B–O Dynamic Covalent Bond-Enabled Polyphenol-Mediated Macroporous Resin Efficiently Separating Boron Isotopes

The separation of boron isotopes (<sup>10</sup>B/<sup>11</sup>B) is challenging due to the much smaller relative mass difference between the <sup>10</sup>B- and <sup>11</sup>B-bearing compounds. Herein, we report an efficient separation of <sup>10</sup>B by polyphenol-mediated macroporous resin (BWT-MR). The phenolic hydroxyl groups of BWT-MR chelate with B of B(OH)<sub>3</sub> into tetrahedral sp<sup>3</sup> hybridized B-phenolic hydroxyl complexes. Then the isotope exchange reaction between <sup>10</sup>B of B(OH)<sub>3</sub> and <sup>11</sup>B in <sup>11</sup>B-phenolic hydroxyl complexes is facilitated for the breaking of the B-O dynamic covalent bond of <sup>11</sup>B-phenolic hydroxyl complexes and rebuilding of the B-O dynamic covalent bond of <sup>10</sup>B-phenolic hydroxyl complexes, leading to the enrichment of <sup>10</sup>B on BWT-MR. The corresponding single-stage separation factor is high up to 1.043. Moreover, the flow-through separation in the fixed bed enables experimental validation for practical industrial applications, achieving a high <sup>10</sup>B abundance (21.64%). This work paves the way for the exploitation of more efficient enrichment of <sup>10</sup>B for sustainable nuclear energy and biomedical research.

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Publication Details

Journal
Langmuir
Published
2025-08-20
DOI
https://doi.org/10.1021/acs.langmuir.5c02806
Primary Topic
Chemical Synthesis and Characterization
Type
article
Field-Weighted Citation Impact
0.00

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article

B–O Dynamic Covalent Bond-Enabled Polyphenol-Mediated Macroporous Resin Efficiently Separating Boron Isotopes

Xian Liu, Junling Guo, Ningbo Pang, Xuepin Liao et al.
Langmuir
Chemical Synthesis and Characterization
article

B–O Dynamic Covalent Bond-Enabled Polyphenol-Mediated Macroporous Resin Efficiently Separating Boron Isotopes

Xian Liu, Junling Guo, Ningbo Pang, Xuepin Liao, Xiaoling Wang, Jiali Cheng
article en

Abstract

The separation of boron isotopes (<sup>10</sup>B/<sup>11</sup>B) is challenging due to the much smaller relative mass difference between the <sup>10</sup>B- and <sup>11</sup>B-bearing compounds. Herein, we report an efficient separation of <sup>10</sup>B by polyphenol-mediated macroporous resin (BWT-MR). The phenolic hydroxyl groups of BWT-MR chelate with B of B(OH)<sub>3</sub> into tetrahedral sp<sup>3</sup> hybridized B-phenolic hydroxyl complexes. Then the isotope exchange reaction between <sup>10</sup>B of B(OH)<sub>3</sub> and <sup>11</sup>B in <sup>11</sup>B-phenolic hydroxyl complexes is facilitated for the breaking of the B-O dynamic covalent bond of <sup>11</sup>B-phenolic hydroxyl complexes and rebuilding of the B-O dynamic covalent bond of <sup>10</sup>B-phenolic hydroxyl complexes, leading to the enrichment of <sup>10</sup>B on BWT-MR. The corresponding single-stage separation factor is high up to 1.043. Moreover, the flow-through separation in the fixed bed enables experimental validation for practical industrial applications, achieving a high <sup>10</sup>B abundance (21.64%). This work paves the way for the exploitation of more efficient enrichment of <sup>10</sup>B for sustainable nuclear energy and biomedical research.

LangmuirVol. 41(34)
Sichuan University (CN)
National Natural Science Foundation of China, Sichuan University, State Key Laboratory of Polymer Materials Engineering, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 73%
Chemical Synthesis and Characterization
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