Postsynthetic functionalization of 3D covalent organic frameworks

David N. Bunck; William R. Dichtel

doi:10.1039/c3cc40358k

Postsynthetic functionalization of 3D covalent organic frameworks

David N. Bunck, William R. Dichtel^*

^*Corresponding author for this work

Chemistry

Research output: Contribution to journal › Article › peer-review

89 Scopus citations

Abstract

We demonstrate a tandem truncation–functionalization strategy using the 3D covalent organic framework, COF-102. Allyl groups incorporated within the pore walls were subjected to thiol–ene coupling conditions, achieving high conversions and maintaining the crystallinity and permanent porosity of the parent framework.

Original language	English (US)
Pages (from-to)	2457-2459
Number of pages	3
Journal	Chemical Communications
Volume	49
Issue number	24
DOIs	https://doi.org/10.1039/c3cc40358k
State	Published - Feb 26 2013

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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title = "Postsynthetic functionalization of 3D covalent organic frameworks",

abstract = "We demonstrate a tandem truncation–functionalization strategy using the 3D covalent organic framework, COF-102. Allyl groups incorporated within the pore walls were subjected to thiol–ene coupling conditions, achieving high conversions and maintaining the crystallinity and permanent porosity of the parent framework.",

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JO - Journal of the Chemical Society D: Chemical Communications

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Postsynthetic functionalization of 3D covalent organic frameworks

Abstract

ASJC Scopus subject areas

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