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Mixed-ligand tris-chelates

However, a number of tris-chelate mixed ligand Cr(III) complexes do exhibit a correlation of the same signs between the lowest frequency 2E component and the major 4E component.119,120,122,123 This relation has been verified by examining the CD for diastereomers of [Cr(en)x(diamine)3 x]3 + (x = 0, 1, 2), c/i-[Cr(NH3)2 (diamine)2]3 +, where the diamines used were (R)- or (5)-propylenediamine and (IR,2R)- or (15,250-1,2-traras-cyclohexanediamine. The differences in CD patterns between each pair of the diastereomers were accounted for by separability and additivity of the configurational and conformational CD contributions. The CD in the spin-allowed 4T2 <— 4A2 transitions shows a positive major component (4E) for the configurational contribution and a minor negative (4Ai) and major positive (4E) components from the lower frequency side for the conformational contribution as shown in Figure 5.30. [Pg.171]

The sensitivity of the method can be increased by addition of gelatine (e = 7.5-10 ) [51]. Hafnium has been extracted with CHCI3 from HCl medium as the chelate complex with N-tolyl-p-methoxybenzohydroxamic acid, and the XO added has given a mixed-ligand complex (e = 8.4-10 ) [52]. In a similar way Zr was determined with the use of tri-n-butylacetohydroxamic acid [53]. [Pg.477]


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Chelate ligands

Chelated ligand

Ligands chelation

Ligands mixed

Tri ligands

Tris ligands

Tris-chelates

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