scholarly journals Synthesis of some new Rhodium complexes containing diaryl chalcogenide ligands and their uses as catalysts in hydrosilylation of alkenes

2021 ◽  
Vol 2063 (1) ◽  
pp. 012022
Author(s):  
Ali Z Al-Rubaie ◽  
Zaki N Kadhim ◽  
Majeed Y Al-Luaibi ◽  
Luma Sabri

Abstract Diaryl Chalcogenides (i.e. Ar2E where Ar = 4-CH3C6H4, 4-BrC6H4, E= S, Se and Te) were reacted with [RhCl(CO)2]2 and rhodium(III) chloride trihydrate to give compounds of type [RhCl(CO)2(Ar2E)] and [RhCl3(Ar2E)3], respectively. All compounds were characterized by IR, NMR, and mass spectroscopic data. Attempts to prepare hydroxyapatite (HAp) supported rhodium catalyst by using different methods were unsuccessful. Complexes [RhCl(CO)2((4-R-C6H4)2S)], [RhCl(CO)2((4-R-C6H4)2Se)] and [RhCl(CO)2((4-R-C6H4)2Te), where R= CH3 or Br], were evaluated as catalysts for hydrosilylation of allyl phenyl ether and 1-decene. They showed good catalytic activities for hydrosilylation of alkenes with triethoxysilane.

2009 ◽  
Vol 54 (5) ◽  
pp. 1610-1612 ◽  
Author(s):  
Norihito Hiyoshi ◽  
Yoshio Masuda ◽  
Osamu Sato ◽  
Aritomo Yamaguchi ◽  
Chandrashekhar V. Rode ◽  
...  

2006 ◽  
Vol 106 (3-4) ◽  
pp. 133-138 ◽  
Author(s):  
Norihito Hiyoshi ◽  
Tomoya Inoue ◽  
Chandrashekhar V. Rode ◽  
Osamu Sato ◽  
Masayuki Shirai

2007 ◽  
Vol 46 (27) ◽  
pp. 5202-5205 ◽  
Author(s):  
Hiroshi Fujiwara ◽  
Yoshiyuki Ogasawara ◽  
Kazuya Yamaguchi ◽  
Noritaka Mizuno

2007 ◽  
Vol 72 (4) ◽  
pp. 468-474 ◽  
Author(s):  
Peter T. Witte

Nitriles are converted to primary amines with high selectivity using a newly developed alumina-supported rhodium catalyst. The high selectivity is obtained without any additives, which are often used to prevent the formation of higher amines. The catalyst is active under mild conditions in various solvents, which makes it specifically suitable for use in pharmaceutical applications or for other substrates that can react with additives like strong acids or bases.


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