N-Doped Sub-3 nm Co Nanoparticles as Highly Efficient and Durable Aerobic Oxidative Coupling Catalysts

Chemistry - An Asian Journal

Volumn 11, Issue 18, 2016, Pages 2594-2601

  Han, Junxing ^a   Gu, Feifei ^b   Li, Yuchao ^a,c  

^a INSTITUTE OF PROCESS ENGINEERING   (China)

^b BEIJING CITY UNIVERSITY   (China)

^c UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

aldehydes; cobalt; methanol; nitrogen; oxidative coupling

Indexed keywords

ALDEHYDES; CARBON; CATALYSTS; COATINGS; COBALT; DOPING (ADDITIVES); ESTERS; LEACHING; MELAMINE FORMALDEHYDE RESINS; METHANOL; NANOPARTICLES; NITROGEN; SULFURIC ACID;

CATALYTIC EFFICIENCIES; COORDINATION STRUCTURES; HEMIACETAL INTERMEDIATE; NANOPARTICLE CATALYSTS; NITROGEN ATMOSPHERES; OXIDATIVE COUPLINGS; SULFURIC ACID LEACHING; SULFURIC ACID SOLUTION;

MOLECULAR OXYGEN;

EID: 84987624439     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201600921     Document Type: Article

References (50)

1. B. N. Zope, D. D. Hibbitts, M. Neurock, R. J. Davis, Science 2010, 330, 74–78;
2. L. Kesavan, R. Tiruvalam, M. H. A. Rahim, M. I. Saiman, D. I. Enache, R. L. Jenkins, N. Dimitratos, J. A. Lopez-Sanchez, S. H. Taylor, D. W. Knight, C. J. Kiely, G. J. Hutchings, Science 2011, 331, 195–199.
3. B. J. Xu, X. Y. Liu, J. Haubrich, R. J. Madix, C. M. Friend, Nat. Chem. 2010, 2, 61–65;
4. B. J. Xu, R. J. Madix, C. M. Friend, J. Am. Chem. Soc. 2010, 132, 16571–16580;
5. B. J. Xu, X. Y. Liu, J. Haubrich, R. J. Madix, C. M. Friend, Angew. Chem. Int. Ed. 2009, 48, 4206–4209;
6. Angew. Chem. 2009, 121, 4270–4273;
7. B. J. Xu, J. Haubrich, C. G. Freyschlag, R. J. Madix, C. M. Friend, Chem. Sci. 2010, 1, 310–314.
8. Y. Mikami, A. Takeda, M. Oh-Kita, US pat. 5 892 102, 1999;
9. S. Yamamatsu, T. Yamaguchi, K. Yokota, O. Nagano, M. Chono, A. Aoshima, Catal. Surv. Asia 2010, 14, 124–131.
10. B. R. Travis, M. Sivakumar, G. O. Hollist, B. Borhan, Org. Lett. 2003, 5, 1031–1034;
11. R. Gopinath, B. Barkakaty, B. Talukdar, B. K. Patel, J. Org. Chem. 2003, 68, 2944–2947;
12. K. Ekoue-Kovi, C. Wolf, Chem. Eur. J. 2008, 14, 6302–6315.
13. S. Gowrisankar, H. Neuman, M. Beller, Angew. Chem. Int. Ed. 2011, 50, 5139–5143;
14. Angew. Chem. 2011, 123, 5245–5249;
15. C. Liu, J. Wang, L. K. Meng, Y. Deng, Y. Li, A. W. Lei, Angew. Chem. Int. Ed. 2011, 50, 5144–5148;
16. Angew. Chem. 2011, 123, 5250–5254;
17. B. H. Wang, W. L. Ran, W. J. Sun, K. Wang, Ind. Eng. Chem. Res. 2012, 51, 3932–3938.
18. M. Nielsen, H. Junge, A. Kammer, M. Beller, Angew. Chem. Int. Ed. 2012, 51, 5711–5713;
19. Angew. Chem. 2012, 124, 5809–5811;
20. J. Zhang, G. Leitus, Y. Ben-David, D. Milstein, J. Am. Chem. Soc. 2005, 127, 10840–10841;
21. C. Gunanathan, L. J. W. Shimon, D. Milstein, J. Am. Chem. Soc. 2009, 131, 3146–3147.
22. N. Yamamoto, Y. Obora, Y. Ishii, J. Org. Chem. 2011, 76, 2937–2941.
23. C. Marsden, E. Taarning, D. Hansen, L. Johansen, S. K. Klitgaard, K. Egeblad, C. H. Christensen, Green Chem. 2008, 10, 168–170;
24. K. Suzuki, T. Yamaguchi, K. Matsushita, C. Iitsuka, J. Miuya, T. Akaogi, H. Ishida, ACS Catal. 2013, 3, 1845–1849;
25. P. Liu, C. Li, E. J. M. Hensen, Chem. Eur. J. 2012, 18, 12122–12129;
26. J. X. Han, S. J. Zhang, J. Zhang, R. Y. Yan, RSC Adv. 2014, 4, 58769–58772.
27. R. Jasinski, Nature 1964, 201, 1212–1213.
28. Y. Y. Liang, Y. G. Li, H. L. Wang, J. G. Zhou, J. Wang, T. Regier, H. J. Dai, Nat. Mater. 2011, 10, 780–786.
29. G. Wu, K. L. More, C. M. Johnston, P. Zelenay, Science 2011, 332, 443–447.
30. H. Y. Jin, J. Wang, D. F. Su, Z. Z. Wei, Z. F. Pang, Y. Wang, J. Am. Chem. Soc. 2015, 137, 2688–2694.
31. R. V. Jagadeesh, N. Junge, M. Beller, Nat. Commun. 2014, 5, 4123–4130.
32. X. J. Cui, Y. H. Li, S. Bachmann, M. Scalone, A. E. Surkus, K. Junge, C. Topf, M. Beller, J. Am. Chem. Soc. 2015, 137, 10652–10658.
33. D. Banerjee, R. V. Jagadeesh, K. Junge, M. M. Pohl, J. Radnik, A. Bruckner, M. Beller, Angew. Chem. Int. Ed. 2014, 53, 4359–4363;
34. Angew. Chem. 2014, 126, 4448–4452.
35. R. V. Jagadeesh, A. E. Surkus, H. Junge, M. M. Pohl, J. Radnik, J. Rabeah, H. Huan, V. Schunemann, A. Bruckner, M. Beller, Science 2013, 342, 1073–1076;
36. F. A. Westerhaus, R. V. Jagadeesh, G. Wienhofer, M. M. Pohl, J. Radnik, A. E. Surkus, J. Rabeah, K. Junge, H. Junge, M. Nielsen, A. Bruckner, M. Beller, Nat. Chem. 2013, 5, 537–543;
37. R. V. Jagadeesh, T. Stemmler, A. E. Surkus, H. Junge, K. Junge, M. Beller, Nat. Protoc. 2015, 10, 548–557.
38. R. V. Jagadeesh, H. Junge, M. M. Pohl, J. Radnik, A. Bruckner, M. Beller, J. Am. Chem. Soc. 2013, 135, 10776–10782;
39. R. V. Jagadeesh, T. Stemmler, A. E. Surkus, M. Bauer, M. M. Pohl, J. Radnik, K. Junge, H. Junge, A. Bruckner, M. Beller, Nat. Protoc. 2015, 10, 916–926.
40. H. L. Fei, J. C. Dong, M. J. Arellana-Jiménez, G. L. Ye, N. D. Kim, E. L. G. Samuel, Z. W. Peng, Z. Zhu, F. Qin, J. M. Bao, M. J. Yacaman, P. M. Ajayan, D. L. Chen, J. M. Tour, Nat. Commun. 2015, 6, 8668–8675;
41. Y. C. Wang, Y. J. Lai, L. Song, Z. Y. Zhou, J. G. Liu, Q. Wang, X. D. Yang, C. Chen, W. Shi, Y. P. Zheng, M. Rauf, S. G. Sun, Angew. Chem. Int. Ed. 2015, 54, 9907–9910;
42. Angew. Chem. 2015, 127, 10045–10048.
43. G. Wu, D. Y. Li, C. S. Dai, D. L. Wang, N. Li, Langmuir 2008, 24, 3566–3575.
44. J. Han, Y. J. Sa, Y. Shim, M. Choi, N. Park, S. H. Joo, S. Park, Angew. Chem. Int. Ed. 2015, 54, 12622–12626;
45. Angew. Chem. 2015, 127, 12813–12817;
46. Z. S. Wu, L. Chen, J. Z. Liu, K. Parvez, H. W. Liang, J. Shu, H. Sachdev, R. Graf, X. L. Feng, K. Mullen, Adv. Mater. 2014, 26, 1450–1455;
47. J. Casanovas, J. M. Ricart, J. Rubio, F. Illas, J. M. Jimenez-Mateos, J. Am. Chem. Soc. 1996, 118, 8071–8076.
48. J. X. Han, S. J. Zhang, Y. C. Li, R. Y. Yan, Catal. Sci. Technol. 2015, 5, 2076–2080.
49. S. Y. Kim, W. H. Suh, J. H. Choi, Y. S. Yi, S. K. Lee, G. D. Stucky, J. K. Kang, J. Mater. Chem. A 2014, 2, 2227–2232;
50. C. T. Hung, N. Yu, C. T. Chen, P. H. Wu, X. Han, Y. S. Kao, T. C. Liu, Y. Chu, F. Deng, A. Zheng, S. B. Liu, J. Mater. Chem. A 2014, 2, 20030–20037.