Bulletin of the Chemical Society of Japan
Online ISSN : 1348-0634
Print ISSN : 0009-2673
 
Chemistry of Anthracene–Acetylene Oligomers. XXI. Structures and Stereochemistry of Chiral Anthracene–Acetylene Dimers with an Intra-Annular Alkoxy Group
Takuya TsuyaTetsuo IwanagaShinji Toyota
Author information
JOURNALS RESTRICTED ACCESS

Volume 86 (2013) Issue 1 Pages 138-145

Details
View on the journal site Contact us
Abstract

Anthracene–acetylene cyclic dimers having a methoxy or an ethoxy group at the intra-annular position were synthesized by cross-coupling reactions. DFT calculations suggested that the alkoxy–alkyl groups were perpendicular to the planar rigid framework leading to a chiral structure. The enantiomers were resolved by chiral HPLC and their chiroptical properties were characterized by optical rotation and CD spectral measurements. Their absolute stereochemistries were assigned by the theoretical calculation of CD spectra by using the TDDFT method. Kinetic measurements revealed that the barriers to enantiomerization were 122 and >142 kJ mol−1 for the methoxy and ethoxy compounds, respectively. The structures and stereochemistries are compared with those of intra-annular alkyl derivatives.

Information related to the author
© 2013 The Chemical Society of Japan
Previous article Next article

Recently visited articles
feedback
Top