Sidebands in dynamic angle spinning (DAS) and double rotation (DOR) NMR
A theory of dynamic angle spinning (DAS) and double rotation (DOR) NMR is described using average Hamiltonian and irreducible tensor methods. Sideband intensities in DAS and DOR spectra are analyzed by both the moment and Bessel function methods, and general formulae are derived. Results show that t...
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Veröffentlicht in: | Solid state nuclear magnetic resonance 1992-12, Vol.1 (5), p.267-295 |
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description | A theory of dynamic angle spinning (DAS) and double rotation (DOR) NMR is described using average Hamiltonian and irreducible tensor methods. Sideband intensities in DAS and DOR spectra are analyzed by both the moment and Bessel function methods, and general formulae are derived. Results show that the DAS moments depend on the relative rotor phase between the first and the second evolution periods, whereas the second and third DOR moments are independent of the relative phase between the inner and outer rotors. Sideband intensities in DAS spectra also depend on the relative rotor phases between evolution at the first and second angles, as well as on the ratio of time spent at each angle. Sideband intensities and phases in DOR spectra are related to the relative rotor phases between the inner and outer rotors, and the sideband pattern is determined by the ratio of the inner and outer rotor spinning speeds. An inversion symmetry of the odd numbered DOR sidebands at the relative rotor phase
γ
r = 0°, 180° permits the elimination of these sidebands. Finally, numerical simulations are implemented and shown to agree with experimental results. Quadrupolar parameters can therefore be recovered either by calculating the second and third moments or by simulating the sideband intensities and phases. |
doi_str_mv | 10.1016/0926-2040(92)90047-D |
format | Article |
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γ
r = 0°, 180° permits the elimination of these sidebands. Finally, numerical simulations are implemented and shown to agree with experimental results. Quadrupolar parameters can therefore be recovered either by calculating the second and third moments or by simulating the sideband intensities and phases.</description><identifier>ISSN: 0926-2040</identifier><identifier>EISSN: 1527-3326</identifier><identifier>DOI: 10.1016/0926-2040(92)90047-D</identifier><identifier>PMID: 1365742</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>central transition ; double rotation ; dynamic-angle spinning ; Magnetic Resonance Spectroscopy - methods ; Models, Chemical ; Models, Theoretical ; Molecular Structure ; Oxalates - chemistry ; Perchlorates - chemistry ; quadrupolar nuclei ; Rotation ; Rubidium - chemistry ; spinning sidebands</subject><ispartof>Solid state nuclear magnetic resonance, 1992-12, Vol.1 (5), p.267-295</ispartof><rights>1992</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-e285271af90743ee4b3fec413a355620501f6b66475fc6a2b7ab1a0c57f85b233</citedby><cites>FETCH-LOGICAL-c357t-e285271af90743ee4b3fec413a355620501f6b66475fc6a2b7ab1a0c57f85b233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0926-2040(92)90047-D$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1365742$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, B.Q.</creatorcontrib><creatorcontrib>Baltisberger, J.H.</creatorcontrib><creatorcontrib>Wu, Y.</creatorcontrib><creatorcontrib>Samoson, A.</creatorcontrib><creatorcontrib>Pines, A.</creatorcontrib><title>Sidebands in dynamic angle spinning (DAS) and double rotation (DOR) NMR</title><title>Solid state nuclear magnetic resonance</title><addtitle>Solid State Nucl Magn Reson</addtitle><description>A theory of dynamic angle spinning (DAS) and double rotation (DOR) NMR is described using average Hamiltonian and irreducible tensor methods. Sideband intensities in DAS and DOR spectra are analyzed by both the moment and Bessel function methods, and general formulae are derived. Results show that the DAS moments depend on the relative rotor phase between the first and the second evolution periods, whereas the second and third DOR moments are independent of the relative phase between the inner and outer rotors. Sideband intensities in DAS spectra also depend on the relative rotor phases between evolution at the first and second angles, as well as on the ratio of time spent at each angle. Sideband intensities and phases in DOR spectra are related to the relative rotor phases between the inner and outer rotors, and the sideband pattern is determined by the ratio of the inner and outer rotor spinning speeds. An inversion symmetry of the odd numbered DOR sidebands at the relative rotor phase
γ
r = 0°, 180° permits the elimination of these sidebands. Finally, numerical simulations are implemented and shown to agree with experimental results. Quadrupolar parameters can therefore be recovered either by calculating the second and third moments or by simulating the sideband intensities and phases.</description><subject>central transition</subject><subject>double rotation</subject><subject>dynamic-angle spinning</subject><subject>Magnetic Resonance Spectroscopy - methods</subject><subject>Models, Chemical</subject><subject>Models, Theoretical</subject><subject>Molecular Structure</subject><subject>Oxalates - chemistry</subject><subject>Perchlorates - chemistry</subject><subject>quadrupolar nuclei</subject><subject>Rotation</subject><subject>Rubidium - chemistry</subject><subject>spinning sidebands</subject><issn>0926-2040</issn><issn>1527-3326</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKw0AUhgdRar28gUJW0i6ic59mI5RWq1AttLoeJpOTMtJOaiYR-vZObdGdm3Pg_P-5fQhdEXxLMJF3OKMypZjjXkb7GcZcpeMj1CWCqpQxKo9R99dyis5C-MAYK8JkB3ViFIrTLposXAG58UVInE-KrTdrZxPjlytIwsZ57_wy6Y2Hi34sFklRtXlU6qoxjat8VGbzfvL6Mr9AJ6VZBbg85HP0_vjwNnpKp7PJ82g4TS0TqkmBDuJ5xJQZVpwB8JyVYDlhhgkhKRaYlDKXkitRWmlorkxODLZClQORU8bO0c1-7qauPlsIjV67YGG1Mh6qNmglBM0EF9HI90ZbVyHUUOpN7dam3mqC9Y6f3sHROzg6o_qHnx7HtuvD_DZfQ_HXtAcW9fu9DvHJLwe1DtaBt1C4Gmyji8r9v-AbiM98EA</recordid><startdate>19921201</startdate><enddate>19921201</enddate><creator>Sun, B.Q.</creator><creator>Baltisberger, J.H.</creator><creator>Wu, Y.</creator><creator>Samoson, A.</creator><creator>Pines, A.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19921201</creationdate><title>Sidebands in dynamic angle spinning (DAS) and double rotation (DOR) NMR</title><author>Sun, B.Q. ; Baltisberger, J.H. ; Wu, Y. ; Samoson, A. ; Pines, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-e285271af90743ee4b3fec413a355620501f6b66475fc6a2b7ab1a0c57f85b233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>central transition</topic><topic>double rotation</topic><topic>dynamic-angle spinning</topic><topic>Magnetic Resonance Spectroscopy - methods</topic><topic>Models, Chemical</topic><topic>Models, Theoretical</topic><topic>Molecular Structure</topic><topic>Oxalates - chemistry</topic><topic>Perchlorates - chemistry</topic><topic>quadrupolar nuclei</topic><topic>Rotation</topic><topic>Rubidium - chemistry</topic><topic>spinning sidebands</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, B.Q.</creatorcontrib><creatorcontrib>Baltisberger, J.H.</creatorcontrib><creatorcontrib>Wu, Y.</creatorcontrib><creatorcontrib>Samoson, A.</creatorcontrib><creatorcontrib>Pines, A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Solid state nuclear magnetic resonance</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, B.Q.</au><au>Baltisberger, J.H.</au><au>Wu, Y.</au><au>Samoson, A.</au><au>Pines, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sidebands in dynamic angle spinning (DAS) and double rotation (DOR) NMR</atitle><jtitle>Solid state nuclear magnetic resonance</jtitle><addtitle>Solid State Nucl Magn Reson</addtitle><date>1992-12-01</date><risdate>1992</risdate><volume>1</volume><issue>5</issue><spage>267</spage><epage>295</epage><pages>267-295</pages><issn>0926-2040</issn><eissn>1527-3326</eissn><abstract>A theory of dynamic angle spinning (DAS) and double rotation (DOR) NMR is described using average Hamiltonian and irreducible tensor methods. Sideband intensities in DAS and DOR spectra are analyzed by both the moment and Bessel function methods, and general formulae are derived. Results show that the DAS moments depend on the relative rotor phase between the first and the second evolution periods, whereas the second and third DOR moments are independent of the relative phase between the inner and outer rotors. Sideband intensities in DAS spectra also depend on the relative rotor phases between evolution at the first and second angles, as well as on the ratio of time spent at each angle. Sideband intensities and phases in DOR spectra are related to the relative rotor phases between the inner and outer rotors, and the sideband pattern is determined by the ratio of the inner and outer rotor spinning speeds. An inversion symmetry of the odd numbered DOR sidebands at the relative rotor phase
γ
r = 0°, 180° permits the elimination of these sidebands. Finally, numerical simulations are implemented and shown to agree with experimental results. Quadrupolar parameters can therefore be recovered either by calculating the second and third moments or by simulating the sideband intensities and phases.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>1365742</pmid><doi>10.1016/0926-2040(92)90047-D</doi><tpages>29</tpages></addata></record> |
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subjects | central transition double rotation dynamic-angle spinning Magnetic Resonance Spectroscopy - methods Models, Chemical Models, Theoretical Molecular Structure Oxalates - chemistry Perchlorates - chemistry quadrupolar nuclei Rotation Rubidium - chemistry spinning sidebands |
title | Sidebands in dynamic angle spinning (DAS) and double rotation (DOR) NMR |
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