Some scientific research about 3491-12-1

Synthetic Route of 3491-12-1, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 3491-12-1 is helpful to your research.

Synthetic Route of 3491-12-1, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 3491-12-1, Name is 4-[4-(4-aminophenoxy)phenoxy]aniline, SMILES is NC1=CC=C(OC2=CC=C(OC3=CC=C(N)C=C3)C=C2)C=C1, belongs to naphthyridines compound. In a article, author is Liu, Zu-Yin, introduce new discover of the category.

A Gold(I) Complex Based on 1,8-Naphthyridine Functionalized N-Heterocyclic Carbene (NHC) and Its Catalytic Activity

A gold complex containing 2,7-bis(mesitylimidazolylidenyl)naphthyridine (NHC-NP) has been synthesized. Thus, reaction of {Ag-3(NHC-NP)(2)} (PF6)(3)] with [Au(Me2S)Cl] provided an unusual digold complex bridged by two NHC-NP, forming a 20-membered dinuclear metallacycle [{Au-2(NHC-NP)(2)Cl-2}-(PF6)(2)] (2) in high yield. This complex was characterized by spectroscopic and elemental analysis. This gold complex is active for the hydrolysis of 2,2,5-trimethyl-1,3-dioxane-5-methanol and can be recycled without losing the activity.

Synthetic Route of 3491-12-1, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 3491-12-1 is helpful to your research.

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