代表论文如下：
[1] “Role of Intermolecular Interactions in Molecular Packing of Alkoxy-Substituted Bis-1,3,4-oxadiazole Derivatives”，Chen， Fangyi；Wang, Yu; Zhang Wanxi; Tian, Taiji；Bai, Binglian；Wang, Haitao*；Bai, Fuquan*; Li, Min*；Crystal Growth & Design 2019, 19, 11, 6100-6113。
The molecular packing, intermolecular interactions, and electron-transporting and photophysical properties of a series symmetrical alkoxy-substituted bis-1,3,4-oxadiazole derivatives (BOXD-o-OCH3, BOXD-m-OCH3, BOXD-D1, and BOXD-T1) are carefully investigated through a combination of experimental techniques and theoretical calculations here.
[2] “Crystal structures, intermolecular interactions and fluorescence properties of a series of symmetrical bi-1,3,4-oxadiazole derivatives”，Chen， Fangyi；Tian, Taiji；Bai, Binglian；Wang, Jian； Wang, Haitao*；Li, Min*；Journal of Materials Chemistry C, 2016, 4(20), 4451-4458。
These investigations provide not only new insight and understanding into molecular packing and its driving force, but also guidance for preparing materials with excellent device performance.
[3] "Controllable molecular aggregation and fluorescence properties of 1,3,4-oxadiazole derivatives", Wang, Haitao；Chen, Fangyi；Jia, Xiaoshi；Liu, Huimin；Ran, Xia；Ravva, Mahesh Kumar；Bai, Fu-Quan；Qu, Songnan；Li, Min*；Zhang, Hong-Xing*；Bredas, Jean-Luc*; Journal of Materials Chemistry C, 2015， 3: 11681-11688。
BOXD-6 molecules can self-assemble into both H- and J-aggregates at moderate concentration (∼10−4 M) and then transit to exclusive J-aggregates at higher concentration (∼10−3 M) in tetrahydrofuran.
[4] "Theoretical and experimental study on intramolecular charge-transfer in symmetric bi-1,3,4-oxadiazole derivatives"，Wang, Haitao；Liu, Huimin；Bai, Fu-Quan；Qu, Songnan；Jia, Xiaoshi；Ran, Xia；Chen, Fangyi；Bai, Binglian；Zhao, Chengxiao； Liu, Zibai；Zhang, Hong-Xing*；Li, Min*；Journal of Photochemistry and Photobiology A: Chemistry, 2015，312：20–27。
The symmetric DAAD arrangement can enhance intramolecular charge-transfer from the side alkoxyl benzene to the central bi-1,3,4-oxadiazole moiety.
[5] "Theoretical study on molecular packing and electronic structure of bi-1,3,4-oxadiazole derivatives"， Wang, Haitao；Bai, Fu-Quan；Jia, Xiaoshi；Cao, Di；Kumar, Ravva Mahesh；Bredas, Jean-Luc；Qu, Songnan；Bai, Binglian；Zhang, Hong-Xing*；Li, Min*；RSC Advances, 2014，4（94）：51942-51949。
One of the energy-minimum structure predicted by intermolecular interaction potential energy surface computed with M062x/6-31G** method resembled very well with the crystal packing.
[6] "Ultrasound-induced controllable morphology and growth dimension in a dihydrazide-based self-assembly system"，Zhang, Yan；Ding, Hao；Wu, Yangfang；Zhang, Chunxue；Bai, Binglian；Wang, Haitao*；Li, Min*；Soft Matter，2014，10（44）：8838-8845。
Ultrasound irradiation has been proved to influence gel properties at micro-levels. Different self-assembled structures from entangled fibers to tube-like structures and nanoparticles can be easily manipulated by tuning irradiation time and water bath temperature.
[7] "Experimental and theoretical study on molecular aggregation and its effect on the photo-physical properties of the mesogenic bi-1,3,4-thiadiazole derivative"，Wang, Haitao；Bai, Fu-Quan；Liu, Huimin；Bai, Binglian；Ran, Xia；Qu, Songnan；Shi, Jianhua；Xie, Dajun；Li, Hui-Ying；Li, Min*；Zhang, Hong-Xing*；Physical Chemistry Chemical Physics，2011，13（20）：9697-9705。
H- and J-aggregates could be formed simultaneously in chloroform solutions of BTD-14 during concentration increase, then transit to exclusive J-aggregates.
