Literature DB >> 15612676

Chiral molecular tweezers.

Michael Harmata1.   

Abstract

In this Account, a summary of our work on the synthesis and chemistry of chiral molecular tweezers and certain related species is presented. The framework around which the structures to be discussed were built was Kagan's ether, a short history of which will be given. Chiral molecular tweezers of various sizes were constructed and shown to exhibit binding to various pi acids. An analysis of chiral recognition was performed using variable temperature chiral high-performance liquid chromatography. It was shown that the chiral discrimination was essentially enthalpic in nature. Other forays into the chemistry of Kagan's ether analogues have also been made through the synthesis of a chiral catalyst and a chiral molecular square.

Entities:  

Year:  2004        PMID: 15612676     DOI: 10.1021/ar030164v

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  12 in total

1.  Molecular recognition of organic ammonium ions in solution using synthetic receptors.

Authors:  Andreas Späth; Burkhard König
Journal:  Beilstein J Org Chem       Date:  2010-04-06       Impact factor: 2.883

Review 2.  Artificial Molecular Machines.

Authors:  Sundus Erbas-Cakmak; David A Leigh; Charlie T McTernan; Alina L Nussbaumer
Journal:  Chem Rev       Date:  2015-09-08       Impact factor: 60.622

3.  Glycoluril-Derived Molecular Clips are Potent and Selective Receptors for Cationic Dyes in Water.

Authors:  Nengfang She; Damien Moncelet; Laura Gilberg; Xiaoyong Lu; Vladimir Sindelar; Volker Briken; Lyle Isaacs
Journal:  Chemistry       Date:  2016-08-05       Impact factor: 5.236

4.  Acyclic Cucurbit[n]uril-type Receptors: Preparation, Molecular Recognition Properties and Biological Applications.

Authors:  Shweta Ganapati; Lyle Isaacs
Journal:  Isr J Chem       Date:  2017-11-14       Impact factor: 3.333

5.  Sequence-selective assembly of tweezer molecules on linear templates enables frameshift-reading of sequence information.

Authors:  Zhixue Zhu; Christine J Cardin; Yu Gan; Howard M Colquhoun
Journal:  Nat Chem       Date:  2010-06-27       Impact factor: 24.427

6.  Preparation, structures and preliminary host-guest studies of fluorinated syn-bis-quinoxaline molecular tweezers.

Authors:  Markus Etzkorn; Jacob C Timmerman; Matthew D Brooker; Xin Yu; Michael Gerken
Journal:  Beilstein J Org Chem       Date:  2010-04-20       Impact factor: 2.883

7.  Molecular cleft or tweezer compounds derived from trioxabicyclo[3.3.1]nonadiene diisocyanate and diacid dichloride.

Authors:  Gert Kollenz; Ralf Smounig; Ferdinand Belaj; David Kvaskoff; Curt Wentrup
Journal:  Beilstein J Org Chem       Date:  2015-01-02       Impact factor: 2.883

Review 8.  A journey in bioinspired supramolecular chemistry: from molecular tweezers to small molecules that target myotonic dystrophy.

Authors:  Steven C Zimmerman
Journal:  Beilstein J Org Chem       Date:  2016-01-25       Impact factor: 2.883

9.  Design and synthesis of a 4-aminoquinoline-based molecular tweezer that recognizes protoporphyrin IX and iron(iii) protoporphyrin IX and its application as a supramolecular photosensitizer.

Authors:  Yosuke Hisamatsu; Naoki Umezawa; Hirokazu Yagi; Koichi Kato; Tsunehiko Higuchi
Journal:  Chem Sci       Date:  2018-08-31       Impact factor: 9.825

10.  How important are dispersion interactions to the strength of aromatic stacking interactions in solution?

Authors:  Jungwun Hwang; Brent E Dial; Ping Li; Michael E Kozik; Mark D Smith; Ken D Shimizu
Journal:  Chem Sci       Date:  2015-05-18       Impact factor: 9.825

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