ChemInform Abstract: EFFECTS OF AXIAL TERT-BUTYL SUBSTITUENTS ON CONFORMATIONS AND GEOMETRIES OF SATURATED SIX-MEMBERED RINGS. CRYSTAL AND MOLECULAR STRUCTURES OF TRANS-2-METHOXY-2-OXO-5-TERT-BUTYL- AND CIS-2,5-DI-TERT-BUTYL-2-THIO-1,3,2-DIOXAPHOSPHORINAN

1979 ◽  
Vol 10 (18) ◽  
Author(s):  
R. W. WARRENT ◽  
C. N. CAUGHLAN ◽  
J. H. HARGIS ◽  
K. C. YEE ◽  
W. G. BENTRUDE
1983 ◽  
Vol 38 (4) ◽  
pp. 485-492 ◽  
Author(s):  
Günter Schmid ◽  
Roland Boese

Abstract The crystal and molecular structures of two isomers of bis(1-tert-butyl-2-methyl-η-1,2-azaborolinyl)cobalt have been determined by single-crystal X-ray diffraction methods. Isomer 1 shows a clockwise, isomer 2 an anti-clockwise conformation of the azaborolinyl rings. In both compounds the azaborolinyl rings have staggered orientations with opposite positions of the tert-butyl groups. The rings in 1 and 2 are slipped so that the three ring carbon atoms are closer to the cobalt atom than the BN groups. The staggered orientation of the ligands in 2 is probably due to a packing effect, as in similar sandwich complexes the anti-clockwise conformers show eclipsed orientation.


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