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Intramolecular OH⋯π hydrogen bonding in 4-substituted 2-allylphenols

Paul Rademacher 1
Paul Rademacher
, 
Levan Khelashvili 1
Levan Khelashvili
10.1070/MC2004v014n06ABEH002033
Published 2004-12-17
Communication , Volume 14, Issue 6, 286-287
8
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Rademacher P., Khelashvili L. Intramolecular OH⋯π hydrogen bonding in 4-substituted 2-allylphenols // Mendeleev Communications. 2004. Vol. 14. No. 6. pp. 286-287.
GOST all authors (up to 50) Copy
Rademacher P., Khelashvili L. Intramolecular OH⋯π hydrogen bonding in 4-substituted 2-allylphenols // Mendeleev Communications. 2004. Vol. 14. No. 6. pp. 286-287.
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TY - JOUR
DO - 10.1070/MC2004v014n06ABEH002033
UR - https://mendcomm.colab.ws/publications/10.1070/MC2004v014n06ABEH002033
TI - Intramolecular OH⋯π hydrogen bonding in 4-substituted 2-allylphenols
T2 - Mendeleev Communications
AU - Rademacher, Paul
AU - Khelashvili, Levan
PY - 2004
DA - 2004/12/17
PB - Mendeleev Communications
SP - 286-287
IS - 6
VL - 14
ER -
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@article{2004_Rademacher,
author = {Paul Rademacher and Levan Khelashvili},
title = {Intramolecular OH⋯π hydrogen bonding in 4-substituted 2-allylphenols},
journal = {Mendeleev Communications},
year = {2004},
volume = {14},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2004v014n06ABEH002033},
number = {6},
pages = {286--287},
doi = {10.1070/MC2004v014n06ABEH002033}
}
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Rademacher, Paul, and Levan Khelashvili. “Intramolecular OH⋯π hydrogen bonding in 4-substituted 2-allylphenols.” Mendeleev Communications, vol. 14, no. 6, Dec. 2004, pp. 286-287. https://mendcomm.colab.ws/publications/10.1070/MC2004v014n06ABEH002033.

Abstract

Conformational analysis of 4-substituted 2-allyphenols 1–10 by B3LYP calculations indicates that the energy and the structure of the intramolecular OH⋯π H-bond show a distinct variation with the substituent.

References

1.
10.1070/MC2004v014n06ABEH002033_bib1
Jeffrey
Hydrogen Bonding in Biological Structures, 1994
2.
10.1070/MC2004v014n06ABEH002033_bib2
Jeffrey
An Introduction To Hydrogen Bonding, 1997
3.
10.1070/MC2004v014n06ABEH002033_bib3
Desiraju
The Weak Hydrogen Bond in Structural Chemistry and Biology, 1999
4.
The Effect of Ortho Substitution on the Absorption of the OH Group of Phenol in the Infrared1
Wulf O.R., Liddel U., Hendricks S.B.
Journal of the American Chemical Society, 1936
6.
P. Rademacher, L. Khelashvili and K. Kowski, in press.
7.
L. Khelashvili, PhD Thesis, University of Duisburg-Essen, 2004.
10.
Intramolecular Hydrogen Bonds to π-Electrons and Other Weakly Basic Groups
Baker A.W., Shulgin A.T.
Journal of the American Chemical Society, 1958
11.
Conformers of o-cis-propenyl phenols
Baker A.W., Shulgin A.T.
Spectrochimica Acta, 1964
13.
The allyl and benzyl groups as hydrogen bond acceptors in derivatives of 2-allylphenol and 2-benzylphenol
Schaefer T., Sebastian R., Wildman T.A.
Canadian Journal of Chemistry, 1979
15.
Ground and excited-state intramolecular interactions in phenol–olefin bichromophoric compounds
Bosch-Montalvá M.T., Domingo L.R., Jiménez M.C., Miranda M.A., Tormos R.
Journal of the Chemical Society Perkin Transactions 2, 1998
19.
10.1070/MC2004v014n06ABEH002033_bib18
Shorter
Correlation Analysis of Organic Reactivity, 1982
20.
10.1070/MC2004v014n06ABEH002033_bib19
Frisch
Gaussian 98, 1998