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Lu SB, Chai H, Ward JS, et al. A 2,3-dialkoxynaphthalene-based naphthocage. Chem Commun (Camb). 2019;56(6):888-891doi: 10.1039/c9cc09585c.
Lu, S. B., Chai, H., Ward, J. S., Quan, M., Zhang, J., Rissanen, K., Luo, R., Yang, L. P., & Jiang, W. (2020). A 2,3-dialkoxynaphthalene-based naphthocage. Chemical communications (Cambridge, England), 56(6), 888-891. https://doi.org/10.1039/c9cc09585c
Lu, Song-Bo, et al. "A 2,3-dialkoxynaphthalene-based naphthocage." Chemical communications (Cambridge, England) vol. 56,6 (2020): 888-891. doi: https://doi.org/10.1039/c9cc09585c
Lu SB, Chai H, Ward JS, Quan M, Zhang J, Rissanen K, Luo R, Yang LP, Jiang W. A 2,3-dialkoxynaphthalene-based naphthocage. Chem Commun (Camb). 2020 Jan 18;56(6):888-891. doi: 10.1039/c9cc09585c. Epub 2019 Dec 20. PMID: 31858093.
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Chem Commun (Camb). 2020 Jan 18;56(6):888-891. doi: 10.1039/c9cc09585c. Epub 2019 Dec 20.

A 2,3-dialkoxynaphthalene-based naphthocage.

Chemical communications (Cambridge, England)

Song-Bo Lu, Hongxin Chai, Jas S Ward, Mao Quan, Jin Zhang, Kari Rissanen, Ray Luo, Liu-Pan Yang, Wei Jiang

Affiliations

  1. Shenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Xueyuan Blvd 1088, Shenzhen, 518055, China. [email protected].
  2. University of Jyväskylä, Department of Chemistry, P. O. Box 35, FI-40014, Jyväskylä, Finland.
  3. Shenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Xueyuan Blvd 1088, Shenzhen, 518055, China. [email protected] and Academy for Advanced Interdisciplinary Studies, Southern University of Science and Technology, Xueyuan Blvd 1088, Shenzhen, 518055, China. [email protected].
  4. Shenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Xueyuan Blvd 1088, Shenzhen, 518055, China. [email protected] and The State Key Laboratory of Molecular Engineering of Polymers, Fudan University, Shanghai, 200433, China.

PMID: 31858093 DOI: 10.1039/c9cc09585c

Abstract

A 2,3-dialkoxynaphthalene-based naphthocage has been synthesized. This naphthocage prefers to bind small organic cations with its low-symmetry conformation, which is in contrast to 2,6-dialkoxynaphthalene-based naphthocages. Self-sorting of these two naphthocages with two structurally similar guests tetramethylammonium and tetraethylammonium was achieved as well.

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