{"title":"复杂各向异性相互作用下基于最优控制的核自旋交叉极化","authors":"Shovik Ray, Venkata SubbaRao Redrouthu, Asif Equbal and Sheetal Kumar Jain","doi":"10.1039/D5CP00096C","DOIUrl":null,"url":null,"abstract":"<p >Cross-polarization is an indispensable part of solid state nuclear magnetic resonance spectroscopy to enhance sensitivity and extract structural information. However, the presence of certain anisotropic interactions, including chemical shift anisotropy and quadrupolar coupling, makes the inter-nuclear spin correlation experiments challenging. This impedes characterization of numerous materials and pharmaceutical compounds containing isotopes, such as <small><sup>19</sup></small>F with large chemical shift anisotropy and <small><sup>6/7</sup></small>Li, <small><sup>23</sup></small>Na, <small><sup>27</sup></small>Al, <em>etc.</em>, with quadrupolar coupling. To address this problem, we introduce a new optimal control simulation-generated pulse sequence for Optimal Polarization Transfer In the presence of Anisotropic Nuclear Spin interactions (OPTIANS). Numerical simulations show high efficiency and robustness against experimental imperfections under a broad range of anisotropic interaction strengths for <small><sup>19</sup></small>F–<small><sup>7</sup></small>Li, <small><sup>19</sup></small>F–<small><sup>23</sup></small>Na, <small><sup>19</sup></small>F–<small><sup>27</sup></small>Al, and <small><sup>19</sup></small>F–<small><sup>13</sup></small>C polarization transfers. The polarization transfer curves show transient oscillations, which make the pulse sequence a quantitative method for dipolar coupling measurements. Experiments on a multi-metal fluoride system validate the predictions of the simulations by showing efficient PT in three spin pairs at varying experimental conditions. Remarkably, this method shows 50% better <small><sup>19</sup></small>F–<small><sup>7</sup></small>Li PT efficiency at 14.1 T compared to the ramped cross-polarization experiment. The underlying polarization transfer mechanism is analyzed using the Fourier transform of the polarization transfer curves revealing that this optimal control method utilizes the chemical shift anisotropy and quadrupolar coupling to facilitate robust and efficient cross-polarization.</p>","PeriodicalId":99,"journal":{"name":"Physical Chemistry Chemical Physics","volume":" 14","pages":" 7016-7027"},"PeriodicalIF":2.9000,"publicationDate":"2025-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimal control-based nuclear spin cross-polarization in the presence of complicating anisotropic interactions†\",\"authors\":\"Shovik Ray, Venkata SubbaRao Redrouthu, Asif Equbal and Sheetal Kumar Jain\",\"doi\":\"10.1039/D5CP00096C\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Cross-polarization is an indispensable part of solid state nuclear magnetic resonance spectroscopy to enhance sensitivity and extract structural information. However, the presence of certain anisotropic interactions, including chemical shift anisotropy and quadrupolar coupling, makes the inter-nuclear spin correlation experiments challenging. This impedes characterization of numerous materials and pharmaceutical compounds containing isotopes, such as <small><sup>19</sup></small>F with large chemical shift anisotropy and <small><sup>6/7</sup></small>Li, <small><sup>23</sup></small>Na, <small><sup>27</sup></small>Al, <em>etc.</em>, with quadrupolar coupling. To address this problem, we introduce a new optimal control simulation-generated pulse sequence for Optimal Polarization Transfer In the presence of Anisotropic Nuclear Spin interactions (OPTIANS). Numerical simulations show high efficiency and robustness against experimental imperfections under a broad range of anisotropic interaction strengths for <small><sup>19</sup></small>F–<small><sup>7</sup></small>Li, <small><sup>19</sup></small>F–<small><sup>23</sup></small>Na, <small><sup>19</sup></small>F–<small><sup>27</sup></small>Al, and <small><sup>19</sup></small>F–<small><sup>13</sup></small>C polarization transfers. The polarization transfer curves show transient oscillations, which make the pulse sequence a quantitative method for dipolar coupling measurements. Experiments on a multi-metal fluoride system validate the predictions of the simulations by showing efficient PT in three spin pairs at varying experimental conditions. Remarkably, this method shows 50% better <small><sup>19</sup></small>F–<small><sup>7</sup></small>Li PT efficiency at 14.1 T compared to the ramped cross-polarization experiment. The underlying polarization transfer mechanism is analyzed using the Fourier transform of the polarization transfer curves revealing that this optimal control method utilizes the chemical shift anisotropy and quadrupolar coupling to facilitate robust and efficient cross-polarization.</p>\",\"PeriodicalId\":99,\"journal\":{\"name\":\"Physical Chemistry Chemical Physics\",\"volume\":\" 14\",\"pages\":\" 7016-7027\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-03-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Physical Chemistry Chemical Physics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/cp/d5cp00096c\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physical Chemistry Chemical Physics","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/cp/d5cp00096c","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Optimal control-based nuclear spin cross-polarization in the presence of complicating anisotropic interactions†
Cross-polarization is an indispensable part of solid state nuclear magnetic resonance spectroscopy to enhance sensitivity and extract structural information. However, the presence of certain anisotropic interactions, including chemical shift anisotropy and quadrupolar coupling, makes the inter-nuclear spin correlation experiments challenging. This impedes characterization of numerous materials and pharmaceutical compounds containing isotopes, such as 19F with large chemical shift anisotropy and 6/7Li, 23Na, 27Al, etc., with quadrupolar coupling. To address this problem, we introduce a new optimal control simulation-generated pulse sequence for Optimal Polarization Transfer In the presence of Anisotropic Nuclear Spin interactions (OPTIANS). Numerical simulations show high efficiency and robustness against experimental imperfections under a broad range of anisotropic interaction strengths for 19F–7Li, 19F–23Na, 19F–27Al, and 19F–13C polarization transfers. The polarization transfer curves show transient oscillations, which make the pulse sequence a quantitative method for dipolar coupling measurements. Experiments on a multi-metal fluoride system validate the predictions of the simulations by showing efficient PT in three spin pairs at varying experimental conditions. Remarkably, this method shows 50% better 19F–7Li PT efficiency at 14.1 T compared to the ramped cross-polarization experiment. The underlying polarization transfer mechanism is analyzed using the Fourier transform of the polarization transfer curves revealing that this optimal control method utilizes the chemical shift anisotropy and quadrupolar coupling to facilitate robust and efficient cross-polarization.
期刊介绍:
Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions.
The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.