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1476777-03-3

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1476777-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1476777-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,7,6,7,7 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1476777-03:
(9*1)+(8*4)+(7*7)+(6*6)+(5*7)+(4*7)+(3*7)+(2*0)+(1*3)=213
213 % 10 = 3
So 1476777-03-3 is a valid CAS Registry Number.

1476777-03-3Downstream Products

1476777-03-3Relevant academic research and scientific papers

Difference in the photophysical properties of a perylenetetracarboxylic diimide dimer and a hexamer linked by the same hexaphenylbenzene group

Xue, Lin,Shi, Yan,Zhang, Liangliang,Li, Xiyou

, p. 3319 - 3326 (2013)

A perylenetetracarboxylic diimide hexamer (6PDI) and a dimer (2PDI) linked with the same hexaphenylbenzene group were prepared, and the structures were fully characterized by 1H NMR spectroscopy, mass spectrometry, and elemental analysis. Due to the similar molecular structure of these two compounds, similar interactions between/among the PDI subunits as well as similar photophysical properties are expected. However, the stationary UV/Vis absorption spectra reveal that the interactions among/between the PDI subunits in 6PDI are significantly stronger than those in 2PDI. This can be attributed to blocked rotation along the long axis of the PDI subunits in 6PDI due to steric hindrance of the two neighboring PDI subunits. The stronger interactions among the PDI subunits in 6PDI lead to long-wavelength emission, which can be assigned to excimer-like excited states. A similar conclusion can also be deduced from the fluorescence quantum yields and the fluorescence lifetimes. Electrochemical studies revealed that interactions between/among the PDI subunits in both 2PDI and 6PDI are still in the range of weak interactions. Ultrafast transient anisotropy decay dynamics revealed that excitation delocalization between the PDI subunits within 2PDI and 6PDI is quick and efficient. More interestingly, delocalization is faster in 6PDI than in 2PDI, probably because of the stronger interactions among the PDI subunits in the former. Interacting with Diimides: A perylenetetracarboxylic diimide (PDI) dimer and a hexamer linked with the same hexaphenylbenzene group are prepared. Despite the similar relative orientation of the neighboring PDI units in these two compounds, stronger interactions among the PDI units within the hexamer are found. The excitation delocalization between the PDI subunits is faster in the hexamer than in the dimer.

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