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ethyl 5-N-[N'-pentyl-1,6,7,12-tetra(p-tert-butylphenoxy)perylene-3,4:9,10-bis(dicarboximide)]pentyl malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1046791-02-9

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1046791-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1046791-02-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,7,9 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1046791-02:
(9*1)+(8*0)+(7*4)+(6*6)+(5*7)+(4*9)+(3*1)+(2*0)+(1*2)=149
149 % 10 = 9
So 1046791-02-9 is a valid CAS Registry Number.

1046791-02-9Downstream Products

1046791-02-9Relevant academic research and scientific papers

Fullerene C60-perylene-3,4:9,10-bis(dicarboximide) light-harvesting dyads: spacer-length and bay-substituent effects on intramolecular singlet and triplet energy transfer

Baffreau, Jerome,Leroy-Lhez, Stephanie,Anh, Nguyen Van,Williams, Rene M.,Hudhomme, Pietrick

, p. 4974 - 4992 (2008)

Novel covalent fullerene C60-perylene-3,4:9,10- bis(dicarboximide) (C60)-PDI) dyads (1-4) were synthesized and characterized. Their electrochemical and photophysical properties were investigated. Electrochemical studies show that the reduction potential of PDI can be tuned relative to C60 by molecular engineering through altering the substituents on the PDI bay region. It was demonstrated using steady-state and time-resolved spectroscopy that a quantitative, photoinduced energy transfer takes place from the PDI moiety, acting as a light-harvesting antenna, to the C60 unit, playing the role of energy acceptor. The baysubstitution (tetrachloro [1 and 2] or tetra-tert-butylphenoxy [3 and 4]) of the PDI antenna and the linkage length (C2 [1 and 3] or C5 [2 and 4]) to the C60 acceptor are important parameters in the kinetics of energy transfer. Femtosecond transient absorption spectroscopy indicates singlet-singlet energy-transfer times (from the PDI to the C 60 unit) of 0.4 and 5 ps (1), 4.5 and 27 ps (2), 0.8 and 12 ps (3), and 7 and 50 ps (4), these values being ascribed to two different conformers for each C60-PDI system. Subsequent triplet-triplet energy-transfer times (from the C60 unit to the PDI) are slower and in the order of 0.8 ns (1), 6.2 ns (2), 2.7 ns (3), and 9 ns (4). Nanosecond transient absorption spectroscopy of final PDI triplet states show a marked influence of the bay substitution (tetrachloro- or tetra-tert-butylphenoxy), and tripletstate lifetimes (10-20 us) and the PDI triplet quantum yields (0.75-0.52) were estimated. The spectroscopy showed no substantial solvent effect upon comparing toluene (non-polar) to benzonitrile (polar), indicating that no electron transfer is occurring in these systems.

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