Multi walled carbon nanotubes supported N-heterocyclic carbene-cobalt (II) as a novel, efficient and inexpensive catalyst for the Mizoroki-Heck reaction

Catalysis Communications

Volumn 77, Issue , 2016, Pages 1-4

  Hajipour, Abdol R ^a,b   Khorsandi, Zahra ^a  

^a ISFAHAN UNIVERSITY OF TECHNOLOGY   (Iran)

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

Heterogonous catalyst; Mizoroki Heck; MWCNTs; NHC ligand

Indexed keywords

CARBON; CARBON NANOTUBES; CATALYST ACTIVITY; CATALYSTS; CHEMICAL REACTIONS; COBALT; COBALT COMPOUNDS; NANOTUBES; ORGANIC COMPOUNDS; PHOSPHORUS COMPOUNDS; YARN;

CATALYST STRUCTURES; COBALT COMPLEXES; MIZOROKI-HECK; MIZOROKI-HECK REACTION; MWCNTS; N-HETEROCYCLIC CARBENES; NHC LIGANDS; NORMAL CONDITION;

MULTIWALLED CARBON NANOTUBES (MWCN);

EID: 84954556149     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2015.12.027     Document Type: Article

References (35)

1. R.F. Heck Acc. Chem. Res. 12 1979 146 151
2. Á. Molnár Chem. Rev. 111 2011 2251 2320
3. R.R. Bader, P. Baumeister, and H.U. Blaser Chimia 50 1996 99 105
4. S. Ma, H. Wang, K. Gao, and F. Zhao J. Mol. Catal. A Chem. 248 2006 17 20
5. S.G. Babu, N. Neelakandeswari, N. Dharmaraj, S.D. Jackson, and R. Karvembu RSC Adv. 3 2013 7774 7781
6. A.R. Hajipour, and G. Azizi Green Chem. 15 2013 1030 1034
7. Y. Ikeda, T. Nakamura, H. Yorimitsu, and K. Oshima J. Am. Chem. Soc. 124 2002 6514 6515
8. C. Gosmini, J.-M. B'egouin, and A. Moncomble Chem. Commun. 2008 3221 3233
9. A. Slamani, S. Demir, and I. Ozdemir Catal. Commun. 29 2012 141 144
10. M. Ghotbinejad, A.R. Khosropour, I.M. Baltork, M. Moghadam, S. Tangestaninejad, and V. Mirkhani J. Mol. Catal. A Chem. 385 2014 78 84
11. T.W. Ebbesen, H.J. Lezec, H. Hiura, J.W. Bennett, H.F. Ghaemi, and T. Thio Nature 382 1996 54 56
12. Z. Liu, X. Lin, J.Y. Lee, W. Zhang, M. Han, and L.M. Gan Langmuir 18 2002 4054 4060
13. Z. Zarnegar, J. Safari, and Z.M. Kafroudi Catal. Commun. 59 2015 216 221
14. E. Kim, H.S. Jeong, and B.M. Kim Catal. Commun. 46 2014 71 74
15. S. Tangestaninejad, M. Moghadam, V. Mirkhani, I. Mohammadpoor-Baltork, and M.S. Saeedi Appl. Catal. A 381 2010 233 241
16. J.L. Stevens, A.Y. Huang, H. Peng, I.W. Chiang, V.N. Khabashesku, and J.L. Margrave Nano Lett. 3 2003 331 336
17. J. Shen, W. Huang, L. Wu, Y. Hu, and M. Ye Compos. Sci. Technol. 67 2007 3041 3050
18. X. He, F. Zhang, R. Wang, and W. Liu Carbon 45 2007 2559 2563
19. S.K. Movahed, R. Esmatpoursalmani, and A. Bazgir RSC Adv. 4 2014 14586 14591
20. G. Cahiez, and A. Moyeux Chem. Rev. 110 2010 1435 1462
21. O. Schuster, L.R. Yang, H.G. Raubenheimer, and M. Albrecht Chem. Rev. 109 2009 3445 3478
22. R.E. Giudici, and A.H. Hoveyda J. Am. Chem. Soc. 129 2007 3824 3825
23. K. Matsubara, A. Kumamoto, H. Yamamoto, Y. Koga, and S. Kawata J. Organomet. Chem. 727 2013 44 49
24. T. Punniyamurthy, S. Velusamy, and J. Iqbal Chem. Rev. 105 2005 2329
25. P. Shukla, Y.-C.H. Hsu, and C.H. Cheng J. Org. Chem. 71 2006 655 658
26. H. Qi, W. Zhang, X. Wang, H. Li, J. Chen, K. Peng, and M. Shao Catal. Commun. 10 2009 1178 1183
27. Z. Zhu, J. Ma, L. Xu, L. Xu, and H. Li ACS Catal. 2 2012 2119 2125
28. P. Zhou, Y. Li, P. Sun, J. Zhou, and J. Bao Chem. Commun. 2007 1418 1420
29. S. Iyer, and V.V. Thakur J. Mol. Catal. A Chem. 157 2000 275 278
30. A.R. Hajipour, and G. Azizi Appl. Organomet. Chem. 29 2015 247 253
31. A.R. Hajipour, and G. Azizi Synlett 24 2013 254 258
32. A.R. Hajipour, E. Boostani, and F. Mohammadsaleh RSC Adv. 5 2015 24742 24748
33. A.Z. Wilczewska, and I. Misztalewska Organometallics 33 2014 5203 5208
34. D. Cincic, and B. Kaitner CrystEngComm 13 2011 4351 4357
35. M. Navidi, B. Movassagh, and S. Rayati Appl. Catal. A 452 2013 24 28