Synthesis of Novel Asymmetric Zinc (II) Phthalocyanines Bearing Octadecyloxyl and Glucosyl Groups

A novel asymmetric zinc (II) phthalocyanine substituted by one lipophilic octadecyloxyl group and three hydrophilic glucosyl groups was synthesized. Using Q-TOF MS, the major byproducts formed during the deprotection processes were identified. An improved procedure was worked out to convert these by...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Pei, Zhang, Shufen, Han, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254961/
https://www.ncbi.nlm.nih.gov/pubmed/19783951
http://dx.doi.org/10.3390/molecules14093688
_version_ 1783373847074963456
author Zhang, Pei
Zhang, Shufen
Han, Gang
author_facet Zhang, Pei
Zhang, Shufen
Han, Gang
author_sort Zhang, Pei
collection PubMed
description A novel asymmetric zinc (II) phthalocyanine substituted by one lipophilic octadecyloxyl group and three hydrophilic glucosyl groups was synthesized. Using Q-TOF MS, the major byproducts formed during the deprotection processes were identified. An improved procedure was worked out to convert these byproducts to the desired product in quantitative yield.
format Online
Article
Text
id pubmed-6254961
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Molecular Diversity Preservation International
record_format MEDLINE/PubMed
spelling pubmed-62549612018-11-30 Synthesis of Novel Asymmetric Zinc (II) Phthalocyanines Bearing Octadecyloxyl and Glucosyl Groups Zhang, Pei Zhang, Shufen Han, Gang Molecules Communication A novel asymmetric zinc (II) phthalocyanine substituted by one lipophilic octadecyloxyl group and three hydrophilic glucosyl groups was synthesized. Using Q-TOF MS, the major byproducts formed during the deprotection processes were identified. An improved procedure was worked out to convert these byproducts to the desired product in quantitative yield. Molecular Diversity Preservation International 2009-09-18 /pmc/articles/PMC6254961/ /pubmed/19783951 http://dx.doi.org/10.3390/molecules14093688 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Communication
Zhang, Pei
Zhang, Shufen
Han, Gang
Synthesis of Novel Asymmetric Zinc (II) Phthalocyanines Bearing Octadecyloxyl and Glucosyl Groups
title Synthesis of Novel Asymmetric Zinc (II) Phthalocyanines Bearing Octadecyloxyl and Glucosyl Groups
title_full Synthesis of Novel Asymmetric Zinc (II) Phthalocyanines Bearing Octadecyloxyl and Glucosyl Groups
title_fullStr Synthesis of Novel Asymmetric Zinc (II) Phthalocyanines Bearing Octadecyloxyl and Glucosyl Groups
title_full_unstemmed Synthesis of Novel Asymmetric Zinc (II) Phthalocyanines Bearing Octadecyloxyl and Glucosyl Groups
title_short Synthesis of Novel Asymmetric Zinc (II) Phthalocyanines Bearing Octadecyloxyl and Glucosyl Groups
title_sort synthesis of novel asymmetric zinc (ii) phthalocyanines bearing octadecyloxyl and glucosyl groups
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254961/
https://www.ncbi.nlm.nih.gov/pubmed/19783951
http://dx.doi.org/10.3390/molecules14093688
work_keys_str_mv AT zhangpei synthesisofnovelasymmetriczinciiphthalocyaninesbearingoctadecyloxylandglucosylgroups
AT zhangshufen synthesisofnovelasymmetriczinciiphthalocyaninesbearingoctadecyloxylandglucosylgroups
AT hangang synthesisofnovelasymmetriczinciiphthalocyaninesbearingoctadecyloxylandglucosylgroups

Ejemplares similares