supported by National Natural Science Foundation of China (No. 51603055)
A novel electron acceptor, namely, tetra-phthalimide end-fused bifluorenylidene(3 D-imide) was designed and synthesized. In comparison to its framework analogue 12,12'-bidibenzo[b,h]fluorenylidene(BF-3), the electron ...
supported by 2017 Natural Science Foundation of Shanghai (No. 17ZR1402400);National Program for Thousand Young Talents of China;the Shanghai Pujiang Program (No. 15PJ1402600);the Natural Science Foundation of Shanghai (No. 17ZR1447100);the Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning
Understanding of the role of supramolecular chirality for tuning material optoelectronic properties has been restricted by the limited number of cases. A particular challenge is to impose supramolecular chirality onto...
the National Science Foundation(No.20674005);the Flat-Panel Display Special Project of China 863 Plan(No.2008AA03A318);Projects of Chinese National Science and Technology Tackling Key Problems(No.2007BAE31B02)
A novel series of chiral dopants synthesized from(S)-1,2-propanediol and mesogenic carboxylic acids were characterized by FT-IR,~1H NMR,elemental analysis and their helical twisting properties were investigated by dop...
supported by the National Natural Science Foundation(No.20674005);the Flat-Panel Display Special Project of China 863 Plan(No.2008AA03A318);Projects of Chinese National Science and Technology Tackling Key Problems(No.2007BAE31B02);Program of National Laboratory of Electro-Optics System Technology(No.9140C150102090C1501).
In this study, a novel series of chiral 1,2-propanediol derivatives with different terminal alkyl chain length were synthesized and characterized by FT-IR, ^1H NMR and DSC. After doped into a nematic liquid crystal ho...
supported by the National Basic Research Program of China(No.2007CB613301);the National Natural Science Foundation(No.20674005);the Program of Beijing Municipal Science and Technology(No.Y0405004040121).
In this study, right-handed dicinnamate isosorbide was synthesized via the esterification reaction betweefi optically active isosorbide and cinnamate. The chiral dopant was characterized by FT-IR, ^1H NMR, elemental a...