Low Catalyst Loading Research Articles

Polyalkenamers as Drop-In Additives for Ring-Opening Metathesis Polymerization: A Promising Upcycling Paradigm.

We report a distinct strategy to upcycle waste polyalkenamers such as polybutadiene into new, performance-advantaged materials by using them as drop-in additives for ring-opening metathesis polymerization (ROMP). The polyalkenamers serve as competent chain-transfer agents in ROMPs of common classes of cyclic olefin monomers, facilitating good molecular weight control, allowing low Ru catalyst loadings, and enabling efficient incorporation of the polyalkenamer into the synthesized polymeric material. We successfully demonstrate ROMP using model polyalkenamers and translate these learnings to leverage commercial polybutadiene and acrylonitrile butadiene styrene (ABS) as chain transfer agents for ROMP copolymerizations. Critically, our strategy is shown to be highly efficient and operationally simple, quantitatively incorporating the polyalkenamer and inheriting aspects of its thermomechanical performance. Our results highlight a promising pathway for the upcycling of polyalkenamers and provide an alternative to existing deconstruction and functional upcycling strategies.

In situ decorated pd NPs on Triazin-encapsulated Fe3O4/SiO2-NH2 as magnetic catalyst for the synthesis of diaryl ethers and oxidation of sulfides

This article is devoted to the synthesis of a new magnetic palladium catalyst that has been immobilized on A-TT-Pd coated-magnetic Fe3O4 nanoparticles. Such surface functionalization of magnetic particles is a promising method to bridge the gap between heterogeneous and homogeneous catalysis approaches. The structure, morphology, and physicochemical properties of the particles were characterized through different analytical techniques, including TEM, FT-IR, XRD, SEM, EDS, TGA-DTG, ICP, and VSM techniques. The obtained Fe3O4@SiO2@A-TT-Pd performance can show excellent catalytic activity for the synthesis of diaryl ethers and oxidation of sulfides, and the corresponding products were obtained with high yields. The advantages of this catalyst include a simple test method, green reaction conditions, no use of dangerous solvents, short reaction time, low catalyst loading, and reusability. Also, the nanocatalyst was easily separated from the reaction mixture with the help of a bar magnet and recovered and reused several times without loss of stability and activity.

NiII, PdII and PtII pincer complexes of 2-(diphenylphosphanyl)-N-(2-(diphenyl-phosphanyl)benzyl)benzamide: synthesis, reactivity and catalytic studies.

In this article, the synthesis of bis(phosphine), o-Ph2PC6H4C(O)N(H)CH2C6H4PPh2-o (1) (hereafter referred to as "PCNHCP" and its anionic form as "PCNCP") and its group 10 metal chemistry and catalytic studies are described. PCNHCP (1) on reaction with NiCl2(DME) and PdCl2(COD) afforded pincer complexes, [MCl{(PCNCP)κ3-P,N,P}] (M = Ni, 2; Pd, 3). A similar reaction of 1 with PtCl2(COD) yielded a chelate complex, [PtCl2{(PCNHCP)κ2-P,P}] (4), which on further treatment with LiHMDS produced the 1,2-azaphospholene-phosphine complex, [PtCl(Ph){(o-P(Ph)C6H4CONCH2C6H4PPh2-o)κ2-P,P}] (5) via P-C/P-N bond metathesis. Passing dry HCl gas through the solution of 5 resulted in benzene elimination to form [PtCl2{(o-P(Ph)C6H4CONCH2C6H4PPh2-o)κ2-P,P}] (6). Treatment of 1 with PtCl2(COD) and Pt(Cl)(Me)(COD) in the presence of a base resulted in pincer complexes [PtX{(PCNCP)κ3-P,N,P}] (X = Cl, 7; Me, 8). Nickel complex 2 catalyzed the Suzuki-Miyaura cross coupling reaction between bromobenzene and phenyl boronic acid to give the corresponding biphenyls in good yield. The platinum complex 5 showed good catalytic activity towards regio- and stereoselective hydroboration of terminal alkynes. Both the catalytic reactions were performed under mild reaction conditions with a very low catalyst loading.

Photoreductive N-N Homocoupling Catalyzed by a Superphotoreductant.

Azines are valuable synthons or target molecules in organic synthesis. In this work, we report that CBZ6 could work as a photoreductive catalyst for the N-N homocoupling of oximes in high efficiency. This therefore enabled convenient access to a large variety of azines from the corresponding aryl and alkyl ketones, as well as aryl aldehydes in up to 99% yield. 2,4-Dinitrophenoxyl was used as the recyclable auxiliary and the CBZ6 photocatalyst could also be recycled. These together with the low catalyst loading (2 mol % of CBZ6), the short reaction time (4 h), and the nontoxic DMSO solvent make the current process a sustainable and practical alternative to the classic methods.

Intermolecular Gold‐Catalyzed Nitrene Transfer Employing Aryl Azides: An Access to 7‐Functionalized 2‐Aminoindoles

AbstractWe report on intermolecular gold‐catalyzed nitrene transfer, utilizing o‐functionalized aryl azides as nitrene transfer reagents. This catalytic reaction provides a modular route to 7‐functionalized 2‐aminoindoles. Due to the optimized reaction conditions (toluene, 80–100 °C), a variety of functional substituents proved compatible (36 examples; yields up to 98%). The reaction can be performed using both homogeneous and heterogeneous catalytic variants with a low catalyst loading (1 mol %). The synthetic potential of the obtained products was illustrated by post‐modifications of the indole backbone and peripheral substituents. A plausible reaction mechanism includes the generation of intermediate α‐imino carbenes directly from the o‐functionalized aryl azides or other nitrene sources, such as anthranils or benzofuroxans, which form during the reaction in the cases of the specific aryls.

“One‐Stone, Two‐Birds”: Zinc‐Rich Metal–Organic Frameworks as Precursors for High‐Entropy Zn‐Air Battery Electrocatalysts with Hierarchical Pore Structures

AbstractThe active sites of inexpensive transition metal electrocatalysts are sparse and singular, thus high‐entropy alloys composed of non‐precious metals have attracted considerable attention due to their multi‐component synergistic effects. However, the facile synthesis of high‐entropy alloy composites remains a challenge. Herein, we report a “one‐stone, two‐birds” method utilizing zinc (Zn)‐rich metal–organic frameworks as precursors, by virtue of the low boiling point of Zn (907 °C) and its high volatility in alloys, high‐entropy alloy carbon nanocomposite with a layered pore structure was ultimately synthesized. The experimental results demonstrate that the volatilization of zinc can prevent metal agglomeration and contribute to the formation of uniformly dispersed high‐entropy alloy nanoparticles at slower pyrolysis and cooling rates. Simultaneously, the volatilization of Zn plays a crucial role in creating the hierarchically porous structure. Compared to the zinc‐free HEA/NC‐1, the HEA/NC‐5 derived from the precursor containing 0.8 Zn exhibit massive micropores and mesopores. The resulting nanocomposites represent a synergistic effect between highly dispersed metal catalytic centers and hierarchical adsorption sites, thus achieving excellent electrocatalytic oxygen reduction performance with low catalyst loading compared to commercial Pt/C. This convenient zinc‐rich precursor method can be extended to the production of more high‐entropy alloys and various application fields.

"One-Stone, Two-Birds": Zinc-Rich Metal-Organic Frameworks as Precursors for High-Entropy Zn-Air Battery Electrocatalysts with Hierarchical Pore Structures.

The active sites of inexpensive transition metal electrocatalysts are sparse and singular, thus high-entropy alloys composed of non-precious metals have attracted considerable attention due to their multi-component synergistic effects. However, the facile synthesis of high-entropy alloy composites remains a challenge. Herein, we report a "one-stone, two-birds" method utilizing zinc (Zn)-rich metal-organic frameworks as precursors, by virtue of the low boiling point of Zn (907 °C) and its high volatility in alloys, high-entropy alloy carbon nanocomposite with a layered pore structure was ultimately synthesized. The experimental results demonstrate that the volatilization of zinc can prevent metal agglomeration and contribute to the formation of uniformly dispersed high-entropy alloy nanoparticles at slower pyrolysis and cooling rates. Simultaneously, the volatilization of Zn plays a crucial role in creating the hierarchically porous structure. Compared to the zinc-free HEA/NC-1, the HEA/NC-5 derived from the precursor containing 0.8 Zn exhibit massive micropores and mesopores. The resulting nanocomposites represent a synergistic effect between highly dispersed metal catalytic centers and hierarchical adsorption sites, thus achieving excellent electrocatalytic oxygen reduction performance with low catalyst loading compared to commercial Pt/C. This convenient zinc-rich precursor method can be extended to the production of more high-entropy alloys and various application fields.

Organophotocatalytic Regioselective Silylation/Germylation and Cascade Cyclization of N-Alkenyl α-CF3 Acrylamides: Access to Densely Functionalized 4-Pyrrolin-2-ones.

We report an organophotoredox-catalyzed silylation/germylation cascade cyclization of N-alkenyl α-CF3 acrylamides under mild conditions. N-Aminopyridinium salts act as hydrogen atom transfer reagents under photoredox catalysis in the generation of silyl and germyl radicals. An array of silyl- and germyl-substituted 3-CF3-4-pyrrolin-2-one derivatives were constructed in a shorter reaction time with low catalyst loading in good to excellent yields at room temperature. Importantly, this protocol is amenable to the late-stage diversification of bioactive molecules, as well as to large-scale synthesis.

Ruthenium-Catalyzed Synthesis of 2-Pyrazolines via Acceptorless Dehydrogenative Coupling of Allylic Alcohols with Hydrazines.

Described herein is the synthesis of 2-pyrazolines via acceptorless dehydrogenative coupling of allylic alcohols with hydrazines based on a Ru3(CO)12/NHC-phosphine-phosphine ligand L catalytic system. The reaction not only exhibits low catalyst loading (only 0.3 mol %), wide substrate scope, good to excellent yields, and high selectivity but also omits the use of sacrificial hydrogen acceptor with only H2 and H2O as byproducts, making the reaction green and atom-economical.

Photooxidation of Toluene Derivatives under HAT and ROS Synergy.

The valorization of toluene offers a dual solution by addressing its environmental impact while also facilitating the synthesis of a diverse array of valuable fine chemicals and pharmaceutical intermediates, thus ensuring both ecological sustainability and economic viability. We report herein a synergistic approach that harmonizes hydrogen atom transfer (HAT) process with the generation of reactive oxygen species (ROS) under mild condition and low catalyst loading, which enables the efficient synthesis of a broad spectrum of esteemed benzoic acid derivatives and aryl ketones through the photocatalytic oxidation of toluene derivatives. Mechanistic elucidation reveals that the HAT reagent anthraquinone has both the capabilities to abstract hydrogen atoms and the ability to generate singlet oxygen 1O2 during energy transfer with triplet oxygen 3O2, and the combination of these two potencies significantly improves the catalytic efficiency of the reaction. This study not only introduces the amalgamation of HAT with ROS generation but also delineates a systematic approach for the selection of HAT reagents with energy transfer proficiency for ROS generation in catalytic oxidation reactions.

Photocatalytic Cascade Trifluoromethylation/Cyclization : Selective Synthesis of Trifluoroethylated Benzopyran and Benzopyranone Derivatives

We have realized the photocatalytic radical cascade cyclization reaction, enabling the one‐step synthesis of rare trifluoroethyl benzopyran derivatives with a wide variety of structures and excellent yields. Furthermore, the approach exhibits low catalyst load, strong regional control and wide applicability under mild conditions. The selectivity of this transformation is influenced by the length of the carbon chain of the benzaldehyde, as demonstrated by the density functional theory calculations. Additionally, scaling up the photocatalytic process can be easily accomplished.

Iodine-Catalyzed Carbonyl-Alkyne Metathesis Reactions.

The reaction between aldehydes or ketones and alkynes-the carbonyl-alkyne metathesis-constitutes a very useful strategy for the synthesis of α,β-unsaturated carbonyls. We now demonstrate that iodine is a highly efficient catalyst for both the intra- and intermolecular metathesis reaction in very small concentrations (0.1-1 mol %). Our protocol outperforms other catalytic systems, is operationally very simple, cheap, metal-free, and tolerates a large variety of functional groups (e. g., -CN, -CO2Me, -Br, -OH) at very low catalyst loadings. We can furthermore show that iodine-catalyzed carbonyl-alkyne metatheses can be combined with other iodine-catalyzed reactions in one-pot procedures to afford larger and more complex molecular structures. Finally, our mechanistic studies indicate that the iodonium ion is the active catalyst under the reaction conditions.

ATRP with ppb Concentrations of Photocatalysts.

In atom transfer radical polymerization (ATRP), dormant alkyl halides are intermittently activated to form growing radicals in the presence of a CuI/L/X-CuII/L (activator/deactivator) catalytic system. Recently developed very active copper complexes could decrease the catalyst concentration to ppm level. However, unavoidable radical termination results in irreversible oxidation of the activator to the deactivator species, leading to limited monomer conversions. Therefore, successful ATRP at a low catalyst loading requires continuous regeneration of the activators. Such a regenerative ATRP can be performed with various reducing agents under milder reaction conditions and with catalyst concentrations diminished in comparison to conventional ATRP. Photoinduced ATRP (PhotoATRP) is one of the most efficient methods of activator regeneration. It initially employed UV irradiation to reduce the air-stable excited X-CuII/L deactivators to the activators in the presence of sacrificial electron donors. Photocatalysts (PCs) can be excited after absorbing light at longer wavelengths and, due to their favorable redox potentials, can reduce X-CuII/L to CuI/L. Herein, we present the application of three commercially available xanthene dyes as ATRP PCs: rose bengal (RB), rhodamine B (RD), and rhodamine 6G (RD-6G). Even at very low Cu catalyst concentrations (50 ppm), they successfully controlled PhotoATRP. Well-defined polymers with preserved livingness were prepared under green LED irradiation, with subppm concentrations ([PC] ≥ 10 ppb) of RB and RD-6G or 5 ppm of RD. Interestingly, these PCs efficiently controlled ATRP at wavelengths longer than their absorption maxima but required higher loadings. Polymerizations proceeded with high initiation efficiencies, yielding polymers with narrow molecular weight distributions and high chain-end fidelity. UV-vis, fluorescence, and laser flash photolysis studies helped to elucidate the mechanism of the processes involved in the dual-catalytic systems, comprising parts per million of Cu complexes and parts per billion of PCs.

Ni‐Catalyzed [2+2+2] Cycloaddition of Alkynes to Form Arenes and Pyridines at Low Catalyst Loadings

Ni‐Catalyzed [2+2+2] Cycloaddition of Alkynes to Form Arenes and Pyridines at Low Catalyst Loadings

Divergent Annulations of 5,6‐Dihydro‐4H‐1,2‐Oxazine N‐Oxides and Enol Diazoacetates for the Switchable Chemoselective Synthesis of Fused 1,2‐Oxazine Derivatives

Reactions of 5,6‐dihydro‐4H‐1,2‐oxazine N‐oxides with enol diazoacetates were studied. A particular reaction path depends on the amount of catalyst and the order of the addition of the substrates. Use of Rh2(Oct)4 (2 mol.%) leads to chemoselective [3+3]‐annulation producing 1,2‐oxazine‐fused 1,2‐oxazine derivatives. With lower catalyst loadings (0.03 mol.%) enol diazoacetates are converted to cyclopropene derivatives, which in situ react with 1,2‐oxazine N‐oxides via tandem [3+2]‐cycloaddition‐rearrangement producing oxazine‐fused aziridines. Both transformations showed a wide substrate scope and produced target products with good yields and diastereoselectivity, thus allowing selective preparation of these rare heterocyclic systems. A mechanistic rationale for observed chemo‐ and stereo‐ selectivities was proposed.

Cooperative Diarylborinic Acid/Chloride-Catalyzed Formal SNi Reaction of cis-4-Hydroxymethyl-1,2-Cyclopentene Oxides.

A catalytic formal SNi reaction was designed to achieve stereoretentive products for cis-4-hydroxymethyl-1,2-cyclopentene oxides by using diarylborinic acid as a dual role catalyst and chloride as a catalytic transient nucleophile through a double-displacement mechanism. This reaction offers the advantages of a low catalyst loading of 0.1 mol % and wide substrate scope, even including N-substituents. The use of chiral boron acid as a catalyst for this reaction was also attempted.

Alkylaluminum Complexes Featuring Bridged Bis-Formylfluorenimide Ligands for Hydroboration of Aldehyde, Ketone, and Imines.

Three bis-formylfluorenimide ligands with different bridging groups were designed and synthesized, leading to the successful preparation of six novel alkylaluminum complexes through their reaction with alkylaluminum reagents (AlMe3 or AlEt3). Complexes 1 and 2 were obtained by the reaction of 1,2-propylene-bridged diamine (L1) with AlMe3 or AlEt3. By reacting 1,2-cyclohexylene-bridged diamine (L2) with AlMe3 or AlEt3 to obtain complexes 3 and 4. The above ligands formed a bidentate four-coordinate structure with alkylaluminum, which involved the elimination of one alkyl group as the ligand reacted with alkylaluminum. The complexes 5 and 6 were synthesized through the reaction of 1,2-phenylene-bridged diamine (L3) with AlEt3 in toluene or tetrahydrofuran. Notably, L3 exhibited unique reactivity compared with the other ligands, which formed a tridentate four-coordinated structure when reacting with alkylaluminum. The formation of the tridentate complex resulted from the introduction of a benzimidazole derivative or tetrahydrofuran (THF) molecule along with the elimination of two alkyl groups during its coordination with alkylaluminum. All complexes were characterized via 1H NMR, 13C NMR, and elemental analysis, with structural determination confirmed through X-ray. Furthermore, the catalytic activity in the hydroboration reaction of aldehyde, ketone, and imines was investigated with these complexes as catalysts. Among them, complex 1 demonstrated excellent catalytic performance (up to 99% yield) and broad substrate compatibility (more than 30 substrates) at low catalyst loading (1 mol %) under mild reaction conditions.

Expeditious and selective synthesis of 2,4,5-trialkyl-1H-imdazoles and benzimidazoles via multicomponent one-pot reaction catalyzed by Schiff base dioxomolybdenum(VI) complex

Imidazoles and benzimidazoles are privileged heterocyclic compounds that can be extensively found in medicinal and materials chemistry, however, the experimental procedures for their synthesis are limited to multicomponent condensation reactions and normally are strongly dependent upon the desired substitution pattern, consequently several procedures with different conditions and catalysts are available in literature. Accordingly, the development of synthetic methodologies to afford these compounds remains a very attractive research problem. In this regard, dioxomolybdenum based catalysts are emerging as versatile and non-expensive reagents for a myriad of chemically relevant transformations. Within this context, an expedient and efficient synthesis of 2,4,5-trialkyl-1H-imidazoles and benzimidazoles from a multicomponent one-pot condensation has been developed with a tridentate Schiff base dioxomolybdenum(VI) complex, resulting in an efficient, simple and readily available catalyst to promote the aforementioned reaction. This reaction offers advantages such as good to excellent yields, good selectivity of products, low catalyst loadings and simple reaction work-up.

Ag nanoparticles on arginine-cyanoguanidine functionalized magnetic g-C3N4: A catalyst for nitroaromatic hydrogenation and regioselective click reactions

This study describes the development of a novel hybrid nanocatalyst that was obtained by doping magnetic g-C3N4 with Ag nanoparticles and modifying it with arginine and cyanoguanidine (Ag@Fe3O4-g-C3N4-Arg-CG). Comprehensive characterization of the nanocatalyst using techniques such as FTIR, XRD, SEM, and TGA confirmed its structural and morphological properties. The catalytic efficiency of the synthesized nanostructure was evaluated in two key reactions: the reduction of nitroaromatic compounds and a click reaction for 1,2,3-triazole synthesis. The results demonstrate that Ag@Fe3O4-g-C3N4-Arg-CG effectively reduced various nitroaromatic compounds to substituted anilines at room temperature using NaBH4 as the reducing agent. Nitrobenzene reduction did not proceed in aprotic solvents such as acetonitrile, CH2Cl2, and dimethylformamide, whereas it exhibited a high reaction yield in protic solvents such as ethanol and water. The highest yield (100 %) was observed in water at 50 °C using H2O solvent. Additionally, the nanohybrid exhibited significant potential for “green” click chemistry by efficiently synthesizing 1,2,3-triazoles under mild conditions, with low catalyst loading. Its magnetic properties facilitated easy recovery, and the catalyst maintained high activity over six cycles, making it suitable for sustainable applications in organic transformations.

Ligand‐Controlled Regioselective Hydroacylation Reactions of Methylenecyclobutanes under Rhodium Catalysis

AbstractIn this study, we report a Rh(I)/dppf catalytic system that can tune the regioselectivity of methylenecyclobutanes. Under the optimal reaction conditions, a series of 1,3‐disubstituted cyclobutanes were prepared in high yields (up to 95%) with excellent regioselectivity (>20:1 r.r.). Scale‐up synthesis of the cyclobutane product at a low catalyst loading (2 mol%) demonstrates the robustness of this dppf‐controlled hydroacylation.