Chemistry is an experimental science, Name: 4-[4-(4-aminophenoxy)phenoxy]aniline, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 3491-12-1, Name is 4-[4-(4-aminophenoxy)phenoxy]aniline, molecular formula is C18H16N2O2, belongs to naphthyridine compound. In a document, author is Li, Lei.
A Polypyridyl-Based Layered Complex as Dual-Functional Co-catalyst for Photo-Driven Organic Dyes Degradation and Water Splitting
With the ever-increasing concerns on environmental pollution and energy crisis, it is of great urgency to develop high-performance photocatalyst to eliminate organic pollutants from wastewater and produce hydrogen via water splitting. Herein, a polypyridyl-based mixed covalent Cu-I/II complex with triangular {Cu-3} and rhombic {Cu2Cl4} subunits alternately extended by mixed SCN- and Cl- heterobridges [Cu-4(DNP)(SCN)Cl-4](n) (1) [DNP = 2,6-bis(1,8-naphthyridine-2-yl)pyridine] was solvothermally synthesized and employed as a dual-functional co-photocatalyst. Resulting from a narrowed band-gap of 1.07 eV with suitable redox potential and unsaturated Cu-I/II sites, the complex together with H2O2 can effectively degrade Rhodamine B and methyl orange up to 87.4 and 88.2%, respectively. Meanwhile, the complex mixed with H2PtCl6 can also accelerate the photocatalytic water splitting in the absence of a photosensitizer with the hydrogen production rate of 27.5 mu mol.g(-1).h(-1). These interesting findings may provide informative hints for the design of the multiple responsive photocatalysts.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 3491-12-1. Name: 4-[4-(4-aminophenoxy)phenoxy]aniline.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem