Kang Heun Kag, Kang Dong Eun, Boo Bong Hyun, Yoo Suk Jae, Lee Jae Kwang, Lim Edward C
Department of Chemistry, Chungnam National University, Daejeon 305-764, Korea.
J Phys Chem A. 2005 Aug 11;109(31):6799-804. doi: 10.1021/jp058019h.
A concerted computational and experimental study has been undertaken to probe the conformational structure and excited-state dynamics of bis(9-fluorenyl)methane (BFM). We have observed that the relative intensity of the delayed excimer fluorescence of BFM is greatly enhanced in comparison with that of the normal fluorescence. This is presumably because the relative concentration of the triplet excimer is enhanced in comparison with the singlet excimer. B3LYP DFT/6-31G(d) calculations indicate that the sandwich conformer of BFM in the singlet ground state is unstable, whereas that in the triplet excited state has a bound state, being very slightly higher in internal and Gibbs free energies than that of the lowest state of the near-orthogonal conformer.
已开展了一项计算与实验相结合的研究,以探究双(9-芴基)甲烷(BFM)的构象结构和激发态动力学。我们观察到,与正常荧光相比,BFM延迟准分子荧光的相对强度大大增强。据推测,这是因为三重态准分子的相对浓度相对于单重态准分子有所增加。B3LYP密度泛函理论/6-31G(d)计算表明,BFM在单重态基态的夹心构象不稳定,而在三重态激发态具有束缚态,其内能和吉布斯自由能比近正交构象的最低态略高。