Selective CO2 Capture in Metal–Organic Frameworks with Azine-Functionalized Pores Generated by Mechanosynthesis
Source abstract
Abstract
Two new three-dimensional porous Zn(II)-based metal–organic frameworks, containing azine-functionalized pores, have been readily and quickly isolated via mechanosynthesis, by using a nonlinear dicarboxylate and linear N-donor ligands. The use of nonfunctionalized and methyl-functionalized N-donor ligands has led to the formation of frameworks with different topologies and metal–ligand connectivities and therefore different pore sizes and accessible volumes. Despite this, both metal–organic frameworks (MOFs) possess comparable BET surface areas and CO 2 uptakes at 273 and 298 K at 1 bar. The network with narrow and interconnected pores in three dimensions shows greater affinity for CO 2 compared to the network with one-dimensional and relatively large pores—attributable to the more effective interactions with the azine groups.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications · Carbon Dioxide Capture Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Islamic Republic of Iran
ICN2 − Institut Catala de Nanociencia i Nanotecnologia, Campus UAB, 08193 Bellaterra (Barcelona), Spain
Service de Cristallochimie, Institut de Chimie des Substances Naturelles-CNRS, Bât 27, 1 Avenue de la Terrasse, 91190 Gif sur Yvette, France
Institució Catalana de Recerca i Estudis Avançats (ICREA), 08100 Barcelona, Spain
References (42)
Show source-provided references
1. Petit J. R. · Nature · 1999 · 399 · 42910.1038/20859 ↗
2. http://www.iea.org/.
3. Ahmed A. · J. Mater. Chem. A · 2013 · 1 · 327610.1039/c2ta01125e ↗
4. Yang S. · Nat. Chem. · 2012 · 4 · 88710.1038/nchem.1457 ↗
5. Wu H. · Chem.—Eur. J. · 2010 · 16 · 1395110.1002/chem.201002683 ↗
6. An J. · Nat. Commun. · 2012 · 3
7. D’Alessandro D. M. · Angew. Chem., Int. Ed. · 2010 · 49 · 605810.1002/anie.201000431 ↗
8. Zhang Z. · Chem. Commun. · 2013 · 49 · 65310.1039/C2CC35561B ↗
9. Sumida K. · Chem. Rev. · 2012 · 112 · 72410.1021/cr2003272 ↗
10. Li T. · Chem. Sci. · 2013 · 4 · 174610.1039/c3sc22207a ↗
11. Angamuthu R. · Science · 2010 · 327 · 31310.1126/science.1177981 ↗
12. Xue D. X. · J. Am. Chem. Soc. · 2013 · 135 · 766010.1021/ja401429x ↗
13. Vaidhyanathan R. · Science · 2010 · 330 · 65010.1126/science.1194237 ↗
14. Stylianou K. C. · Chem. Commun. · 2011 · 47 · 338910.1039/c0cc05559j ↗
15. McDonald T. M. · J. Am. Chem. Soc. · 2012 · 134 · 705610.1021/ja300034j ↗
16. An J. · J. Am. Chem. Soc. · 2010 · 132 · 3810.1021/ja909169x ↗
17. Yuan B. · Chem. Commun. · 2012 · 48 · 113510.1039/C2CC16923A ↗
18. Corma A. · Chem. Rev. · 2010 · 110 · 460610.1021/cr9003924 ↗
19. Demessence A. · J. Am. Chem. Soc. · 2009 · 131 · 878410.1021/ja903411w ↗
20. Gao W.-Y. · Chem. Commun. · 2012 · 48 · 889810.1039/c2cc34380k ↗
21. Lan A. · Angew. Chem., Int. Ed. · 2009 · 48 · 233410.1002/anie.200804853 ↗
22. Pramanik S. · J. Am. Chem. Soc. · 2011 · 133 · 415310.1021/ja106851d ↗
23. Vaidhyanathan R. · Angew. Chem., Int. Ed. · 2006 · 45 · 649510.1002/anie.200602242 ↗
24. Li J. R. · Coord. Chem. Rev. · 2011 · 255 · 179110.1016/j.ccr.2011.02.012 ↗
25. Gassensmith J. J. · J. Am. Chem. Soc. · 2011 · 133 · 1531210.1021/ja206525x ↗
26. Ramsahye N. A. · Adsorption. · 2007 · 13 · 46110.1007/s10450-007-9025-5 ↗
27. Yuan W. · Angew. Chem., Int. Ed. · 2010 · 49 · 391610.1002/anie.200906965 ↗
28. Friscic T. · CrystEngComm · 2009 · 11 · 74310.1039/b822934c ↗
29. Fujii K. · Chem. Commun. · 2010 · 46 · 757210.1039/c0cc02635b ↗
30. Beldon P. J. · Angew. Chem., Int. Ed. · 2010 · 49 · 964010.1002/anie.201005547 ↗
31. Friščić T. · Angew. Chem., Int. Ed. · 2010 · 49 · 71210.1002/anie.200906583 ↗
32. Cliffe M. J. · Chem. Sci. · 2012 · 3 · 249510.1039/C2SC20344H ↗
33. Friscic T. · Chem. Soc. Rev. · 2012 · 41 · 349310.1039/c2cs15332g ↗
34. Bennett T. D. · J. Am. Chem. Soc. · 2011 · 133 · 1454610.1021/ja206082s ↗
35. Yuan W. B. · CrystEngComm · 2010 · 12 · 351510.1039/c0ce00216j ↗
36. Spek A. L. · J. Appl. Crystallogr. · 2003 · 36 · 710.1107/S0021889802022112 ↗
37. Bhattacharya B. · Dalton Trans. · 2014 · 43 · 227210.1039/C3DT52266K ↗
38. Stylianou K. C. · J. Am. Chem. Soc. · 2012 · 134 · 2046610.1021/ja308995t ↗
39. Nugent P. · Nature · 2013 · 495 · 8010.1038/nature11893 ↗
40. Bae Y.-S. · J. Mater. Chem. · 2009 · 19 · 213110.1039/b900390h ↗
41. Dincǎ M. · J. Am. Chem. Soc. · 2005 · 127 · 937610.1021/ja0523082 ↗
42. Burd S. D. · J. Am. Chem. Soc. · 2012 · 134 · 366310.1021/ja211340t ↗