Citation:
	            
		            ZHANG  Hui, WANG  Xian-Ying, CHEN  Lei-Qi, FANG  Xue-Ming, GAO  Jing-Xing XU Zhi-Gu(608), . Absolute Asymmetry Synthesis and Resolution Mechanism of Chiral cis-bromoamminebis(ethylenediamine) cobalt(III) Bromide[J]. Acta Physico-Chimica Sinica,
							;2006, 22(05): 608-615.
						
							doi:
								10.1016/S1872-1508(06)60021-1
						
					
				
					
				
	        
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	                	The absolute asymmetric synthesis of the title complexes Λ-(+)D-cis-[CoBr(NH3)(en)2]Br2(1) and Δ-(-)D-cis-[CoBr(NH3)(en)2]Br2(2)(en=1,2-ethylenediamine) as well as the improved optical resolution of cis-[CoBr(NH3)(en)2]Br2·2H2O(3) are described in detail. The products were characterized by means of elemental analysis, TG-DTA, optical rotation, UV-Vis, and CD spectra. The distribution of enantiomeric excess(ee) of cis-[CoBr(NH3)(en)2]Br2 in the absolute asymmetric synthesis was obtained by the measurements of their CD spectra. It was found that the complete resolution of rac-cis-[CoBr(NH3)(en)2]Br2·2H2Owas achieved by use of NH4(d-BCS) (ammonium d-α-bromocamphor-π-sulfonate) or NH4(l-BCS) while NH4(dl-BCS) could only be partially resolved by chiral cis-[CoBr(NH3)(en)2]Br2 at the same condition. It is deduced that there are notable differences in the chiral discrimination of the reciprocal resolution between cis-[CoBr(NH3)(en)2]Br2 and NH4BCS.Moreover, a new“catalysis-crystal induction”mechanismin the preparation of the chiral Co(III) complex is put forward.
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