4-Cyano-4'-pentylbiphenyl

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search
4-Cyano-4'-pentylbiphenyl
Skeletal formula of 4-cyano-4'-pentylbiphenyl
Space-filling model of the 4-cyano-4'-pentylbiphenyl molecule
Names
Other names
4'-Amyl-4-biphenylcarbonitrile, 4'-Pentyl-4-biphenylcarbonitrile, 4-Amyl-4'-cyanobiphenyl
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.050.068
EC Number
  • 255-093-2
Properties
C18H19N
Molar mass 249.357 g·mol−1
Appearance Colorless if isotropic or cloudy white if nematic
Density 1.008 g/mL
Hazards
Safety data sheet [1]
GHS pictograms GHS07: Harmful
GHS Signal word Warning
H302, H312, H315, H319, H332, H335
P261, P264, P270, P271, P280, P301+312, P302+352, P304+312, P304+340, P305+351+338, P312, P321, P322, P330, P332+313, P337+313, P362, P363, P403+233, P405, P501
NFPA 704 (fire diamond)
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilHealth code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
1
2
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is ☑Y☒N ?)
Infobox references

4-Cyano-4'-pentylbiphenyl is a commonly used nematic liquid crystal with the chemical formula C18H19N. It frequently goes by the common name 5CB. 5CB was first synthesized by George William Gray, Ken Harrison, and J.A. Nash at the University of Hull in 1972 and at the time it was the first member of the cyanobiphenyls.[1][2] The liquid crystal was discovered after Gray's group received a grant from the UK Ministry of Defence to find a liquid crystal that had liquid crystal phases near room temperature with the specific intention of using them in liquid crystal displays. The molecule is about 20 Å long. The liquid crystal 5CB undergoes a phase transition from a crystalline state to a nematic state at 24 °C and it goes from a nematic to an isotropic state at 35 °C.[3]

Production[edit]

5CB is produced by modifying biphenyl in a linear manner. First Br2 is added to the biphenyl to introduce a bromine atom to the end of the moiety. Next aluminium chloride and C4H9COCl is added to the sample, followed by the addition of potassium hydroxide and NH2NH2. By this point the molecule will have a bromine atom on one end of the rigid core and C5H11 on the other end. Finally, introduction of copper(I) cyanide and DMF results in the removal of the bromine and its replacement with CN, yielding 5CB.[4]

Notes[edit]

  1. ^ Gray, Harrison & Nash 1973, pp. 130–131
  2. ^ Collings & Hird 1997, p. 53
  3. ^ BAROIS, Philippe (1996-02-10). "Cristaux liquides". Techniques de l'Ingénieur (in French). p. 5.
  4. ^ Collings & Hird 1997, pp. 151–152

References[edit]

  • Barois, Philippe (1996). Cristaux liquides. Techniques de l'ingénieur. ref. article : a1325.
  • Collings, Peter J.; Hird, Michael (1997). Gray, George William; Goodby, J. W.; Fukuda, A. (eds.). Introduction to Liquid Crystals: Chemistry and Physics. Taylor and Francis Ltd. ISBN 0-7484-0643-3.
  • Gray, George William (January 1998). "Reminiscences from a life with liquid crystals". Liquid Crystals. 24 (1): 5–14. doi:10.1080/026782998207523.
  • Gray, George William; Harrison, Ken J.; Nash, J A. (1973). "New family of nematic liquid crystals for displays". Electronics Letters. 9 (6): 130–131. doi:10.1049/el:19730096.
  • Seo, D. S.; Matsuda, H.; Oh-Ide, T.; Kobayashi, S. (1993). "Alignment of Nematic Liquid Crystal(5CB) on the Treated Substrates: Characterization of Orientation Films, Generation of Pretilt Angles, and Surface Anchoring Strength". Molecular Crystals and Liquid Crystals. 224 (1): 13–31. doi:10.1080/10587259308032475.
  • Vill, Volkmar (January 1998). "Grey levels in the history of liquid crystals". Liquid Crystals. 24 (1): 21–24. doi:10.1080/026782998207541.

External links[edit]