Supramolecular chemistry and the control of the crystallization behavior by the choice of the counter-ion. Part 11. The stereochemistry and crystallization architecture of [(tren)Co(NO2)2]A (I), [(tren)Co(ox)]A (II), [(en)2Co(ox)]A (III) and [trans-(pn)2Co(NO2)2]A (IV), with A=[trans-(NH3)2Co(NO2)4]
Author:
Publisher
Elsevier BV
Subject
General Chemical Engineering,General Chemistry
Reference23 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. V. Clavic Dissymmetry in Coordination Compounds. IV. A Neutron Diffraction Study of K[trans-Co(NH3)2(NO2)4]
3. 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
4. The Phenomenon of Conglomerate Crystallization. XXI. Clavic Dissymmetry in Coordination Compounds. XIX. A Topological Investigation of the Conformational and Configurational Characteristics of Racemic [Cis-β-Co(trien)(N02)2][trans-Co(NH3)2(No2)4]·H2O
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