solution, which is much better than IrO₂/C and RuO₂/C and is the best iron‐based OER catalyst free of active metals such as Ni, Co, or precious metals.     

Electrodeposition of (hydro)oxides for an oxygen evolution electrode

Electrochemical water splitting is a promising technology for hydrogen production and sustainable energy conversion, but the electrolyzers that are currently available do not have anodic electrodes that are robust enough and highly active for the oxygen evolution reaction (OER). Electrodeposition provides a feasible route for preparing freestanding OER electrodes with high active site utilization, fast mass transport and a simple fabrication process, which is highly attractive from both academic and commercial points of view. This minireview focuses on the recent electrodeposition strategies for metal (hydro)oxide design and water oxidation applications. First, the intrinsic advantages of electrodeposition in comparison with traditional technologies are introduced. Then, the unique properties and underlying principles of electrodeposited metal (hydro)oxides in the OER are unveiled. In parallel, illustrative examples of the latest advances in materials structural design, controllable synthesis, and mechanism understanding through the electrochemical synthesis of (hydro)oxides are presented. Finally, the latest representative OER mechanism and electrodeposition routes for OER catalysts are briefly overviewed. Such observations provide new insights into freestanding (hydro)oxides electrodes prepared via electrodeposition, which show significant practical application potential in water splitting devices. We hope that this review will provide inspiration for researchers and stimulate the development of water splitting technology.

This minireview looks at recent electrodeposition strategies for metal (hydro)oxide design and water oxidation applications, unveiling the unique properties and underlying principles of electrodeposited metal (hydro)oxides in the OER.     

Low‐Coordinate Iridium Oxide Confined on Graphitic Carbon Nitride for Highly Efficient Oxygen Evolution

Highly active and durable electrocatalysts for the oxygen evolution reaction (OER) is greatly desired. Iridium oxide/graphitic carbon nitride (IrO₂/GCN) heterostructures are designed with low‐coordinate IrO₂ nanoparticles (NPs) confined on superhydrophilic highly stable GCN nanosheets for efficient acidic OER. The GCN nanosheets not only ensure the homogeneous distribution and confinement of IrO₂ NPs but also endows the heterostructured catalyst system with a superhydrophilic surface, which can maximize the exposure of active sites and promotes mass diffusion. The coordination number of Ir atoms is decreased owing to the strong interaction between IrO₂ and GCN, leading to lattice strain and increment of electron density around Ir sites and hence modulating the attachment between the catalyst and reaction intermediates. The optimized IrO₂/GCN heterostructure delivers not only by far the highest mass activity among the reported IrO₂‐based catalysts but also decent durability.     

Charge accumulation kinetics in multi-redox molecular catalysts immobilised on TiO2

Multi-redox catalysis requires the accumulation of more than one charge carrier and is crucial for solar energy conversion into fuels and valuable chemicals. In photo(electro)chemical systems, however, the necessary accumulation of multiple, long-lived charges is challenged by recombination with their counterparts. Herein, we investigate charge accumulation in two model multi-redox molecular catalysts for proton and CO₂ reduction attached onto mesoporous TiO₂ electrodes. Transient absorption spectroscopy and spectroelectrochemical techniques have been employed to study the kinetics of photoinduced electron transfer from the TiO₂ to the molecular catalysts in acetonitrile, with triethanolamine as the hole scavenger. At high light intensities, we detect charge accumulation in the millisecond timescale in the form of multi-reduced species. The redox potentials of the catalysts and the capacity of TiO₂ to accumulate electrons play an essential role in the charge accumulation process at the molecular catalyst. Recombination of reduced species with valence band holes in TiO₂ is observed to be faster than microseconds, while electron transfer from multi-reduced species to the conduction band or the electrolyte occurs in the millisecond timescale. Finally, under light irradiation, we show how charge accumulation on the catalyst is regulated as a function of the applied bias and the excitation light intensity.

Using transient spectroelectrochemical techniques, we investigate multiply reduced states of molecular catalysts on titania photoelectrodes as a function of the applied bias and the light intensity.     

Enhanced ammonia oxidation on BDD induced by inhibition of oxygen evolution reaction

Electrochemical oxidation of ammonia (NH₃ and NH₄ ⁺ ) on boron-doped diamond (BDD) electrode was studied using differential electrochemical mass-spectrometry (DEMS) and chronoamperometry. Electro-oxidation of ammonia induces inhibition of the oxygen evolution reaction (OER) due to adsorption of the ammonia oxidation products on the BDD surface. The inhibition of the OER enhances ammonia electro-oxidation, which becomes the main reaction. The amino radicals, formed during ammonia oxidation, trigger a reaction chain in which molecular oxygen dissolved in solution is involved in the ammonia electro-oxidation. Nitrogen, nitrous oxide, and nitrogen dioxide were detected as the ammonia oxidation products, with nitrogen being the main gaseous product of the oxidation.     

Photocatalytic redox-neutral hydroxyalkylation of N-heteroaromatics with aldehydes

Hydroxyalkylation of N-heteroaromatics with aldehydes was achieved using a binary hybrid catalyst system comprising an acridinium photoredox catalyst and a thiophosphoric acid organocatalyst. The reaction proceeded through the following sequence: (1) photoredox-catalyzed single-electron oxidation of a thiophosphoric acid catalyst to generate a thiyl radical, (2) cleavage of the formyl C–H bond of the aldehyde substrates by a thiyl radical acting as a hydrogen atom transfer catalyst to generate acyl radicals, (3) Minisci-type addition of the resulting acyl radicals to N-heteroaromatics, and (4) a spin-center shift, photoredox-catalyzed single-electron reduction, and protonation to produce secondary alcohol products. This metal-free hybrid catalysis proceeded under mild conditions for a wide range of substrates, including isoquinolines, quinolines, and pyridines as N-heteroaromatics, as well as both aromatic and aliphatic aldehydes, and tolerated various functional groups. The reaction was applicable to late-stage derivatization of drugs and their leads.

Hydroxyalkylation of N-heteroaromatics with aldehydes was achieved using a binary hybrid catalyst system comprising an acridinium photoredox catalyst and a thiophosphoric acid organocatalyst.     

Effects of ruthenium hydride species on primary amine synthesis by direct amination of alcohols over a heterogeneous Ru catalyst

Heterogeneously catalysed synthesis of primary amines by direct amination of alcohols with ammonia has long been an elusive goal. In contrast to reported Ru-based catalytic systems, we report that Ru–MgO/TiO₂ acts as an effective heterogeneous catalyst for the direct amination of a variety of alcohols to primary amines at low temperatures of ca. 100 °C without the introduction of H₂ gas. The present system could be applied to a variety of alcohols and provides an efficient synthetic route for 2,5-bis(aminomethyl)furan (BAMF), an attention-getting biomonomer. The high catalytic performance can be rationalized by the reactivity tuning of Ru–H species using MgO. Spectroscopic measurements suggest that MgO enhances the reactivity of hydride species by electron donation from MgO to Ru.

Ru–MgO/TiO₂ exhibited high catalytic performance for direct amination of alcohols based on the acceleration effects of MgO.     

Electrochemical comparison between IrO2 prepared by thermal treatment of iridium metal and IrO2 prepared by thermal decomposition of H2IrCl6 solution

The surface redox activities, the oxygen evolution reaction (OER), the oxidation of formic acid (FA) and the anodic stability have been investigated and compared on IrO₂ electrodes prepared by two techniques: the thermal decomposition of H₂IrCl₆ precursor (TDIROF) and the thermal treatment of metallic iridium (TOIROF). It was found, that the surface redox activities involved on both IrO₂-based electrodes are similar. Concerning the oxygen evolution reaction and the oxidation of formic acid, both films show similar mechanism.The electrode stability measurements have shown that both films are not corroded under strong OER or organics oxidation conditions and therefore, to summarize, both IrO₂-based films exhibit similar electrochemical behaviours.     

Optimization of Active Sites via Crystal Phase,Composition, and Morphology for Efficient Low-Iridium Oxygen Evolution Catalysts

Reducing the amount of iridium in oxygen evolution electrocatalysts without compromising their catalytic performances is one of the major requirements in proton-exchange-membrane water electrolyzers. Herein, with the help of theoretical studies, we show that anatase-type TiO₂-IrO₂ solid solutions possess more active iridium catalytic sites for the oxygen evolution reaction (OER) than IrO₂, the benchmark OER catalyst. Note that the same is not observed for their rutile-type counterparts. However, owing to their thermodynamic metastability, anatase-type TiO₂-IrO₂ solid solutions are generally hard to synthesize. Our theoretical studies demonstrate that such catalytically active anatase-type solid-solution phases can be created in situ on the surfaces of readily available SrTiO₃-SrIrO₃ solid solutions during electrocatalysis in acidic solution as the solution can etch away Sr atoms. We experimentally show this with porous SrTiO₃-SrIrO₃ solid-solution nanotubes synthesized by a facile synthetic route that contain 56 % less iridium than IrO₂ yet show an order of magnitude higher apparent catalytic activity for OER in acidic solution.     

A diketopyrrolopyrrole dye-based dyad on a porous TiO2 photoanode for solar-driven water oxidation

Dye-sensitised photoanodes modified with a water oxidation catalyst allow for solar-driven O₂ evolution in photoelectrochemical cells. However, organic chromophores are generally considered unsuitable to drive the thermodynamically demanding water oxidation reaction, mainly due to their lack of stability upon photoexcitation. Here, the synthesis of a dyad photocatalyst (DPP-Ru) consisting of a diketopyrrolopyrrole chromophore (DPPdye) and ruthenium-based water oxidation catalyst (RuWOC) is described. The DPP-Ru dyad features a cyanoacrylic acid anchoring group for immobilisation on metal oxides, strong absorption in the visible region of the electromagnetic spectrum, and photoinduced hole transfer from the dye to the catalyst unit. Immobilisation of the dyad on a mesoporous TiO₂ scaffold was optimised, including the use of a TiCl₄ pretreatment method as well as employing chenodeoxycholic acid as a co-adsorbent, and the assembled dyad-sensitised photoanode achieved O₂ evolution using visible light (100 mW cm⁻², AM 1.5G, λ > 420 nm). An initial photocurrent of 140 μA cm⁻² was generated in aqueous electrolyte solution (pH 5.6) under an applied potential of +0.2 V vs. NHE. The production of O₂ has been confirmed by controlled potential electrolysis with a faradaic efficiency of 44%. This study demonstrates that metal-free dyes are suitable light absorbers in dyadic systems for the assembly of water oxidising photoanodes.

Construction of a water oxidising photoanode with an organic chromophore-catalyst dyad.     

Redox mediators accelerate electrochemically-driven solubility cycling of molecular transition metal complexes

The solubility of molecular transition metal complexes can vary widely across different redox states, leaving these compounds vulnerable to electron transfer-initiated heterogenization processes in which oxidation or reduction of the soluble form of the redox couple generates insoluble molecular deposits. These insoluble species can precipitate as suspended nanoparticles in solution or, under electrochemical conditions, as an electrode-adsorbed material. While this electrochemically-driven solubility cycling is technically reversible, the reverse electron transfer to regenerate the soluble redox couple state is a practical challenge if sluggish electron transfer kinetics result in a loss of electronic communication between the molecular deposits and the electrode. In this work, we present an example of this electrochemically-driven solubility cycling, report a novel strategy for catalytically enhancing the oxidation of the insoluble material using homogeneous redox mediators, and develop the theoretical framework for analysing and digitally simulating the action of a homogeneous catalyst on a heterogeneous substrate via cyclic voltammetry. First, a mix of electrochemical and spectroscopic methods are used to characterize an example of this electrochemically-driven solubility cycling which is based on the two-electron reduction of homogeneous [Ni(P^Ph₂N^Ph₂)₂(CH₃CN)]²⁺ (P^Ph₂N^Ph₂ = 1,3,5,7-tetraphenyl-1,5-diaza-3,7-diphosphacyclooctane). The limited solubility of the doubly-reduced product in acetonitrile leads to precipitation and deposition of molecular [Ni(P^Ph₂N^Ph₂)₂]. While direct oxidation of this heterogeneous [Ni(P^Ph₂N^Ph₂)₂] at the electrode surface is possible, this electron transfer is kinetically limited. We demonstrate how a freely diffusing redox mediator (ferrocene) – which shuttles electrons between the electrode and the molecular material – can be used to overcome these slow electron transfer kinetics, enabling catalytic regeneration of soluble [Ni(P^Ph₂N^Ph₂)₂]²⁺. Finally, mathematical models are developed that describe the current–potential response for a generic EC′ mechanism involving a homogeneous catalyst and surface-adsorbed substrate. This novel strategy has the potential to enable reversible redox chemistry for heterogeneous, molecular deposits that are adsorbed on the electrode or suspended as nanoparticles in solution.

We present an example of electrochemically-driven solubility cycling of a molecular transition metal complex and report a novel strategy for catalytically enhancing the oxidation of an insoluble material using homogeneous redox mediators.     

The dome of gold nanolized for catalysis

Gold is noble in bulk but turns out to be a superior catalyst at the nanoscale when supported on oxides, in particular titania. The critical thickness for activity, namely two-layer gold particles on titania, observed two decades ago represents one of the most influential mysteries in the recent history of heterogeneous catalysis. By developing a Bayesian optimization controlled global potential energy surface exploration tool with machine learning potential, here we determine the atomic structures of gold particles within ∼2 nm on a TiO₂ surface. We show that the smallest stable Au nanoparticle is Au₂₄ which is pinned on the oxygen-rich TiO₂ and exhibits an unprecedented dome architecture made by a single-layer Au sheet but with an apparent two-atomic-layer height. Importantly, this has the highest activity for CO oxidation at room temperature. The physical origin of the high activity is the outstanding electron storage ability of the nano-dome, which activates the lattice oxygen of the oxide. The determined CO oxidation mechanism, the simulated rate and the fitted apparent energy barrier are consistent with known experimental facts, providing key evidence for the presence of both the high-activity Au dome and the low-activity close-packed Au particles in real catalysts. The future direction for the preparation of active and stable Au-based catalysts is thus outlined.

The smallest stable Au particle Au₂₄O₄ on TiO₂ surface is determined by the machine learning assisted global optimization, exhibiting a dome architecture made by a single-layer sheet and the highest activity for CO oxidation at room temperature.     

Highly efficient ammonia synthesis at low temperature over a Ru–Co catalyst with dual atomically dispersed active centers

The desire for a carbon-free society and the continuously increasing demand for clean energy make it valuable to exploit green ammonia (NH₃) synthesis that proceeds via the electrolysis driven Haber–Bosch (eHB) process. The key for successful operation is to develop advanced catalysts that can operate under mild conditions with efficacy. The main bottleneck of NH₃ synthesis under mild conditions is the known scaling relation in which the feasibility of N₂ dissociative adsorption of a catalyst is inversely related to that of the desorption of surface N-containing intermediate species, which leads to the dilemma that NH₃ synthesis could not be catalyzed effectively under mild conditions. The present work offers a new strategy via introducing atomically dispersed Ru onto a single Co atom coordinated with pyrrolic N, which forms RuCo dual single-atom active sites. In this system the d-band centers of Ru and Co were both regulated to decouple the scaling relation. Detailed experimental and theoretical investigations demonstrate that the d-bands of Ru and Co both become narrow, and there is a significant overlapping of t_2g and e_g orbitals as well as the formation of a nearly uniform Co 3d ligand field, making the electronic structure of the Co atom resemble that of a “free-atom”. The “free-Co-atom” acts as a bridge to facilitate electron transfer from pyrrolic N to surface Ru single atoms, which enables the Ru atom to donate electrons to the antibonding π* orbitals of N₂, thus resulting in promoted N₂ adsorption and activation. Meanwhile, H₂ adsorbs dissociatively on the Co center to form a hydride, which can transfer to the Ru site to cause the hydrogenation of the activated N₂ to generate N₂H_x (x = 1–4) intermediates. The narrow d-band centers of this RuCo catalyst facilitate desorption of surface *NH₃ intermediates even at 50 °C. The cooperativity of the RuCo system decouples the sites for the activation of N₂ from those for the desorption of *NH₃ and *N₂H_x intermediates, giving rise to a favorable pathway for efficient NH₃ synthesis under mild conditions.

The desire for a carbon-free society and the continuously increasing demand for clean energy make it valuable to exploit green ammonia (NH₃) synthesis that proceeds via the electrolysis driven Haber–Bosch (eHB) process.     

Probing the electronic and mechanistic roles of the μ4-sulfur atom in a synthetic CuZ model system

Nitrous oxide (N₂O) contributes significantly to ozone layer depletion and is a potent greenhouse agent, motivating interest in the chemical details of biological N₂O fixation by nitrous oxide reductase (N₂OR) during bacterial denitrification. In this study, we report a combined experimental/computational study of a synthetic [4Cu:1S] cluster supported by N-donor ligands that can be considered the closest structural and functional mimic of the Cu_Z catalytic site in N₂OR reported to date. Quantitative N₂ measurements during synthetic N₂O reduction were used to determine reaction stoichiometry, which in turn was used as the basis for density functional theory (DFT) modeling of hypothetical reaction intermediates. The mechanism for N₂O reduction emerging from this computational modeling involves cooperative activation of N₂O across a Cu/S cluster edge. Direct interaction of the μ₄-S ligand with the N₂O substrate during coordination and N–O bond cleavage represents an unconventional mechanistic paradigm to be considered for the chemistry of Cu_Z and related metal–sulfur clusters. Consistent with hypothetical participation of the μ₄-S unit in two-electron reduction of N₂O, Cu K-edge and S K-edge X-ray absorption spectroscopy (XAS) reveal a high degree of participation by the μ₄-S in redox changes, with approximately 21% S 3p contribution to the redox-active molecular orbital in the highly covalent [4Cu:1S] core, compared to approximately 14% Cu 3d contribution per copper. The XAS data included in this study represent the first spectroscopic interrogation of multiple redox levels of a [4Cu:1S] cluster and show high fidelity to the biological Cu_Z site.

Experimental data and computational modeling indicates an active role for the bridging sulfide ligand in a synthetic Cu_Z model.     

Pseudo-potentiostatic electrolysis by potential buffering induced by the oxygen evolution reaction

A new approach is proposed in order to perform electrochemical oxidation of organics by working under galvanostatic conditions with the potential ‘buffered’ by the competing side reaction of oxygen evolution (OER). According to this process the working potential is fixed by the nature of electrode material and is buffered during organics oxidation by the side reaction of OER. This principle has been used for the selective oxidation of some model organic compounds on Ti/IrO₂ anode.     

A chiral cobalt(ii) complex catalyzed enantioselective aza-Piancatelli rearrangement/Diels–Alder cascade reaction

A chiral N,N′-dioxide/cobalt(ii) complex catalyzed highly diastereoselective and enantioselective tandem aza-Piancatelli rearrangement/intramolecular Diels–Alder reaction has been disclosed. Various valuable hexahydro-2a,5-epoxycyclopenta[cd]isoindoles bearing six contiguous stereocenters have been obtained in good yields with excellent diastereo- and enantio-selectivities from a wide range of both readily available 2-furylcarbinols and N-(furan-2-ylmethyl)anilines.

An asymmetric aza-Piancatelli rearrangement/Diels–Alder cascade reaction between 2-furylcarbinols and N-(furan-2-ylmethyl)anilines was realized by using a chiral N,N′-dioxide/cobalt(ii) complex catalyst.     

Water oxidation kinetics of nanoporous BiVO4 photoanodes functionalised with nickel/iron oxyhydroxide electrocatalysts

In this work, spectroelectrochemical techniques are employed to analyse the catalytic water oxidation performance of a series of three nickel/iron oxyhydroxide electrocatalysts deposited on FTO and BiVO₄, at neutral pH. Similar electrochemical water oxidation performance is observed for each of the FeOOH, Ni(Fe)OOH and FeOOHNiOOH electrocatalysts studied, which is found to result from a balance between degree of charge accumulation and rate of water oxidation. Once added onto BiVO₄ photoanodes, a large enhancement in the water oxidation photoelectrochemical performance is observed in comparison to the un-modified BiVO₄. To understand the origin of this enhancement, the films were evaluated through time-resolved optical spectroscopic techniques, allowing comparisons between electrochemical and photoelectrochemical water oxidation. For all three catalysts, fast hole transfer from BiVO₄ to the catalyst is observed in the transient absorption data. Using operando photoinduced absorption measurements, we find that water oxidation is driven by oxidised states within the catalyst layer, following hole transfer from BiVO₄. This charge transfer is correlated with a suppression of recombination losses which result in remarkably enhanced water oxidation performance relative to un-modified BiVO₄. Moreover, despite similar electrocatalytic behaviour of all three electrocatalysts, we show that variations in water oxidation performance observed among the BiVO₄/MOOH photoanodes stem from differences in photoelectrochemical and electrochemical charge accumulation in the catalyst layers. Under illumination, the amount of accumulated charge in the catalyst is driven by the injection of photogenerated holes from BiVO₄, which is further affected by the recombination loss at the BiVO₄/MOOH interface, and thus leads to deviations from their behaviour as standalone electrocatalysts.

Elucidating the role of charge accumulation and reaction kinetics in governing the performance of Ni/Fe oxyhydroxides as electrocatalysts and as co-catalysts on BiVO₄ photoanodes water oxidation.     

General and selective synthesis of primary amines using Ni-based homogeneous catalysts

The development of base metal catalysts for industrially relevant amination and hydrogenation reactions by applying abundant and atom economical reagents continues to be important for the cost-effective and sustainable synthesis of amines which represent highly essential chemicals. In particular, the synthesis of primary amines is of central importance because these compounds serve as key precursors and central intermediates to produce value-added fine and bulk chemicals as well as pharmaceuticals, agrochemicals and materials. Here we report a Ni-triphos complex as the first Ni-based homogeneous catalyst for both reductive amination of carbonyl compounds with ammonia and hydrogenation of nitroarenes to prepare all kinds of primary amines. Remarkably, this Ni-complex enabled the synthesis of functionalized and structurally diverse benzylic, heterocyclic and aliphatic linear and branched primary amines as well as aromatic primary amines starting from inexpensive and easily accessible carbonyl compounds (aldehydes and ketones) and nitroarenes using ammonia and molecular hydrogen. This Ni-catalyzed reductive amination methodology has been applied for the amination of more complex pharmaceuticals and steroid derivatives. Detailed DFT computations have been performed for the Ni-triphos based reductive amination reaction, and they revealed that the overall reaction has an inner-sphere mechanism with H₂ metathesis as the rate-determining step.

A Ni-triphos based homogeneous catalyst enabled the synthesis of all kinds of primary amines by reductive amination of carbonyl compounds with ammonia and hydrogenation of nitroarenes.     

N2Phos – an easily made,highly effective ligand designed for ppm level Pd-catalyzed Suzuki–Miyaura cross couplings in water

A new biaryl phosphine-containing ligand from an active palladium catalyst for ppm level Suzuki–Miyaura couplings, enabled by an aqueous micellar reaction medium. A wide array of functionalized substrates including aryl/heteroaryl bromides are amenable, as are, notably, chlorides. The catalytic system is both general and highly effective at low palladium loadings (1000–2500 ppm or 0.10–0.25 mol%). Density functional theory calculations suggest that greater steric congestion in N₂Phos induces increased steric crowding around the Pd center, helping to destabilize the 2 : 1 ligand–Pd(0) complex more for N₂Phos than for EvanPhos (and less bulky ligands), and thereby favoring formation of the 1 : 1 ligand–Pd^o complex that is more reactive in oxidative addition to aryl chlorides.

A new, biaryl phosphine-containing ligand, N₂Phos, forms a 1 : 1 complex with Pd resulting in an active catalyst at the ppm level for Suzuki–Miyaura couplings in water, enabled by an aqueous micellar medium. Notably, aryl chlorides are shown to be amenable substrates.