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ADDITION OF PHENYLACETYLENE TO THE MIXED-CHALCOGENIDE COMPOUNDS (CO)(6)FE-2(MU-SETE), (CO)(6)FE-2(MU-SSE), AND (CO)(6)FE-2(MU-STE) - STRUCTURAL CHARACTERIZATION OF (CO)(6)FE-2(MU-SEC(H)=C(PH)TE)

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Title ADDITION OF PHENYLACETYLENE TO THE MIXED-CHALCOGENIDE COMPOUNDS (CO)(6)FE-2(MU-SETE), (CO)(6)FE-2(MU-SSE), AND (CO)(6)FE-2(MU-STE) - STRUCTURAL CHARACTERIZATION OF (CO)(6)FE-2(MU-SEC(H)=C(PH)TE)
 
Creator MATHUR, P
HOSSAIN, MM
UMBARKAR, S
SATYANARAYANA, CVV
TAVALE, SS
PURANIK, VG
 
Subject acetylenic bond reduction
carbonyl-compounds
metal-clusters
ligands
complex
se
fe2(co)6(mu-se2)
organosulfur
construction
reactivity
 
Description From the room-temperature reaction of the mixed-chalcogenide compound Fe-2(CO)(6)(mu-SeTe) with phenylacetylene two isomeric products were isolated, Fe-2(CO)(6){mu SeC(H)=C-(Ph)Te} (1) and Fe-2(CO)6{mu-SeC(Ph)=C(H)Te} (2). Fe-2(CO)(6)(mu-SSe) reacted with phenylacetylene to form Fe-2(CO)(6){mu-SC(Ph)=C(H)Se} (3). The room-temperature reaction of Fe-2(CO)(6)(mu-STe) with phenylacetylene also yielded two isomeric products, Fe-2(CO)(6)(mu-SC-(H)=C(Ph)Te) (4) and Fe-2(CO)(6)(mu-SC(Ph)=C(H)Te) (5). In ah of these reactions, the homochalcogenide compounds Fe-2(CO)(6)(mu-EC(H)=C(Ph)E) (E = Se, Te, E = S, Se, and E = S, Te, respectively) were also formed in trace amounts. The new compounds 1-5 were characterized by IR and H-1, C-13, Se-77, and Te-125 NMR spectroscopy. Compound 1 was structurally characterized by single-crystal X-ray diffraction methods. It crystallized in the triclinic space group P $($) over bar$$ 1 with a = 7.773(9) Angstrom, b = 10.635(9) Angstrom, c = 12.010(10) Angstrom, a = 104.99(10)degrees, beta = 102.86(11)degrees, gamma = 106.38(9)degrees, V = 872.1(8) Angstrom(3), Z = 2, and D(calc) = 2.241 g cm(-3).Full-matrix least-squares refinement of 1 converged to R = 0.077 and R(w) = 0.086.
 
Publisher AMER CHEMICAL SOC
 
Date 2011-07-13T15:26:22Z
2011-12-26T12:47:56Z
2011-12-27T05:42:18Z
2011-07-13T15:26:22Z
2011-12-26T12:47:56Z
2011-12-27T05:42:18Z
1995
 
Type Article
 
Identifier ORGANOMETALLICS, 14(2), 959-963
0276-7333
http://dx.doi.org/10.1021/om00002a049
http://dspace.library.iitb.ac.in/xmlui/handle/10054/3707
http://hdl.handle.net/10054/3707
 
Language en