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[Cu(2,9-di-s-butyl-4,7-diphenyl-1,10-phenanthroline)(10,10'-(2,8-dimethylphenoxathiine-4,6-diyl)bis(2,8-dimethyl-10H-phenoxaphosphinine))]PF6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1529758-64-2

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1529758-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1529758-64-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,9,7,5 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1529758-64:
(9*1)+(8*5)+(7*2)+(6*9)+(5*7)+(4*5)+(3*8)+(2*6)+(1*4)=212
212 % 10 = 2
So 1529758-64-2 is a valid CAS Registry Number.

1529758-64-2Downstream Products

1529758-64-2Relevant academic research and scientific papers

A noble-metal-free system for photocatalytic hydrogen production from water

Mejia, Esteban,Luo, Shu-Ping,Karnahl, Michael,Friedrich, Aleksej,Tschierlei, Stefanie,Surkus, Annette-Enrica,Junge, Henrik,Gladiali, Serafino,Lochbrunner, Stefan,Beller, Matthias

supporting information, p. 15972 - 15978 (2014/04/03)

A series of heteroleptic copper(I) complexes with bidentate PP and NN chelate ligands was prepared and successfully applied as photosensitizers in the light-driven production of hydrogen, by using [Fe3(CO)12] as a water-reduction catalyst (WRC). These systems efficiently reduces protons from water/THF/triethylamine mixtures, in which the amine serves as a sacrificial electron donor (SR). Turnover numbers (for H) up to 1330 were obtained with these fully noble-metal-free systems. The new complexes were electrochemically and photophysically characterized. They exhibited a correlation between the lifetimes of the MLCT excited state and their efficiency as photosensitizers in proton-reduction systems. Within these experiments, considerably long excited-state lifetimes of up to 54μs were observed. Quenching studies with the SR, in the presence and absence of the WRC, showed that intramolecular deactivation was more efficient in the former case, thus suggesting the predominance of an oxidative quenching pathway.

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