Superparamagnetic polymer composite microspheres supported Schiff base palladium complex: An efficient and reusable catalyst for the Suzuki coupling reactions

Chemical Engineering Journal

Volumn 287, Issue , 2016, Pages 241-251

  Yuan, Dingzhong ^a   Chen, Long ^a   Yuan, Ligang ^a   Liao, Shijun ^a   Yang, Mengmei ^a   Zhang, Qinghua ^a  

^a EAST CHINA UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

Heterogeneous catalyst; Palladium; Superparamagnetic polymer composite microspheres; Suzuki coupling reactions

Indexed keywords

CATALYST ACTIVITY; CATALYSTS; CHEMICAL REACTIONS; COMPOSITE MATERIALS; EMULSIFICATION; EMULSION POLYMERIZATION; FOURIER TRANSFORM INFRARED SPECTROSCOPY; HIGH RESOLUTION TRANSMISSION ELECTRON MICROSCOPY; MAGNETISM; MICROSPHERES; PALLADIUM; PALLADIUM COMPOUNDS; SUPERPARAMAGNETISM; TRANSMISSION ELECTRON MICROSCOPY; X RAY DIFFRACTION;

FOURIER TRANSFORM INFRARED; HETEROGENEOUS CATALYST; PALLADIUM COMPLEXES; POLYMER COMPOSITE; SCHIFF BASE CATALYSTS; SOAP-FREE EMULSION POLYMERIZATION; SUZUKI COUPLING REACTION; VIBRATING SAMPLE MAGNETOMETER;

CATALYST SUPPORTS;

EID: 84947968576     PISSN: 13858947     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cej.2015.10.081     Document Type: Article

References (52)

1. Miyaura N., Suzuki A. Chem. Rev. 1995, 95:2457-2483.
2. Suzuki A. J. Organomet. Chem. 1999, 576:147-168.
3. Molnar A. Chem. Rev. 2011, 111:2251-2320.
4. Fihri A., Bouhrara J.-M., Nekoueishahraki B., Basset M., Polshettiwar V. Chem. Soc. Rev. 2011, 40:5181-5203.
5. Han F.-S. Chem. Soc. Rev. 2013, 42:5270-5298.
6. Fleckenstein C.A., Plenio H. Green Chem. 2007, 9:1287-1291.
7. Marziale A.N., Faul S.H., Reiner S.H.T., Schneider S., Eppinger J. Green Chem. 2010, 12:35-38.
8. Anderson K.W., Buchwald S.L. Angew. Chem. Int. Ed. 2005, 44:6173-6177.
9. Tu T., Wang Z.X., Liu X.Y. Dalton Trans. 2010, 39:10598-10600.
10. Roy S., Plenio H. Adv. Synth. Catal. 2010, 352:1014-1022.
11. Godoy F., Segarra C., Poyatos M., Peris E. Organometallics 2011, 30:684-688.
12. Herrmann W.A., Ofele K., Schneider S.K., Herdtweck E., Hoffmann S.D. Angew. Chem. Int. Ed. 2006, 45:3859-3862.
13. Wass D.F., Haddow M.F., Hey T.W., Guy A.O., Russell C.A., Wingad R.L., Green M. Chem. Commun. 2007, 2704-2706.
14. Feng X.J., Yan M., Zhang T., Liu Y., Bao M. Green Chem. 2010, 12:1758-1766.
15. Xi C.J., Wu Y.W., Yan X.Y. J. Organomet. Chem. 2008, 693:3842-3846.
16. Kawamura K., Haneda S., Gan Z., Eda K., Hayashi M. Organometallics 2008, 27:3748-3752.
17. Haneda S., Ueba C., Eda K., Hayashi M. Adv. Synth. Catal. 2007, 349:833-835.
18. Yao Q., Zabawa M., Woo J., Zheng C. J. Am. Chem. Soc. 2007, 129:3088-3089.
19. Mehendale N.C., Sietsma J.R.A., De Jong K.P., Van Walree C.A., Gebbink R.J.M.K., Van Koten G. Adv. Synth. Catal. 2007, 349:2619-2630.
20. Zhang J., Zhao G.-F., Popovic Z., Lu Y., Liu Y. Mater. Res. Bull. 2010, 45:1648-1653.
21. Kantam M.L., Srinivas P., Yadav J., Likhar P.R., Bhargava S. J. Org. Chem. 2009, 74:4882-4885.
22. Rao G.K., Kumar A., Kumar B., Kumar D., Singh A.K. Dalton Trans. 2012, 41:1931-1937.
23. Bohade S.R., Waghmode S.B. Tetrahedron Lett. 2008, 49:3423-3429.
24. Borhade S.R., Waghmode S.B. Indian J. Chem. 2010, 49B:565-572.
25. Huang R., Shaughnessy K.H. Organometallics 2006, 25:4105-4112.
26. He Y., Cai C. Catal. Commun. 2011, 12:678-683.
27. Islam S.M., Mondal P., Tuhina K., Roy A.S., Mondal S., Hossain K. J. Inorg. Organomet. Polym. 2010, 20:264-277.
28. Cho H.-J., Jung S.W., Kong S., Park S.-J., Lee S.-M., Lee Y.-S. Adv. Synth. Catal. 2014, 356:1056-1064.
29. Dhara K., Sarkar K., Srimani D., Saha S.K., Chattopadhyay P., Bhaumik A. Dalton Trans. 2010, 39:6395-6402.
30. Veisi H., Manesh A.A., Eivazi N., Faraji A.R. RSC Adv. 2015, 5:20098-20107.
31. Bhunia S., Sen R., Koner S. Inorg. Chim. Acta 2010, 363:3993-3999.
32. Bui N.T., Dang T.B., Le H.V., Phan N.T.S. Chin. J. Catal. 2011, 32:1667-1676.
33. Beygzadeh M., Alizadeh A., Khodaei M.M., Kordestani D. Catal. Commun. 2013, 32:86-91.
34. Sobhani S., Ghasemzadeh M.S., Honarmand M., Zarifi F. RSC Adv. 2014, 4:44166-44174.
35. Yuan D.Z., Chen B.B. Chin. Org. Chem. 2014, 34:1630-1638.
36. Navidi M., Rezaei N., Movassagh B. J. Organomet. Chem. 2013, 743:63-69.
37. Saha D., Sen R., Maity T., Koner S. Langmuir 2013, 29:3140-3151.
38. Stevens P.D., Fan J.D., Gardimalla H.M.R., Yen M., Gao Y. Org. Lett. 2005, 7:2085-2088.
39. Wang Z., Yu Y., Zhang Y.X., Li S.Z., Qian H., Lin Z.Y. Green Chem. 2015, 17:413-420.
40. Yuan D.Z., Zhang H.P. Appl. Catal. A: General 2014, 475:249-255.
41. Bukowska A., Bukowski W., Noworol I. J. Appl. Polym. Sci. 2007, 106:3800-3807.
42. Latha A.G., George B.K., Kannnan K.G., Ninan K.N. J. Appl. Polym. Sci. 1991, 43:1159-1163.
43. Shao N.Z., Gao S.T., Feng C., Zhang H.Y., Wang C., Wang Z. RSC Adv. 2013, 3:21863-21868.
44. Scheuermann G.M., Rumi L.G., Steurer P., Bannwarth W., Mülhaupt R. J. Am. Chem. Soc. 2009, 131:8262-8270.
45. Karimi B., Akhavan P.F. Inorg. Chem. 2011, 50:6063-6072.
46. Widegren J.A., Finke R.G. J. Mol. Catal. A: Chem. 2003, 198:317-341.
47. Phan N.T.S., Van der Sluy M., Jones C.W. Adv. Synth. Catal. 2006, 348:609-679.
48. Rebek J., Brown D., Zimmerman S. J. Am. Chem. Soc. 1975, 97:454-455.
49. Rebek J., Gavina F. J. Am. Chem. Soc. 1974, 69:7112-7114.
50. Kim J.-H., Kim J.-W., Shokouhimerhr M., Lee Y.-S. J. Org. Chem. 2005, 70:6714-6720.
51. Islam S.M., Mondal P., Tuhina K., Roy A.S., Mondal S., Hossain D. J. Inorg. Organomet. Polym. 2010, 20:264-277.
52. Park J.H., Raza F., Jeon S.-J., Kim H.-I., Kang T.W., Yim D., Kim J.-H. Tetrahedron Lett. 2014, 55:3426-3430.