F. Ciuchi et al., SELF-RECOGNITION AND SELF-ASSEMBLY OF FOLIC-ACID SALTS - COLUMNAR LIQUID-CRYSTALLINE POLYMORPHISM AND THE COLUMN GROWTH-PROCESS, Journal of the American Chemical Society, 116(16), 1994, pp. 7064-7071
Alkaline folates in water, with or without added NaCl, form columnar m
esophases; the columns are composed of a stacked array of folate tetra
mers held together by Hoogsteen-type hydrogen bonds and stacking inter
actions. There is a considerable difference in both the liquid crystal
line polymorphism and the columnar characteristics in pure water and t
hose in 1 mol L(-1) NaCl solutions. In pure water, the tetramer-tetram
er interaction is weak, the columnar length changes slowly with the fo
late concentration, and only the hexagonal mesophase is observed. In 1
mol L(-1) NaCl, the tetramer-tetramer interaction is stronger, a chol
esteric mesophase is observed, and, even at relatively low folate conc
entration, the length of the columns is significant (ca. 20 disks at t
he isotropic-to-cholesteric transition). In both cases, the columns ar
e finite at all concentrations investigated. The formation of a choles
teric mesophase with a pitch of ca. 14 mu m indicates that the tetrame
rs do not pile up in register but are rotated one with respect to the
other to give a chiral column similar both to the four-stranded helix
of poly(G) and to the columnar aggregates formed by homoguanylic oligo
deoxynucleotides.