Highly Porous Metalloporphyrin Covalent Ionic Frameworks with Well‐Defined Cooperative Functional Groups as Excellent Catalysts for CO2 Cycloaddition. Issue 38 (5th June 2019)
- Record Type:
- Journal Article
- Title:
- Highly Porous Metalloporphyrin Covalent Ionic Frameworks with Well‐Defined Cooperative Functional Groups as Excellent Catalysts for CO2 Cycloaddition. Issue 38 (5th June 2019)
- Main Title:
- Highly Porous Metalloporphyrin Covalent Ionic Frameworks with Well‐Defined Cooperative Functional Groups as Excellent Catalysts for CO2 Cycloaddition
- Authors:
- Liu, Jiahui
Zhao, Guoying
Cheung, Ocean
Jia, Lina
Sun, Zhenyu
Zhang, Suojiang - Abstract:
- Abstract: The development of multifunctional heterogeneous catalysts with high porosity and remarkable catalytic activity still remains a challenge. Herein, four highly porous metalloporphyrin covalent ionic frameworks (CIFs) were synthesized by coupling 5, 10, 15, 20‐tetrakis(4‐nitrophenyl)porphyrin (TNPP) with 3, 8‐diamino‐6‐phenylphenanithridine (NPPN) or 5, 5′‐diamino‐2, 2′‐bipyridine (NBPy) followed by ionization with bromoethane (C2 H5 Br) or dibromoethane (C2 H4 Br2 ) and then metalization with Zn or Co. The resulting CIFs showed high efficiency in catalyzing the cycloaddition of propylene oxide (PO) with CO2 to form propylene carbonate (PC). All of the Zn‐containing CIF catalysts were able to catalyze the cycloaddition reaction with a PC yield greater than 97 %. The TNPP/NBPy (CIF2) catalyst ionized with C2 H4 Br2 and metalized with Zn (Zn‐CIF2‐C2 H4 ) exhibited the highest catalytic activity among the synthesized catalysts. The high catalytic performance of Zn‐CIF2‐C2 H4 is related to its high porosity (577 m 2 g −1 ), high Br:metal ratio (1:3.89), and excellent synergistic action between the Lewis acidic Zn sites and the nucleophilic Br − ions. Zn‐CIF2‐C2 H4 is sufficiently stable that greater than 94 % PC yield could be obtained even after six cycles. In addition, Zn‐CIF2‐C2 H4 could catalyze the cycloaddition of several other epoxides with CO2 . These highly porous materials are promising multifunctional and efficient catalysts for industrially relevantAbstract: The development of multifunctional heterogeneous catalysts with high porosity and remarkable catalytic activity still remains a challenge. Herein, four highly porous metalloporphyrin covalent ionic frameworks (CIFs) were synthesized by coupling 5, 10, 15, 20‐tetrakis(4‐nitrophenyl)porphyrin (TNPP) with 3, 8‐diamino‐6‐phenylphenanithridine (NPPN) or 5, 5′‐diamino‐2, 2′‐bipyridine (NBPy) followed by ionization with bromoethane (C2 H5 Br) or dibromoethane (C2 H4 Br2 ) and then metalization with Zn or Co. The resulting CIFs showed high efficiency in catalyzing the cycloaddition of propylene oxide (PO) with CO2 to form propylene carbonate (PC). All of the Zn‐containing CIF catalysts were able to catalyze the cycloaddition reaction with a PC yield greater than 97 %. The TNPP/NBPy (CIF2) catalyst ionized with C2 H4 Br2 and metalized with Zn (Zn‐CIF2‐C2 H4 ) exhibited the highest catalytic activity among the synthesized catalysts. The high catalytic performance of Zn‐CIF2‐C2 H4 is related to its high porosity (577 m 2 g −1 ), high Br:metal ratio (1:3.89), and excellent synergistic action between the Lewis acidic Zn sites and the nucleophilic Br − ions. Zn‐CIF2‐C2 H4 is sufficiently stable that greater than 94 % PC yield could be obtained even after six cycles. In addition, Zn‐CIF2‐C2 H4 could catalyze the cycloaddition of several other epoxides with CO2 . These highly porous materials are promising multifunctional and efficient catalysts for industrially relevant reactions. Abstract : Biomimetic heterogeneous catalysts : Multifunctional metalloporphyrin covalent ionic frameworks with a highly porous structure for cooperative catalysis by Lewis acidic metal sites and nucleophilic Br − ions showed efficient catalytic activity in CO2 cycloaddition to epoxides (see figure), and the catalytic performance could be further enhanced by altering the functional groups and the BET surface area. … (more)
- Is Part Of:
- Chemistry. Volume 25:Issue 38(2019)
- Journal:
- Chemistry
- Issue:
- Volume 25:Issue 38(2019)
- Issue Display:
- Volume 25, Issue 38 (2019)
- Year:
- 2019
- Volume:
- 25
- Issue:
- 38
- Issue Sort Value:
- 2019-0025-0038-0000
- Page Start:
- 9052
- Page End:
- 9059
- Publication Date:
- 2019-06-05
- Subjects:
- carbon dioxide -- covalent ionic frameworks -- cycloaddition -- heterogeneous catalysis -- porphyrins
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201900992 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 17483.xml