Addition of small molecules to (.eta.-C5H5)2Rh2(CO)(CF3C2CF3). 6. Formation of the .mu.-alkylidene complexes (.eta.-C5H5)2Rh2(.mu.-CO)(.mu.-CHR)(.mu.-CF3C2CF3) (R = CO2Et, SiMe3, CF3, or CH:CH4) and coupling reactions of the alkyne and carbene ligands within these complexes. X-ray crystal structure of (.eta.-C5H5)2Rh2(CO){C(CF3)C(CF3)CH(CO2Et)}

1987 ◽  
Vol 6 (6) ◽  
pp. 1240-1246 ◽  
Author(s):  
Ron S. Dickson ◽  
Gary D. Fallon ◽  
Susan M. Jenkins ◽  
Rhonda J. Nesbit

Author(s):  
Tilman Lechel ◽  
Irene Brüdgam ◽  
Hans-Ulrich Reissig

A series of trifluoromethyl-substituted 3-alkoxypyridinol derivatives has been deprotected to furnish pyridine-3,4-diol derivatives in good yields. The X-ray crystal structure analysis proved that a 1:1 mixture of pyridine-3,4-diols and their pyridin-4-one tautomers exist in the solid state. Subsequent conversion into bis(perfluoroalkanesulfonate)s were smoothly achieved. The obtained compounds were used as substrates for palladium-catalyzed coupling reactions. Fluorescence measurements of the biscoupled products showed a maximum of emission in the violet region of the spectrum.



2000 ◽  
Vol 78 (11) ◽  
pp. 1399-1404
Author(s):  
Thoralf Gross ◽  
Helmut Reinke ◽  
Hartmut Oehme

Protodesilylation of diphenylsilane with trifluoromethanesulfonic acid and subsequent reaction of the obtained bis(trifluoromethanesulfonyloxy)silane with tris(trimethylsilyl)silyllithium (1) (molar ratio 1:2) afforded bis[tris(trimethylsilyl)silyl]silane (8). Methyl-bis[tris(trimethylsilyl)silyl]silane (3) and phenyl-bis[tris(trimethylsilyl)silyl]silane (10) were obtained by coupling reactions of 1 with MeHSiCl2 or PhHSiCl2, respectively, (2:1). By treatment with HCBr3, the H-silanes 3, 8, and10 were converted into the bromosilanes [(Me3Si)3Si]2SiR1R2 (9: R1 = R2 = Br; 11: R1 = Me, R2 = Br; 12: R1 = Ph, R2 = Br). X-ray crystal structure analyses, performed for 3, 10 and 12, confirmed the expected distortions of the molecular skeletons of the compounds. Thus, e.g., in 10, the spatial demand of the two extended hemispherical hypersilyl groups forces a widening of the Si-Si-Si angle at the central Si atom to a value of 128.3°.Key words: silanes, sterically congested, bis(hypersilyl)silanes, hypersilylsilanes, bis(hypersilyl)germanes, tris(trimethylsilyl)silylsilanes.





Polyhedron ◽  
1992 ◽  
Vol 11 (4) ◽  
pp. 431-441 ◽  
Author(s):  
M.M.Taqui Khan ◽  
N.H. Khan ◽  
R.I. Kureshy ◽  
K. Venkatasubramanian


Author(s):  
Jacques Levisalles ◽  
Francoise Rose-Munch ◽  
Henri Rudler ◽  
Jean-Claude Daran ◽  
Yves Dromzee ◽  
...  


2011 ◽  
Vol 7 ◽  
pp. 555-564 ◽  
Author(s):  
Lian-jun Liu ◽  
Feijun Wang ◽  
Wenfeng Wang ◽  
Mei-xin Zhao ◽  
Min Shi

Axially chiral mono(NHC)–Pd(II) and mono(NHC)–Au(I) complexes with one side shaped 1,1'-biphenyl backbone have been prepared from chiral 6,6'-dimethoxybiphenyl-2,2'-diamine. The complexes were characterized by X-ray crystal structure diffraction. The Pd(II) complex showed good catalytic activities in the Suzuki–Miyaura and Heck–Mizoroki coupling reactions, and the (S)-Au(I) complexes also showed good catalytic activities in the asymmetric intramolecular hydroamination reaction to give the corresponding product in moderate ee.



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