Simple exploration of N-Cyclohexylmaleimide

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One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 1631-25-0, Name is N-Cyclohexylmaleimide, formurla is C10H13NO2. In a document, author is Moya, Sergio A., introducing its new discovery. Safety of N-Cyclohexylmaleimide.

Synthesis and characterization of new complexes of the type [Ru(CO)(2)Cl-2 (2-phenyl-1,8-naphthyridine-kN) (2-phenyl-1,8-naphthyridine-kN ‘)]. Preliminary applications in homogeneous catalysis

Novel ruthenium (II) complexes were prepared containing 2-phenyl-1,8-naphthyridine derivatives. The coordination modes of these ligands were modified by addition of coordinating solvents such as water into the ethanolic reaction media. Under these conditions 1,8-naphthyridine (napy) moieties act as monodentade ligands forming unusual [Ru(CO)(2)Cl-2(eta(1)-2-phenyl-1,8-naphthyridine-kN)(eta(1)-2-phenyl-1,8-naphthyridine-kN ‘)] complexes. The reaction was reproducible when different 2-phenyl-1,8-naphthyridine derivatives were used. On the other hand, when dry ethanol was used as the solvent we obtained complexes with napy moieties acting as a chelating ligand. The structures proposed for these complexes were supported by NMR spectra, and the presence of two ligands in the [Ru(CO)(2)Cl-2(eta(1)-2-phenyl-1,8-naphthyridine-kN)(eta(1)-2-phenyl-1,8-naphthyridine-kN ‘)] type complexes was confirmed using elemental analysis. All complexes were tested as catalysts in the hydroformylation of styrene showing moderate activity in N,N ‘-dimethylformamide. Copyright (C) 2008 John Wiley & Sons, Ltd.

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Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem