Minoru Yamaji, Kazuyoshi Shima, Jun Nishimura and Haruo Shizuka
The formation and decay processes of triplet naphthalenophanes (3NP*) sensitized by triplet benzophenone (3BP*) have been investigated by means of laser photolysis techniques. It was found that the dynamic behaviour of 3NP* markedly depends on their molecular conformations. For the cases of NP with tetramethylene chains (tNP), triplet energy transfer from 3BP* occurred to produce triplet tNP (3tNP*). The triplet–triplet (T–T) absorption spectrum of syn-tNP having full-overlapped naphthalene moieties (parallel form) consisted of local (430 nm) and excimer triplet (580 nm) absorption bands. For anti-tNP with partially overlapped naphthalene moieties (antiparallel form), only the local T–T absorption was observed. The efficiency (ϕTET) of triplet energy transfer was determined to be unity for syn-tNP while 0.76 for anti-tNP. The rate constants for the quenching of 3BP* (kq) and triplet energy transfer (kTET) were determined. At high BP concentrations, it was shown that the decay processes of 3tNP* mainly proceeded via a triplet exciplex between 3tNP* and BP regardless of their molecular structures. For the cases of NP with a cyclobutane ring (cNP, tilted form), after triplet energy transfer from 3BP*, the bond dissociation of the cyclobutane ring of 3cNP* subsequently took place to give the corresponding triplet biradicals.