fragmentation study of the Rhodamine 610 cation using visible-laser desorption ionization
The fragmentation of a potential visible matrix-assisted laser desorption ionization: Rhodamine 610 was studied under 532 nm visible irradiation, as a function of anion counter ion. It was found that at a fixed fluence, the chloride salt produced fewer fragments than those formed with ClO₄ ⁻ or BF₄...
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| Veröffentlicht in: | Journal of mass spectrometry. 2010-08, Vol.45 (8), p.909-914 |
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| container_issue | 8 |
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| container_title | Journal of mass spectrometry. |
| container_volume | 45 |
| creator | Yang, C.Y Hu, X.K Loboda, A.V Lipson, R.H |
| description | The fragmentation of a potential visible matrix-assisted laser desorption ionization: Rhodamine 610 was studied under 532 nm visible irradiation, as a function of anion counter ion. It was found that at a fixed fluence, the chloride salt produced fewer fragments than those formed with ClO₄ ⁻ or BF₄ ⁻. Evidence presented suggests that the degree of fragmentation is inversely proportional to the strength of the contact ion pair in the solid state; that is, more energy is deposited into the radical cation which can lead to fragmentation when less energy is required to separate the ion pair. Similar results were found for salts of Rhodamine 6G. Copyright © 2010 John Wiley & Sons, Ltd. |
| doi_str_mv | 10.1002/jms.1779 |
| format | Article |
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It was found that at a fixed fluence, the chloride salt produced fewer fragments than those formed with ClO₄ ⁻ or BF₄ ⁻. Evidence presented suggests that the degree of fragmentation is inversely proportional to the strength of the contact ion pair in the solid state; that is, more energy is deposited into the radical cation which can lead to fragmentation when less energy is required to separate the ion pair. Similar results were found for salts of Rhodamine 6G. 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Mass Spectrom</addtitle><description>The fragmentation of a potential visible matrix-assisted laser desorption ionization: Rhodamine 610 was studied under 532 nm visible irradiation, as a function of anion counter ion. It was found that at a fixed fluence, the chloride salt produced fewer fragments than those formed with ClO₄ ⁻ or BF₄ ⁻. Evidence presented suggests that the degree of fragmentation is inversely proportional to the strength of the contact ion pair in the solid state; that is, more energy is deposited into the radical cation which can lead to fragmentation when less energy is required to separate the ion pair. Similar results were found for salts of Rhodamine 6G. Copyright © 2010 John Wiley & Sons, Ltd.</description><subject>anion effect</subject><subject>cation fragmentation</subject><subject>Cations</subject><subject>Cations - chemistry</subject><subject>Chemistry</subject><subject>Chlorides</subject><subject>Desorption</subject><subject>Exact sciences and technology</subject><subject>Fragmentation</subject><subject>Fragments</subject><subject>Ion pairs</subject><subject>Ionization</subject><subject>Mass spectrometry</subject><subject>matrices</subject><subject>Organic chemistry</subject><subject>Reactivity and mechanisms</subject><subject>Rhodamine</subject><subject>Rhodamine dyes</subject><subject>Rhodamines - chemistry</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</subject><subject>Temperature</subject><subject>visible-MALDI</subject><issn>1076-5174</issn><issn>1096-9888</issn><issn>1096-9888</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90Mtu1DAUBuAIgWgpSDwBZINgk3JOfF-iFkpRCxItQrCxnNieuuQytRNgePomndCuYGHZkj-dy59lTxH2EaB8fdmmfRRC3ct2ERQvlJTy_vwWvGAo6E72KKVLAFCK8ofZTgmcSi7YbvbNR7NqXTeYIfRdnobRbvLe58OFyz9f9Na0oXM5R8jrrRhT6Fb5z5BC1biiMcnF3LrUx_XN93TCnxv5OHvgTZPck-Xey87fvT0_eF-cfDo6PnhzUtSUMlVwySR6Z0lpgTJGPSfeIgOKRGJljbXMg0MCJTCmnOC-QusqakpvCC3JXvZyW3Yd-6vRpUG3IdWuaUzn-jFpQRWgmBae5Kv_SuQCieJcyjtaxz6l6Lxex9CauNEIek5cT4nrOfGJPluqjlXr7C38G_EEXizApNo0U95dHdKdI4iCq7lQsXW_QuM2_2yoP5yeLY0XH9Lgft96E39oLohg-uvHI02-n0oBeKjn9Z9vvTe9Nqs4zfDlrIQpWZSSCQHkGsOirsU</recordid><startdate>201008</startdate><enddate>201008</enddate><creator>Yang, C.Y</creator><creator>Hu, X.K</creator><creator>Loboda, A.V</creator><creator>Lipson, R.H</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><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>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>201008</creationdate><title>fragmentation study of the Rhodamine 610 cation using visible-laser desorption ionization</title><author>Yang, C.Y ; Hu, X.K ; Loboda, A.V ; Lipson, R.H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4459-68581fed32d04554f63fd15041381bdadd5f0e13020559e76fb1deb4a2fa3423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>anion effect</topic><topic>cation fragmentation</topic><topic>Cations</topic><topic>Cations - chemistry</topic><topic>Chemistry</topic><topic>Chlorides</topic><topic>Desorption</topic><topic>Exact sciences and technology</topic><topic>Fragmentation</topic><topic>Fragments</topic><topic>Ion pairs</topic><topic>Ionization</topic><topic>Mass spectrometry</topic><topic>matrices</topic><topic>Organic chemistry</topic><topic>Reactivity and mechanisms</topic><topic>Rhodamine</topic><topic>Rhodamine dyes</topic><topic>Rhodamines - chemistry</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</topic><topic>Temperature</topic><topic>visible-MALDI</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, C.Y</creatorcontrib><creatorcontrib>Hu, X.K</creatorcontrib><creatorcontrib>Loboda, A.V</creatorcontrib><creatorcontrib>Lipson, R.H</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><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><collection>MEDLINE - Academic</collection><jtitle>Journal of mass spectrometry.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, C.Y</au><au>Hu, X.K</au><au>Loboda, A.V</au><au>Lipson, R.H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>fragmentation study of the Rhodamine 610 cation using visible-laser desorption ionization</atitle><jtitle>Journal of mass spectrometry.</jtitle><addtitle>J. Mass Spectrom</addtitle><date>2010-08</date><risdate>2010</risdate><volume>45</volume><issue>8</issue><spage>909</spage><epage>914</epage><pages>909-914</pages><issn>1076-5174</issn><issn>1096-9888</issn><eissn>1096-9888</eissn><abstract>The fragmentation of a potential visible matrix-assisted laser desorption ionization: Rhodamine 610 was studied under 532 nm visible irradiation, as a function of anion counter ion. It was found that at a fixed fluence, the chloride salt produced fewer fragments than those formed with ClO₄ ⁻ or BF₄ ⁻. Evidence presented suggests that the degree of fragmentation is inversely proportional to the strength of the contact ion pair in the solid state; that is, more energy is deposited into the radical cation which can lead to fragmentation when less energy is required to separate the ion pair. Similar results were found for salts of Rhodamine 6G. Copyright © 2010 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>20648675</pmid><doi>10.1002/jms.1779</doi><tpages>6</tpages></addata></record> |
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| ispartof | Journal of mass spectrometry., 2010-08, Vol.45 (8), p.909-914 |
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| source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
| subjects | anion effect cation fragmentation Cations Cations - chemistry Chemistry Chlorides Desorption Exact sciences and technology Fragmentation Fragments Ion pairs Ionization Mass spectrometry matrices Organic chemistry Reactivity and mechanisms Rhodamine Rhodamine dyes Rhodamines - chemistry Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods Temperature visible-MALDI |
| title | fragmentation study of the Rhodamine 610 cation using visible-laser desorption ionization |
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