Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 61, Issue 31, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202202597
Keywords
Gas Adsorption; Organic Crystals; Porous Organic Salts; Recrystallization; Void Structures
Categories
Funding
- MEXT, Japan [20H02548, 21J30005, 22K14732]
- Kurata Grants from the Hitachi Global Foundation [1431]
- Mizuho Foundation for the Promotion of Sciences
- Mishima Kaiun Memorial Foundation
- Nipponham
- FUSO Innovative Technology Fund
- Grants-in-Aid for Scientific Research [21J30005, 20H02548] Funding Source: KAKEN
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Porous organic salts (POSs) are porous organic materials formed by self-assembly of aromatic sulfonic acids and amines through hydrogen bonding. They have high solubility and recyclability. By introducing substituents, the void structure and environment of POSs can be controlled, significantly affecting their gas adsorption behavior.
Porous organic salts (POSs) are porous organic materials, in which various aromatic sulfonic acids and amines are regularly self-assembled by charge-assisted hydrogen bonding. POSs exhibit high solubility in highly polar solvents. Therefore, they are prepared via facile recrystallization and exhibit high recyclability. In this study, tetrahedral-structured tetrasulfonic acid and triphenylmethylamine (TPMA) were combined to construct POSs with rigid diamond networks called diamondoid porous organic salts (d-POSs). Furthermore, by introducing substituents (e.g., F, Cl, Br, or I) at the para-positions of benzene rings of TPMA, these substituents were exposed on the void surface of d-POSs, and their diamond networks were distorted. This induced the formation of a variety of void structures and environments in the d-POSs, which significantly affected their gas adsorption behavior. In particular, the d-POS from TPMA substituted by fluorine exhibited very high CO2 adsorption of 182 mL(STP) g(-1) at 1 atm in all-organic porous materials.
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