Sophisticated Design of Covalent Organic Frameworks with Controllable Bimetallic Docking for a Cascade Reaction

Chemistry - A European Journal

Volumn 22, Issue 27, 2016, Pages 9087-9091

  Leng, Wenguang ^a   Peng, Yongsheng ^a   Zhang, Jianqiang ^a   Lu, Hui ^a   Feng, Xiao ^b   Ge, Rile ^a   Dong, Bin ^a   Wang, Bo ^b   Hu, Xiangping ^a   Gao, Yanan ^a  

^a DALIAN INSTITUTE OF CHEMICAL PHYSICS   (China)

^b BEIJING INSTITUTE OF TECHNOLOGY   (China)

Author keywords

cascade reactions; covalent organic frameworks; heterogeneous catalysis; metal loading; nitrogen ligands

Indexed keywords

CATALYSIS; CATALYST ACTIVITY; CATALYTIC OXIDATION; CHEMICAL OXYGEN DEMAND; LIGANDS; METAL COMPLEXES; METAL IONS; METALS; NITROGEN; ORGANOMETALLICS; RHODIUM COMPOUNDS; SURFACE REACTIONS;

CASCADE REACTIONS; COVALENT ORGANIC FRAMEWORKS; HETEROGENEOUS CATALYST; METAL LOADINGS; NITROGEN LIGAND; SELECTIVE COORDINATION; SYNTHETIC PROCEDURES; TWO DIMENSIONAL (2 D);

PALLADIUM COMPOUNDS;

EID: 84971236460     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201601334     Document Type: Article

References (42)

1. A. P. Côté, A. I. Benin, N. W. Ockwig, M. O'Keeffe, A. J. Matzger, O. M. Yaghi, Science 2005, 310, 1166–1170.
2. H. M. El-Kaderi, J. R. Hunt, J. L. Mendoza-Cortés, A. P. Côté, R. E. Taylor, M. O'Keeffe, O. M. Yaghi, Science 2007, 316, 268–272.
3. X. Feng, X. S. Ding, D. L. Jiang, Chem. Soc. Rev. 2012, 41, 6010–6022.
4. S. Y. Ding, W. Wang, Chem. Soc. Rev. 2013, 42, 548–568.
5. S. Y. Ding, J. Gao, Q. Wang, Y. Zhang, W. G. Song, C. Y. Su, W. Wang, J. Am. Chem. Soc. 2011, 133, 19816–19822.
6. H. Xu, X. Chen, J. Gao, J. B. Lin, M. Addicoat, S. Irle, D. L. Jiang, Chem. Commun. 2014, 50, 1292–1294.
7. P. Pachfule, S. Kandambeth, D. Díaz Díaz, R. Banerjee, Chem. Commun. 2014, 50, 3169–3172.
8. P. Pachfule, M. K. Panda, S. Kandambeth, S. M. Shivaprasad, D. Díaz Díaz, R. Banerjee, J. Mater. Chem. A 2014, 2, 7944–7952.
9. Q. R. Fang, S. Gu, J. Zheng, Z. B. Zhuang, S. L. Qiu, Y. S. Yan, Angew. Chem. Int. Ed. 2014, 53, 2878–2882;
10. Angew. Chem. 2014, 126, 2922–2926.
11. K. N. Zhang, O. K. Farha, J. T. Hupp, S. T. Nguyen, ACS Catal. 2015, 5, 4859–4866.
12. Y. G. Zhang, J. Y. Ying, ACS Catal. 2015, 5, 2681–2691.
13. Y. G. Zhang, S. N. Riduan, Chem. Soc. Rev. 2012, 41, 2083–2094.
14. S. S. Han, H. Furukawa, O. M. Yaghi, W. A. Goddard III, J. Am. Chem. Soc. 2008, 130, 11580–11581.
15. H. Furukawa, O. M. Yaghi, J. Am. Chem. Soc. 2009, 131, 8875–8883.
16. C. J. Doonan, D. J. Tranchemontagne, T. G. Glover, J. R. Hunt, O. M. Yaghi, Nat. Chem. 2010, 2, 235–238.
17. H. P. Ma, H. Ren, S. Meng, Z. J. Yan, H. Y. Zhao, F. X. Sun, G. S. Zhu, Chem. Commun. 2013, 49, 9773–9775.
18. M. G. Rabbani, A. K. Sekizkardes, Z. Kahveci, T. E. Reich, R. S. Ding, H. M. El-Kaderi, Chem. Eur. J. 2013, 19, 3324–3328.
19. S. Dalapati, S. B. Jin, J. Gao, Y. H. Xu, A. Nagai, D. L. Jiang, J. Am. Chem. Soc. 2013, 135, 17310–17313.
20. J. Zhang, L. B. Wang, N. Li, J. F. Liu, W. Zhang, Z. B. Zhang, N. C. Zhou, X. L. Zhu, CrystEngComm 2014, 16, 6547–6551.
21. S. Wan, J. Guo, J. Kim, H. Ihee, D. L. Jiang, Angew. Chem. Int. Ed. 2008, 47, 8826–8830;
22. Angew. Chem. 2008, 120, 8958–8962.
23. S. Wan, J. Guo, J. Kim, H. Ihee, D. L. Jiang, Angew. Chem. Int. Ed. 2009, 48, 5439–5442;
24. Angew. Chem. 2009, 121, 5547–5550.
25. X. Feng, L. Chen, Y. Honsho, O. Saengsawang, L. L. Liu, L. Wang, A. Saeki, S. Irle, S. Seki, Y. P. Dong, D. L. Jiang, Adv. Mater. 2012, 24, 3026–3031.
26. E. L. Spitler, J. W. Colson, F. J. Uribe-Romo, A. R. Woll, M. R. Giovino, A. Saldivar, W. R. Dichtel, Angew. Chem. Int. Ed. 2012, 51, 2623–2627;
27. Angew. Chem. 2012, 124, 2677–2681.
28. M. Dogru, M. Handloser, F. Auras, T. Kunz, D. Medina, A. Hartschuh, P. Knochel, T. Bein, Angew. Chem. Int. Ed. 2013, 52, 2920–2924;
29. Angew. Chem. 2013, 125, 2992–2996.
30. L. Chen, K. Furukawa, J. Gao, A. Nagai, T. Nakamura, Y. P. Dong, D. L. Jiang, J. Am. Chem. Soc. 2014, 136, 9806–9809.
31. C. R. DeBlase, K. E. Silberstein, T. T. Truong, H. D. Abruña, W. R. Dichtel, J. Am. Chem. Soc. 2013, 135, 16821–16824.
32. L. Stegbauer, K. Schwinghammer, B. V. Lotsch, Chem. Sci. 2014, 5, 2789–2793.
33. X. Chen, N. Huang, J. Gao, H. Xu, F. Xu, D. L. Jiang, Chem. Commun. 2014, 50, 6161–6163.
34. L. Y. Chen, S. Rangan, J. Li, H. F. Jiang, Y. W. Li, Green Chem. 2014, 16, 3978–3985.
35. A. Nagai, Z. Q. Guo, X. Feng, S. B. Jin, X. Chen, X. S. Ding, D. L. Jiang, Nat. Commun. 2011, 2, 536.
36. Figure SThis bipyridine-free 2D imine-linked COF product was poorly crystalline with a low surface area (17). However, it was still synthesized for comparison with the different sorts of X % BPy COFs to illustrate the role of the bipyridine units towards the docking metals.
37. A. A. Tregubov, K. Q. Vuong, E. Luais, J. J. Gooding, B. A. Messerle, J. Am. Chem. Soc. 2013, 135, 16429–16437.
38. 2 was determined by Material Studio Geometry Optimization by using the CASTED calculation module component built-in the Material Studio software.
39. S. K. Goforth, R. C. Walroth, L. McElwee-White, Inorg. Chem. 2013, 52, 5692–5701.
40. M. Sakai, M. Ueda, N. Miyaura, Angew. Chem. Int. Ed. 1998, 37, 3279–3281;
41. Angew. Chem. 1998, 110, 3475–3477.
42. R. A. Sheldon, Catal. Today 2015, 247, 4–13.