Synthesis and Protonation Constants of an Amide-Based Chelating Cyclophane
1
Departamento de Investigación en Polímeros y Materiales. Universidad de Sonora. Apartado Postal 130, Col Centro.83000. Hermosillo, Sonora, México
2
Centro de Investigaciones Químicas, Universidad Autónoma del Estado de Morelos. 62209. Cuernavaca, Morelos, México
*
Author to whom correspondence should be addressed.
Molbank 2006, 2006(6), M519; https://doi.org/10.3390/M519
Received: 21 July 2006 / Accepted: 29 September 2006 / Published: 1 December 2006
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
This is an open access article distributed under the Creative Commons Attribution License
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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- Supplementary File 1:
m519.mol 3D structure (MOL, 5 KB)
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3D structure generated by CORINA by Molecular Networks. - Supplementary File 2:
m519.mol (INCHI, 2 KB)
- Supplementary File 3:
m519.mol (MOL, 5 KB)
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