Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation

A rapid and efficient method for preparation of C2-symmetrical 1,3,5-triazine polycarboxylate ligands was developed. The reactions included either selective mono- or di-substitution of 2,4,6-trichloro-1,3,5-triazine with various nucleophiles containing carboxyl group(s), followed by nucleophilic dis...

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Main Authors: Funfuenha W., Phakhodee W., Pattarawarapan M.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-84903854342&partnerID=40&md5=f3d289f31cc4a3e3d904d5c9ab9a20a8
http://cmuir.cmu.ac.th/handle/6653943832/4890
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-48902014-08-30T02:55:55Z Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation Funfuenha W. Phakhodee W. Pattarawarapan M. A rapid and efficient method for preparation of C2-symmetrical 1,3,5-triazine polycarboxylate ligands was developed. The reactions included either selective mono- or di-substitution of 2,4,6-trichloro-1,3,5-triazine with various nucleophiles containing carboxyl group(s), followed by nucleophilic displacement of the remained chloride(s) in aqueous media under microwave irradiation. Novel C2-symmetrical tripodal ligands were afforded in good yields and purities under short reaction time with simple work-up, which are potentially useful as structural directing units in metal-organic frameworks. © 2014 Elsevier Ltd. All rights reserved. 2014-08-30T02:55:55Z 2014-08-30T02:55:55Z 2014 Article in Press 00404020 10.1016/j.tet.2014.06.127 TETRA http://www.scopus.com/inward/record.url?eid=2-s2.0-84903854342&partnerID=40&md5=f3d289f31cc4a3e3d904d5c9ab9a20a8 http://cmuir.cmu.ac.th/handle/6653943832/4890 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description A rapid and efficient method for preparation of C2-symmetrical 1,3,5-triazine polycarboxylate ligands was developed. The reactions included either selective mono- or di-substitution of 2,4,6-trichloro-1,3,5-triazine with various nucleophiles containing carboxyl group(s), followed by nucleophilic displacement of the remained chloride(s) in aqueous media under microwave irradiation. Novel C2-symmetrical tripodal ligands were afforded in good yields and purities under short reaction time with simple work-up, which are potentially useful as structural directing units in metal-organic frameworks. © 2014 Elsevier Ltd. All rights reserved.
format Article
author Funfuenha W.
Phakhodee W.
Pattarawarapan M.
spellingShingle Funfuenha W.
Phakhodee W.
Pattarawarapan M.
Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
author_facet Funfuenha W.
Phakhodee W.
Pattarawarapan M.
author_sort Funfuenha W.
title Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_short Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_full Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_fullStr Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_full_unstemmed Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_sort facile and efficient synthesis of c2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-84903854342&partnerID=40&md5=f3d289f31cc4a3e3d904d5c9ab9a20a8
http://cmuir.cmu.ac.th/handle/6653943832/4890
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