One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Quality Control of 1,8-Diazanaphthalene, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 254-60-4, Name is 1,8-Diazanaphthalene, molecular formula is C8H6N2
[{Rh(Nbd)Cl)2] (Nbd = norbomadiene) reacts with o-(diphenylphosphane)benzaldehyde in benzene solution to give the rhodium(III) complex [Rh(Cl)(C7H9){o-PPh2(C 6H4CO)}]n (1), where C7H 9 is a nortricyclyl (Ntyl) group. Complex 1 reacts with various bidentate N-donors, such as biacetyldihydrazone, 2,2?-bipyridine, 8-aminoquinoline, 2-(aminomethyl)-pyridine, or pyridine, to afford nortricyclyl [Rh(Cl){o-PPh2(C6H4CO)}(Ntyl)(NN)] complexes. The presence of the nortricyclyl group and the structure of the complexes have been confirmed by NMR spectroscopy and, in one case, by single-crystal X-ray diffraction. Nortricyclyl complexes containing bidentate N-donors are also formed by the reaction in benzene of PPh2(o-C6H 4CHO) with the corresponding [Rh(Cl)(Nbd)(NN)] compounds prepared “in situ”. (Rh(Cl)-(Nbd)(bipy)| prepared “in situ” reacts with PPh2(o-C6H4CH O) in methanol to give the complex [Rh(Cl){o-PPh2(C6H4CO)}(C 7H9(bipy)], where C7H9 is a norbomenyl (Nbyl) group. This compound has been fully characterized by NMR spectroscopy. A proposal for the selective production of the norbomenyl and the nortricydyl derivatives is presented. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Quality Control of 1,8-Diazanaphthalene, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 254-60-4, in my other articles.
Reference£º
1,109-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N103 – PubChem