journal article·2020-03-18Open access

Synthesis of a Porous C3N-Derived Framework with High Yield by Gallic Acid Cross-Linking Using Salt Melts

Zhihong Tian, Tobias Heil, Johannes Schmidt, Shaokui Cao, Markus Antonietti

ACS Applied Materials & Interfaces· Volume 12· Issue 11

Abstract

Porous carbon/nitrogen frameworks are an emerging class of noble organic materials with a wide range of potential applications. However, the design and controlled synthesis of those materials are still a challenge. Herein, we present the rational design of such a system with high microporosity, specific surface areas of up to 946 m2 g-1, and excellent condensation yields. The obtained noble frameworks were used for the delivery of larger organic molecules and changed the melting behavior of some daily drug molecules along their highly polarizable surfaces.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications · Advanced Photocatalysis Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001, P. R. China

Department of Colloid Chemistry, Max Planck Institute of Colloids and Interfaces, Potsdam 14476, Germany

Technical University of Berlin, Institute of Chemistry, Hardenberg str. 40, Berlin 10623, Germany

Funding

Zhengzhou University · Max-Planck-Gesellschaft

References (40)

Show source-provided references
1. 10.1002/adma.20170683610.1002/adma.201706836 ↗
2. 10.1021/ja109856y10.1021/ja109856y ↗
3. 10.1002/anie.20171342910.1002/anie.201713429 ↗
4. 10.1126/sciadv.140012910.1126/sciadv.1400129 ↗
5. 10.1038/ncomms597310.1038/ncomms5973 ↗
6. 10.1016/j.electacta.2016.10.05010.1016/j.electacta.2016.10.050 ↗
7. 10.1038/nenergy.2016.7010.1038/nenergy.2016.70 ↗
8. 10.1021/acs.accounts.5b0001010.1021/acs.accounts.5b00010 ↗
9. 10.1038/nmat231710.1038/nmat2317 ↗
10. 10.1126/science.aaa314510.1126/science.aaa3145 ↗
11. 10.1038/ncomms748610.1038/ncomms7486 ↗
12. 10.1016/j.carbon.2013.04.04310.1016/j.carbon.2013.04.043 ↗
13. 10.1002/adma.20160562510.1002/adma.201605625 ↗
14. 10.1073/pnas.160531811310.1073/pnas.1605318113 ↗
15. 10.1039/C8TA03213K10.1039/C8TA03213K ↗
16. 10.1021/acs.chemmater.8b0468310.1021/acs.chemmater.8b04683 ↗
17. 10.1021/acs.chemmater.8b0140910.1021/acs.chemmater.8b01409 ↗
18. 10.1016/j.tca.2015.02.01610.1016/j.tca.2015.02.016 ↗
19. 10.1039/C6TA09580A10.1039/C6TA09580A ↗
20. 10.1002/anie.20171116910.1002/anie.201711169 ↗
21. 10.1002/anie.20180435910.1002/anie.201804359 ↗
22. 10.1002/anie.20141023410.1002/anie.201410234 ↗
23. 10.1039/c3ee41444b10.1039/c3ee41444b ↗
24. 10.1021/ja803708s10.1021/ja803708s ↗
25. 10.1016/j.drudis.2007.09.00510.1016/j.drudis.2007.09.005 ↗
26. 10.1016/j.colsurfb.2018.09.08010.1016/j.colsurfb.2018.09.080 ↗
27. 10.1016/j.ijpharm.2013.05.06110.1016/j.ijpharm.2013.05.061 ↗
28. 10.1016/j.ijpharm.2014.07.02410.1016/j.ijpharm.2014.07.024 ↗
29. 10.1016/j.jpba.2015.11.00310.1016/j.jpba.2015.11.003 ↗
30. 10.1016/j.ijpharm.2013.05.01610.1016/j.ijpharm.2013.05.016 ↗
31. 10.1016/j.ijpharm.2010.07.04010.1016/j.ijpharm.2010.07.040 ↗
32. 10.1038/s41467-018-04910-510.1038/s41467-018-04910-5 ↗
33. 10.1021/jacs.7b0092510.1021/jacs.7b00925 ↗
34. 10.1039/C4CE00878B10.1039/C4CE00878B ↗
35. 10.1016/j.jconrel.2018.03.03110.1016/j.jconrel.2018.03.031 ↗
36. 10.1021/cm960118810.1021/cm9601188 ↗
37. 10.1016/j.ejpb.2017.03.00210.1016/j.ejpb.2017.03.002 ↗
38. 10.1021/cg200492w10.1021/cg200492w ↗
39. 10.1126/sciadv.aax078010.1126/sciadv.aax0780 ↗
40. 10.1021/acsami.8b1182510.1021/acsami.8b11825 ↗