A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Application In Synthesis of 3-Bromo-1,10-phenanthroline, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 66127-01-3, Name is 3-Bromo-1,10-phenanthroline, molecular formula is C12H7BrN2. In a Article, authors is Brodie, Craig R.，once mentioned of 66127-01-3
We report the synthesis, resolution and characterisation of a number of novel ruthenium(II) complexes. Four mononuclear complexes, [Ru(dpq) 2(3-Br-phen)]2+, [Ru(dpq)2(4-Cl-phen)] 2+, [Ru(dpq)2(5-Cl-phen)]2+ and [Ru(dpq) 2(phen)]2+ were synthesised (dpq = dipyrido[3,2-d: 2?,3?-f]quinoxaline, phen = 1,10-phenanthroline, 3-Br-phen = 3-bromo-1,10-phenanthroline, 4-Cl-phen = 4-chloro-1,10-phenanthroline, 5-Cl-phen = 5-chloro-1,10-phenanthroline). These complexes were resolved using the chiral TRISPHAT anion, [tris(tetrachlorocatecholato)phosphate(V)]-. Racemic mononuclear complexes were used in the synthesis of the racemic dinuclear complexes, [{Ru(dpq)2}2mu-(phen-n-SOS-n-phen)] 4+ (SOS = 2-mercaptoethyl ether, n = 3, 4 or 5). Resolved mononuclear complexes were used to synthesise stereoselectively the DeltaDelta- and LambdaLambda-enantiomers of their respective dinuclear complexes. All metal complexes were characterised by 1H NMR, ESI-MS, UV/Vis and luminescence spectroscopy. Resolved metal complexes were further characterised using CD spectroscopy and chiral 1H NMR titrations. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about is helpful to your research. Application In Synthesis of 3-Bromo-1,10-phenanthroline
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI