{"title":"Identifying and Quantifying Borate Environments in Borosilicate Glasses: <sup>11</sup>B NMR-Peak Assignments Assisted by Double-Quantum Experiments.","authors":"Baltzar Stevensson, Peng Lv, Mattias Edén","doi":"10.1021/acs.jpcb.4c06721","DOIUrl":null,"url":null,"abstract":"<p><p>We discuss the prospects for accurate <sup>11</sup>B magic-angle-spinning (MAS) nuclear magnetic resonance (NMR) spectral deconvolutions for reaching beyond the readily extracted borate speciations offered by the integrated resonances of the coexisting B<sup>[3]</sup> and B<sup>[4]</sup> species of the respective BO<sub>3</sub> and BO<sub>4</sub> network groups in borosilicate (BS) glasses. We critically review hitherto proposed <sup>11</sup>B<sup>[3]</sup> and <sup>11</sup>B<sup>[4]</sup> NMR-peak assignments relating to their neighboring Si, B<sup>[3]</sup> and B<sup>[4]</sup> species, as quantified by MAS NMR spectral deconvolution. Guidance to these resonance assignments was offered from double-quantum-single-quantum (2Q-1Q) <sup>11</sup>B MAS NMR experiments that inform about the B<sup>[<i>p</i>]</sup>-O-B<sup>[<i>q</i>]</sup> network linkages. The NMR spectral deconvolutions from two BS glass series with low nonbridging oxygen (NBO) contents and fixed molar ratios <i>n</i><sub>Si</sub>/<i>n</i><sub>B</sub> = {1.0, 2.0} but variable network-modifying cations of alkali metals and Mg<sup>2+</sup> revealed a dominance of B<sup>[4]</sup>-O-Si linkages, yet with a significant dependence on the BO<sub>3</sub> population of the glass, which was rationalized by the different propensities for B<sup>[4]</sup>-O-{Si, B<sup>[3]</sup>, B<sup>[4]</sup>} linkage formation. For BS glasses with comparable B and Si contents, we recommend three-peak deconvolutions of the <sup>11</sup>B<sup>[4]</sup> spectral region, whose <sup>11</sup>B<sup>[4]</sup>(<i>m</i>Si) sites differ in their (average) numbers of <i>m</i> B<sup>[4]</sup>-O-Si and 4 - <i>m</i> B<sup>[4]</sup>-O-B<sup>[<i>p</i>]</sup> bonds, where B<sup>[<i>p</i>]</sup> may assume B<sup>[3]</sup> <i>or</i> B<sup>[4]</sup>. We also discuss the structural origin of the two rather arbitrarily classified \"ring\" and \"non-ring\" B<sup>[3]</sup> entities, where 2Q-1Q <sup>11</sup>B NMR suggests the former to primarily constitute BO<sub>3</sub> groups that coexist with BO<sub>4</sub> moieties in (superstructural) ring units largely devoid of bonds to Si, whereas the \"non-ring\" B<sup>[3]</sup> sites involve linkages to all of B<sup>[3]</sup>, B<sup>[4]</sup>, and Si, with B<sup>[3]</sup>-O-Si linkages prevailing. The limitations of <sup>11</sup>B NMR spectral deconvolutions are discussed, including the remaining challenges in analyzing NBO-rich BS glasses.</p>","PeriodicalId":60,"journal":{"name":"The Journal of Physical Chemistry B","volume":" ","pages":"12651-12667"},"PeriodicalIF":2.8000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry B","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpcb.4c06721","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/10 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
We discuss the prospects for accurate 11B magic-angle-spinning (MAS) nuclear magnetic resonance (NMR) spectral deconvolutions for reaching beyond the readily extracted borate speciations offered by the integrated resonances of the coexisting B[3] and B[4] species of the respective BO3 and BO4 network groups in borosilicate (BS) glasses. We critically review hitherto proposed 11B[3] and 11B[4] NMR-peak assignments relating to their neighboring Si, B[3] and B[4] species, as quantified by MAS NMR spectral deconvolution. Guidance to these resonance assignments was offered from double-quantum-single-quantum (2Q-1Q) 11B MAS NMR experiments that inform about the B[p]-O-B[q] network linkages. The NMR spectral deconvolutions from two BS glass series with low nonbridging oxygen (NBO) contents and fixed molar ratios nSi/nB = {1.0, 2.0} but variable network-modifying cations of alkali metals and Mg2+ revealed a dominance of B[4]-O-Si linkages, yet with a significant dependence on the BO3 population of the glass, which was rationalized by the different propensities for B[4]-O-{Si, B[3], B[4]} linkage formation. For BS glasses with comparable B and Si contents, we recommend three-peak deconvolutions of the 11B[4] spectral region, whose 11B[4](mSi) sites differ in their (average) numbers of m B[4]-O-Si and 4 - m B[4]-O-B[p] bonds, where B[p] may assume B[3]or B[4]. We also discuss the structural origin of the two rather arbitrarily classified "ring" and "non-ring" B[3] entities, where 2Q-1Q 11B NMR suggests the former to primarily constitute BO3 groups that coexist with BO4 moieties in (superstructural) ring units largely devoid of bonds to Si, whereas the "non-ring" B[3] sites involve linkages to all of B[3], B[4], and Si, with B[3]-O-Si linkages prevailing. The limitations of 11B NMR spectral deconvolutions are discussed, including the remaining challenges in analyzing NBO-rich BS glasses.
期刊介绍:
An essential criterion for acceptance of research articles in the journal is that they provide new physical insight. Please refer to the New Physical Insights virtual issue on what constitutes new physical insight. Manuscripts that are essentially reporting data or applications of data are, in general, not suitable for publication in JPC B.