1435520-65-2

Usage

Uses

Used in Organic Synthesis:
Pd(dsbp)2 is used as a catalyst for various organic synthesis reactions, including cross-coupling reactions and C-H activation. Its high catalytic activity and selectivity make it a valuable tool in the field of organometallic chemistry and catalysis.
Used in Pharmaceutical Industry:
Pd(dsbp)2 is used as a catalyst in the synthesis of pharmaceutical compounds, enabling the efficient production of complex molecules with high selectivity and yield.
Used in Chemical Research:
Pd(dsbp)2 is employed as a catalyst in academic and industrial research settings, facilitating the development of new synthetic methods and the discovery of novel chemical compounds.
Used in Material Science:
Pd(dsbp)2 is utilized as a catalyst in the synthesis of advanced materials, such as polymers, nanoparticles, and other functional materials, contributing to the development of new technologies and applications in various industries.

Upstream product

• 53189-26-7 palladium(II) acetate trimer 
• 1445085-50-6 [1,1'-biphenyl]-2-aminium methanesulfonate 
• 127384-48-9 palladium acetate nitrite 
• 90-41-5 2-phenylaniline 
• 3375-31-3 palladium diacetate 

Downstream Products

• 1445085-92-6 C₂₂H₃₂NP*C₁₃H₁₃NO₃PdS 
• 1445085-97-1 C₃₉H₃₂OP₂*C₁₃H₁₃NO₃PdS 
• 1445086-02-1 C₁₈H₁₅P*C₁₃H₁₃NO₃PdS 
• 1445086-07-6 C₂₁H₂₁P*C₁₃H₁₃NO₃PdS 
• 1445086-12-3 C₁₈H₃₃P*C₁₃H₁₃NO₃PdS 
• 1445086-17-8 C₁₂H₂₇P*C₁₃H₁₃NO₃PdS 
• 1445086-28-1 C₃₄H₂₈FeP₂*C₁₃H₁₃NO₃PdS 
• 1445085-55-1 ((2-dicyclohexylphosphino-2',4’,6’-triisopropyl-1,1‘-biphenyl)[2-(2‘-amino-1,1‘-biphenyl)]palladium(II) methanesulfonate) 
• 1445085-66-4 C₄₁H₅₅NPPd⁽¹⁺⁾*CH₃O₃S^(1-) 
• 1445085-77-7 C₃₀H₄₃O₂P*C₁₃H₁₃NO₃PdS 
• 1445085-82-4 C₂₆H₃₅O₂P*C₁₃H₁₃NO₃PdS 
• 1445085-87-9 C₂₆H₃₆NP*C₁₃H₁₃NO₃PdS 

Relevant academic research and scientific papers

Can Palladium Acetate Lose Its "saltiness"? Catalytic Activities of the Impurities in Palladium Acetate

Commercially available palladium acetate often contains two major impurities, whose presence can impact the overall catalytic efficacy. This systematic study provides a comparison of the differences in catalytic activity of pure palladium acetate, Pd3(OAc)6, with the two impurities: Pd3(OAc)5(NO2) and polymeric [Pd(OAc)2]n in a variety of cross-coupling reactions. The solid state 13C NMR spectra of all three compounds in conjunction with DFT calculations confirm their reported geometries.

Design and preparation of new palladium precatalysts for C-C and C-N cross-coupling reactions

A series of easily prepared, phosphine-ligated palladium precatalysts based on the 2-aminobiphenyl scaffold have been prepared. The role of the precatalyst-associated labile halide (or pseudohalide) in the formation and stability of the palladacycle has been examined. It was found that replacing the chloride in the previous version of the precatalyst with a mesylate leads to a new class of precatalysts with improved solution stability and that are readily prepared from a wider range of phosphine ligands. The differences between the previous version of precatalyst and that reported here are explored. In addition, the reactivity of the latter is examined in a range of C-C and C-N bond forming reactions.