IF 2.8 2区 化学 Q3 CHEMISTRY, PHYSICAL
The Journal of Physical Chemistry B Pub Date : 2024-12-19 Epub Date: 2024-12-10 DOI:10.1021/acs.jpcb.4c06721
Baltzar Stevensson, Peng Lv, Mattias Edén
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引用次数: 0

摘要

我们讨论了准确的 11B 魔术角旋转(MAS)核磁共振(NMR)光谱解旋的前景,以超越硼硅酸盐(BS)玻璃中各自的 BO3 和 BO4 网络基团中共存的 B[3] 和 B[4] 物种的综合共振所提供的易于提取的硼酸盐规格。我们对迄今为止提出的与相邻 Si、B[3] 和 B[4] 物种有关的 11B[3] 和 11B[4] NMR 峰分配进行了批判性回顾,并通过 MAS NMR 光谱解卷积进行了量化。双量子-单量子 (2Q-1Q) 11B MAS NMR 实验为这些共振分配提供了指导,这些实验提供了有关 B[p]-O-B[q] 网络链接的信息。两个 BS 玻璃系列的 NMR 光谱解旋结果显示,它们的非桥氧(NBO)含量较低,固定摩尔比 nSi/nB = {1.0, 2.0} 但碱金属和 Mg2+ 的网络修饰阳离子可变时,B[4]-O-Si 连接占主导地位,但这与玻璃中的 BO3 数量有很大关系,B[4]-O-{Si、B[3]、B[4]} 连接形成的不同倾向使其合理化。对于 B 和 Si 含量相当的 BS 玻璃,我们建议对 11B[4] 光谱区进行三峰解旋,其 11B[4](mSi) 位点在 m B[4]-O-Si 和 4 - m B[4]-O-B[p] 键的(平均)数量上有所不同,其中 B[p] 可以是 B[3] 或 B[4]。我们还讨论了 "环状 "和 "非环状 "B[3] 实体的结构来源,2Q-1Q 11B NMR 表明前者主要由 BO3 基团构成,这些基团与 BO4 分子共存于(超结构)环单元中,基本上没有与 Si 的键,而 "非环状 "B[3] 位点涉及与所有 B[3]、B[4]和 Si 的连接,其中以 B[3]-O-Si 连接为主。本文讨论了 11B NMR 光谱解旋的局限性,包括在分析富含 NBO 的 BS 玻璃时仍然面临的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identifying and Quantifying Borate Environments in Borosilicate Glasses: 11B NMR-Peak Assignments Assisted by Double-Quantum Experiments.

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.

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来源期刊
CiteScore
5.80
自引率
9.10%
发文量
965
审稿时长
1.6 months
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.
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