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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