| 主要论文 | 1) Feng X., Xu Z., Hu Z., Qi C., Luo   D., Zhao X., Mu Z., Redshaw C., Lam J. W. Y., Ma D., Tang B. Z.*, “Pyrene-based blue emitters with aggregationinduced   emission features for high-performance organic light-emitting diodes:, J.   Mater. Chem. C, 2019, 7,   2283-2290. 2) Islam M. M. Hu   Z., Wang Q.,  Redshaw C., Feng   X.*, “Pyrene-based Aggregation-induced Emission Luminogens and their   Applications”, Mater. Chem. Front.,   2019, DOI: 10.1039/C9QM00090A. 3) Feng X., Li, Y. He X., Liu, H.,   Zhao Z., Kwok R. T. K., Elsegood M. R. J., Lam J. W. Y., Tang B. Z.* “A Substitution-Dependent Light-Up Fluorescence Probe   for Selectively Detecting Fe3+ Ions and Its Cell Imaging Application”, Adv. Funct. Mater., 2018, 1802833 4) Feng X., Qi C. Feng H.-T., Zhao   Z., Sung H. H. Y., Williams I. D., Kwok R. T. K., Elsegood M. R. J., Lam J.   W. Y., Tang B. Z.* “Dual   fluorescence of tetraphenylethylene substituted pyrenes with   aggregation-induced emission characteristics for white-light emission” Chem. Sci., 2018, 9, 5679–5687 5) Wang, C.-Z., Feng X.,* Kowsera, Z., Wu C.,   Akther T., Elsegood M. R. J., Redshaw C., Yamato T., Dyes Pigments, 2018, 153, 125–131. 6) Wang C.-Z., Ihiyanagi H.,   Sakaguchi K., Feng X.,* Elsegood   M. J., Redshaw C., Yamato T.* A pyrene-based approach to tune emission color   from blue to yellow,   Journal of   Organic Chemistry, 2017, 82, 7176−7182. 7) Wang, C.-Z., Noda   Y., Wu C.; Feng X.,*   Venkatesan P., Cong H., Elsegood M. R. J., Warwick T. G., Teat   S. J.; Redshaw C.; Yamato T., Multiple   Photoluminescence from Pyrene-Fused Hexaarylbenzenes with   Aggregation-Enhanced Emission Features, Asian   J. Org. Chem., 2018, 7, 444 – 450 8) Feng   X.,* Hu J.-Y., Redshaw   C.,   Yamato T.* Functionalization of   Pyrene To Prepare Luminescent Materials—Typical Examples of Synthetic   Methodology, Chem. Eur. J. 2016, 22, 11898 – 11916.  9) Wang C.-Z., Kihara, R., Feng X.,* Thuéry, P., Redshaw C., Yamato T.* Synthesis, Structure and   Photophysical Properties of Pyrene–based [5]Helicenes: an Experimental and   Theoretical Study, ChemistrySelect , 2017, 2, 1436–1441. 10) Feng   X., Seto N., Wang C.-Z., Matsumoto, T., Tanaka   J., Wei X.-.F., Elsegood, Mark R. J., Horsburgh L., Redshaw C., Yamato T.*   Extended p-Conjugated Pyrene Derivatives: Structural, Photophysical and   Electrochemical Properties, ChemistrySelect,   2016, 1, 1926- 1932. 11) Feng X., Tomiyasu, H., Hu J.-Y.,   Wei X., Redshaw C., Elsegood M. R. J., Horsburgh L., Teat S. J.,   Yamato T.*   Regioselective substitution at the 1,3- and 6,8-positions of pyrene for the   construction of small dipolar molecules.   Journal of Organic Chemistry,2015, 80, 10973–10978.  12) Feng X., Hu J.-Y., Wei X., Redshaw   C., Yamato T.*   Influence of substituent position on thermal properties, photoluminescence   and morphology of pyrene-fluorene derivatives. Journal of Molecular Structure, 2015, 1086, 216-222. 13) Feng X., Hu J.-Y., Tomiyasu H., Tao   Z., Redshaw C., Elsegood M. R. J., Horsburgh L., Teat S. J., Wei X.-F., Yamato   T.*Iron (III)   bromide catalyzed bromination of 2-tertbutylpyrene and corresponding   positiondependent aryl-functionalized pyrene derivatives. RSC Advances, 2015, 5, 8835-8848. 14) Feng X., Hu J-Y., Tomiyasu H., Seto   N., Redshaw C., Elsegood Mark R. J., Yamato T.*Synthesis and photophysical   properties of novel butterfly-shaped blue emitters based on pyrene, Organic & Biomolecular Chemistry, 2013, 11, 8366-8374. 15) Feng X., Iwanaga F., Hu J-Y.,   Tomiyasu H., Nakano M., Redshaw C., Elsegood Mark R. J., Yamato   T.* An   Efficient Approach to the Synthesis of Novel Pyrene-Fused Azaacenes, Organic Letters, 2013,  15, 3594-3597.  16) Feng X., Hu J-Y., Iwanaga F., Seto   N., Redshaw C., Elsegood M. R. J., Yamato T.* Blue-Emitting Butterfly-Shaped   1,3,5,9-Tetraarylpyrenes: Synthesis, Crystal Structures and Photophysical   Properties, Organic Letters, 2013, 15, 1318-1321.  17) Feng X., Hu J-Y., Yi L., Seto N.,   Tao Z., Redshaw C., Elsegood M. R. J., Yamato T.* Pyrene-Based Y-shaped   Solid-State Blue Emitters: Synthesis, Characterization, and   Photoluminescence, Chemistry - An Asian   Journal, 2012, 7, 2854-2863.  18) Feng X., Chen K., Zhang Y.-Q., Xue   S.-F., Zhu Q.-J., Tao Z., Day A. I.,Stable cucurbit[5]uril MOF structures as   "beaded" rings built on a p-hydroxybenzoic acid template-a small   molecule absorption material, CrystEngComm,   2011, 13, 5049-5051 (Hot article) . 19) Feng X., Du H., Chen K., Xiao X.,   Luo S.-X., Xue S.-F., Zhang Y.-Q., Zhu Q.-J, Tao Z, Zhang X.-Y., Design and   Synthesis of Self-assembly Supramolecular Entities Based on Noncovalent   Interaction of Cucurbit[5]uril, Metal Ions, and Hydroxybenzene or Its   Derivatives, Crystal Growth &   Design, 2010, 10, 2901-2907. 20) Feng X., Li Z.-F., Xue S.-F., Tao   Z., Zhu Q.-J., Zhang Y.-Q., Liu J.-X., Complexation of   Cyclohexanocucurbit[6]uril with Cadmium Ions: X-ray Crystallographic and   Electrochemical Study, Inorganic.   Chemistry,2010, 49, 7638-7640.  21) Feng   X., Lu X.-J., Xue S.-F., Zhang Y.-Q., Tao Z.,   Zhu Q.-J., A novel two-dimensional network formed by complexation of   cucurbituril with cadmium ions, Inorganic   Chemistry Communications,2009,   12, 849-852. 
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