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Restriction of the rotational relaxation of a butadiyne-bridged porphyrin dimer in ultrathin filmsстатья
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: 23 августа 2019 г.
- Авторы: Shokurov Alexander V., Meshkov Ivan N., Bulach Véronique, Gorbunova Yulia G., Hosseini Mir Wais, Tsivadze Aslan Yu, Arslanov Vladimir V., Selektor Sofia L.
- Журнал: New Journal of Chemistry
- Том: 43
- Номер: 28
- Год издания: 2019
- Издательство: Royal Society of Chemistry
- Местоположение издательства: United Kingdom
- Первая страница: 11419
- Последняя страница: 11425
- DOI: 10.1039/c9nj01807g
- Аннотация: The dynamic behaviour of a porphyrin dimer, based on the covalent linkage of two macrocyclic moieties with a butadiyne connector, was studied in thin films by UV-Vis and emission spectroscopies. The degree of π-conjugation through control of intramolecular motion was investigated without employing extreme conditions such as cryogenic temperatures or high viscosity. By exploiting the propensity of the dimer to bind axial ligands through Zn–N bonds, it was shown that the co-planar and orthogonal conformations of the dimer may be stabilized in ultrathin films at the air/water interface. Furthermore, using the Langmuir–Blodgett technique, monolayer-thick matrix-free films on solid substrates containing the porphyrin dimer were obtained. In the latter case, the dimer exists in either an exclusively co-planar state or a mixture of conformational states depending on the nature of the axial ligand: 1,4-diazabicyclo[2.2.2]-octane (DABCO) or 4-aminomethylpyridine (AMP).
- Добавил в систему: Мешков Иван Николаевич