Loading…
Spirocyclic Nitroxide Biradicals: Synthesis and Evaluation as Dynamic Nuclear Polarizing Agents
A method for the synthesis of rigid nitroxide biradicals with various spatial orientations between the radical centers is reported. Diketones were employed as substrates for tin amine protocol (SnAP) reagents to provide the parent spirocyclic diamines. Oxidation by peroxyacids provided the correspon...
Saved in:
Published in: | Helvetica chimica acta 2020-12, Vol.103 (12), p.n/a |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3179-bb24adbbdeed88dd59cc3aea56ae44122c3dd2ea7d91d6e83649fce8ea6035f93 |
---|---|
cites | cdi_FETCH-LOGICAL-c3179-bb24adbbdeed88dd59cc3aea56ae44122c3dd2ea7d91d6e83649fce8ea6035f93 |
container_end_page | n/a |
container_issue | 12 |
container_start_page | |
container_title | Helvetica chimica acta |
container_volume | 103 |
creator | Jackl, Moritz K. Gordon, Christopher P. Copéret, Christophe Bode, Jeffrey W. |
description | A method for the synthesis of rigid nitroxide biradicals with various spatial orientations between the radical centers is reported. Diketones were employed as substrates for tin amine protocol (SnAP) reagents to provide the parent spirocyclic diamines. Oxidation by peroxyacids provided the corresponding nitroxide biradicals. A set of four different biradicals with various interelectron distances and torsion angles between the radical planes was synthesized using this method. The exact geometries were determined by X‐ray crystallography and the biradicals were investigated by EPR spectroscopy and evaluated for their dynamic nuclear polarization (DNP) performance. 1H‐DNP enhancements in the range of 1.2–2.1 at 14.1 Tesla (600 MHz spectrometer) were achieved. This synthetic methodology opens a promising alternative to access nitroxide biradicals with various torsional angles and inter radical distances. |
doi_str_mv | 10.1002/hlca.202000179 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2468994311</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2468994311</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3179-bb24adbbdeed88dd59cc3aea56ae44122c3dd2ea7d91d6e83649fce8ea6035f93</originalsourceid><addsrcrecordid>eNqFkE1LAzEQhoMoWKtXzwHPW5PsZ7zVWq1QVKiCtzCbzLYp292a7Krrr3dLRY-eBobneWd4CTnnbMQZE5erUsNIMMEY46k8IAMeCxGIJI0PyaDfZQHj8vWYnHi_7hkpWTogarG1rtadLq2mD7Zx9ac1SK-tA2M1lP6KLrqqWaG3nkJl6PQdyhYaW1cUPL3pKtjszFaXCI4-1SU4-2WrJR0vsWr8KTkq-hQ8-5lD8nI7fZ7Mgvnj3f1kPA902D8b5LmIwOS5QTRZZkwstQ4BIU4Ao4gLoUNjBEJqJDcJZmESyUJjhpCwMC5kOCQX-9ytq99a9I1a162r-pNKREkmZRRy3lOjPaVd7b3DQm2d3YDrFGdqV6Lalah-S-wFuRc-bIndP7SazSfjP_cbI4F4OQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2468994311</pqid></control><display><type>article</type><title>Spirocyclic Nitroxide Biradicals: Synthesis and Evaluation as Dynamic Nuclear Polarizing Agents</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Jackl, Moritz K. ; Gordon, Christopher P. ; Copéret, Christophe ; Bode, Jeffrey W.</creator><creatorcontrib>Jackl, Moritz K. ; Gordon, Christopher P. ; Copéret, Christophe ; Bode, Jeffrey W.</creatorcontrib><description>A method for the synthesis of rigid nitroxide biradicals with various spatial orientations between the radical centers is reported. Diketones were employed as substrates for tin amine protocol (SnAP) reagents to provide the parent spirocyclic diamines. Oxidation by peroxyacids provided the corresponding nitroxide biradicals. A set of four different biradicals with various interelectron distances and torsion angles between the radical planes was synthesized using this method. The exact geometries were determined by X‐ray crystallography and the biradicals were investigated by EPR spectroscopy and evaluated for their dynamic nuclear polarization (DNP) performance. 1H‐DNP enhancements in the range of 1.2–2.1 at 14.1 Tesla (600 MHz spectrometer) were achieved. This synthetic methodology opens a promising alternative to access nitroxide biradicals with various torsional angles and inter radical distances.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.202000179</identifier><language>eng</language><publisher>Zürich: Wiley Subscription Services, Inc</publisher><subject>Angles (geometry) ; biradicals ; Crystallography ; Diamines ; Diketones ; DNP ; EPR ; Nitroxide ; Oxidation ; Polarization ; Reagents ; SnAP ; Spatial distribution ; Spectroscopy ; spiro compounds ; Substrates ; Synthesis ; Tin</subject><ispartof>Helvetica chimica acta, 2020-12, Vol.103 (12), p.n/a</ispartof><rights>2020 Wiley‐VHCA AG, Zurich, Switzerland</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3179-bb24adbbdeed88dd59cc3aea56ae44122c3dd2ea7d91d6e83649fce8ea6035f93</citedby><cites>FETCH-LOGICAL-c3179-bb24adbbdeed88dd59cc3aea56ae44122c3dd2ea7d91d6e83649fce8ea6035f93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Jackl, Moritz K.</creatorcontrib><creatorcontrib>Gordon, Christopher P.</creatorcontrib><creatorcontrib>Copéret, Christophe</creatorcontrib><creatorcontrib>Bode, Jeffrey W.</creatorcontrib><title>Spirocyclic Nitroxide Biradicals: Synthesis and Evaluation as Dynamic Nuclear Polarizing Agents</title><title>Helvetica chimica acta</title><description>A method for the synthesis of rigid nitroxide biradicals with various spatial orientations between the radical centers is reported. Diketones were employed as substrates for tin amine protocol (SnAP) reagents to provide the parent spirocyclic diamines. Oxidation by peroxyacids provided the corresponding nitroxide biradicals. A set of four different biradicals with various interelectron distances and torsion angles between the radical planes was synthesized using this method. The exact geometries were determined by X‐ray crystallography and the biradicals were investigated by EPR spectroscopy and evaluated for their dynamic nuclear polarization (DNP) performance. 1H‐DNP enhancements in the range of 1.2–2.1 at 14.1 Tesla (600 MHz spectrometer) were achieved. This synthetic methodology opens a promising alternative to access nitroxide biradicals with various torsional angles and inter radical distances.</description><subject>Angles (geometry)</subject><subject>biradicals</subject><subject>Crystallography</subject><subject>Diamines</subject><subject>Diketones</subject><subject>DNP</subject><subject>EPR</subject><subject>Nitroxide</subject><subject>Oxidation</subject><subject>Polarization</subject><subject>Reagents</subject><subject>SnAP</subject><subject>Spatial distribution</subject><subject>Spectroscopy</subject><subject>spiro compounds</subject><subject>Substrates</subject><subject>Synthesis</subject><subject>Tin</subject><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LAzEQhoMoWKtXzwHPW5PsZ7zVWq1QVKiCtzCbzLYp292a7Krrr3dLRY-eBobneWd4CTnnbMQZE5erUsNIMMEY46k8IAMeCxGIJI0PyaDfZQHj8vWYnHi_7hkpWTogarG1rtadLq2mD7Zx9ac1SK-tA2M1lP6KLrqqWaG3nkJl6PQdyhYaW1cUPL3pKtjszFaXCI4-1SU4-2WrJR0vsWr8KTkq-hQ8-5lD8nI7fZ7Mgvnj3f1kPA902D8b5LmIwOS5QTRZZkwstQ4BIU4Ao4gLoUNjBEJqJDcJZmESyUJjhpCwMC5kOCQX-9ytq99a9I1a162r-pNKREkmZRRy3lOjPaVd7b3DQm2d3YDrFGdqV6Lalah-S-wFuRc-bIndP7SazSfjP_cbI4F4OQ</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Jackl, Moritz K.</creator><creator>Gordon, Christopher P.</creator><creator>Copéret, Christophe</creator><creator>Bode, Jeffrey W.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>202012</creationdate><title>Spirocyclic Nitroxide Biradicals: Synthesis and Evaluation as Dynamic Nuclear Polarizing Agents</title><author>Jackl, Moritz K. ; Gordon, Christopher P. ; Copéret, Christophe ; Bode, Jeffrey W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3179-bb24adbbdeed88dd59cc3aea56ae44122c3dd2ea7d91d6e83649fce8ea6035f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Angles (geometry)</topic><topic>biradicals</topic><topic>Crystallography</topic><topic>Diamines</topic><topic>Diketones</topic><topic>DNP</topic><topic>EPR</topic><topic>Nitroxide</topic><topic>Oxidation</topic><topic>Polarization</topic><topic>Reagents</topic><topic>SnAP</topic><topic>Spatial distribution</topic><topic>Spectroscopy</topic><topic>spiro compounds</topic><topic>Substrates</topic><topic>Synthesis</topic><topic>Tin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jackl, Moritz K.</creatorcontrib><creatorcontrib>Gordon, Christopher P.</creatorcontrib><creatorcontrib>Copéret, Christophe</creatorcontrib><creatorcontrib>Bode, Jeffrey W.</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Helvetica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jackl, Moritz K.</au><au>Gordon, Christopher P.</au><au>Copéret, Christophe</au><au>Bode, Jeffrey W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spirocyclic Nitroxide Biradicals: Synthesis and Evaluation as Dynamic Nuclear Polarizing Agents</atitle><jtitle>Helvetica chimica acta</jtitle><date>2020-12</date><risdate>2020</risdate><volume>103</volume><issue>12</issue><epage>n/a</epage><issn>0018-019X</issn><eissn>1522-2675</eissn><abstract>A method for the synthesis of rigid nitroxide biradicals with various spatial orientations between the radical centers is reported. Diketones were employed as substrates for tin amine protocol (SnAP) reagents to provide the parent spirocyclic diamines. Oxidation by peroxyacids provided the corresponding nitroxide biradicals. A set of four different biradicals with various interelectron distances and torsion angles between the radical planes was synthesized using this method. The exact geometries were determined by X‐ray crystallography and the biradicals were investigated by EPR spectroscopy and evaluated for their dynamic nuclear polarization (DNP) performance. 1H‐DNP enhancements in the range of 1.2–2.1 at 14.1 Tesla (600 MHz spectrometer) were achieved. This synthetic methodology opens a promising alternative to access nitroxide biradicals with various torsional angles and inter radical distances.</abstract><cop>Zürich</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/hlca.202000179</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0018-019X |
ispartof | Helvetica chimica acta, 2020-12, Vol.103 (12), p.n/a |
issn | 0018-019X 1522-2675 |
language | eng |
recordid | cdi_proquest_journals_2468994311 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Angles (geometry) biradicals Crystallography Diamines Diketones DNP EPR Nitroxide Oxidation Polarization Reagents SnAP Spatial distribution Spectroscopy spiro compounds Substrates Synthesis Tin |
title | Spirocyclic Nitroxide Biradicals: Synthesis and Evaluation as Dynamic Nuclear Polarizing Agents |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T13%3A15%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Spirocyclic%20Nitroxide%20Biradicals:%20Synthesis%20and%20Evaluation%20as%20Dynamic%20Nuclear%20Polarizing%20Agents&rft.jtitle=Helvetica%20chimica%20acta&rft.au=Jackl,%20Moritz%20K.&rft.date=2020-12&rft.volume=103&rft.issue=12&rft.epage=n/a&rft.issn=0018-019X&rft.eissn=1522-2675&rft_id=info:doi/10.1002/hlca.202000179&rft_dat=%3Cproquest_cross%3E2468994311%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3179-bb24adbbdeed88dd59cc3aea56ae44122c3dd2ea7d91d6e83649fce8ea6035f93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2468994311&rft_id=info:pmid/&rfr_iscdi=true |