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A [2]catenane displaying pirouetting motion triggered by debenzylation and locked by chloride anion recognition

Research output: Contribution to Journal/Magazine › Journal article › peer-review

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A [2]catenane displaying pirouetting motion triggered by debenzylation and locked by chloride anion recognition. / Evans, Nicholas H.; Serpell, Christopher J.; Beer, Paul D.
In: Chemistry - A European Journal, Vol. 17, No. 28, 07.2011, p. 7734-7738.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Evans, NH, Serpell, CJ & Beer, PD 2011, 'A [2]catenane displaying pirouetting motion triggered by debenzylation and locked by chloride anion recognition', Chemistry - A European Journal, vol. 17, no. 28, pp. 7734-7738. https://doi.org/10.1002/chem.201101033

APA

Evans, N. H., Serpell, C. J., & Beer, P. D. (2011). A [2]catenane displaying pirouetting motion triggered by debenzylation and locked by chloride anion recognition. Chemistry - A European Journal, 17(28), 7734-7738. https://doi.org/10.1002/chem.201101033

Vancouver

Evans NH, Serpell CJ, Beer PD. A [2]catenane displaying pirouetting motion triggered by debenzylation and locked by chloride anion recognition. Chemistry - A European Journal. 2011 Jul;17(28):7734-7738. doi: 10.1002/chem.201101033

Author

Evans, Nicholas H. ; Serpell, Christopher J. ; Beer, Paul D. / A [2]catenane displaying pirouetting motion triggered by debenzylation and locked by chloride anion recognition. In: Chemistry - A European Journal. 2011 ; Vol. 17, No. 28. pp. 7734-7738.

Bibtex

@article{c89dc5d8ac2740c98b92dd88b8f59500,
title = "A [2]catenane displaying pirouetting motion triggered by debenzylation and locked by chloride anion recognition",
abstract = "Chloride locks the rings: Debenzylation of a chloride-templated N-benzyl pyridinium catenane, allows for a 180° “pirouetting” of the rings in the resulting neutral pyridyl catenane (see scheme). The catenane may be returned to its original co-conformation by chloride recognition as evidenced in solution and in the solid state.",
keywords = "anions, catenanes, molecular devices, supramolecular chemistry, template synthesis, SELECTIVITY, ROTAXANE, RING",
author = "Evans, {Nicholas H.} and Serpell, {Christopher J.} and Beer, {Paul D.}",
year = "2011",
month = jul,
doi = "10.1002/chem.201101033",
language = "English",
volume = "17",
pages = "7734--7738",
journal = "Chemistry - A European Journal",
issn = "0947-6539",
publisher = "Wiley-VCH Verlag",
number = "28",

}

RIS

TY - JOUR

T1 - A [2]catenane displaying pirouetting motion triggered by debenzylation and locked by chloride anion recognition

AU - Evans, Nicholas H.

AU - Serpell, Christopher J.

AU - Beer, Paul D.

PY - 2011/7

Y1 - 2011/7

N2 - Chloride locks the rings: Debenzylation of a chloride-templated N-benzyl pyridinium catenane, allows for a 180° “pirouetting” of the rings in the resulting neutral pyridyl catenane (see scheme). The catenane may be returned to its original co-conformation by chloride recognition as evidenced in solution and in the solid state.

AB - Chloride locks the rings: Debenzylation of a chloride-templated N-benzyl pyridinium catenane, allows for a 180° “pirouetting” of the rings in the resulting neutral pyridyl catenane (see scheme). The catenane may be returned to its original co-conformation by chloride recognition as evidenced in solution and in the solid state.

KW - anions

KW - catenanes

KW - molecular devices

KW - supramolecular chemistry

KW - template synthesis

KW - SELECTIVITY

KW - ROTAXANE

KW - RING

U2 - 10.1002/chem.201101033

DO - 10.1002/chem.201101033

M3 - Journal article

VL - 17

SP - 7734

EP - 7738

JO - Chemistry - A European Journal

JF - Chemistry - A European Journal

SN - 0947-6539

IS - 28

ER -