ARTICLES

Synthesis of 10B-Enriched Borane Lewis Base Adducts

  • Shasha Liang ,
  • Yanna Ma ,
  • Xuenian Chen
Expand
  • a College of Chemistry, Zhengzhou University, Zhengzhou 450001
    b School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007
* Corresponding authors. E-mail: ;

Received date: 2023-02-28

  Revised date: 2023-04-25

  Online published: 2023-04-26

Supported by

National Natural Science Foundation of China(22171246); National Natural Science Foundation of China(22271256)

Abstract

In nature, boron is composed of a mixture of two stable isotopes, 10B (19.78%) and 11B (80.22%). The isotopical 10B-enriched compounds play important roles in many fields, such as the nuclear industry and cancer radiate treatment. Therefore, the syntheses of such kind of compounds is of important significance. These isotopical 10B-enriched compounds can be prepared from 10B-enriched boranes, however, the synthetic methods of such boranes are few. Herein, the synthetic methods of 10B-enriched Na10BH4, THF•10BH3, DMS•10BH3, DMA•10BH3, NH310BH3, Me3N•10BH3, Ph3P•10BH3, and IPr•10BH3 were developed. Firstly, Na10BH4 was synthesized with commercially available 10B(OH)3 as starting material based on the modified literature methods. Then the reaction of Na10BH4 and I2 provided 10B2H6, which could rapidly react with different Lewis bases to afford corresponding L•10BH3. Undoubtedly, these approaches provide convenient ways for the synthesis of 10B-enriched compounds.

Cite this article

Shasha Liang , Yanna Ma , Xuenian Chen . Synthesis of 10B-Enriched Borane Lewis Base Adducts[J]. Chinese Journal of Organic Chemistry, 2023 , 43(5) : 1772 -1776 . DOI: 10.6023/cjoc202302032

References

[1]
Gao, C.; Xuan, Q.; Song, Q. Chin. J. Chem. 2021, 39, 2504.
[2]
(a) Bose, S. K.; Mao, L.; Kuehn, L.; Radius, U.; Nekvinda, J.; Santos, W. L.; Westcott, S. A.; Steel, P. G.; Marder, T. B. Chem. Rev. 2021, 121, 13238.
[2]
(b) Tucker, C. E.; Davidson, J.; Knochel, P. J. Org. Chem. 1992, 57, 3482.
[3]
(a) Hill, T. G.; Godfroid, R. A.; White, J. P.; Shore, S. G. Inorg. Chem. 1991, 30, 2952.
[3]
(b) Sivaev, I. B.; Bregadze, V. I.; Sj?berg, S. Collect. Czech. Chem. Commun. 2002, 67, 679.
[3]
(c) Miller, H. C.; Miller, N. E.; Muetterties, E. L. J. Am. Chem. Soc. 1963, 85, 3885
[3]
(d) Chen, X.-M.; Ma, N.; Liu, X.-R.; Wei, C.; Cui, C.-C.; Cao, B.-L.; Guo, Y.; Wang, L.-S.; Gu, Q.; Chen, X. Angew. Chem., Int. Ed. 2019, 58, 2720.
[3]
(e) Chen, X.-M.; Ma, N.; Zhang, Q.-F; Wang, J.; Feng, X.; Wei, C.; Wang, L.-S.; Zhang, J.; Chen, X. J. Am. Chem. Soc. 2018, 140, 6718.
[3]
(f) Ma, Y.-N.; Gao, Y.; Ma, Y.; Wang, Y.; Ren, H.; Chen, X. J. Am. Chem. Soc. 2022, 144, 8371.
[3]
(g) Ma, Y.-N.; Ren, H.; Wu, Y.; Li, N.; Chen, F.; Chen, X. J. Am. Chem. Soc. 2023, 145, 7331.
[3]
(h) Ge, Y.; Qiu, Z.; Xie, Z. Acta Chim. Sinica 2022, 80, 432. (in Chinese)
[3]
(葛懿修, 邱早早, 谢作伟, 化学学报, 2022, 80, 432.)
[3]
(i) Zhang, J.; Xie, Z. Sci. Sin. Chim. 2023, 53, 312. (in Chinese)
[3]
(张洁, 谢作伟, 中国科学: 化学, 2023, 53, 312.)
[4]
(a) Zhao, Q.; Dewhurst, R. D.; Braunschweig, H.; Chen, X. Angew. Chem., Int. Ed. 2019, 58, 3268.
[4]
(b) Peng, J.; Song, Y.; Wang, Y.; Liu, Z.; Chen, X. Org. Chem. Front. 2022, 9, 1536.
[4]
(c) Ju, M.-Y.; Guo, Y.; Chen, X.-M.; Chen, X. Inorg. Chem. 2021, 60, 7101
[4]
(d) Miao, Y.; Kang, J.-X.; Ma, Y.-N.; Chen, X. Green Chem. 2021, 23, 3595.
[4]
(e) Guo, Y.; Wang, R.-Y.; Kang, J.-X.; Ma, Y.-N.; Xu, C.-Q.; Li, J.; Chen, X. Nat. Commun. 2021, 12, 5964.
[5]
(a) Yang, J.; Li, Z.; Zhu, S. Chin. J. Org. Chem. 2017, 37, 2481. (in Chinese)
[5]
(杨吉民, 李子奇, 朱守非, 有机化学, 2017, 37, 2481.)
[5]
(b) Huang, M.-Y.; Zhu, S.-F. Chem. Catal. 2022, 2, 3112.
[5]
(c) Huang, M.-Y.; Zhu, S.-F. Chem. Sci. 2021, 12, 15790.
[5]
(d) Cheng, Q.; Xu, H.; Zhu, S.; Zhou, Q. Acta Chim. Sinica 2015, 73, 326. (in Chinese)
[5]
(程清卿, 许唤, 朱守非, 周其林, 化学学报, 2015, 73, 326.)
[6]
(a) Moss, R. L. Appl. Radiat. Isot. 2017, 88, 2.
[6]
(b) Li, J.; Tu, Z.; Liu, Z. Sci. Sin. Chim. 2020, 50, 1296. (in Chinese)
[6]
(李纪元, 涂智宇, 刘志博, 中国科学: 化学, 2020, 50, 1296.)
[7]
(a) Safronov, A. V.; Jalisatgi, S. S.; Hawthorne, M. F. Inorg. Chem. 2016, 55, 5116.
[7]
(b) Adams, L.; Hosmane, S. N.; Eklund, J. E.; Wang, J.; Hosmane, N. S. J. Am. Chem. Soc. 2002, 124, 7292.
[8]
(a) Narayana, C.; Periasamy, M. A. J. Organomet. Chem. 1987, 323, 145.
[8]
(b) Zhu, Y.; Widjaja, E.; Sia, S. L. P.; Wang, Z.; Carpenter, K.; Maguire, J. A.; Hosmane, N. S.; Hawthorne, M. F. J. Am. Chem. Soc. 2007, 129, 6507.
[9]
Chen, X.; Bao, X.; Billet, B.; Shore, S. G.; Zhao, J.-C. Chem.-Eur. J. 2012, 18, 11994.
[10]
Kikuchi, T.; Nobuta, Y.; Umeda, J.; Yamamoto, Y.; Ishyama, T.; Miyaura, N. Tetrahedron 2008, 64, 4967.
[11]
(a) Stock, A.; Kuss, E. Ber. Dtsch. Chem. Ges. 1923, 56, 789.
[11]
(b) Shore, S. G.; Boddeker, K. W. Inorg. Chem. 1964, 3, 914.
[11]
(c) Chen, X.; Bao, X.; Zhao, J.; Shore, S. G. J. Am. Chem. Soc. 2011, 133, 14172.
[12]
Hermanek, S. Chem. Rev. 1992, 92, 325.
Outlines

/