Literature DB >> 24037374

A chiral indolocarbazole foldamer displaying strong circular dichroism responsive to anion binding.

Dan A Kim1, Philjae Kang, Moon-Gun Choi, Kyu-Sung Jeong.   

Abstract

A chiral foldamer that consists of three indolocarbazoles and chiral amide residues folds into a helical conformation with the orientation bias, thus displaying characteristic CD signals. The X-ray crystal structure of its chloride complex was found to be a left-handed (M-) helix which stacks to give one-dimensional columnar arrays.

Entities:  

Year:  2013        PMID: 24037374     DOI: 10.1039/c3cc45989f

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  4 in total

Review 1.  Ion and molecular recognition using aryl-ethynyl scaffolding.

Authors:  Chris L Vonnegut; Blakely W Tresca; Darren W Johnson; Michael M Haley
Journal:  Chem Asian J       Date:  2015-01-13

Review 2.  Helical Anion Foldamers in Solution.

Authors:  Eric A John; Casey J Massena; Orion B Berryman
Journal:  Chem Rev       Date:  2020-02-10       Impact factor: 60.622

3.  Anion-coordination-driven single-double helix switching and chiroptical molecular switching based on oligoureas.

Authors:  Hongfei Li; Lei Kou; Lin Liang; Boyang Li; Wei Zhao; Xiao-Juan Yang; Biao Wu
Journal:  Chem Sci       Date:  2022-04-07       Impact factor: 9.969

4.  Anion binding studies on receptors derived from the indolo[2,3-a]carbazole scaffold having different binding cavity sizes.

Authors:  Guzmán Sánchez; David Curiel; Alberto Tárraga; Pedro Molina
Journal:  Sensors (Basel)       Date:  2014-07-31       Impact factor: 3.576

  4 in total

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