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  4. Optical stability of axially chiral push-pull-substituted buta-1,3dienes: Effect of a single methyl group on the C60 surface
 
research article

Optical stability of axially chiral push-pull-substituted buta-1,3dienes: Effect of a single methyl group on the C60 surface

Yamada, M.
•
Rivera-Fuentes, P.
•
Bernd Schweizer, W.
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2010
Angewandte Chemie International Edition

A new spin on C60: Axially chiral, pushpull buta-1,3-diene chromophores conjugated to vicinally methylated fullerenes (see picture) have high barriers of rotation about their chiral axes. These high barriers allowed their optical resolution and the determination of the absolute configuration by comparison of experimental and calculated circular dichroism spectra. The methyl group is rigidly fixed upon the surface of the carbon sphere and is responsible for the high rotational barriers. (Figure Presented). © 2010 Wiley-VCH Verlag GmbH & Co. KGaA.

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Type
research article
DOI
10.1002/anie.200906853
Scopus ID

2-s2.0-77952340098

Author(s)
Yamada, M.
Rivera-Fuentes, P.
Bernd Schweizer, W.
Diederich, F.
Date Issued

2010

Publisher

Wiley-VCH Verlag GmbH

Published in
Angewandte Chemie International Edition
Volume

49

Issue

20

Start page

3532

End page

3535

Subjects

Absolute configuration

•

Axial chirality

•

Buta-1-3-dienes

•

Carbon Spheres

•

Charge-transfer chromophores

•

Chirality

•

Chromophores

•

Circular dichroism

•

Circular dichroism spectra

•

Copying

•

Dichroism

•

Enantiomers

•

Fullerenes

•

Methyl group

•

Methylated fullerenes

•

Olefins

•

Optical resolution

•

Optical stability

•

optical stability axially chiral push pull substituted butadiene

•

Organic polymers

•

Rotational barriers

•

Spin-on

•

Stereochemistry

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LOCBP  
Available on Infoscience
October 30, 2019
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/162511
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