The phenomenon of conglomerate crystallization. VIII. Spontaneous resolution in coordination compounds. VI. The chiral behaviour of [trans-(P, or M)-Co(NH3)2 (NO2)4]− anions, dissymmetric by virtue of their propeller conformation
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Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry
Reference10 articles.
1. The phenomenon of conglomerate crystallization.III [1]. Spontaneous resolution in coordination compounds.III [1]. The structures and absolute configuration of Λ(δλδ) [(-)589-cis-α-(triethylenetetraamine) Co(NO2)2]Cl· H2O (I), Λ(δλδ)[(-)589− cis-bis-ethylenediamine Co(NO)2)2]Cl (II) and of K[trans-Co(NH3)2(NO2)4] (III)stereoisomers displaying CLAVIC dissymmetry
2. The phenomenon of conglomerate crystallization. IV. The structure and absolute configuration of [Λ(δλ)(−)589-cis-Co(en)2(NO2)2][trans-Co(NH3)2(NO2)4] a substance containing clavic dyssymmetric cations and anions
3. The Phenomenon of Conglomerate Crystallization. V. Clavic Dissymmetry in Coordination Compounds. IV. A Neutron Diffraction Study of K[trans-Co(NH3)2(NO2)4]
4. Chiroptical properties of trans-dichlorotetrakis(pyridine)cobalt(III) ion. A fixed propeller conformation
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4. The Phenomenon of Conglomerate Crystallization. Part 44. Counterion Control of Crystallization Pathway Selection. Part VI. The Crystallization Behavior of [Co(abap)(NO2)2]Cl (I), [Co(abap)(NO2)2]ClO4 (II), [Co(abap)(NO2)2]PF6·H2O (III) and [Co(abap)(NO2)2]I·H2O (IV);Fundamental Principles of Molecular Modeling;1996
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