Synthesis and properties of chiral internally branched PAMAM-dendrimers
Improved synthetic methodology for the synthesis of internally branched chiral poly(amidoamine) (PAMAM) dendrons and dendrimers has been developed and the compounds have been characterized by NMR spectroscopy, IR spectroscopy, and optical rotation measurements. The dendrons and dendrimers show incre...
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Veröffentlicht in: | Tetrahedron 2015-02, Vol.71 (7), p.1109-1116 |
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creator | Petersen, Johannes F. Tortzen, Christian G. Pittelkow, Michael Christensen, Jørn B. |
description | Improved synthetic methodology for the synthesis of internally branched chiral poly(amidoamine) (PAMAM) dendrons and dendrimers has been developed and the compounds have been characterized by NMR spectroscopy, IR spectroscopy, and optical rotation measurements. The dendrons and dendrimers show increased degree of internal hydrogen bonding upon increasing generation and the presence of different types of amide-protons in the compounds is indicative of the existence of a tertiary structure in these PAMAM-dendrimers.
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doi_str_mv | 10.1016/j.tet.2014.12.080 |
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[Display omitted]</description><subject>Amide coupling</subject><subject>Branched</subject><subject>Convergent synthesis</subject><subject>Dendrimer</subject><subject>Dendrimers</subject><subject>Hydrogen bonding</subject><subject>Infrared radiation</subject><subject>Internal branching</subject><subject>NMR spectroscopy</subject><subject>Optical activity</subject><subject>Optical properties</subject><subject>Optical rotation</subject><subject>Synthesis (chemistry)</subject><issn>0040-4020</issn><issn>1464-5416</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kEFLAzEQhYMoWKs_wNsevew6kya7WzyVolVoUVDPIU0mNGWbrUkq9N-7Us-e5vK-x5uPsVuECgHr-22VKVccUFTIK2jhjI1Q1KKUAutzNgIQUArgcMmuUtoCACKfjNji_RjyhpJPhQ622Md-TzF7SkXvCrPxUXeFD5li0F13LNZRB7MhW7zNVrNVaSnY6HcU0zW7cLpLdPN3x-zz6fFj_lwuXxcv89myNKKBXGouOE1MbUkYK7leY9satwarEa2RE4kNgUNNtWwdoXQgm9Y5Ig0GUOrJmN2deoelXwdKWe18MtR1OlB_SAobIerptBYwRPEUNbFPKZJT-2GrjkeFoH6lqa0apKlfaQq5GqQNzMOJoeGHb09RJeMpGLI-ksnK9v4f-gejq3Wg</recordid><startdate>20150218</startdate><enddate>20150218</enddate><creator>Petersen, Johannes F.</creator><creator>Tortzen, Christian G.</creator><creator>Pittelkow, Michael</creator><creator>Christensen, Jørn B.</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20150218</creationdate><title>Synthesis and properties of chiral internally branched PAMAM-dendrimers</title><author>Petersen, Johannes F. ; Tortzen, Christian G. ; Pittelkow, Michael ; Christensen, Jørn B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-a242e3c6de4cd52ab188cfb0da11dc53517e0f1ae658fe15f0578ffeea0c015a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Amide coupling</topic><topic>Branched</topic><topic>Convergent synthesis</topic><topic>Dendrimer</topic><topic>Dendrimers</topic><topic>Hydrogen bonding</topic><topic>Infrared radiation</topic><topic>Internal branching</topic><topic>NMR spectroscopy</topic><topic>Optical activity</topic><topic>Optical properties</topic><topic>Optical rotation</topic><topic>Synthesis (chemistry)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Petersen, Johannes F.</creatorcontrib><creatorcontrib>Tortzen, Christian G.</creatorcontrib><creatorcontrib>Pittelkow, Michael</creatorcontrib><creatorcontrib>Christensen, Jørn B.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Tetrahedron</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Petersen, Johannes F.</au><au>Tortzen, Christian G.</au><au>Pittelkow, Michael</au><au>Christensen, Jørn B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and properties of chiral internally branched PAMAM-dendrimers</atitle><jtitle>Tetrahedron</jtitle><date>2015-02-18</date><risdate>2015</risdate><volume>71</volume><issue>7</issue><spage>1109</spage><epage>1116</epage><pages>1109-1116</pages><issn>0040-4020</issn><eissn>1464-5416</eissn><abstract>Improved synthetic methodology for the synthesis of internally branched chiral poly(amidoamine) (PAMAM) dendrons and dendrimers has been developed and the compounds have been characterized by NMR spectroscopy, IR spectroscopy, and optical rotation measurements. The dendrons and dendrimers show increased degree of internal hydrogen bonding upon increasing generation and the presence of different types of amide-protons in the compounds is indicative of the existence of a tertiary structure in these PAMAM-dendrimers.
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subjects | Amide coupling Branched Convergent synthesis Dendrimer Dendrimers Hydrogen bonding Infrared radiation Internal branching NMR spectroscopy Optical activity Optical properties Optical rotation Synthesis (chemistry) |
title | Synthesis and properties of chiral internally branched PAMAM-dendrimers |
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