Multicomponent One-pot Reactions Towards the Synthesis of Stereoisomers of Dipicolylamine Complexes

Reported are multi‐component one‐pot syntheses of chiral complexes [M(LROR′)Cl2] or [M(LRSR′)Cl2] from the mixture of an N‐substituted ethylenediamine, pyridine‐2‐carboxaldehyde, a primary alcohol or thiol and MCl2 utilizing in‐situ formed cyclized Schiff bases where a C−O bond, two stereocenters, a...

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Veröffentlicht in:Chemistry, an Asian journal an Asian journal, 2016-01, Vol.11 (1), p.128-135
Hauptverfasser: Raje, Sakthi, Gurusamy, Sureshbabu, Koner, Abhishek, Mehrotra, Sonam, Jennifer, Samson Jegan, Vasudev, Prema G., Butcher, Ray J., Angamuthu, Raja
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container_issue 1
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container_title Chemistry, an Asian journal
container_volume 11
creator Raje, Sakthi
Gurusamy, Sureshbabu
Koner, Abhishek
Mehrotra, Sonam
Jennifer, Samson Jegan
Vasudev, Prema G.
Butcher, Ray J.
Angamuthu, Raja
description Reported are multi‐component one‐pot syntheses of chiral complexes [M(LROR′)Cl2] or [M(LRSR′)Cl2] from the mixture of an N‐substituted ethylenediamine, pyridine‐2‐carboxaldehyde, a primary alcohol or thiol and MCl2 utilizing in‐situ formed cyclized Schiff bases where a C−O bond, two stereocenters, and three C−N bonds are formed (M=Zn, Cu, Ni, Cd; R=Et, Ph; R′=Me, Et, nPr, nBu). Tridentate ligands LROR′ and LRSR′ comprise two chiral centers and a hemiaminal ether or hemiaminal thioether moiety on the dipicolylamine skeleton. Syn‐[Zn(LPhOMe)Cl2] precipitates out readily from the reaction mixture as a major product whereas anti‐[Zn(LPhOMe)Cl2] stays in solution as minor product. Both syn‐[Zn(LPhOMe)Cl2] and anti‐[Zn(LPhOMe)Cl2] were characterized using NMR spectroscopy and mass spectrometry. Solid‐state structures revealed that syn‐[Zn(LPhOMe)Cl2] adopted a square pyramidal geometry while anti‐[Zn(LPhOMe)Cl2] possesses a trigonal bipyramidal geometry around the Zn centers. The scope of this method was shown to be wide by varying the components of the dynamic coordination assembly, and the structures of the complexes isolated were confirmed by NMR spectroscopy, mass spectrometry, and X‐ray crystallography. Syn complexes were isolated as major products with ZnII and CuII, and anti complexes were found to be major products with NiII and CdII. Hemiaminals and hemiaminal ethers are known to be unstable and are seldom observed as part of cyclic organic compounds or as coordinated ligands assembled around metals. It is now shown, with the support of experimental results, that linear hemiaminal ethers or thioethers can be assembled without the assistance of Lewis acidic metals in the multi‐component assembly, and a possible pathway of the formation of hemiaminal ethers has been proposed. We belong to the Zinpyr family: Hemiaminals and hemiaminal ethers are known to be unstable and are seldom observed as part of cyclic organic compounds or as coordinated ligands assembled around metals. It is now shown that linear hemiaminal ethers or thioethers can be assembled without the assistance of Lewis acidic metals. Multicomponent one‐pot reactions offer a new route towards the synthesis of stereoisomers of new dipicolylamine complexes.
doi_str_mv 10.1002/asia.201500889
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Tridentate ligands LROR′ and LRSR′ comprise two chiral centers and a hemiaminal ether or hemiaminal thioether moiety on the dipicolylamine skeleton. Syn‐[Zn(LPhOMe)Cl2] precipitates out readily from the reaction mixture as a major product whereas anti‐[Zn(LPhOMe)Cl2] stays in solution as minor product. Both syn‐[Zn(LPhOMe)Cl2] and anti‐[Zn(LPhOMe)Cl2] were characterized using NMR spectroscopy and mass spectrometry. Solid‐state structures revealed that syn‐[Zn(LPhOMe)Cl2] adopted a square pyramidal geometry while anti‐[Zn(LPhOMe)Cl2] possesses a trigonal bipyramidal geometry around the Zn centers. The scope of this method was shown to be wide by varying the components of the dynamic coordination assembly, and the structures of the complexes isolated were confirmed by NMR spectroscopy, mass spectrometry, and X‐ray crystallography. Syn complexes were isolated as major products with ZnII and CuII, and anti complexes were found to be major products with NiII and CdII. Hemiaminals and hemiaminal ethers are known to be unstable and are seldom observed as part of cyclic organic compounds or as coordinated ligands assembled around metals. It is now shown, with the support of experimental results, that linear hemiaminal ethers or thioethers can be assembled without the assistance of Lewis acidic metals in the multi‐component assembly, and a possible pathway of the formation of hemiaminal ethers has been proposed. We belong to the Zinpyr family: Hemiaminals and hemiaminal ethers are known to be unstable and are seldom observed as part of cyclic organic compounds or as coordinated ligands assembled around metals. It is now shown that linear hemiaminal ethers or thioethers can be assembled without the assistance of Lewis acidic metals. 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Asian J</addtitle><description>Reported are multi‐component one‐pot syntheses of chiral complexes [M(LROR′)Cl2] or [M(LRSR′)Cl2] from the mixture of an N‐substituted ethylenediamine, pyridine‐2‐carboxaldehyde, a primary alcohol or thiol and MCl2 utilizing in‐situ formed cyclized Schiff bases where a C−O bond, two stereocenters, and three C−N bonds are formed (M=Zn, Cu, Ni, Cd; R=Et, Ph; R′=Me, Et, nPr, nBu). Tridentate ligands LROR′ and LRSR′ comprise two chiral centers and a hemiaminal ether or hemiaminal thioether moiety on the dipicolylamine skeleton. Syn‐[Zn(LPhOMe)Cl2] precipitates out readily from the reaction mixture as a major product whereas anti‐[Zn(LPhOMe)Cl2] stays in solution as minor product. Both syn‐[Zn(LPhOMe)Cl2] and anti‐[Zn(LPhOMe)Cl2] were characterized using NMR spectroscopy and mass spectrometry. Solid‐state structures revealed that syn‐[Zn(LPhOMe)Cl2] adopted a square pyramidal geometry while anti‐[Zn(LPhOMe)Cl2] possesses a trigonal bipyramidal geometry around the Zn centers. The scope of this method was shown to be wide by varying the components of the dynamic coordination assembly, and the structures of the complexes isolated were confirmed by NMR spectroscopy, mass spectrometry, and X‐ray crystallography. Syn complexes were isolated as major products with ZnII and CuII, and anti complexes were found to be major products with NiII and CdII. Hemiaminals and hemiaminal ethers are known to be unstable and are seldom observed as part of cyclic organic compounds or as coordinated ligands assembled around metals. It is now shown, with the support of experimental results, that linear hemiaminal ethers or thioethers can be assembled without the assistance of Lewis acidic metals in the multi‐component assembly, and a possible pathway of the formation of hemiaminal ethers has been proposed. We belong to the Zinpyr family: Hemiaminals and hemiaminal ethers are known to be unstable and are seldom observed as part of cyclic organic compounds or as coordinated ligands assembled around metals. It is now shown that linear hemiaminal ethers or thioethers can be assembled without the assistance of Lewis acidic metals. Multicomponent one‐pot reactions offer a new route towards the synthesis of stereoisomers of new dipicolylamine complexes.</description><subject>Chemistry</subject><subject>chiral complexes</subject><subject>dipicolylamine</subject><subject>Ligands</subject><subject>Mass spectrometry</subject><subject>nitrogen ligands</subject><subject>one-pot synthesis</subject><subject>Scientific imaging</subject><subject>zinc complexes</subject><issn>1861-4728</issn><issn>1861-471X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkMtO3DAUQC3UCiiw7RJF6oZNprYTP7KcTukA4iExPLqzHOdGmCZxaieC-XsMAyPEhtW9ss49sg5C3wmeEIzpTx2snlBMGMZSFhtom0hO0lyQv1_WO5Vb6FsI9xgzigu5ibYozwljlG4jczY2gzWu7V0H3ZBcdJD2bkguQZvBui4kV-5B-yokwx0ki2UXR7AhcXWyGMCDs8G14F8efts-mpplo1vbQTKL0gYeIeyir7VuAuy9zh10_efwanaUnl7Mj2fT09QwmRcpGKppVpCcS16ykohMMpITWgtNBYdKZFzEFSQztGC8pKbmmOSVKHWFJc2zHXSw8vbe_R8hDKq1wUDT6A7cGBQRPEaSkuOI_viA3rvRd_F3kYplOMsIjdRkRRnvQvBQq97bVvulIlg951fP-dU6fzzYf9WOZQvVGn_rHYFiBTzYBpaf6NR0cTx9L09XtzYM8Li-1f6f4iITTN2ez9VlfvNrJk_O1Tx7An7AoIA</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Raje, Sakthi</creator><creator>Gurusamy, Sureshbabu</creator><creator>Koner, Abhishek</creator><creator>Mehrotra, Sonam</creator><creator>Jennifer, Samson Jegan</creator><creator>Vasudev, Prema G.</creator><creator>Butcher, Ray J.</creator><creator>Angamuthu, Raja</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201601</creationdate><title>Multicomponent One-pot Reactions Towards the Synthesis of Stereoisomers of Dipicolylamine Complexes</title><author>Raje, Sakthi ; Gurusamy, Sureshbabu ; Koner, Abhishek ; Mehrotra, Sonam ; Jennifer, Samson Jegan ; Vasudev, Prema G. ; Butcher, Ray J. ; Angamuthu, Raja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5849-ec2a23914686b5b173851412f7a276ed73677a2e85c2956b2cf6014d7bad08243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Chemistry</topic><topic>chiral complexes</topic><topic>dipicolylamine</topic><topic>Ligands</topic><topic>Mass spectrometry</topic><topic>nitrogen ligands</topic><topic>one-pot synthesis</topic><topic>Scientific imaging</topic><topic>zinc complexes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raje, Sakthi</creatorcontrib><creatorcontrib>Gurusamy, Sureshbabu</creatorcontrib><creatorcontrib>Koner, Abhishek</creatorcontrib><creatorcontrib>Mehrotra, Sonam</creatorcontrib><creatorcontrib>Jennifer, Samson Jegan</creatorcontrib><creatorcontrib>Vasudev, Prema G.</creatorcontrib><creatorcontrib>Butcher, Ray J.</creatorcontrib><creatorcontrib>Angamuthu, Raja</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry, an Asian journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raje, Sakthi</au><au>Gurusamy, Sureshbabu</au><au>Koner, Abhishek</au><au>Mehrotra, Sonam</au><au>Jennifer, Samson Jegan</au><au>Vasudev, Prema G.</au><au>Butcher, Ray J.</au><au>Angamuthu, Raja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multicomponent One-pot Reactions Towards the Synthesis of Stereoisomers of Dipicolylamine Complexes</atitle><jtitle>Chemistry, an Asian journal</jtitle><addtitle>Chem. 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Both syn‐[Zn(LPhOMe)Cl2] and anti‐[Zn(LPhOMe)Cl2] were characterized using NMR spectroscopy and mass spectrometry. Solid‐state structures revealed that syn‐[Zn(LPhOMe)Cl2] adopted a square pyramidal geometry while anti‐[Zn(LPhOMe)Cl2] possesses a trigonal bipyramidal geometry around the Zn centers. The scope of this method was shown to be wide by varying the components of the dynamic coordination assembly, and the structures of the complexes isolated were confirmed by NMR spectroscopy, mass spectrometry, and X‐ray crystallography. Syn complexes were isolated as major products with ZnII and CuII, and anti complexes were found to be major products with NiII and CdII. Hemiaminals and hemiaminal ethers are known to be unstable and are seldom observed as part of cyclic organic compounds or as coordinated ligands assembled around metals. It is now shown, with the support of experimental results, that linear hemiaminal ethers or thioethers can be assembled without the assistance of Lewis acidic metals in the multi‐component assembly, and a possible pathway of the formation of hemiaminal ethers has been proposed. We belong to the Zinpyr family: Hemiaminals and hemiaminal ethers are known to be unstable and are seldom observed as part of cyclic organic compounds or as coordinated ligands assembled around metals. It is now shown that linear hemiaminal ethers or thioethers can be assembled without the assistance of Lewis acidic metals. Multicomponent one‐pot reactions offer a new route towards the synthesis of stereoisomers of new dipicolylamine complexes.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>26415522</pmid><doi>10.1002/asia.201500889</doi><tpages>8</tpages></addata></record>
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source Wiley Online Library All Journals
subjects Chemistry
chiral complexes
dipicolylamine
Ligands
Mass spectrometry
nitrogen ligands
one-pot synthesis
Scientific imaging
zinc complexes
title Multicomponent One-pot Reactions Towards the Synthesis of Stereoisomers of Dipicolylamine Complexes
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