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Molbank 2006, 2006(6), M519; doi:10.3390/M519

Synthesis and Protonation Constants of an Amide-Based Chelating Cyclophane

Departamento de Investigación en Polímeros y Materiales. Universidad de Sonora. Apartado Postal 130, Col Centro.83000. Hermosillo, Sonora, México
Centro de Investigaciones Químicas, Universidad Autónoma del Estado de Morelos. 62209. Cuernavaca, Morelos, México
Author to whom correspondence should be addressed.
Received: 21 July 2006 / Accepted: 29 September 2006 / Published: 1 December 2006
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Note: In lieu of an abstract, this is an excerpt from the first page.


Our research group have reported that, under high dilution conditions, condensation reactions between 4,4’-ethylenebis(2,6-morpholinedione), 1, and aromatic diamines gave a new series of tetraaza chelating cylophanes, which have amide and aromatic groups in the ring framework and pendant carboxymethyl groups [1].[...] View Full-Text
Keywords: Cyclophane; potentiometry; protonation; amine; anhydride; condensation Cyclophane; potentiometry; protonation; amine; anhydride; condensation

Figure 1

This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Altamirano-Coronado, J.C.; Godoy-Alcántar, C.; Medrano, F. Synthesis and Protonation Constants of an Amide-Based Chelating Cyclophane. Molbank 2006, 2006, M519.

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