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Molecular nanotechnologies of gelatin-immobilization using macrocyclic metal chelates

This article is a review of recent developments in the self-assembled nanostructures based on chelate coordination compounds. Molecular nanotechnologies of self-assembly of 3d-element aza- and thiazametalmacrocyclic complexes that happen in nanoreactors on the basis of metal hexacyanoferrate(II) gel...

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Autor principal: Mikhailov, Oleg V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918507/
https://www.ncbi.nlm.nih.gov/pubmed/24516711
http://dx.doi.org/10.3402/nano.v5.21485
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author Mikhailov, Oleg V.
author_facet Mikhailov, Oleg V.
author_sort Mikhailov, Oleg V.
collection PubMed
description This article is a review of recent developments in the self-assembled nanostructures based on chelate coordination compounds. Molecular nanotechnologies of self-assembly of 3d-element aza- and thiazametalmacrocyclic complexes that happen in nanoreactors on the basis of metal hexacyanoferrate(II) gelatin-immobilized matrix under their contact with water solutions containing various (N,O,S)-donor atomic ligands and organic compounds having one or two carbonyl groups have been considered in this review. It has been noted that the assortment of macrocyclic metal chelates obtained as a result of using molecular nanotechnologies in such specific conditions considerably differs from the assortment of metal chelates formed at the conditions traditional for chemical synthesis.
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spelling pubmed-39185072014-02-10 Molecular nanotechnologies of gelatin-immobilization using macrocyclic metal chelates Mikhailov, Oleg V. Nano Rev Review Article This article is a review of recent developments in the self-assembled nanostructures based on chelate coordination compounds. Molecular nanotechnologies of self-assembly of 3d-element aza- and thiazametalmacrocyclic complexes that happen in nanoreactors on the basis of metal hexacyanoferrate(II) gelatin-immobilized matrix under their contact with water solutions containing various (N,O,S)-donor atomic ligands and organic compounds having one or two carbonyl groups have been considered in this review. It has been noted that the assortment of macrocyclic metal chelates obtained as a result of using molecular nanotechnologies in such specific conditions considerably differs from the assortment of metal chelates formed at the conditions traditional for chemical synthesis. Co-Action Publishing 2014-02-07 /pmc/articles/PMC3918507/ /pubmed/24516711 http://dx.doi.org/10.3402/nano.v5.21485 Text en © 2014 Oleg V. Mikhailov http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Mikhailov, Oleg V.
Molecular nanotechnologies of gelatin-immobilization using macrocyclic metal chelates
title Molecular nanotechnologies of gelatin-immobilization using macrocyclic metal chelates
title_full Molecular nanotechnologies of gelatin-immobilization using macrocyclic metal chelates
title_fullStr Molecular nanotechnologies of gelatin-immobilization using macrocyclic metal chelates
title_full_unstemmed Molecular nanotechnologies of gelatin-immobilization using macrocyclic metal chelates
title_short Molecular nanotechnologies of gelatin-immobilization using macrocyclic metal chelates
title_sort molecular nanotechnologies of gelatin-immobilization using macrocyclic metal chelates
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918507/
https://www.ncbi.nlm.nih.gov/pubmed/24516711
http://dx.doi.org/10.3402/nano.v5.21485
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