BINOL Macrocycle Derivatives: Synthesis of New Dinaphthyl Sulfide Aza Oxa Thia Crowns (Lariats)

In this research work, dinaphthyl sulfide diester was prepared from the reaction of 1,1′-thiobis (2-hydroxy naphthalene) and methylchloroacetate. Its aza-macrocyclic derivative was synthesized from the reaction of dinaphthyl sulfide diester and diethylenetriamine. Lariats were prepared from the reac...

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Main Authors: Abbas Shockravi, Shahram Mehdipour-Ataei, Esmael Rostami
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2013/598937
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author Abbas Shockravi
Shahram Mehdipour-Ataei
Esmael Rostami
author_facet Abbas Shockravi
Shahram Mehdipour-Ataei
Esmael Rostami
author_sort Abbas Shockravi
collection DOAJ
description In this research work, dinaphthyl sulfide diester was prepared from the reaction of 1,1′-thiobis (2-hydroxy naphthalene) and methylchloroacetate. Its aza-macrocyclic derivative was synthesized from the reaction of dinaphthyl sulfide diester and diethylenetriamine. Lariats were prepared from the reaction of chloroamides (four derivatives) and initial macrocycle. Chloroamides were synthesized from the reaction of amines (aniline, benzylamine, 8-amino quinoline and 4-amino azobenzene) and chloroacetyl chloride. All the materials were identified by IR, 1H NMR, 13C NMR, and mass spectroscopies, and elemental analysis.
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institution Kabale University
issn 2090-9063
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publishDate 2013-01-01
publisher Wiley
record_format Article
series Journal of Chemistry
spelling doaj-art-ab3085a0489a4c8f9b1af222d233b44b2025-02-03T01:01:44ZengWileyJournal of Chemistry2090-90632090-90712013-01-01201310.1155/2013/598937598937BINOL Macrocycle Derivatives: Synthesis of New Dinaphthyl Sulfide Aza Oxa Thia Crowns (Lariats)Abbas Shockravi0Shahram Mehdipour-Ataei1Esmael Rostami2Faculty of Chemistry, Tarbiat Moallem University, Mofatteh Avenue, No. 49, Tehran 15614, IranPolyurethanes & Advanced Polymeric Materials Department, Faculty of Polymer Science, Iran Polymer & Petrochemical Institute (IPPI), P.O. Box 14965/115, Tehran, IranDepartment of Chemistry, Payame Noor University, P.O. Box 19395-3697, Tehran 19569, IranIn this research work, dinaphthyl sulfide diester was prepared from the reaction of 1,1′-thiobis (2-hydroxy naphthalene) and methylchloroacetate. Its aza-macrocyclic derivative was synthesized from the reaction of dinaphthyl sulfide diester and diethylenetriamine. Lariats were prepared from the reaction of chloroamides (four derivatives) and initial macrocycle. Chloroamides were synthesized from the reaction of amines (aniline, benzylamine, 8-amino quinoline and 4-amino azobenzene) and chloroacetyl chloride. All the materials were identified by IR, 1H NMR, 13C NMR, and mass spectroscopies, and elemental analysis.http://dx.doi.org/10.1155/2013/598937
spellingShingle Abbas Shockravi
Shahram Mehdipour-Ataei
Esmael Rostami
BINOL Macrocycle Derivatives: Synthesis of New Dinaphthyl Sulfide Aza Oxa Thia Crowns (Lariats)
Journal of Chemistry
title BINOL Macrocycle Derivatives: Synthesis of New Dinaphthyl Sulfide Aza Oxa Thia Crowns (Lariats)
title_full BINOL Macrocycle Derivatives: Synthesis of New Dinaphthyl Sulfide Aza Oxa Thia Crowns (Lariats)
title_fullStr BINOL Macrocycle Derivatives: Synthesis of New Dinaphthyl Sulfide Aza Oxa Thia Crowns (Lariats)
title_full_unstemmed BINOL Macrocycle Derivatives: Synthesis of New Dinaphthyl Sulfide Aza Oxa Thia Crowns (Lariats)
title_short BINOL Macrocycle Derivatives: Synthesis of New Dinaphthyl Sulfide Aza Oxa Thia Crowns (Lariats)
title_sort binol macrocycle derivatives synthesis of new dinaphthyl sulfide aza oxa thia crowns lariats
url http://dx.doi.org/10.1155/2013/598937
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AT esmaelrostami binolmacrocyclederivativessynthesisofnewdinaphthylsulfideazaoxathiacrownslariats