Electric Literature of 13104-56-8, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.13104-56-8, Name is 4′-(4-Methoxyphenyl)-2,2′:6′,2”-terpyridine, molecular formula is C22H17N3O. In a article，once mentioned of 13104-56-8
Rhodium-terpyridine catalyzed redox-neutral depolymerization of lignin in water
Simple rhodium terpyridine complexes were found to be suitable catalysts for the redox neutral cleavage of lignin in water. Apart from cleaving lignin model compounds into ketones and phenols, the catalytic system could also be applied to depolymerize dioxasolv lignin and lignocellulose, affording aromatic ketones as the major monomer products. The (hemi)cellulose components in the lignocellulose sample remain almost intact during lignin depolymerization, providing an example of a “lignin-first” process under mild conditions. Mechanistic studies suggest that the reaction proceeds via a rhodium catalyzed hydrogen autotransfer process.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 13104-56-8, and how the biochemistry of the body works.Electric Literature of 13104-56-8
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI