A5064693345- Luminescence and Fluorescent Materials
- Covalent Organic Framework Applications
- Conducting polymers and applications
- Perovskite Materials and Applications
- Organic Electronics and Photovoltaics
- Metal-Organic Frameworks: Synthesis and Applications
- Advanced Nanomaterials in Catalysis
- Catalytic C–H Functionalization Methods
- Surface Chemistry and Catalysis
- Nerve injury and regeneration
- Supramolecular Self-Assembly in Materials
- Photopolymerization techniques and applications
- Advanced Photocatalysis Techniques
- Neuroscience and Neural Engineering
- Organic Light-Emitting Diodes Research
- Porphyrin and Phthalocyanine Chemistry
- Nanoparticle-Based Drug Delivery
- Advanced Polymer Synthesis and Characterization
- Nanoplatforms for cancer theranostics
Nanyang Technological University
2016-2019
Direct C–H arylation enables “greener” synthesis of π-conjugated small molecules and polymers without tedious preactivation bonds.
Conjugated porous polymers with narrow bandgaps, tunable morphologies, porosities and optoelectronic properties are synthesized <italic>via</italic> facile direct arylation polymerization.
Triazine-based conjugated porous polymers were synthesised by direct arylation polymerization and used as photocatalysts for aerobic oxidation of benzylamine.
We report multiscale structured fibers and patterned films based on a semiconducting polymer, poly(3-hexylthiophene) (P3HT), as photoconductive biointerfaces to promote neuronal stimulation upon light irradiation. The micro/nanoscale structures of P3HT used for interfacing include nanofibers with an average diameter 100 nm, microfibers about 1 μm, lithographically stripes width 3, 25, 50 respectively. effect irradiation provides electrical differentiation directed growth. Our results...
Conjugated microporous polymers are synthesized <italic>via</italic> facile direct arylation polymerization, resulting in conjugated networks with hierarchical porosity and a narrow bandgap of 1.5 eV.
Thiophene-flanked π-conjugated building blocks are often used in the design of linear conjugated polymers as they leverage reactivity thiophene numerous C–C coupling reactions to include a variety donor and acceptor molecules backbone. However, this strategy has been rarely for synthesis porous (CPPs) until recently. In article, we report facile characterization library CPPs synthesized via versatile synthetic scheme C–H direct arylation polymerization that involves commercially available...
Theranostic agents incorporating diagnostic and therapeutic together play crucial roles in clinical cancer treatment. On the one hand, near-infrared (NIR) fluorescence imaging strategies are expected to provide high-resolution real-time structural molecular information with deep penetration biological tissues vivo. other photothermal therapy (PTT) offers a highly efficient treatment negligible safety concerns. To combine strengths of both NIR PTT for simultaneous therapy, we report type...
ABSTRACT Wide‐bandgap π‐conjugated donor‐acceptor (D‐A) alternating copolymers consisting of benzo[1,2‐c:4,5‐c']dithiophene‐4,8‐dione (BDTD) as the electron‐accepting building block have demonstrated outstanding performances in organic bulk heterojunction (BHJ) solar cell devices. But synthesis these polymers has been largely limited to conventional polymerization techniques, particularly Stille‐coupling based polycondensations, which often involve tedious preactivation C‐H bonds using...
We report a solution-processable π-conjugated molecular building block (denoted as PhDPP) consisting of rigid and planar core phenyl-flanked diketopyrrolopyrrole "soft" branched alkoxy chains that endow the solubility in variety organic solvents. Intermolecular hydrogen bonding PhDPP was revealed nonpolar solvents above threshold concentration below critical point temperature. The strong intermolecular interaction mainly contributed by hydrogen-bonding π–π between molecules promoted...