B.M. Fung, Tat-Hung Tong, Thilo Dollase, Matthew L. Magnuson
{"title":"具有捕获延迟的固态质子核磁共振谱线变窄","authors":"B.M. Fung, Tat-Hung Tong, Thilo Dollase, Matthew L. Magnuson","doi":"10.1006/jmra.1996.0213","DOIUrl":null,"url":null,"abstract":"<div><p>Organic solids have extensive proton–proton dipolar interactions, and their<sup>1</sup>H NMR linewidths are very large even with magic-angle spinning at moderate speeds. Recently it has been shown that substantial narrowing of the proton linewidths of organic solids can be achieved by using single-pulse excitation with acquisition delay or spin echo [S. Ding and C. A. McDowell,<em>J. Magn. Reson. A</em>111, 212 (1994); 115, 141 (1995); 117, 171 (1995)]. This interesting line-narrowing phenomenon has been further examined through the study of several amino acids, their deuterated analogs, and some aromatic compounds. The results confirm that narrow proton peaks are observed with long acquisition delay, and the peaks appear in the appropriate chemical-shift ranges for organic protons (0–10 ppm with respect to tetramethylsilane). However, except for some special cases, the observed peaks cannot be assigned to individual types of protons based on chemical-shift considerations only. To explore the reason for the line narrowing, the effect of acquisition delay on the<sup>19</sup>F linewidth of CaF<sub>2</sub>was also studied and compared with that on the<sup>1</sup>H linewidths of organic solids. It is suggested that the broad proton peak in an organic solid is a superposition of numerous transitions. These transitions have different linewidths, and the narrow peaks in the spectrum remain observable with long acquisition delays.</p></div>","PeriodicalId":16165,"journal":{"name":"Journal of Magnetic Resonance, Series A","volume":"123 1","pages":"Pages 56-63"},"PeriodicalIF":0.0000,"publicationDate":"1996-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/jmra.1996.0213","citationCount":"9","resultStr":"{\"title\":\"Line Narrowing in Solid-State Proton NMR with Acquisition Delay\",\"authors\":\"B.M. Fung, Tat-Hung Tong, Thilo Dollase, Matthew L. Magnuson\",\"doi\":\"10.1006/jmra.1996.0213\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Organic solids have extensive proton–proton dipolar interactions, and their<sup>1</sup>H NMR linewidths are very large even with magic-angle spinning at moderate speeds. Recently it has been shown that substantial narrowing of the proton linewidths of organic solids can be achieved by using single-pulse excitation with acquisition delay or spin echo [S. Ding and C. A. McDowell,<em>J. Magn. Reson. A</em>111, 212 (1994); 115, 141 (1995); 117, 171 (1995)]. This interesting line-narrowing phenomenon has been further examined through the study of several amino acids, their deuterated analogs, and some aromatic compounds. The results confirm that narrow proton peaks are observed with long acquisition delay, and the peaks appear in the appropriate chemical-shift ranges for organic protons (0–10 ppm with respect to tetramethylsilane). However, except for some special cases, the observed peaks cannot be assigned to individual types of protons based on chemical-shift considerations only. To explore the reason for the line narrowing, the effect of acquisition delay on the<sup>19</sup>F linewidth of CaF<sub>2</sub>was also studied and compared with that on the<sup>1</sup>H linewidths of organic solids. It is suggested that the broad proton peak in an organic solid is a superposition of numerous transitions. These transitions have different linewidths, and the narrow peaks in the spectrum remain observable with long acquisition delays.</p></div>\",\"PeriodicalId\":16165,\"journal\":{\"name\":\"Journal of Magnetic Resonance, Series A\",\"volume\":\"123 1\",\"pages\":\"Pages 56-63\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1996-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1006/jmra.1996.0213\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Magnetic Resonance, Series A\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1064185896902132\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Magnetic Resonance, Series A","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1064185896902132","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Line Narrowing in Solid-State Proton NMR with Acquisition Delay
Organic solids have extensive proton–proton dipolar interactions, and their1H NMR linewidths are very large even with magic-angle spinning at moderate speeds. Recently it has been shown that substantial narrowing of the proton linewidths of organic solids can be achieved by using single-pulse excitation with acquisition delay or spin echo [S. Ding and C. A. McDowell,J. Magn. Reson. A111, 212 (1994); 115, 141 (1995); 117, 171 (1995)]. This interesting line-narrowing phenomenon has been further examined through the study of several amino acids, their deuterated analogs, and some aromatic compounds. The results confirm that narrow proton peaks are observed with long acquisition delay, and the peaks appear in the appropriate chemical-shift ranges for organic protons (0–10 ppm with respect to tetramethylsilane). However, except for some special cases, the observed peaks cannot be assigned to individual types of protons based on chemical-shift considerations only. To explore the reason for the line narrowing, the effect of acquisition delay on the19F linewidth of CaF2was also studied and compared with that on the1H linewidths of organic solids. It is suggested that the broad proton peak in an organic solid is a superposition of numerous transitions. These transitions have different linewidths, and the narrow peaks in the spectrum remain observable with long acquisition delays.