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{(E)-[(3-N-isopropylcarbazolyl)dimethylsilyl]ethenyl}benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1613577-83-5

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1613577-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1613577-83-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,3,5,7 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1613577-83:
(9*1)+(8*6)+(7*1)+(6*3)+(5*5)+(4*7)+(3*7)+(2*8)+(1*3)=175
175 % 10 = 5
So 1613577-83-5 is a valid CAS Registry Number.

1613577-83-5Downstream Products

1613577-83-5Relevant academic research and scientific papers

Intramolecular charge transfer photoemission of a silicon-based copolymer containing carbazole and divinylbenzene chromophores. Electron transfer across silicon bridges

Bayda, Malgorzata,Ludwiczak, Monika,Hug, Gordon L.,Majchrzak, Mariusz,Marciniec, Bogdan,Marciniak, Bronislaw

, p. 4750 - 4758 (2014/07/21)

A new copolymer consisting of N-isopropylcarbazole/dimethylsilylene bridge/divinylbenzene units was synthesized and characterized. Dual fluorescence was observed in this copolymer in polar solvents. The absence of the second band at the lower transition energy of the two emission maxima in nonpolar solvents and the quantitative correlation of the lower-energy emission band maxima with solvent polarity indicate that the lower-energy emission band arises from an intramolecular charge transfer (ICT) state. A series of model compounds was synthesized to investigate the source of the charge transfer. It was found that the Si-bridged dyad with a single N-isopropylcarbazole and a single divinylbenzene was the minimum structure necessary to observe dual luminescence. The lack of dual luminescence in low-temperature glasses indicates that the ICT requires a conformation change in the copolymer. Analogous behavior in the Si-bridged dyad suggests that the ICT in the copolymer is across the silicon bridge. Results from time-resolved luminescence measurements with picosecond and subnanosecond excitation were used to support the thesis that twisted charge-transfer states are the likely source of the observed dual luminescence.

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