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Metal complexes with macrocyclic ligands. Part XXXIV . Geometrical and conformational changes during the on/off reaction of the side chain in the Cu II complex of 11‐(3‐aminopropyl)‐1,4,7,11‐tetraazacyclotetradecane
Author(s) -
Schiegg André,
Riesen Andreas,
Kaden Thomas A.
Publication year - 1991
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19910740809
Subject(s) - chemistry , protonation , deprotonation , perchlorate , dissociation (chemistry) , crystallography , metal , side chain , macrocyclic ligand , ligand (biochemistry) , stereochemistry , ion , crystal structure , organic chemistry , biochemistry , receptor , polymer
Solution studies of the Cu 2+ complex with 11‐(3‐aminopropyl)‐1,4,7,11‐tetraazacyclotetradecane(L) indicate that, depending on the pH and on the age of the solution, different species are present. Dissolving the solid [CuL](ClO 4 ) 2 in slightly acidic solution gives the protonated complex AH , characterized by an absorption maximum at 574 nm, by a relatively fast proton‐induced dissociation kinetics and by the typical colour change in basic solution to give the deprolonated form A with coordinated side chain. AH slowly interconverts in acidic solution to a new species BH , which has an absorption maximum at 547 nm, and which is kineticaily more stable against acid dissociation and shows no coordination of the amino group of the side chain. In alkaline solution, however, the deprotonated form B deliver A in a base induced reaction. The X‐ray diffraction studies of A and BH allow to determine the geometry of the metal ion and the configuration of the macrocycle. In A , the Cu 2+ is pentacoordinated by the five N‐atoms of the ligand and the macrocycle is in the RRSR configuration, whereas in BH the Cu 2+ is octahedrally coordinated by the four N‐atoms of the macrocycle and two axial perchlorate O‐atoms with the macrocycle in the RRRS configuration. The amino group of the side chain is protonated and not coordinated. Thus, the on/off equilibrium of the side chain not only changes the geometry of the metal ion, as is generally found, but also alters the macrocyclic moiety.