Tin–iron carbonyl clusters from the reaction of stannane, SnH4, with Fe2(CO)9; the crystal structure of SnFe5(CO)19

1989 ◽  
Vol 372 (1) ◽  
pp. 25-32 ◽  
Author(s):  
Skelten G. Anema ◽  
Kenneth M. Mackay ◽  
Brian K. Nicholson
1984 ◽  
Vol 23 (10) ◽  
pp. 1363-1368 ◽  
Author(s):  
Allesandro Ceriotti ◽  
Paolo Chini ◽  
Allesandro Fumagalli ◽  
Thomas F. Koetzle ◽  
Giuliano Longoni ◽  
...  

2005 ◽  
Vol 358 (5) ◽  
pp. 1521-1530 ◽  
Author(s):  
Alberto Cabrera ◽  
Esther Delgado ◽  
Cesar Pastor ◽  
Miguel A. Maestro ◽  
Félix Zamora

1981 ◽  
Vol 210 (1) ◽  
pp. C1-C4 ◽  
Author(s):  
Henri Patin ◽  
Gerard Mignani ◽  
Christian Mahe ◽  
Jean-Yves Le Marouille ◽  
Alain Benoit ◽  
...  

1990 ◽  
Vol 385 (3) ◽  
pp. 387-398 ◽  
Author(s):  
Brian F.G. Johnson ◽  
Rajesh Khattar ◽  
Jack Lewis ◽  
Paul R. Raithby ◽  
Maria J. Rosales

2011 ◽  
Vol 396-398 ◽  
pp. 2485-2488
Author(s):  
Bao Hua Zhu ◽  
Guo Hua Xu ◽  
Zhi Wei Xia

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.


ChemSusChem ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 3252-3260
Author(s):  
Chuanshuai Li ◽  
Ahibur Rahaman ◽  
Weihua Lin ◽  
Hassan Mourad ◽  
Jie Meng ◽  
...  

1989 ◽  
Vol 363 (1-2) ◽  
pp. 181-188 ◽  
Author(s):  
Gianfranco Ciani ◽  
Massimo Moret ◽  
Angelo Sironi ◽  
Secondo Martinengo

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