Photoreactivities of two kinds of bimolecular crystals formed from acridine and phenothiazine

Hideko Koshima*, Yang Wang, Teruo Matsuura, Ikuko Miyahara, Hisashi Mizutani, Ken Hirotsu, Tsuyoshi Asahi, Hiroshi Masuhara

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

A yellow crystal 3 and a red crystal 4 simultaneously crystallize from a solution of acridine 1 and phenothiazine 2 in acetonitrile. Similar N ⋯ H-N hydrogen bonding pairs of 1 and 2 are formed in the two crystals. The 3:4 crystal 3 has a slightly uncommon molecular arrangement of which four acridine molecules out of twelve are disordered in the unit cell. The 1:1 crystal 4 has a more rigid packing of the hydrogen bonding pairs. Irradiation of 3 gives a photoadduct 5 as the sole product, whereas 4 shows almost no photoreactivity. The occurrence of photoinduced electron transfer has been confirmed by the measurement of transient absorption spectra of the crystals 3 and 4. However, the two-stage decay of the transient absorption of 3 with lifetimes of 2 and 50 ps is different from that of 4 with a single short lifetime of 2 ps. Upon irradiating 3, electron transfer, proton transfer and subsequent radical coupling occur over the shortest distance of 4.1 Å between the preradical carbon and nitrogen atoms in the crystal lattice followed by dehydrogenation to afford the product 5. In the case of the red crystal 4, the radical coupling is difficult because of the longer coupling distance of 5.6 Åand the more restricted movement in the rigid crystal lattice. The results indicate that the observed photochemical behaviour of 3 and 4 are controlled by the molecular arrangement in the crystal lattice.

Original languageEnglish
Pages (from-to)2033-2038
Number of pages6
JournalJournal of the Chemical Society. Perkin Transactions 2
Issue number10
DOIs
StatePublished - 1 Jan 1997

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