ChemInform Abstract: STRUCTURAL STUDIES OF STERIC EFFECTS IN PHOSPHINE COMPLEXES. 5. SYNTHESIS AND D CRYSTAL AND MOLECULAR STRUCTURES OF THE DIMERS BIS(ACETATO)(TRICYCLOHEXYLPHOSPHINE)MERCURY(II) AND BIS(ACETATO)(TRI-O-TOLYLPHOSPHINE)MERCURY(II)

1979 ◽  
Vol 10 (50) ◽  
Author(s):  
E. C. ALYEA ◽  
S. A. DIAS ◽  
G. FERGUSON ◽  
M. A. KHAN ◽  
P. J. ROBERTS
ChemInform ◽  
1990 ◽  
Vol 21 (2) ◽  
Author(s):  
L. N. ITO ◽  
J. D. SWEET ◽  
A. M. MUETING ◽  
L. H. PIGNOLET ◽  
M. F. J. SCHOONDERGANG ◽  
...  

1961 ◽  
Vol 39 (8) ◽  
pp. 1638-1644 ◽  
Author(s):  
J. Trotter

The structures of m-dinitrobenzene and p-dinitrobenzene have been refined by three-dimensional (Fo—Fc) syntheses. The results indicate that both nitro groups in each molecule are twisted 11° out of the aromatic plane, about the C—N bonds, in contrast to nitrobenzene, where the whole molecule is completely planar. These molecular configurations are shown to be in accord with those which might be expected from intramolecular steric effects. The dimensions of the three molecules have also been compared.


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