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Structure Determination of Photoproducts of Anthracenes with (Arylmethoxymethyl) Sidechains

✍ Scribed by Silvia Dobis; Dieter Schollmeyer; Chunmei Gao; Derong Cao; Herbert Meier


Book ID
102175410
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
229 KB
Volume
2007
Category
Article
ISSN
1434-193X

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✦ Synopsis


Abstract

Irradiation of 9‐(arylmethoxymethyl)anthracenes 3 leads either to a cyclomer and cyclodimer mixture (3a → 4a,5a), to selectively formed dimers (3b → 5b), or a selectively formed cyclomer (3c → 4c). The [4Ο€+4Ο€]cyclodimerization is under the conditions used a regioselective head‐to‐tail process. In the crystals of the dimers 5a,b, the sidechains are attached in an antiperiplanar position related to the CC bonds generated in the dimerization. In solutions, however, the structures consist of three rotamers the equilibration of which was studied by temperature‐dependent NMR spectra. (Β© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)


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