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Reactivity studies of monoacetylide species towards chalcogen-bridged mixed-metal clusters:: Synthesis and characterisation of [(η5-C5H5)2Fe2RuM2(CO)6(μ3-E)2{μ4-CC(Ph)C(Ph)C}] (M=Mo, W; E=S, Se) and [(η5-C5H5)2Fe2Ru2M2(CO)9(μ3-E)2{μ-CCPh}2] (M=W, E=S, Se)

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Title Reactivity studies of monoacetylide species towards chalcogen-bridged mixed-metal clusters:: Synthesis and characterisation of [(η5-C5H5)2Fe2RuM2(CO)6(μ3-E)2{μ4-CC(Ph)C(Ph)C}] (M=Mo, W; E=S, Se) and [(η5-C5H5)2Fe2Ru2M2(CO)9(μ3-E)2{μ-CCPh}2] (M=W, E=S, Se)
 
Creator MATHUR, PRADEEP
CHIMALAKONDA, SRINIVASU
MOAWIA, AHMED O
PURANIK, VEDAVATI G
UMBARKAR, SHUBHANGI B
 
Subject cluster
mixed metal
monoacetylide
chalcogen
crystal structure
 
Description Thermolysis of a toluene solution containing [Fe2Ru(CO)9(μ3-E)2] (E=S or Se) and [(η5-C5H5)M(CO)3(C6-point triple bond; length half of m-dashCPh)] (M=Mo or W) results in coupling of monoacetylide ligands and formation of new mixed-metal clusters [(η5-C5H5)2Fe2RuM2(CO)6(μ3-E)2{μ4-CC(Ph)C(Ph)C}] (M=Mo, E=S 1 or Se 2; M=W, E=S 3 or Se 4) and [(η5-C5H5)2Fe2Ru2M2(CO)9(μ3-E)2{μ-CCPh}2] (M=W, E=S 5 or Se 6). Compounds 1–6 have been characterised by IR and 1H- and 13C-NMR spectroscopy. Structures of 1 and 5 have been established crystallographically. Compound 1 features a tail-to-tail type of coupling of two acetylide groups on a Fe2RuMoS2 core and compound 5 is a hexanuclear Fe–Ru–W mixed-metal cluster with two uncoupled acetylide groups.
 
Publisher Elsevier
 
Date 2009-03-09T07:44:26Z
2011-11-25T18:52:12Z
2011-12-26T13:06:57Z
2011-12-27T05:54:56Z
2009-03-09T07:44:26Z
2011-11-25T18:52:12Z
2011-12-26T13:06:57Z
2011-12-27T05:54:56Z
2002
 
Type Article
 
Identifier Journal of Organometallic Chemistry 659(1-2), 196-201
0022-328X
http://dx.doi.org/10.1016/S0022-328X(02)01768-0
http://hdl.handle.net/10054/907
http://dspace.library.iitb.ac.in/xmlui/handle/10054/907
 
Language en