Enantiomer resolution, barrier to ring inversion, circular dichroism spectrum and absolute configuration of cycloocta[2,1-b: 3,4-b′]dipyridine

Author(s):  
Parviz Rashidi-Ranjbar ◽  
Jan Sandström ◽  
Henry N. C. Wong ◽  
Xiu Chun Wang
1991 ◽  
Vol 45 ◽  
pp. 1076-1079 ◽  
Author(s):  
Tihamér Hargitai ◽  
Per Reinholdsson ◽  
Jan Sandström ◽  
Carsten M. Nielsen ◽  
Hugh Brian Dunford ◽  
...  

1981 ◽  
Vol 34 (12) ◽  
pp. 2499 ◽  
Author(s):  
LR Gahan ◽  
AM Sargeson

The synthesis of a potentially hexadentate ligand 2,2',2''-[(cyclohexane-l,3,5-triyl)trithio]tris(ethanamine) (atch) is described. The ligand forms a hexadentate cobalt(III) complex which has been resolved into its catoptric forms. The (+)520-[Co(atch)]3+ complex displays a strikingly large dichroism in the region of the first ligand field transition in the circular dichroism spectrum with Δε480+ 11.9 mol-1 1. cm-1 and has been assigned the Λ absolute configuration by comparisons of the circular dichroism with those of similar complexes of known absolute configuration. Attempts to cap the complex by using nitromethane and formaldehyde under basic conditions are described.


1983 ◽  
Vol 36 (5) ◽  
pp. 1037 ◽  
Author(s):  
IRC Bick ◽  
MA Hai ◽  
VA Patrick ◽  
AH White

The crystal structure of the alkaloid aristoserratine,* C20H24N2O, has been determined by single-crystal X-ray diffraction methods at 295 K, the structure being refined to a residual of 0.034 for 1107 independent 'observed' reflections. Crystals are monoclinic, P21, a 14.836(5), b 8.568(3), c 6.633(3) �, β 98.05(3)�, Z 2. The relative configuration is established and, by inference, by comparison of the circular dichroism spectrum with that of aristoteline, the absolute configuration is assigned.


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