22844-32-2

Upstream product

• 186581-53-3 diazomethane 
• 54522-77-9 trans-β-(9-phenanthryl)acrylic acid 
• 4707-71-5 Phenanthrene-9-carboxaldehyde 
• 573-17-1 9-bromophenanthrene 
• 292638-85-8 acrylic acid methyl ester 

Relevant academic research and scientific papers

Synthesis and Immobilization of Metal Nanoparticles Using Photoactive Polymer-Decorated Zeolite L Crystals and Their Application in Catalysis

A facile route to generate Au and Pd nanoparticles (NPs) on zeolite L crystals decorated with photoactive polymer brushes is described. The polymers used in this approach serve a dual role: Upon irradiation with UV light, they release highly reducing ketyl radicals in a Norrish-Type-I reaction. These radicals serve as one electron donors to reduce metal salts to the corresponding metal NPs. At the same time the polymer shell stabilizes the in situ generated metal NPs. It is shown that the zeolite-polymer-NP composites can be used as recyclable catalysts for the oxidation of benzylic alcohols to aldehydes and the stereoselective semihydrogenation of alkynes to Z-alkenes. The polymer shell in these hybrid catalysts protects the NPs from aggregation and also alters their catalytic properties. (Figure presented.).

The [RPPhPd as a catalyst precursor for the heck cross-coupling reaction by in situ formation of stabilized Pd(0) nanoparticles

Pd(II) anionic, square planar complexes of the type [RPPhPdl, where X = Cl, Br, have been applied for the first time as a catalyst precursor for the Heck reaction carried out in DMF at 140 °C. The highest yield was obtained for the most reducible ones, [MePPhPdrl, in DMF in the presence of NaHCOas a base. It was found that during the reaction, phosphonium halide stabilized Pd(0) nanoparticles of about 10 nm, which have been formed in situ from the palladium(II) precursor and Pd(0) colloidal nanoparticles acts as the reservoir for Pd(II) species via activation of the metal surface through the oxidative addition of aryl halides. Georg Thieme Verlag Stuttgart New York.

Accelerated Heck reaction using ortho-palladated complex in a nonaqueous ionic liquid with controlled microwave heating

The activity of {Pd[C6H2(CH2CH 2NH2)-(OMe)2,3,4] (μ-Br)}2 complex was investigated in the Heck-Mizoroki C-C cross-coupling reaction under conventional heating and microwave irradiation conditions in molten salt tetrabutylammonium bromide as the solvent and promoter at 130 °C. This complex in these conditions is an active and efficient catalyst for the Heck reaction of aryl iodides, bromides and even chlorides, and also arenesulfonyl chlorides. Copyright

Application of dimeric cyclopalladated complex of tribenzylamine as an efficient catalyst in the Heck cross-coupling reaction

The activity of [Pd{C6H4(CH2N(CH 2Ph)2)} (μ-Br)]2 complex was investigated in the Heck-Mizoroki C-C cross-coupling reaction. This complex is an active and efficient catalyst for the Heck reaction of aryl iodides, bromides and even chlorides and also arenesulfonyl chlorides. The cross-coupled products were produced in excellent yields in short reaction time using a catalytic amount of [Pd{C6H4(CH2N(CH2Ph)2) (μ-Br)]2 complex in NMP at 130 °C.

Heck coupling reaction using monomeric ortho-palladated complex of 4-methoxy- benzoylmethylenetriphenylphosphorane under microwave irradiation

The activity of [Pd(C6H4CH2 NH 2-κ2-C-N)PPh3MOBPPY]OTf complex, A (MOBPPY = 4-methoxybenzoylmethylenetriphenyl- phosphoraneylide), was investigated in the Heck-Mizoroki C-C cross-coupling reaction under conventional heating and microwave irradiation conditions. The complex is an active and efficient catalyst for the Heck reaction of aryl halides. The yields were excellent using a catalytic amount of [Pd(C6H4CH 2 NH2-κ2-C-N)PPh3MOBPPY]OTf complex in N-methyl-2-pyrrolidinone (NMP) at 130 °C and 600 W. In comparison to conventional heating conditions, the reactions under microwave irradiation gave higher yields in shorter reaction times. Copyright