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ChemInform Abstract: Thermally Induced Cyclodehydrogenation of Biaryls: A Simple Radical Reaction or a Sequence of Rearrangements?

✍ Scribed by J. CIOSLOWSKI; P. PISKORZ; D. MONCRIEFF


Book ID
101866102
Publisher
John Wiley and Sons
Year
2010
Weight
26 KB
Volume
29
Category
Article
ISSN
0931-7597

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✦ Synopsis


Thermally Induced Cyclodehydrogenation of Biaryls: A Simple Radical Reaction or a Sequence of Rearrangements?

-The first direct radical pathway from 1-phenylnaphthalene to fluoranthene predominates at lower temperatures. The second pathway involves an arylaryne/anellated cyclopentadienylidenecarbene mechanism. The third pathway involves direct equilibration and is associated with very high activation energies, so that an operation under normal pyrolytic conditions is not probable. -(CIOSLOWSKI,


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