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1569542-91-1

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1569542-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569542-91-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,5,4 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1569542-91:
(9*1)+(8*5)+(7*6)+(6*9)+(5*5)+(4*4)+(3*2)+(2*9)+(1*1)=211
211 % 10 = 1
So 1569542-91-1 is a valid CAS Registry Number.

1569542-91-1Downstream Products

1569542-91-1Relevant articles and documents

Aging and ball-milling as low-energy and environmentally friendly methods for the synthesis of Pd(II) photosensitizers

Juribasic, Marina,Halasz, Ivan,Babic, Darko,Cincic, Dominik,Plavec, Janez,Curic, Manda

, p. 1227 - 1234 (2014)

Simple and efficient solid-state synthetic methods, aging and ball milling (liquid-assisted grinding, LAG), have been employed to achieve reactions of triphenylphosphine (tpp) and 1,1′-bis(diphenylphosphino)ferrocene (dppf) with dicyclopalladated azobenzenes (DMF)PdCl(μ-R1C 6H3N=NC6H3R2)PdCl(DMF), R1 = H, OCH3, N(CH3)2 and R 2 = H, NO2. For the first time the aging processes have been applied in the formation of Pd(II) heteroleptic complexes. Both synthetic procedures lead to four types of tetra- or pentacoordinated complexes (tpp)PdCl{(μ-Cl)(μ-R1C6H3N=NC 6H3R2)}Pd(tpp) 1A-3A, (tpp) 2PdCl(μ-R1C6H3N=NC 6H3R2)PdCl(tpp)2 1B-3B, PdCl{(μ-Cl)(μ-R1C6H3N=NC 6H3R2)}Pd(dppf) 1C-3C, and (dppf)PdCl(μ- R1C6H3N=NC6H3R 2)PdCl(dppf) 1D-3D, in which azobenzenes simultaneously act as monodentate C- and bidentate C,N-donors (A, B, and C complexes) or, for the first time, only as double C-donors (D complexes). Although their formation requires complex intramolecular transformations, aging and ball milling have been proved to be efficient synthetic methods. All products have been fully characterized in solid state and solution. Solid-state structures of complexes have been resolved by a single crystal or powder X-ray diffraction (PXRD) and solid-state NMR spectroscopy. Their electronic structures have been rationalized by the quantum-chemical calculations. The structural features of complexes and their stability in solutions have been evaluated by 1H and 31P NMR spectroscopy along with the ESI-MS spectrometry. The absorption and emission properties of complexes have been studied, and the nature of their electronic transitions in the low energy region has been examined by TD-DFT calculations. Significant fluorescence observed for the complexes with 4-dimethylamino-4′-nitroazobenzene ligand at room temperature in solid state and/or in the solution makes them interesting for potential applications as photoactive units in optical devices.

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