Loading…
EPR-correlated dipolar spectroscopy by Q-band chirp SIFTER
While two-dimensional correlation spectra contain more information as compared to one-dimensional spectra, typical spectral widths encountered in electron paramagnetic resonance (EPR) spectroscopy largely restrict the applicability of correlation techniques. In essence, the monochromatic excitation...
Saved in:
Published in: | Physical chemistry chemical physics : PCCP 2016-08, Vol.18 (33), p.23111-2312 |
---|---|
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-c485t-31800e419f6cb514c2ee6b786d664c66dadc94668a87bbe14d714897535bf5ce3 |
---|---|
cites | cdi_FETCH-LOGICAL-c485t-31800e419f6cb514c2ee6b786d664c66dadc94668a87bbe14d714897535bf5ce3 |
container_end_page | 2312 |
container_issue | 33 |
container_start_page | 23111 |
container_title | Physical chemistry chemical physics : PCCP |
container_volume | 18 |
creator | Doll, Andrin Jeschke, Gunnar |
description | While two-dimensional correlation spectra contain more information as compared to one-dimensional spectra, typical spectral widths encountered in electron paramagnetic resonance (EPR) spectroscopy largely restrict the applicability of correlation techniques. In essence, the monochromatic excitation pulses established in pulsed EPR often cannot uniformly excite the entire spectrum. Here, this restriction is alleviated for nitroxide spin labels at Q-band microwave frequencies around 35 GHz. This is achieved by substitution of monochromatic pulses by frequency-swept chirp pulses tailored for uniform excitation. Unwanted interference effects brought by this substitution are analyzed for a pair of electron spins with secular dipolar coupling. Experimentally, the dipole-dipole interaction can be separated from other interactions by a constant-time Zeeman-compensated solid echo sequence called SIFTER. Such SIFTER experiments usually yield a one-dimensional dipolar spectrum. EPR-correlated dipolar spectra can be obtained when the four pulses are replaced by chirp pulses. These two-dimensional spectra encode additional information on the geometrical arrangement of the two spin labels. With the excitation parameters achieved by a home-built Q-band spectrometer capable of frequency-swept excitation, unwanted interference effects can be largely neglected for the examined model compound with a spin-spin distance of 4 nm. The experimentally obtained correlation pattern conforms to the expectation based on the inter-spin geometry of the investigated rigid model compound.
Frequency-swept chirp pulses uniformly excite the nitroxide spectrum at Q-band frequencies, which allows for acquisition of two-dimensional spectra correlating the dipolar spectrum to the EPR spectrum. |
doi_str_mv | 10.1039/c6cp03067j |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1812439081</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1812439081</sourcerecordid><originalsourceid>FETCH-LOGICAL-c485t-31800e419f6cb514c2ee6b786d664c66dadc94668a87bbe14d714897535bf5ce3</originalsourceid><addsrcrecordid>eNqNkdFLwzAQh4MoTqcvvit9FKGaLMk19U3KppOBc87nklxS7OjWmnQP---tbs5XuYc7uI8f3HeEXDB6yyhP7xCwoZxCsjggJ0wAj1OqxOF-TqBHTkNYUEqZZPyY9AaJSBmn4oTcD6ezGGvvXaVbZyNbNnWlfRQah62vA9bNJjKb6DU2emUj_Ch9E72NR_Ph7IwcFboK7nzX--R9NJxnT_Hk5XGcPUxiFEq2MWeKUidYWgAayQQOnAOTKLAAAgGstpgKAKVVYoxjwiZMqDSRXJpCouN9cr3NbXz9uXahzZdlQFdVeuXqdciZ4lKqruAfKBsI3tlhHXqzRbG7MnhX5I0vl9pvckbzb615Btn0R-tzB1_tctdm6ewe_fXYAZdbwAfcb__-wr8AHsB55Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1812439081</pqid></control><display><type>article</type><title>EPR-correlated dipolar spectroscopy by Q-band chirp SIFTER</title><source>Royal Society of Chemistry</source><creator>Doll, Andrin ; Jeschke, Gunnar</creator><creatorcontrib>Doll, Andrin ; Jeschke, Gunnar</creatorcontrib><description>While two-dimensional correlation spectra contain more information as compared to one-dimensional spectra, typical spectral widths encountered in electron paramagnetic resonance (EPR) spectroscopy largely restrict the applicability of correlation techniques. In essence, the monochromatic excitation pulses established in pulsed EPR often cannot uniformly excite the entire spectrum. Here, this restriction is alleviated for nitroxide spin labels at Q-band microwave frequencies around 35 GHz. This is achieved by substitution of monochromatic pulses by frequency-swept chirp pulses tailored for uniform excitation. Unwanted interference effects brought by this substitution are analyzed for a pair of electron spins with secular dipolar coupling. Experimentally, the dipole-dipole interaction can be separated from other interactions by a constant-time Zeeman-compensated solid echo sequence called SIFTER. Such SIFTER experiments usually yield a one-dimensional dipolar spectrum. EPR-correlated dipolar spectra can be obtained when the four pulses are replaced by chirp pulses. These two-dimensional spectra encode additional information on the geometrical arrangement of the two spin labels. With the excitation parameters achieved by a home-built Q-band spectrometer capable of frequency-swept excitation, unwanted interference effects can be largely neglected for the examined model compound with a spin-spin distance of 4 nm. The experimentally obtained correlation pattern conforms to the expectation based on the inter-spin geometry of the investigated rigid model compound.
Frequency-swept chirp pulses uniformly excite the nitroxide spectrum at Q-band frequencies, which allows for acquisition of two-dimensional spectra correlating the dipolar spectrum to the EPR spectrum.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/c6cp03067j</identifier><identifier>PMID: 27491304</identifier><language>eng</language><publisher>England</publisher><subject>Chirp ; Correlation ; Excitation ; Excitation spectra ; Interference ; Labels ; Spectra ; Spectroscopy</subject><ispartof>Physical chemistry chemical physics : PCCP, 2016-08, Vol.18 (33), p.23111-2312</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-31800e419f6cb514c2ee6b786d664c66dadc94668a87bbe14d714897535bf5ce3</citedby><cites>FETCH-LOGICAL-c485t-31800e419f6cb514c2ee6b786d664c66dadc94668a87bbe14d714897535bf5ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27491304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Doll, Andrin</creatorcontrib><creatorcontrib>Jeschke, Gunnar</creatorcontrib><title>EPR-correlated dipolar spectroscopy by Q-band chirp SIFTER</title><title>Physical chemistry chemical physics : PCCP</title><addtitle>Phys Chem Chem Phys</addtitle><description>While two-dimensional correlation spectra contain more information as compared to one-dimensional spectra, typical spectral widths encountered in electron paramagnetic resonance (EPR) spectroscopy largely restrict the applicability of correlation techniques. In essence, the monochromatic excitation pulses established in pulsed EPR often cannot uniformly excite the entire spectrum. Here, this restriction is alleviated for nitroxide spin labels at Q-band microwave frequencies around 35 GHz. This is achieved by substitution of monochromatic pulses by frequency-swept chirp pulses tailored for uniform excitation. Unwanted interference effects brought by this substitution are analyzed for a pair of electron spins with secular dipolar coupling. Experimentally, the dipole-dipole interaction can be separated from other interactions by a constant-time Zeeman-compensated solid echo sequence called SIFTER. Such SIFTER experiments usually yield a one-dimensional dipolar spectrum. EPR-correlated dipolar spectra can be obtained when the four pulses are replaced by chirp pulses. These two-dimensional spectra encode additional information on the geometrical arrangement of the two spin labels. With the excitation parameters achieved by a home-built Q-band spectrometer capable of frequency-swept excitation, unwanted interference effects can be largely neglected for the examined model compound with a spin-spin distance of 4 nm. The experimentally obtained correlation pattern conforms to the expectation based on the inter-spin geometry of the investigated rigid model compound.
Frequency-swept chirp pulses uniformly excite the nitroxide spectrum at Q-band frequencies, which allows for acquisition of two-dimensional spectra correlating the dipolar spectrum to the EPR spectrum.</description><subject>Chirp</subject><subject>Correlation</subject><subject>Excitation</subject><subject>Excitation spectra</subject><subject>Interference</subject><subject>Labels</subject><subject>Spectra</subject><subject>Spectroscopy</subject><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkdFLwzAQh4MoTqcvvit9FKGaLMk19U3KppOBc87nklxS7OjWmnQP---tbs5XuYc7uI8f3HeEXDB6yyhP7xCwoZxCsjggJ0wAj1OqxOF-TqBHTkNYUEqZZPyY9AaJSBmn4oTcD6ezGGvvXaVbZyNbNnWlfRQah62vA9bNJjKb6DU2emUj_Ch9E72NR_Ph7IwcFboK7nzX--R9NJxnT_Hk5XGcPUxiFEq2MWeKUidYWgAayQQOnAOTKLAAAgGstpgKAKVVYoxjwiZMqDSRXJpCouN9cr3NbXz9uXahzZdlQFdVeuXqdciZ4lKqruAfKBsI3tlhHXqzRbG7MnhX5I0vl9pvckbzb615Btn0R-tzB1_tctdm6ewe_fXYAZdbwAfcb__-wr8AHsB55Q</recordid><startdate>20160817</startdate><enddate>20160817</enddate><creator>Doll, Andrin</creator><creator>Jeschke, Gunnar</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20160817</creationdate><title>EPR-correlated dipolar spectroscopy by Q-band chirp SIFTER</title><author>Doll, Andrin ; Jeschke, Gunnar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-31800e419f6cb514c2ee6b786d664c66dadc94668a87bbe14d714897535bf5ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Chirp</topic><topic>Correlation</topic><topic>Excitation</topic><topic>Excitation spectra</topic><topic>Interference</topic><topic>Labels</topic><topic>Spectra</topic><topic>Spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Doll, Andrin</creatorcontrib><creatorcontrib>Jeschke, Gunnar</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</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>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Doll, Andrin</au><au>Jeschke, Gunnar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EPR-correlated dipolar spectroscopy by Q-band chirp SIFTER</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><addtitle>Phys Chem Chem Phys</addtitle><date>2016-08-17</date><risdate>2016</risdate><volume>18</volume><issue>33</issue><spage>23111</spage><epage>2312</epage><pages>23111-2312</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>While two-dimensional correlation spectra contain more information as compared to one-dimensional spectra, typical spectral widths encountered in electron paramagnetic resonance (EPR) spectroscopy largely restrict the applicability of correlation techniques. In essence, the monochromatic excitation pulses established in pulsed EPR often cannot uniformly excite the entire spectrum. Here, this restriction is alleviated for nitroxide spin labels at Q-band microwave frequencies around 35 GHz. This is achieved by substitution of monochromatic pulses by frequency-swept chirp pulses tailored for uniform excitation. Unwanted interference effects brought by this substitution are analyzed for a pair of electron spins with secular dipolar coupling. Experimentally, the dipole-dipole interaction can be separated from other interactions by a constant-time Zeeman-compensated solid echo sequence called SIFTER. Such SIFTER experiments usually yield a one-dimensional dipolar spectrum. EPR-correlated dipolar spectra can be obtained when the four pulses are replaced by chirp pulses. These two-dimensional spectra encode additional information on the geometrical arrangement of the two spin labels. With the excitation parameters achieved by a home-built Q-band spectrometer capable of frequency-swept excitation, unwanted interference effects can be largely neglected for the examined model compound with a spin-spin distance of 4 nm. The experimentally obtained correlation pattern conforms to the expectation based on the inter-spin geometry of the investigated rigid model compound.
Frequency-swept chirp pulses uniformly excite the nitroxide spectrum at Q-band frequencies, which allows for acquisition of two-dimensional spectra correlating the dipolar spectrum to the EPR spectrum.</abstract><cop>England</cop><pmid>27491304</pmid><doi>10.1039/c6cp03067j</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1463-9076 |
ispartof | Physical chemistry chemical physics : PCCP, 2016-08, Vol.18 (33), p.23111-2312 |
issn | 1463-9076 1463-9084 |
language | eng |
recordid | cdi_proquest_miscellaneous_1812439081 |
source | Royal Society of Chemistry |
subjects | Chirp Correlation Excitation Excitation spectra Interference Labels Spectra Spectroscopy |
title | EPR-correlated dipolar spectroscopy by Q-band chirp SIFTER |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T23%3A21%3A56IST&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=EPR-correlated%20dipolar%20spectroscopy%20by%20Q-band%20chirp%20SIFTER&rft.jtitle=Physical%20chemistry%20chemical%20physics%20:%20PCCP&rft.au=Doll,%20Andrin&rft.date=2016-08-17&rft.volume=18&rft.issue=33&rft.spage=23111&rft.epage=2312&rft.pages=23111-2312&rft.issn=1463-9076&rft.eissn=1463-9084&rft_id=info:doi/10.1039/c6cp03067j&rft_dat=%3Cproquest_cross%3E1812439081%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c485t-31800e419f6cb514c2ee6b786d664c66dadc94668a87bbe14d714897535bf5ce3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1812439081&rft_id=info:pmid/27491304&rfr_iscdi=true |