Research Fields:
Synthesis of Triphyrin and metallotriphyrin complexes.
Research Projects:
1. National Natural Science Foundation of China No. 21301074, 2014.01-2016.12
2. National Science Foundation of Jiangsu Province No. BK20130483, 2013.09-2016.09
3. China Postdoctoral Science Foundation funded project No. 2013M540415, 2013.09-2015.09
4. Colleges and universities in Jiangsu Province Natural Science Research on the project No. 13KJB150010
5. Programs of Senior Talent Foundation of Jiangsu University
Publications:
(1)
Zhaoli Xue, D. Kuzuhara, S. Ikeda, Y. Sakakibara, K. Ohkubo, N. Aratani, T. Okujima, H. Uno, S. Fukuzumi, H. Yamada, “η
5-Cyclopentadienyliron(II)–[14]Triphyrin(2.1.1) Sandwich Compounds: Synthesis, Characterization, and Stable Redox Interconversion,”
Angewandte Chemie
International Edition,
2013,
52, 7306-7309
(2)
Zhaoli Xue, S. Ikeda, D. Kuzuhara, T. Okujima, H. Uno, H. Yamada, “Synthesis and Characterization of New Platinum(II) and Platinum(IV) Triphyrin Complexes,”
Inorganic Chemistry,
2013,
52, 1688 – 1690.
(3)
ZhaoLi Xue Z. Shen, J. Mack, D. Kuzuhara, H. Yamada, T. Okujima, N. Ono, X. Z. You, N. Kobayashi, “A Facile One-Pot Synthesis of Meso-Aryl-Substituted [14]Triphyrin(2.1.1),”
Journal of American Chemical Society,
2008,
130, 16478 – 16479. (
Highlight by
Angewandte Chemie
International Edition,
2009,
48, 3592 – 3594).
(4)
Zhaoli Xue, J. Mack, H. Lu, L. Zhang, X. Z. You, D. Kuzuhara, M. Stillman, H. Yamada, S. Yamauchi, N. Kobayashi, Z. Shen, “The Synthesis and Properties of Free-Base [14]Triphyrin(2.1.1) Compounds and the Formation of Subporphyrinoid Metal Complexes,”
Chemistry-A European Journal,
2011,
17, 4396 – 4407. (Selected as
VIP and
Inside Cover,
Spotlight by
Angewandte Chemie
International Edition,
2011,
50, 3592 – 3594).
(5) D. Kuzuhara,
Zhaoli Xue, S. Mori, T. Okujima, H. Uno, N. Aratani, H. Yamada, “Synthesis and properties of Boron Complexes of [14]Triphyrin(2.1.1),”
Chemical Communications,
2013,
49, 8955 – 8957.
(6) Y. Sung, J. Lim,
Zhaoli Xue, Z. Shen, D. Kim, “Comparative Photophysical Properties Between Bicyclo[2.2.2]octadiene (BCOD)- and Benzo-Fused Free-Base Triphyrins (2.1.1),”
Chemical Communications,
2011,
47, 12616 – 12618.
(7) D. Kuzuhara, H. Yamada,
ZhaoLi Xue, T. Okujima, S. Mori, Z. Shen, H. Uno, “New Synthesis of Meso-Free-[14]Triphyrin(2.1.1) by McMurry Coupling and its Derivatization to Mn(I) and Re(I) Complexes,”
Chemical Communications,
2011,
47, 722 – 724.
(8) Y. Iima, D. Kuzuhara,
Zhaoli Xue, H. Uno, S. Akimoto, H. Yamada, K. Tominaga, “Photophysical Properties of Triphyrin(2.1.1) Investigated by Time-Resolved Fluorescence Measurements,”
Chemical Physics Letter,
2011,
513, 67 – 71.
(9) H. J. Xu, J. Mark, D. Wu,
Zhaoli Xue, A. B. Descalzo, K. Rurack, Z. Shen, “Synthesis and properties of fused-ring-expanded porphyrins that were core-Modified with group 16 heteroatoms,”
Chemistry-A European Journal,
2012,
18, 16844 – 16867.
(10) H. Lu,
Zhaoli Xue, J. Mack, Z. Shen, X. Z. You, N. Kobayashi, “Specific Cu
2+-Induced J-Aggregation and Hg
2+-Induced Fluorescence Enhancement Based on BODIPY,”
Chemical Communications,
2010,
46, 3565 – 3567.
(11) A. B. Descalzo, H. Xu,
Zhaoli Xue, K. Hoffmann, Z. Shen, M. G. Weller, X. Z. You, K. Rurack, “Phenanthrene-Fused Boron-Dipyrromethenes as Bright Long-Wavelength Fluorophores,”
Organic Letters,
2008,
10, 1581 – 1584.
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