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  4. The Torsional Barriers of 2-Hydroxy- and 2-Fluorobiphenyl: Small but Measurable
 
research article

The Torsional Barriers of 2-Hydroxy- and 2-Fluorobiphenyl: Small but Measurable

Mazzanti, Andrea
•
Lunazzi, Lodovico
•
Ruzziconi, Renzo
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2010
Chemistry - A European Journal

By making use of a novel diastereotopicity probe, namely C(CF3)(2)OH, it has been possible to measure by very low temperature F-19 NMR spectroscopy the elusive aryl aryl rotation barriers of biphenyls bearing an OH or F group in one rill position. The experimental values (5.4 and 4.4 kcal mol(-1), respectively) are matched by those from ab initio calculations (5.3 and 4.3 kcal mol(-1), respectively).

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Type
research article
DOI
10.1002/chem.200903372
Web of Science ID

WOS:000281312800031

Author(s)
Mazzanti, Andrea
Lunazzi, Lodovico
Ruzziconi, Renzo
Spizzichino, Sara
Schlosser, Manfred  
Date Issued

2010

Published in
Chemistry - A European Journal
Volume

16

Start page

9186

End page

9192

Subjects

ab initio calculations

•

biphenyls

•

diastereotopicity probes

•

NMR spectroscopy

•

steric hindrance

•

Dynamic Nmr

•

Stereochemical Consequences

•

Conformational-Analysis

•

Absolute-Configuration

•

Internal-Rotation

•

Arylboronic Acids

•

Carbon-Carbon

•

Methyl-Ether

•

Stereodynamics

•

Atropisomers

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
SB  
Available on Infoscience
December 16, 2011
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/75246
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