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New mesomorphic organocyclosiloxanes II. Thermal behaviour and mesophase structure of organocyclohexasiloxanesстатья
Информация о цитировании статьи получена из
Web of Science,
Scopus
Статья опубликована в журнале из списка Web of Science и/или Scopus
Дата последнего поиска статьи во внешних источниках: 18 марта 2017 г.
- Авторы: Matukhina Elena V., Shchegolikhina Olga I., Molodtsova Yulia A., Pozdniakova Yulia A., Lyssenko Konstantin A., Vasil’ev Viktor G., Buzin Mikhail I., Katsoulis Dimitris E.
- Журнал: Liquid Crystals
- Том: 31
- Номер: 3
- Год издания: 2004
- Издательство: Taylor & Francis
- Местоположение издательства: United Kingdom
- Первая страница: 401
- Последняя страница: 420
- DOI: 10.1080/02678290410001665986
- Аннотация: Investigations of thermotropic phase transitions performed on organocyclosiloxanes [PhSi(O)OSiR]6, where R is Me3, Me2(CH2Cl) or Me2(CH≃CH2), have revealed that all these hexamers are mesomorphic compounds. The hexamers exhibit uncommon polymesomorphic behaviour forming two quite different mesomorphic structures. The molecular arrangement in the low temperature (LT) modification is characterized by two-dimensional (2D) long-range order with hexagonal packing. The X-ray diffraction pattern and peculiarities of molecular packing in the crystal lead us to suggest that the LT-mesophase is columnar, presumably of the Colhd type. The LT-mesophase is formed by dimeric moieties, which associate with each other in column-like substructures, the ring planes not orthogonal to the stack axis. The high temperature (HT) mesophase is a plastic crystal (3D-order), where molecules take up positions in a face-centred cubic lattice. This is a very uncommon example of thermal behaviour for plastic crystals that provides a unique opportunity to bridge the gap between plastic crystalline and liquid crystalline mesomorphic behaviour. The thermal and structural properties of the mesophases depend upon the type of side groups of the hexamers. The size of the ring also affects the phase behaviour and the mesomorphic structure. This conclusion is consistent with data obtained by us earlier for cyclotetrasiloxanes.
- Добавил в систему: Щеголихина Ольга Ивановна