TY - JOUR
T1 - Constructing multicomponent materials containing cavitands, and phosphonium and imidazolium cations
AU - Ling, Irene
AU - Alias, Yatimah
AU - Sobolev, Alexandre N.
AU - Raston, Colin L.
PY - 2009/10/7
Y1 - 2009/10/7
N2 - Bis-imidazolium cations, 1,1′-[1,4-phenylenebis(methylene)]bis(3-R- 1H-imidazolium-1-yl), (R = methyl or n-butyl), form discrete multicomponent complexes in water with various phosphonium cations, anionic /?-sulfonatocalix[4]arene, and aquated gadolinium(III) ions. The terminal alkyl groups, R, reside in the cavities of the calixarenes, with two calixarenes either adjacent to each other, where they face the same direction and are in the same bilayer arrangement made of calixarenes and phosphonium cations, or where they face opposite directions. Here the calixarenes are similarly part of a bilayer arrangement, or they are part of an extended structure which can. be regarded as being built from the assembly of supermol.ecul.es or "molecular capsules", [(bis-imidazolium)⊂(p-sulfonatocalix[4]arene)2], which are π-stacked through the calixarenes in a head-to-tail fashion. The nature of the product depends on the length of the terminal alkyl group, and the choice of phosphonium cation.
AB - Bis-imidazolium cations, 1,1′-[1,4-phenylenebis(methylene)]bis(3-R- 1H-imidazolium-1-yl), (R = methyl or n-butyl), form discrete multicomponent complexes in water with various phosphonium cations, anionic /?-sulfonatocalix[4]arene, and aquated gadolinium(III) ions. The terminal alkyl groups, R, reside in the cavities of the calixarenes, with two calixarenes either adjacent to each other, where they face the same direction and are in the same bilayer arrangement made of calixarenes and phosphonium cations, or where they face opposite directions. Here the calixarenes are similarly part of a bilayer arrangement, or they are part of an extended structure which can. be regarded as being built from the assembly of supermol.ecul.es or "molecular capsules", [(bis-imidazolium)⊂(p-sulfonatocalix[4]arene)2], which are π-stacked through the calixarenes in a head-to-tail fashion. The nature of the product depends on the length of the terminal alkyl group, and the choice of phosphonium cation.
UR - http://www.scopus.com/inward/record.url?scp=70350236290&partnerID=8YFLogxK
U2 - 10.1021/cg900710c
DO - 10.1021/cg900710c
M3 - Article
AN - SCOPUS:70350236290
SN - 1528-7483
VL - 9
SP - 4497
EP - 4503
JO - Crystal Growth & Design
JF - Crystal Growth & Design
IS - 10
ER -