1334536-32-1Relevant articles and documents
Influence of N-Alkyl Substituents and Counterions on the Structural and Mesomorphic Properties of Guanidinium Salts: Experiment and Quantum Chemical Calculations
Butschies, Martin,Sauer, Sven,Kessler, Elena,Siehl, Hans-Ullrich,Claasen, Birgit,Fischer, Peter,Frey, Wolfgang,Laschat, Sabine
, p. 3752 - 3765 (2010)
A series of N-4-(4'-alkoxybiphenyl)-N',N',N",N"-tetramethylguanidinium salts was synthesized with varying alkoxy chain lengths and additional N-alkyl substituents, each with a number of different counterions. X-ray crystal-structure analyses of 1b I, 1b PF6, 2a I, and 4a I reveal bilayer structures in the solid state and, for the 1b and 1b PF6 salts, a hydrogen-bond-type connectivity between the guanidinium N-H group and the anion is found. For the N-alkyl homologues 2a I and 4a I the anion is still oriented close to the head group, although at a larger distance. Ion pairs are present also in solution, as demonstrated by 1H NMR: the N-H chemical shift shows a good linear correlation with the radius, and hence the hardness, of the anion. The intramolecular conformational flexibility of 1b I, 2b I, 3b I, and 4b I was studied by temperature-dependent 1H NMR spectroscopy and discrete activation barriers were determined for rotations about each of the three C-N partial double bonds of the guanidinium core. The relative heights of the individual barriers change between the N-H and the N-alkylguanidinium salts. A fourth barrier is observed for the rotation about the N-biphenyl bond. DFT calculations of charge densities show that the positive charge resides primarily on the central carbon atom. Rotational barriers were calculated for N'-substituted 2-amino-1,3-dimethylimidazolidinium cations as models, and are in qualitatively good agreement with the NMR data. Mesomorphic properties were studied by differential-scanning calorimetry, polarizing optical microscopy, and X-ray diffraction (WAXS/SAXS). All liquid-crystalline guanidinium salts exhibit smectic A mesophases. Clearing temperatures show a linear correlation with the anionic radius. Substitution of the N-H group with methyl, ethyl, or propyl results in decreasing mesophase widths and a concomitant shrinkage of the layer spacings.The anion makes the difference: The synthesis of various guanidinium salts with varying alkoxy chain lengths and additional N-alkyl substituents is reported (see picture). Mesomorphic properties are studied by differential-scanning calorimetry, polarizing optical microscopy, and X-ray diffraction. All liquid-crystalline guanidinium salts exhibit smectic A mesophases.
