The thermotropic smectic phases of amphiphilic 2-(trans-4--alkylcyclohexyl)-propane-1,3-diols were investigated by means of small- and wide-angle x-ray scattering and values of the smectic (bi-)layer spacing, the orientational order parameters and , the orientational distribution function as well as the intralayer correlation length were extracted from the scattering profiles. The results for the octyl homolog indicate that these smectic phases combine a very high degree of smectic one-dimensional-translational order with remarkably low orientational order, the order parameter of which is far below those values typically found in nonamphiphilic smectics. This combination, quite exceptional in thermotropic smectics, most likely originates from the intermolecular hydrogen bonding between the terminal diol groups which seems to be the specific driving force in the formation of the thermotropic smectic structure in these amphiphiles and leads to a type of microphase segregation. Even in the absence of a solvent, the liquid-crystalline ordering of the amphiphilic mesogens comes close to the structure of the so-called neat soaps, found in lyotropic liquid crystals.
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15 July 2005
Research Article|
July 26 2005
Orientational order in smectic liquid-crystalline phases of amphiphilic diols
Frank Giesselmann;
Universität Stuttgart
, Institut für Physikalische Chemie, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
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Roland Germer;
Universität Stuttgart
, Institut für Physikalische Chemie, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
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Alexander Saipa
Alexander Saipa
Universität Stuttgart
, Institut für Physikalische Chemie, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
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Electronic mail: [email protected]
b)
Present address: Siemens VDO Automotive AG, Babenhausen, Germany.
J. Chem. Phys. 123, 034906 (2005)
Article history
Received:
November 29 2004
Accepted:
May 06 2005
Citation
Frank Giesselmann, Roland Germer, Alexander Saipa; Orientational order in smectic liquid-crystalline phases of amphiphilic diols. J. Chem. Phys. 15 July 2005; 123 (3): 034906. https://doi.org/10.1063/1.1943972
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