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phenanthrene

American  
[fuh-nan-threen] / fəˈnæn θrin /

noun

Chemistry.
  1. a colorless, shiny, crystalline, water-insoluble isomer of anthracene, C 1 4 H 1 0 , derived from coal tar: used chiefly in dyestuffs and in the synthesis of drugs.


phenanthrene British  
/ fɪˈnænθriːn /

noun

  1. a colourless crystalline aromatic compound isomeric with anthracene: used in the manufacture of dyes, drugs, and explosives. Formula: C 14 H 10

"Collins English Dictionary — Complete & Unabridged" 2012 Digital Edition © William Collins Sons & Co. Ltd. 1979, 1986 © HarperCollins Publishers 1998, 2000, 2003, 2005, 2006, 2007, 2009, 2012

phenanthrene Scientific  
/ fə-nănthrēn′ /
  1. A colorless, crystalline hydrocarbon obtained by fractional distillation of coal-tar oils and used in dyes, drugs, and explosives. Phenanthrene is an isomer of anthracene and has three benzene rings fused together but not arranged in a straight line. Chemical formula: C 14 H 10 .


Etymology

Origin of phenanthrene

First recorded in 1880–85; phen(o)- + anthr(ac)ene

Example Sentences

Examples are provided to illustrate real-world usage of words in context. Any opinions expressed do not reflect the views of Dictionary.com.

Furthermore, it was demonstrated that the phenyl ether substituent and phenanthrene shelf were forced into a PD stacking interaction in the folded conformation.

From Nature • Mar. 28, 2017

They also investigated certain hydrocarbons occurring in the high boiling point fraction of the coal tar distillate and solved the constitution of phenanthrene.

From Encyclopaedia Britannica, 11th Edition, Volume 10, Slice 4 "Finland" to "Fleury, Andre" by Various

The hydrocarbons are separated from the “Stupp” by means of alcohol, the soluble portion on distillation giving first phenanthrene and then a mixture of pyrene and fluoranthene.

From Encyclopaedia Britannica, 11th Edition, Volume 10, Slice 5 "Fleury, Claude" to "Foraker" by Various

Their names are: benzene, toluene, xylene, phenol, cresol, naphthalene, anthracene, methyl anthracene, phenanthrene and carbazol.

From Creative Chemistry Descriptive of Recent Achievements in the Chemical Industries by Slosson, Edwin E.

An interesting observation by Baeyer, viz. that stilbene, C6H5�CH:CH�C6H5, is very readily oxidized, while phenanthrene is not, supports, in some measure, the views of Bamberger.

From Encyclopaedia Britannica, 11th Edition, Volume 6, Slice 1 "Châtelet" to "Chicago" by Various