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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2013-01-01
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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. |
format | Article |
id | doaj-art-ab3085a0489a4c8f9b1af222d233b44b |
institution | Kabale University |
issn | 2090-9063 2090-9071 |
language | English |
publishDate | 2013-01-01 |
publisher | Wiley |
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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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