Pd EnCat™ 30 Recycling in Suzuki Cross-Coupling Reactions DOI Creative Commons
L. D’Andrea,

Casper Steinmann

Organics, Journal Year: 2024, Volume and Issue: 5(4), P. 443 - 449

Published: Oct. 22, 2024

Pd EnCat™ 30 is a palladium catalyst broadly used in several hydrogenation and cross-coupling reactions. It known for its numerous beneficial features, which include high-yielding performance, easy recovery, reusability. However, the available data regarding recyclability Suzuki coupling reactions are limited to few reaction cycles and, therefore, fail explore full potential. Our work focuses on investigating extent of reusability by measuring performance according isolated yields product. findings demonstrate that can be reused over minimum cycles, advantageous terms cost reduction more sustainable chemical production.

Language: Английский

A new Schiff‐base complex of palladium nanoparticles on modified boehmite with di(pyridin‐2‐yl)methanone as a robust, reusable, and selective nanocatalyst in the C‐C coupling reaction DOI
Bahman Tahmasbi,

Mitra Darabi,

Mohsen Nikoorazm

et al.

Applied Organometallic Chemistry, Journal Year: 2024, Volume and Issue: 38(3)

Published: Jan. 4, 2024

Boehmite is one of the stable phases alumina that easily available, and it also has a variety applications. Therefore in this work, for preparation AlOOH, Sodium hydroxide (NaOH) solutions was added to aluminum nitrate nonahydrate (Al(NO 3 ) .9H 2 O) solution. Then, surface AlOOH modified with (3‐aminopropyl)triethoxysilane (APTES), due high condensation hydroxyl groups on its surface. di(pyridin‐2‐yl)methanone (di(PM)) immobilized toward synthesis Schiff‐base (di(PM)@AlOOH) as heterogeneous ligand. Finally, palladium complex (Pd‐di(PM)@AlOOH) reusable, practical, novel nanocatalyst. Pd‐di(PM)@AlOOH characterized by thermogravimetric analysis (TGA) analysis, Fourier‐transform infrared spectroscopy (FT‐IR), transmission electron microscopy (TEM), scanning microscope (SEM) imaging, energy‐dispersive X‐ray (EDS) wavelength‐dispersive (WDX) inductively coupled plasma (ICP) analysis. After characterization Pd‐di(PM)@AlOOH, performance used highly stable, retrievable, hybrid organic–inorganic catalyst C‐C coupling Suzuki reaction. The hot filtration study revealed acts heterogeneously We found can be recycled five runs without leaching, studied test ICP

Language: Английский

Citations

17

Unlocking the Nucleophilic Functionalization Potential of a Natural Asphalt: Grafting a Pd(0)–Diethanolamine Complex as a Recyclable Catalyst for Upgrading Biaryl Synthesis DOI
Masoud Mohammadi, Mohammad Soleiman‐Beigi

Langmuir, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 2, 2025

This study introduces a novel method for functionalizing natural asphalt, presenting new opportunities upgrading asphaltenes from road to catalyst. The process utilizes metal-free sonobromination technique in acetic acid incorporate carbon-halogen substituents onto asphalt. These sites are then targeted by nucleophilic substitution with diethanolamine, followed complexation Pd(0) create unique palladium complex grafted stabilized serves as heterogeneous and recoverable catalyst the Suzuki reaction. facilitates reaction between aryl boronic acids various

Language: Английский

Citations

4

Cobalt Nanoprism with ppm Level of Palladium as a Synergistic Catalyst for Suzuki- Miyaura Reaction DOI
Mohammad Gholinejad,

Mahboobe Eskandari,

M. Sansano José

et al.

Journal of Molecular Structure, Journal Year: 2025, Volume and Issue: unknown, P. 141364 - 141364

Published: Jan. 1, 2025

Language: Английский

Citations

1

Recent Advances in Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions: Exploration of Catalytic Systems, Reaction Parameters, and Ligand Influences: A Review DOI
Dana A. Kader,

Mohammed Koksh Sidiq,

Salam Ghafour Taher

et al.

Journal of Organometallic Chemistry, Journal Year: 2025, Volume and Issue: unknown, P. 123569 - 123569

Published: Feb. 1, 2025

Language: Английский

Citations

1

Nanodiamond Supported Ultra-Small Palladium Nanoparticles as an Efficient Catalyst for Suzuki Cross-Coupling Reactions DOI Open Access

Radka Pocklanová,

Indrajeet R. Warkad, Robert Prucek

et al.

Catalysts, Journal Year: 2024, Volume and Issue: 14(1), P. 53 - 53

Published: Jan. 12, 2024

A nanocatalyst comprising ultra-small palladium nanoparticles supported on nanodiamonds (ultra-small Pd/rNDs) was fabricated via a reduction of (II) salt oxidized nanodiamond. The prepared catalyst characterized using XRD, XPS, ICP-MS, AAS, and TEM/HRTEM techniques, including STEM-EDS chemical mapping, which revealed that the modified material is combination reduced nanodiamond decorated with nanoparticles. as-prepared well-characterized Pd rNDs displayed superb catalytic activity for Suzuki–Miyaura cross-coupling reactions at low temperature without any toxic solvents, to obtain respective products in good-to-excellent yields (75–98%). easily separated from reaction solution reused four times loss or stability.

Language: Английский

Citations

6

Heterogeneous Catalysts for C–C Bond Formation Reactions DOI
Kusum K. Bania, Subir Biswas, Arpita Devi

et al.

Synlett, Journal Year: 2025, Volume and Issue: unknown

Published: April 9, 2025

Abstract Carbon–carbon (C–C) bond formation reactions have contributed significantly to the construction of numerous important molecules that in various dimensions. Heterogeneous catalysts are recyclable and can convert a chemical reaction with same affinity as homogeneous counterpart provide an economically viable path. This account, therefore, focuses on different types C–C triggered by transition metal supported mostly zeolite-Y few oxide nanocatalysts. The account comprises our recent works devoted performed such heterogeneous including photocatalysts. 1 Introduction 2 Biaryl Synthesis C–Cl Bond Activation 3 3,3′-Bis(indolyl)methanes 4 C2 Trimerization Indoles 5 Cross-Aldol Condensation Reaction 6 Friedel–Crafts Benzylation Naphthol Phenol 7 Oxidative Coupling Naphthols 8 Conclusion

Language: Английский

Citations

0

Sulfoxides as electrophilic substrates in cross-coupling reactions DOI
Rahadian Zainul, Bahaa Fadhil Hamzah, Hussein Ali Al‐Bahrani

et al.

Journal of Sulfur Chemistry, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 14

Published: Feb. 25, 2025

Language: Английский

Citations

0

A Palladium Thiolate-SNS Complex-Catalyst for Mizoroki-Heck Cross-Coupling DOI Creative Commons
Saeed Ataie,

Atousa Khanzadeh,

R. Tom Baker

et al.

Dalton Transactions, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Phosphine-free catalysts for the Mizoroki-Heck cross-coupling reaction offer significant advantages in terms of air and moisture stability. We synthesized two palladium(II) complexes featuring a thiolate-imine-thioether SNS pincer ligand: Pd(κ2-SNSMe)2 (Pd-1) PdI(κ3-SNSMe) (Pd-2). Their catalytic activities were compared, with Pd-2 demonstrating excellent reactivity at low catalyst loading 1.5 mol%, efficiently producing olefin products across various substrates within 5 hours. Conversely, Pd-1 showed no activity due to its isomerization Pd(II)-N2S2 complex via imine C-C bond formation elevated temperatures, which restricted access coordination sites necessary oxidative addition alkene coordination. Heating excess NEt3 affords Pd dithiolate tetramer, [Pd(μ-κ3-SNS)]4via selective C-S activation.

Language: Английский

Citations

0

Highly Dispersed Pd-Nanoparticles in Vanadium Oxide Supported Zeolite-Y for C-C Coupling Reaction through C-Cl Bond Activation DOI

Tonmoy J. Bora,

Nand Kishor Gour, Lakshi Saikia

et al.

Applied Catalysis A General, Journal Year: 2024, Volume and Issue: unknown, P. 120053 - 120053

Published: Dec. 1, 2024

Language: Английский

Citations

1

Hyper-Cross-Linked Pyridine-Functionalized Bis(imino)acenaphthene-N-heterocyclic Carbene (BIAN-NHC) Palladium Catalysts for Superior Suzuki–Miyaura and Buchwald–Hartwig Coupling Reactions DOI

Mengjie Peng,

Hui Gao, Yanlong Gu

et al.

ACS Applied Polymer Materials, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 2, 2024

The design and synthesis of a series palladium-loaded hyper-cross-linked polymer (HCP) catalysts, demonstrating high catalytic activity excellent cycling stability in Suzuki–Miyaura Buchwald–Hartwig coupling reactions is reported. By employing pyridine-functionalized BIAN-NHC as the building unit, HCPs with rich hierarchical pore structures surface areas were prepared. Notably, HCP-BIAN-Pd-2 exhibited superior achieved 99% yield less reactive benzyl chloride, maintaining 95% even after 10 cycles. This study addresses issues cost, toxicity, recyclability associated traditional homogeneous palladium significantly enhancing by selectively introducing ligands. These findings highlight immense potential these catalysts for large-scale production practical applications, underscoring their significant implications field heterogeneous catalysis.

Language: Английский

Citations

1