23523-32-2Relevant articles and documents
Synthetic access to a phosphorescent non-palindromic pincer complex of palladium by a double oxidative addition-comproportionation sequence
Feuerstein, Wolfram,Breher, Frank
supporting information, p. 12589 - 12592 (2020/11/02)
A highly luminescent non-palindromic [(C^C^N)Pd] pincer complex forms upon reacting pyridine-substituted 2,2′-diiodo-biphenyl with [Pd(PPh3)4]. This case study establishes for the first time that the title compound is formed via a double oxidative addition-comproportionation sequence. DFT and TDDFT calculations complement mechanistic and photophysical characterizations.
Oxidative Mechanochemistry: Direct, Room-Temperature, Solvent-Free Conversion of Palladium and Gold Metals into Soluble Salts and Coordination Complexes
Do, Jean-Louis,Tan, Davin,Fri??i?, Tomislav
supporting information, p. 2667 - 2671 (2018/02/06)
Noble metals are valued, critical elements whose chemical activation or recycling is challenging, and traditionally requires high temperatures, strong acids or bases, or aggressive complexation agents. By using elementary palladium and gold, demonstrated here is the use of mechanochemistry for noble-metal activation and recycling by mild, clean, solvent-free, and room-temperature chemistry. The process leads to direct, efficient, one-pot conversion of the metals, including spent catalysts, into either simple water-soluble salts or metal–organic catalysts.
Catalytic Chemoselective and Stereoselective Semihydrogenation of Alkynes to E-Alkenes Using the Combination of Pd Catalyst and ZnI2
Maazaoui, Radhouan,Abderrahim, Raoudha,Chemla, Fabrice,Ferreira, Franck,Perez-Luna, Alejandro,Jackowski, Olivier
supporting information, p. 7544 - 7549 (2019/01/03)
An efficient E-selective semihydrogenation of internal alkynes was developed under low dihydrogen pressure and low reaction temperature from commercially available reagents: Cl2Pd(PPh3)2, Zn0, and ZnI2. Kinetic studies and control experiments underline the significant role of ZnI2 in this process under H2 atmosphere, establishing that the transformation involves syn-hydrogenation followed by isomerization. This simple and easy-to-handle system provides a route to E-alkenes under mild conditions.