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C15H10 See also: hydrocarbon occurring with phenanthrene, See also: pyrene, See also: diphenyl, and other substances in " Stupp " fat (the fat obtained in working up the mercury ores in See also: Idria), and. also in the higher boiling fractions of the See also: coal See also: tar distillate
.
It was discovered by R
.
Fittigin 1878, who, with Gebhard and H
.
Liepmann, elucidated its constitution (see See also: Ann., 1879, 200, p
.
I)
.
The See also: hydrocarbons are separated from the " Stupp " by means of See also: alcohol, the soluble portion on See also: distillation giving first phenanthrene and then a mixture of pyrene and See also: fluoranthene
.
From the tar distillate, the chrysene can be fractionally precipitated, and the fluoranthene can be separated from most of the pyrene by fractional distillation in a partial vacuum
.
In either See also: case the two hydrocarbons are finally separated by fractional See also: crystallization of their picrates, which are then decomposed by See also: ammonia
.
Fluoranthene crystallizes in large slender needles or See also: monoclinic tables, melting at 10g-110° C. and boiling at 250—251° C
.
(6o mm.)
.
It is easily soluble in hot alcohol, See also: ether and See also: carbon bisulphide
.
On oxidation with chromic acid it forms a quinone, C15HSO2, and an a-diphenylene keto-
CeHic
carboxylic acid Cr,H3>CO2H• The picrate melts at 182—183° C
.
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