Literature DB >> 11225870

Calixarenes in analytical and separation chemistry.

R Ludwig1.   

Abstract

Discovered in the 1940's, [1n]metacyclophanes with the common name calix[n]arenes which is derived from for the molecule's shape enjoyed a remarkable interest in almost all fields of chemistry since the 1980's, which is highlighted by several books [1-8]. Over 50 reviews concerning their synthesis, properties and applicabilities were published, many of those with emphasis on organic synthesis and structural properties are cited in [P. 5-6 in 2]. Of interest for analytical chemists are reviews on calixarenes and the structurally related resorcin[n]arenes (or calix[n]resorcarenes) and calixpyrroles concerning potentiometric sensors [9-12], chromo- and fluorophores [13, 14], molecular switches [15], metal ion binding in solution [16-19], redox properties [20] and anion binding [21-24]. Other recent reviews deal with thermodynamic aspects [25], organometallic compounds [26], P-containing calixarenes [27-29], as well as molecular dynamics modeling [30-33]. It is a vital field with over 200 publications per year. Therefore, this article presents only selected results on complexation, solvent extraction and membrane transport with the emphasis on ion and molecular recognition which can be used for analytical purposes, without attempting to cover all available references.

Entities:  

Year:  2000        PMID: 11225870     DOI: 10.1007/s002160051611

Source DB:  PubMed          Journal:  Fresenius J Anal Chem        ISSN: 0937-0633


  8 in total

Review 1.  Nanocaged platforms: modification, drug delivery and nanotoxicity. Opening synthetic cages to release the tiger.

Authors:  Mahdi Karimi; Parham Sahandi Zangabad; Fatemeh Mehdizadeh; Hedieh Malekzad; Alireza Ghasemi; Sajad Bahrami; Hossein Zare; Mohsen Moghoofei; Amin Hekmatmanesh; Michael R Hamblin
Journal:  Nanoscale       Date:  2017-01-26       Impact factor: 7.790

2.  Noncovalent complexation of monoamine neurotransmitters and related ammonium ions by tetramethoxy tetraglucosylcalix[4]arene.

Authors:  Mika Torvinen; Elina Kalenius; Francesco Sansone; Alessandro Casnati; Janne Jänis
Journal:  J Am Soc Mass Spectrom       Date:  2011-12-01       Impact factor: 3.109

Review 3.  Azo group(s) in selected macrocyclic compounds.

Authors:  Ewa Wagner-Wysiecka; Natalia Łukasik; Jan F Biernat; Elżbieta Luboch
Journal:  J Incl Phenom Macrocycl Chem       Date:  2018-01-08       Impact factor: 1.633

4.  Quenching of pyrene fluorescence by calix[4]arene and calix[4]resorcinarenes.

Authors:  Shubha Pandey; Maroof Ali; Anjali Bishnoi; Amir Azam; Siddharth Pandey; H M Chawla
Journal:  J Fluoresc       Date:  2007-12-23       Impact factor: 2.217

5.  Non-covalent calixarene-amino acid complexes formed by MALDI-MS.

Authors:  Michele M Stone; Andreas H Franz; Carlito B Lebrilla
Journal:  J Am Soc Mass Spectrom       Date:  2002-08       Impact factor: 3.109

6.  Host-Guest Extraction of Heavy Metal Ions with p-t-Butylcalix[8]arene from Ammonia or Amine Solutions.

Authors:  Md Hasan Zahir; Shakhawat Chowdhury; Md Abdul Aziz; Mohammad Mizanur Rahman
Journal:  Int J Anal Chem       Date:  2018-07-11       Impact factor: 1.885

7.  Isolation of a Nitromethane Anion in the Calix-Shaped Inorganic Cage.

Authors:  Yuji Kikukawa; Hiromasa Kitajima; Sho Kuwajima; Yoshihito Hayashi
Journal:  Molecules       Date:  2020-12-01       Impact factor: 4.411

8.  A fluorescent calix[4]arene with naphthalene units at the upper rim exhibits long fluorescence emission lifetime without fluorescence quenching.

Authors:  Masaki Takahashi; Naoya Tsuji; Kohei Yazaki; Yoshihisa Sei; Makoto Obata
Journal:  RSC Adv       Date:  2021-03-22       Impact factor: 3.361

  8 in total

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