Ruthenium and Iron Carbonyl Clusters Catalyzed Reduction of N,N-dimethylbenzamide and N,N-diethyl-(3-methyl)benzamide

Article Preview

Abstract:

One new Ruthenium and one known Iron bimetallic carbonyl clusters containing triphos (1,1,1-tris(diphenylphosphinomethyl)ethane) ligand have been prepared as catalyst to study the reduction of amide to amine. All clusters were characterized by elemental analysis, 1HNMR, 31PNMR and IR spectroscopy. The reduction of N,N-dimethylbenzamide and N,N-diethyl-(3-methyl) benzamide catalyzed by Ru and Fe carbonyl clusters were investigated at 100 ~ 110 °C for 24 ~ 28h, polymethylhydrogensiloxane (PMHS) as reduction agent. The products were analysized using GC-MS, IR and UV-vis spectroscopy and an excellent yield (97%) of N,N-diethyl- (3-methyl)benzamine was obtained when using 3 mol% of bimetallic ruthenium carbonyl cluster as catalyst. The data of IR and UV-vis show that the frameworks of clusters are not changed remarkably during the reaction.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 396-398)

Pages:

2485-2488

Citation:

Online since:

November 2011

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2012 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] R. D. Adams, F. A. Cotton, Catalysis by di- and polynuclear metal cluster complexes; Wiley-VCH: New York (1998)

Google Scholar

[2] B. C. Gates, J. Mol. Catal. A: Chem. Vol.163 (2000), p.55

Google Scholar

[3] H. Paul, S. Bhaduri and G.K. Lahiri, Organometallics Vol. 22 (2003), p.3019

Google Scholar

[4] H. Nagashima, C. Itonaga, J. Yasuhara, Y. Motoyama and K. Matsubara, Organometallics Vol. 23 (2004), p.5779

Google Scholar

[5] (a) B. H. Zhu, W. Q. Zhang, B. Hu, Z. G. Bian, Q. Y. Zhao, Y. H. Zhang, Y. Q. Yin, J. Sun, J. Organomet. Chem. Vol. 650 (2002), p.181

Google Scholar

[6] (a) B. H. Zhu, L. Zhang, N. Xiao, J.-B. Chen, Y.-Q. Yin and J. Sun. Inorg. Chim. Acta Vol. 357 (2004), p.864. (b)B. H. Zhu, B. Hu, W. Q. Zhang, Y. Q. Yin, J. Sun. J. Mol. Catal. (China), Vol.19 (2005), p.61

Google Scholar

[7] A. Ricci, Modern Amination Methods, Wiley, New York (2000)

Google Scholar

[8] (a) T. Ohta, M. Kamiya, M. Nobutomo, K. Kusui, I. Furukawa, Bull. Chem. Soc. Jpn., Vol.78 (2005), p.1856

Google Scholar

[9] S. Zhou, K. Junge, D. Addis, S. Das, and M. Beller, Angew. Chem. Int. Ed. Vol. 48 (2009), p.9507

Google Scholar

[10] M.G. Richmond, M. Absi-Halabi, C.U. Pittman Jr., J. Mol. Catal. Vol.22 (1984), p.367

Google Scholar