While the job of a research scientist varies, Product Details of 179324-87-9, most chemistry careers in research are based in laboratories, where research is conducted by teams following scientific methods and standards.179324-87-9, Name is (R)-BoroLeu-(+)-Pinanediol trifluoroacetate, SMILES is CC1(C)[C@@]([H])(C2)C[C@]3([H])[C@](OB([C@H](CC(C)C)N)O3)(C)[C@]12[H].O=C(O)C(F)(F)F, belongs to naphthyridine compound. In a article, author is Li, Lei, introduce new discover of the category.
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.
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Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem