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Absolute configuration of chelate ring

Figure 2-6. The two enantiomeric forms of the chelate ring present in complexes of 1,2-diaminoet-hane. The labels 8 and X describe the absolute configuration of the chelate ring. Figure 2-6. The two enantiomeric forms of the chelate ring present in complexes of 1,2-diaminoet-hane. The labels 8 and X describe the absolute configuration of the chelate ring.
It was recognized quite early that the chelate rings of these ligands could not adopt a planar structure16,17K The more stable gauche conformation may present X or 5 helicity so that substituents fixed on the carbon chain can adopt two non-equivalent positions. If the absolute configuration of such a ligand is determined, as for example in R(—)propylenediamine, one of the two conformations becomes more stable. On... [Pg.6]

This result corresponds to the conformational analysis which predicts 24 as the most stable one. As already mentioned, it is possible to fix the absolute configuration of a given isomer by a suitable choice of substituents. A selection between different geometrical isomers — e.g. on the base of chelate ring size — seems to be less easy. It... [Pg.19]

Figure 1-18 Different ways of viewing the puckering of ethyl-enediamine chelate rings. The ab-S solute configurations A and S are defined. [Reproduced by permission from C. J. Hawkins, Absolute Configurations of Metal Complexes, Wiley, New York, 1971.]... Figure 1-18 Different ways of viewing the puckering of ethyl-enediamine chelate rings. The ab-S solute configurations A and S are defined. [Reproduced by permission from C. J. Hawkins, Absolute Configurations of Metal Complexes, Wiley, New York, 1971.]...

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Absolute configuration

Chelate rings

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