Electronic structure of the lowest excited triplet state of 5,12-naphthacenequinone.

Takuji Shimokage, Tadaaki Ikoma, Kimio Akiyama, Shozo Tero-Kubota

文献索引：Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 58(6) , 1201-8, (2002)

全文：HTML全文

摘要

Continuous-wave time-resolved EPR (cw-TREPR) and pulsed electron nuclear double resonance (ENDOR) studies have been carried out to clarify the electronic structure of the lowest excited triplet (Tl) state of 5,12-naphthacenequinone (5,12-NpQ) as well as 1,4-anthraquinone (1,4-AQ) and 6,13-pentacenequinone (6,13-PeQ). The Tl energy level and the D value of the zero-field splitting (ZFS) parameters only slightly decreased with the increasing pi-conjugated system. The Tl states of these linear para-acenequinones were assigned to the pi pi* character. In triplet 5,12-naphthacenequinone, more than 80% of the unpaired electron spins are localized on the naphthalene aromatic sub-system.