Synthesis, Structure and Anion Sensing Properties of a Dicationic Bis(imidazolium)-Based Cyclophane-Reference-Cited by-同舟云学术

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Synthesis, Structure and Anion Sensing Properties of a Dicationic Bis(imidazolium)-Based Cyclophane

Published:2018-04-09 Issue:13 Volume:3 Page:3855-3859
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Sabater Paula¹,Zapata Fabiola¹,Caballero Antonio¹,Alkorta Ibon²,Ramirez de Arellano Carmen³,Elguero Jose²,Molina Pedro¹^ORCID

Affiliation:

1. Departamento de Química Orgánica; Universidad de Murcia, Campus de Espinardo; E-30100 Murcia Spain

2. Instituto de Química Médica; Consejo Superior de Investigaciones Científicas (CSIC); Juan de la Cierva, 3 E-28006 Madrid Spain

3. Departamento de Química Orgánica; Universidad de Valencia; E-46100 Valencia Spain

Funder

Ministerio de Economía y Competitividad of Spain

FEDER

Fundación Séneca Región de Murcia (CARM)

Comunidad Autónoma de Madrid

University of Murcia

Government of Spain

Publisher

Wiley

Subject

General Chemistry

Reference62 articles.

1. Supramolekulare Chemie von Anionen: von der Erkennung zur chemischen Anwendung

2. Advances in Anion Supramolecular Chemistry: From Recognition to Chemical Applications

3. Anion receptor chemistry: highlights from 2011 and 2012

4. Chromogenic and fluorogenic chemosensors and reagents for anions. A comprehensive review of the years 2010–2011

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1. Can Dative Bond Between Two Anions Possible?;ChemPhysChem;2023-07-31

2. Fluorescent cyclophanes and their applications;Chemical Society Reviews;2022

3. A detailed insight into anion sensing based on intramolecular charge transfer (ICT) mechanism: A comprehensive review of the years 2016 to 2021;Coordination Chemistry Reviews;2021-12

4. Revisiting imidazolium receptors for the recognition of anions: highlighted research during 2010–2019;Chemical Society Reviews;2021

5. A Conceptual DFT Study of Phosphonate Dimers: Dianions Supported by H-Bonds;The Journal of Physical Chemistry A;2020-02-24

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