Volume 127, Issue 43 p. 12700
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Innentitelbild: Regulating Molecular Recognition with C-Shaped Strips Attained by Chirality-Assisted Synthesis (Angew. Chem. 43/2015)

Dr. Xiaoxi Liu

Dr. Xiaoxi Liu

Department of Chemistry, The University of Vermont, Burlington, VT 05405 (USA)

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Zackariah J. Weinert

Zackariah J. Weinert

Department of Chemistry, The University of Vermont, Burlington, VT 05405 (USA)

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Mona Sharafi

Mona Sharafi

Department of Chemistry, The University of Vermont, Burlington, VT 05405 (USA)

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Dr. Chenyi Liao

Dr. Chenyi Liao

Department of Chemistry, The University of Vermont, Burlington, VT 05405 (USA)

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Prof. Jianing Li

Corresponding Author

Prof. Jianing Li

Department of Chemistry, The University of Vermont, Burlington, VT 05405 (USA)

Department of Chemistry, The University of Vermont, Burlington, VT 05405 (USA)Search for more papers by this author
Prof. Severin T. Schneebeli

Corresponding Author

Prof. Severin T. Schneebeli

Department of Chemistry, The University of Vermont, Burlington, VT 05405 (USA)

Department of Chemistry, The University of Vermont, Burlington, VT 05405 (USA)Search for more papers by this author
First published: 17 September 2015

Graphical Abstract

C-förmige molekulare Streifen umgreifen Pillararen-Makrocyclen so ähnlich wie ein Schraubenschlüssel einen Schraubenkopf. In der Zuschrift auf S. 12963 ff. beschreiben S. T. Schneebeli, J. Li et al., wie diese molekularen Pinzetten durch chiralitätsunterstützte Synthese in Form von reinen Enantiomeren erhalten werden. In Gegenwart von Pillararenen und Viologenen bilden die molekularen Streifen ternäre Komplexe, die durch kooperative supramolekulare Wechselwirkungen stabilisiert werden.

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