Nakatsuji Shin'ichi, Ojima Takeo, Akutsu Hiroki, Yamada Jun-ichi
Department of Material Science, Faculty of Science, Himeji Institute of Technology, 3-2-1 Kouto, Kamigori, Hyogo 678-1297, Japan.
J Org Chem. 2002 Feb 8;67(3):916-21. doi: 10.1021/jo010943u.
Anthracene derivatives with several TEMPO radicals (2-4, 10) were prepared, and each photodimerization reaction was investigated. Although the photodimerization was unsuccessful in obtaining the dimers of anthracenes 2 and 3, which could be alternatively prepared in a stepwise manner, the photodimers of anthracenes 4 and 10 were available by the direct photoreaction. The dissociation reaction of the dimers proceeded well by heating them in solution to give the corresponding monomers in each case, and thus the reversible system could be constructed in the latter two systems. While no large difference was observed in their magnetic behaviors between the monomer/dimer pair of 4 and 8, an intriguing difference was found in the magnetic behaviors for the pair of 10 and 11 from ferromagnetic interactions in 10 to the variable magnetic interactions in 11 depending on the solvent molecules incorporated in the crystals.
制备了带有多个TEMPO自由基的蒽衍生物(2 - 4、10),并对每个光二聚反应进行了研究。尽管通过光二聚反应未能成功获得蒽2和3的二聚体,不过它们可以通过逐步方式另行制备,而蒽4和10的光二聚体可通过直接光反应得到。通过在溶液中加热二聚体,其解离反应顺利进行,在每种情况下都得到了相应的单体,因此在后两种体系中可以构建可逆体系。虽然在4和8的单体/二聚体对之间未观察到明显的磁行为差异,但在10和11的对中发现了一个有趣的差异,即从10中的铁磁相互作用到11中取决于晶体中所含溶剂分子的可变磁相互作用。