Related Experiment Video
Updated: May 14, 2026

Microfluidic-based Synthesis of Covalent Organic Frameworks (COFs): A Tool for Continuous Production of COF Fibers and Direct Printing on a Surface
Published on: July 10, 2017
Postsynthetic functionalization of 3D covalent organic frameworks.
David N Bunck1, William R Dichtel
1Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853-1301, USA.
We developed a new method to modify 3D covalent organic frameworks (COFs). This technique successfully functionalized COF-102 while preserving its structure and porosity.
Area of Science:
- Materials Science
- Organic Chemistry
- Nanotechnology
Background:
- Covalent organic frameworks (COFs) are crystalline porous polymers with tunable properties.
- Functionalizing COFs is crucial for tailoring their applications.
- Existing methods often struggle to maintain the structural integrity of COFs during modification.
Purpose of the Study:
- To develop a novel tandem truncation-functionalization strategy for 3D COFs.
- To investigate the modification of pore wall functionalities in COF-102.
- To assess the impact of functionalization on the structural and porous properties of COF-102.
Main Methods:
- Utilized a 3D covalent organic framework, COF-102, as the model system.
- Employed thiol-ene coupling reactions under mild conditions.
- Incorporated allyl groups within the pore walls of COF-102 for functionalization.
Main Results:
- Achieved high conversion rates for the thiol-ene coupling reaction.
- Successfully functionalized the allyl groups within the COF-102 pore walls.
- Demonstrated that the functionalization process preserved the crystallinity of the parent framework.
- Maintained the permanent porosity of the modified COF-102.
Conclusions:
- The tandem truncation-functionalization strategy is effective for modifying 3D COFs.
- This method allows for precise functionalization without compromising the structural integrity of COFs.
- The preserved porosity and crystallinity open avenues for advanced applications of functionalized COFs.
Related Concept Videos
Introduction to Functional Groups
Functional groups are group of atoms with specific chemical properties that occur within organic molecules and sometimes denoted as “R”. Functional groups are found along the carbon backbone of macromolecules can form chains or rings of carbon atoms. Functional groups can “functionalize” a compound by enabling it to adopt different physical and chemical properties.
Types of common functional groups
The table below summarizes some of the major functional groups in organic chemistry. (The...
Structures of Carboxylic Acid Derivatives
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the unhybridized p...
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous overlap of p...
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group with both...
Overview of Advanced Functional Groups
Functional groups are groups of atoms with specific chemical properties that occur within organic molecules and are sometimes denoted as “R”. Functional groups can “functionalize” a compound by enabling it to adopt different physical and chemical properties.
Types of Advanced Functional Groups
The table below summarizes some of the major functional groups in organic chemistry.
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

