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N-(3,5-dimethoxyphenyl)-3-(2-pyridyl)-1,8-naphthalimide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1425192-29-5

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1425192-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1425192-29-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,5,1,9 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1425192-29:
(9*1)+(8*4)+(7*2)+(6*5)+(5*1)+(4*9)+(3*2)+(2*2)+(1*9)=145
145 % 10 = 5
So 1425192-29-5 is a valid CAS Registry Number.

1425192-29-5Downstream Products

1425192-29-5Relevant academic research and scientific papers

Ruthenium(II) complexes bearing a naphthalimide fragment: A modular dye platform for the dye-sensitized solar cell

Pogozhev, Dmitry V.,Bezdek, Mate J.,Schauer, Phil A.,Berlinguette, Curtis P.

, p. 3001 - 3006 (2013/05/08)

Cycloruthenated complexes of the type [RuII(N^N) 2(C^N)]+ (N^N = substituted 2,2′-bipyridine; C^N = substituted 3-(2′-pyridyl)-1,8-naphthalimide ligand) are shown to generate high power conversion efficiencies (PCEs) in the dye-sensitized solar cell (DSSC). It is shown that substitution of the pyridine ring of the C^N ligand with conjugated groups can enhance molar absorption extinction coefficients, while the electron density imparted on the metal center is alleviated by the 1,8-naphthalimide fragment. This latter feature maintains a Ru(III)/Ru(II) redox couple more positive than 0.8 V versus NHE, thereby accommodating regeneration of the oxidized dye by an iodide-based redox mediator. This dye platform can consequently be modulated at various sites to enhance light absorption and suppress recombination between the redox mediator and the TiO2 surface without compromising dye regeneration, thereby maintaining device PCEs as high as 7%. We also introduce a new phosphine-based coadsorbent, bis(2-ethylhexyl)phosphinic acid (BEPA), which is significantly easier to synthesize than the widely used bis(3,3-dimethylbutyl)phosphinic acid (DINHOP) while also facilitating high dye loading.

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