TY - JOUR
T1 - Heterobimetallic Calix[4]arene Complexes
T2 - Interconversion of Dimeric (Ca, Sr or Ba)/TiIV Complexes with a Monomeric K/TiIV Complex
AU - Petrella, Antonella J.
AU - Roberts, Nicholas K.
AU - Raston, Colin L.
AU - Craig, Donald C.
AU - Thornton-Pett, Mark
AU - Lamb, Robert N.
PY - 2003/12/5
Y1 - 2003/12/5
N2 - Reaction of calix[4]arene with alkaline earth metals (Ca/Sr/Ba) in methanol followed by the addition of various titanium(IV) sources afforded novel dimeric 1:1 alkaline earth/titanium(IV) calix[4]arene complexes. In each complex the central core of the crystallographically imposed centrosymmetric dimer consists of a rhombus of alternating alkaline earth metals and μ 3-oxo-centres. Five terminal methanol ligands form seven-coordinate calcium and strontium centres, while the barium centres are bridged by two additional methanol ligands, making them nine-coordinate. Each oxo centre is the apical ligand of a square-pyramidal titanium(IV) centre, whose basal plane ligands are the four phenolate oxygens from a calix[4]arene in the symmetrical cone-conformation. Deprotonation of calix[4]arene with potassium metal, followed by the addition of a titanium(IV) source containing at least one acetylacetonate ligand, formed a mixed potassium/titanium complex based on one calix[4]arene. The potassium cation in this complex binds within the π-basic calix[4]arene cavity, whilst titanium is octahedrally complexed in the exo-position, by four phenolates and one acetylacetonate. The alkaline earth titanium dimers and potassium/titanium monomers could be interconverted merely by changing the solvent, with the appropriate cations and ligands present in solution.
AB - Reaction of calix[4]arene with alkaline earth metals (Ca/Sr/Ba) in methanol followed by the addition of various titanium(IV) sources afforded novel dimeric 1:1 alkaline earth/titanium(IV) calix[4]arene complexes. In each complex the central core of the crystallographically imposed centrosymmetric dimer consists of a rhombus of alternating alkaline earth metals and μ 3-oxo-centres. Five terminal methanol ligands form seven-coordinate calcium and strontium centres, while the barium centres are bridged by two additional methanol ligands, making them nine-coordinate. Each oxo centre is the apical ligand of a square-pyramidal titanium(IV) centre, whose basal plane ligands are the four phenolate oxygens from a calix[4]arene in the symmetrical cone-conformation. Deprotonation of calix[4]arene with potassium metal, followed by the addition of a titanium(IV) source containing at least one acetylacetonate ligand, formed a mixed potassium/titanium complex based on one calix[4]arene. The potassium cation in this complex binds within the π-basic calix[4]arene cavity, whilst titanium is octahedrally complexed in the exo-position, by four phenolates and one acetylacetonate. The alkaline earth titanium dimers and potassium/titanium monomers could be interconverted merely by changing the solvent, with the appropriate cations and ligands present in solution.
KW - Alkaline earth metals
KW - Calixarenes
KW - Heterometallic complexes
KW - Potassium
KW - Titanium
UR - http://www.scopus.com/inward/record.url?scp=0345732164&partnerID=8YFLogxK
U2 - 10.1002/ejic.200300395
DO - 10.1002/ejic.200300395
M3 - Article
AN - SCOPUS:0345732164
SN - 1434-1948
SP - 4153
EP - 4158
JO - European Journal of Inorganic Chemistry
JF - European Journal of Inorganic Chemistry
IS - 23
ER -