Influence of N-Alkyl Substituents and Counterions on the Structural and Mesomorphic Properties of Guanidinium Salts: Experiment and Quantum Chemical Calculations

被引:33
作者
Butschies, Martin [2 ]
Sauer, Sven [2 ]
Kessler, Elena [1 ]
Siehl, Hans-Ullrich [1 ]
Claasen, Birgit [2 ]
Fischer, Peter [2 ]
Frey, Wolfgang [2 ]
Laschat, Sabine [2 ]
机构
[1] Univ Ulm, Inst Organ Chem 1, D-89069 Ulm, Germany
[2] Univ Stuttgart, Inst Organ Chem, D-70569 Stuttgart, Germany
关键词
charge distribution; density functional calculations; internal dynamics; liquid crystals; mesophases; IONIC LIQUID-CRYSTALS; CN-DOUBLE-BONDS; NMR-SPECTROSCOPY; ROTATION; SOLVATION; COMPLEXES; SOLVENTS; CALIBRATION; INVERSION; CRITERIA;
D O I
10.1002/cphc.201000444
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 H-1 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.
引用
收藏
页码:3752 / 3765
页数:14
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