Solvent supramolecular

Makarevic. J. Jokic, M. Peric, B. Tomisic. V. Kojic-Prodic. B. Zinic, M. Bisfamino acid) oxalyl amides as ambidextrous gelators of water and organie solvents, supramolecular gels with temperature dependent assem-bly/dissolution equilibrium. Chem. Eur. J. 2001, 7, 3328-3341. 

Vickery, J.C., Olmstead, M.M., Fung, E.Y. and Balch, A.L. (1997) Solvent-stimulated luminescence from the supramolecular aggregation of a trinuclear gold(I) complex that displays extensive intermolecular Au Au interactions. Angewandte Chemie, 109, 1227-1229 (1997) Angewandte Chemie (International Edition in English), 36, 1179-1181. 

Guo, H., and M. Karplus. 1994. Solvent Influence on the Stability of the Peptide Hydrogen Bond A Supramolecular Cooperative Effect. J. Phys. Chem. 98, 7104-7105. 

Strong intermolecular interactions between active SCO mononuclear building blocks stem from the presence of efficient hydrogen-bonding networks or 7i-7i stacking interactions and have led to abrupt spin transitions [1], sometimes with associated hysteresis [2-4]. Despite the important efforts made by crystal engineers in establishing reliable connections between molecular and supramolecular structures on the basis of intermolecular interactions, the control of such forces is, however, difficult and becomes even more complicated when uncoordinated counter-ions and/or solvent molecules are present in the crystal lattice. 

A second example of homochiral columns formed by discotics are the complexes of tetrazoles (59 and 60) with l,3,5-tris(4,5-dihydroimidazol-2-yl)benzene (61).74 Four molecules self-assemble to give a supramolecular disc and these discs subsequently form columns in nonpolar solvents. Chiral discs were obtained from the self-assembly of the chiral tetrazole (60) with 61. The chirality of the side chains was found to induce a bias in the helic-ity of the supramolecular assembly. Sergeants-and-soldiers measurements75 were performed for which chiral (60) and achiral (59) molecules were mixed. The experiments showed no amplification of chirality, thus revealing that in these systems chirality transfer from the side chains into the column is... 

Several natural and synthetic helical macromolecules such as DNA, polypeptides, and polyisocyanates form, in the appropriate solvent, cholesteric meso-phases. Also self-assembled supramolecular systems formed by guanosine derivatives 2 and 3 (G-wires), which are essentially four-stranded helices (Figure 7.8), behave in a similar way.35... 

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