1. Organic Synthesis 

2. Synthesis of organic functional Materials

3. Molecular Devices

EDUCATION

1987-1991, B.S. Anhui Normal University
1998-2001, M. S. Department of Chemistry,  University of New Mexico, USA
2003-2006, Ph.D. Institute of Chemistry, Chinese Academy of Sciences

   

1.   Axially chiral thermally activated delayed fluorescence emitters enabled by molecular engineering towards high-performance circularly polarized OLEDs，Chemical Engineering Journal，2023，468，143508

2.      Advances in circularly polarized luminescent materials based on axially chiral compounds, J. Photochem. & Photobio., C: Photochem. Rev. 2022, 50, 100500.

3.      Chiral Thermally Activated Delayed Fluorescence-Active Macrocycles Displaying Efficient Circularly Polarized Electroluminescence, CCS Chem. 2022, 178, 10832

4.      Quinoline-based TADF emitters exhibiting aggregation-induced emission for efficient non-doped organic light-emitting diodes，Mater. Chem. Front., 2021, 5, 834

5.      A Green Fluorescent Nitrogen-Doped Aromatic Belt Containing a [6]Cycloparaphenylene Skeleton，Angew. Chem. Int. Ed. 2021, 60, 15291 –15295

6.      Axially chiral thermally activated delayed fluorescent emitter with dual emitting core for highly efficient organic light-emitting diode, Chem. Commun., 2020, 56, 9380

7.      Sign inversions of circularly polarized luminescence for helical compounds by chemically fine-tuning operations, Chem. Commun. 2020, 56, 1863-1866.

8.      Naphthyridine-based thermally activated delayed fluorescence emitters for highly efficient blue OLEDs, Dyes and Pigments，2020，178 ，108324

9.      Advances in helicene derivatives with circularly polarized luminescence，Chem. Commun., 2019, 55, 13793 - 13803

10.   Novel oxacalix[2]arene[2]triazines with thermally activated delayed fluorescence and aggregationinduced emission properties，Chem. Commun., 2019, 55, 9559 

11.   Naphthyridine-based thermally activated delayed fluorescence emitters for multi-color organic light-emitting diodes with low efficiency roll-off，J.Mater. Chem. C, 2019, 7, 4673

12.   1,8-Naphthalimide-based circularly polarized TADF enantiomers as the emitters for efficient orange-red OLEDs，Organic Electronics，2019，70，71–77

13.   Phthalimide-based ‘‘D–N–A’’ emitters with thermally activated delayed fluorescence and isomer-dependent room-temperature phosphorescence properties，Chem. Commun., 2019, 55, 12172

14.   Helicene-Based Illusory Chiral Supramolecular Expression of the Penrose Stairs: Chiroptical Property and Narcissistic Self-Sorting, Eur. J. Inorg. Chem. 2019, 13, 1847–1853.

15.   Metal-free construction of contiguous quaternary stereocentres with a polycyclic framework，Chem. Commun., 2019, 55, 4631

16.   Synthesis, chiroptical properties, and self-assembled nanoparticles of chiral conjugated polymers based on optically stable helical aromatic esters, RSC Adv., 2018, 8, 1014–1021

17.   [5]Helicene derivatives containing aromatic imide moiety: synthesis, structure, and photophysical properties, J. Photochem. Photobio. A: Chem. 2018, 355, 408–413

18.   Insights into the effect of donor ability on photophysical properties of dihydroindeno[2,1c]fluorene-based imide derivatives， Phys.Chem.Chem.Phys., 2018, 20, 7514

19.   Chiral Nanoparticles with Full-Color and White CPL Properties Based on Optically Stable Helical Aromatic Imide Enantiomers, ACS Applied Materials & Interfaces， 2018, 10(9), 8225–8230.

20.   Intense blue circularly polarized luminescence from helical aromatic esters, Chem. Commun. 2017, 53(45), 6093-6096.

21.   A new thioimide-based fluorescent ‘turn-on’ and chromogenic chemodosimeter in acetonitrile and its nanoparticles in water for highly selective and sensitive detection of Hg2+, Chin. J. Chem. 2017, 35(4), 435-441.

22.   Synthesis, Structures, and Photophysical Properties of Difuro-Fused Tetrahydro[5]helicene Imide Derivatives, Asian J. Org. Chem. 2016, 5, 1518–1524.

23.   Benzo[5]helicene-based conjugated polymers: synthesis, photophysical properties, and application for the detection of nitroaromatic explosives, Polym. Chem. 2016, 7, 310–318. (back cover paper)

24.   Helical aromatic imide based enantiomers with full-color circularly polarized luminescence, Chem. Commun., 2016, 52, 9921-9924.

25.   Dialkoxybenzo[j]fluoranthenes: synthesis, structures, photophysical properties, and optical waveguide application, RSC Adv. 2015, 5, 18609–18614.

26.   A dinaphtho[8,1,2-cde:2’,1’,8’-uva]pentacene derivative and analogues: synthesis, structures, photophysical and electrochemical properties, Org. Biomol. Chem. 2015, 13, 7628–7632.

27.   Tetrahydro[5]helicene-based dye with remarkable and reversible acid/base stimulated fluorescence switching properties in solution and solid state, Dyes and Pigments, 2015, 120, 184-189.

28.   Tetrahydro[5]helicene-based full-color emission dyes in both solution and solid state: synthesis, structures, photophysical properties and optical waveguide application, J. Mater. Chem. C 2014, 2(39), 8373–8380.

29.   Tetrahydro[5]helicene thioimide-based fluorescent and chromogenic chemodosimeter for highly selective and sensitive detection of Hg²⁺, Sensors & Actuators: B. Chem. 2014, 202, 583–587.

30.   Dihydroindeno[2,1-c]fluorine-Based Imide Dyes: Synthesis, Structures, Photophysical and Electrochemical Properties, J. Org. Chem. 2014, 79(5), 2139−2147.

31.   Tetrahydro[5]helicene-Based Nanoparticles for Structure-Dependent Cell Fluorescent Imaging, Adv. Funct. Mater. 2014, 24(28), 4405–4412 (front cover paper).

32.   Tetrahydro[5]helicene-based imide dyes with intense fluorescence in both solution and solid state, Chem. Commun. 2014, 50(23), 2993−2995 (inside front cover paper).

33.   A Stimulus-Response and Self-Healing Supramolecular Polymer, Macromol. Chem. Phys. 2013, 214, 1596−1601.

34.   Synthesis, Structures and Optical Properties of Aza[4]helicenes, Eur. J. Org. Chem. 2013, 15, 3059–3066.

35.   Simple, efficient and selective colorimetric sensors for naked eye detection of Hg²⁺, Cu²⁺ and Fe³⁺, RSC Adv. 2012, 2(10), 4415–4420.

36.   Turn-On Fluorescent Sensor for Selective Detection of Zn²⁺, Cd²⁺, and Hg²⁺ in Water, J. Org. Chem. 2012, 77 (7), 3670–3673.

37.   Sulfonylrhodaminehydrazide: A sensitive and selective chromogenicand fluorescent chemodosimeter for copper ion in aqueous media, Dyes and Pigments, 2011, 88(3), 257-261.

38.   Highly sensitive and selective turn-on fluorescent chemosensor for Pb²⁺ and Hg2+ based on a rhodamine–phenylurea conjugate, Chem. Commun. 2010, 46(21), 3765–3767.

39.   Synthesis, Structure and Redox Property of a New Tetrathiafulvalene Based Macrocyclic Compound, Chin. J. Org. Chem. 2009, 29(2), 234-238.

40.   Highly Selective Fluorescence Detection for Mercury (II) Ions in Aqueous Solution Using Water-Soluble Conjugated Polyelectrolytes, Macromol. Rapid Commun. 2008, 29(17), 1467–1471.   

41.   N-(2-Nitrophenylsulfonyl)-N-(4-nitrophenylsulfonyl)methylamine, Acta Cryst. 2008, E64, 1885.  

42.   Highly Effective Phosphate Electrochemical Sensor Based on Tetrathiafulvalene. Chem. Commun. 2005, 38, 4777–4779. (Highlighted as cover picture 封面文章)   

43.   A Novel Multisignaling Optical-Electrochemical Chemosensor for Anions Based on Tetrathiafulvalene, Org. Lett. 2005, 7(21), 4629–4632.

44.   A Novel Approach to the Synthesis of Amino-Sugars. Routes to Selectively Protected 3-Amino-3-deoxy- aldopentoses Based on Pyridium Salt Photochemistry, J. Org. Chem. 2002, 67(10), 3525–3528.

45.   A Concise Synthesis of the (-)-AllosamizolineAminocyclopentitol Based on Pyridinium Salt Photochemistry, Tetrahedron Lett. 2001, 42(29), 4755–4757.