Reference of 148332-36-9, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 148332-36-9, Name is [2,2′:6′,2”-Terpyridine]-4′-carboxylic acid, molecular formula is C16H11N3O2. In a Article，once mentioned of 148332-36-9
Energy transfer in rhodium?ruthenium dimer-of-dimer assemblies
A synthetic route to linear pairs of dirhodium tetracarboxylate ?paddlewheel? dimers bridged by Ru(II) complexes of tridentate ?terpyridine-like? ligands is presented. Three dimer-of-dimer assemblies were synthesized as well as two monomer-of-dimer assemblies. A bis(4?-(4-carboxyphenyl)-terpyridine)Ru(II) complex spanning two dirhodium dimers displays a 26 A separation between the dimers in its X-ray crystal structure. Increased electronic interaction is found for the dimer of dimers without the phenyl groups using bis(4?-(4-carboxy)-terpyridine)Ru(II) as the bridging complex. The addition of one or two of the dirhodium dimers to the Ru photosensitizer leads to an increase in the molar absorptivity in an additive fashion. In the emission profile, the dirhodium tetracarboxylates act as energy transfer traps as the Ru based3MLCT (MLCT = metal-to-ligand charge-transfer) excited state is efficiently quenched by energy transfer from the Ru core to the dirhodium periphery, both at room temperature and low (77 K) temperature.
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.Reference of 148332-36-9, you can also check out more blogs about148332-36-9
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI