Journal
CHEMISTRY-AN ASIAN JOURNAL
Volume 16, Issue 11, Pages 1398-1402Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.202100323
Keywords
Microporous organic polymer; Acyl Sonogashira coupling; Post-synthetic modification; Thiol-yne click reaction; Carbon dioxide conversion
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Funding
- National Research Foundation (NRF) - Ministry of Science and ICT, Republic of Korea [2017M1A2A2043146]
- National Research Council of Science & Technology (NST), Republic of Korea [C140110] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
- National Research Foundation of Korea [4199990213977] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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This study demonstrates the preparation of hollow microporous organic polymer with activated internal alkynes as IR probes by template synthesis at room temperature. The polymer serves as a versatile platform for nonradical thiol-yne click-based main chain PSM and can be used for monitoring the reaction process. Functionalized polymers show efficient adsorption towards Ag+ ions and exhibit excellent performance in CO2 fixation reactions.
This work shows that hollow microporous organic polymer (H-MOP-A) with activated internal alkynes as IR probes can be prepared by template synthesis based on acyl Sonogashira-Hagihara coupling at room temperature. The H-MOP-A is a versatile platform in the main chain PSM based on nonradical thiol-yne click reaction. Moreover, an IR peak of internal alkynes in the H-MOP-A is very intense and could be utilized in the monitoring of thiol-yne click-based main chain PSM. The functionalized H-MOP-A with carboxylic acids (H-MOP-CA) showed efficient adsorption toward Ag+ ions. The resultant H-MOP-CA-Ag showed excellent performance in the CO2 fixation to alpha-alkylidene cyclic compounds.
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