Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Application In Synthesis of (2,2′-Bipyridine)dichloropalladium(II). Introducing a new discovery about 14871-92-2, Name is (2,2′-Bipyridine)dichloropalladium(II)
The organometallic osmium(VI) hydroxo compounds [N(n-Bu) 4][Os(N)(CH2SiMe3)3(OH)], cis and trans isomers of [N(n-Bu)4][Os(N)(CH2SiMe 3)2(OH)2], result from the substitution of chloride for hydroxide ligands in precursor compounds. Depending on the molecular structure, these compounds behave as nucleophiles, Bronsted bases, or Lewis bases in their reactions. One of these, [N(n-Bu) 4][cis-Os(N)-(CH2SiMe3)2(OH) 2], reacts readily with CO2 to produce the carbonate compound [N(n-Bu)4][Os(N)(CH2-SiMe3) 2(CO3)]. The other isomer, [N(n-Bu)4][trans- Os(N)(CH2SiMe3)2(OH)2], reacts with CO2 to slowly form the same carbonate compound. It is protonated by other acids to give the neutral hydroxo dimer {Os(N)(CH2SiMe 3)2(mu-OH)}2. The and isomer of {Os(N)(CH2SiMe3)2(mu-OH)}2 reacts with Pd(bpy)-(OSiMe3)2 to produce the coordinatively unsaturated, heterometallic complex {Os(N)(CH2SiMe3) 2}2(mu3-O)2Pd(bpy). The molecular structure of this complex shows two square-pyramidal osmium groups with an anti arrangement of the apical nitrido ligand and a square-planar palladium(II) center, all connected by the triply bridging oxo groups.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of (2,2′-Bipyridine)dichloropalladium(II), you can also check out more blogs about14871-92-2
Reference：
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method