Chemistry:1,1,4,4-Tetraphenylbutadiene

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1,1,4,4-tetraphenylbutadiene (TPB) is an organic compound with the formula (C
6
H
5
)
2
C=CHCH=C(C
6
H
5
)
2
. Other isomers are possible, but the term usually refers to the derivative of butadiene with two phenyl group on each of the terminal carbon atoms It is a white solid that has attracted some attention as an electroluminescent dye.[1]

The compound was first prepared by double dehydration of the diol.[2]

It glows blue with an emission spectrum peak wavelength at 430 nm,[3] It is useful as a wavelength shifter.[4][5]

1,2,3,4-Tetraphenylbutadiene ((C
6
H
5
)CH=C(C
6
H
5
)C(C
6
H
5
)=CH(C
6
H
5
)
) is also well-known.

References

  1. ↑ Kido, J.; Shionoya, H.; Nagai, K. (1995). "Single-layer white light-emitting organic electroluminescent devices based on dye-dispersed poly( N -vinylcarbazole)". Applied Physics Letters 67 (16): 2281–2283. doi:10.1063/1.115126. Bibcode: 1995ApPhL..67.2281K. .
  2. ↑ A. Orechoff (1914). "Über eine neue Synthese einiger Inden-Derivate". Berichte der Deutschen Chemischen Gesellschaft 47: 89-95. doi:10.1002/cber.19140470114. 
  3. ↑ Burton, W. M; Powell, B. A (1973). "Fluorescence of Tetraphenyl-Butadiene in the Vacuum Ultraviolet". Applied Optics 12 (1): 87–9. doi:10.1364/AO.12.000087. PMID 20125234. Bibcode: 1973ApOpt..12...87B. .
  4. ↑ Wise, Donald Lee; Gary E. Wnek; Debra J. Trantolo; Thomas M. Cooper; Joseph D. Gresser (1998). Photonic Polymer Systems. CRC Press. p. 250. ISBN 978-0-8247-0152-9. https://books.google.com/books?id=CseEUIK6dVkC&q=%221,1,4,4-Tetraphenyl-1,3-butadiene%22&pg=PA250. Retrieved 2009-06-02. 
  5. ↑ Wernick, Miles N.; John N. Aarsvold (2004). Emission Tomography. Academic Press. p. 374. ISBN 978-0-12-744482-6. https://books.google.com/books?id=R5slur_hdfEC&q=%22Tetraphenyl+butadiene%22&pg=PA11. Retrieved 2009-06-02.