Related Experiment Video
Updated: Sep 16, 2025

Constructing Thioether/Vinyl Sulfide-tethered Helical Peptides Via Photo-induced Thiol-ene/yne Hydrothiolation
Published on: August 1, 2018
Spherical Covalent Organic Framework-like Material with a Vinylene Bridge for a Photothermal-Driven Suzuki Coupling
Tianwen Chen1, Li Chen2, Qun Li1
1College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, P.R. China.
None:
Turning a traditional homogeneous reaction into a heterogeneous catalytic process has long been a crucial issue in the chemical industry because of favorable cost reduction from catalyst recycling. Modification of these heterogeneous catalysts could enable various functions that further benefit energy consumption and production efficiency. In this work, a spherical covalent organic framework like (COF-like) material (PDPP-TBP) was developed, which possesses broad light absorption properties and efficient photothermal conversion capabilities, with the highest surface temperature increased by over 70 °C from room temperature under the simulated light irradiation (1 kW m-2, equal to one sun). Palladium nanoparticles (Pd NPs) were successfully loaded onto PDPP-TBP by an impregnation-reduction method, forming photothermal heterogeneous catalyst Pd@PDPP-TBP. Such a composite exhibited high product yield and recyclability in photothermally driven Suzuki-Miyaura cross couplings, implying great potential of Pd@PDPP-TBP for advancing the field of heterogeneous catalysis, particularly in applications requiring environmentally friendly and energy-efficient processes.
More Related Videos
06:49Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
Published on: April 22, 2016
08:51Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Related Concept Videos
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Hybridization of Atomic Orbitals I
[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement