Steady-State and Picosecond Spectroscopy of Li+ or Ca2+ Complexes with a Crowned Merocyanine. Reversible Photorelease of Cations
Steady-State and Picosecond Spectroscopy of Li+ or Ca2+ Complexes with a Crowned Merocyanine. Reversible Photorelease of Cations
复制标题
Li 或 Ca2 与冠部花青配合物的稳态和皮秒光谱。
DOI:
10.1021/jp952783u
复制
发表时间:
1996
期刊:
影响因子:
--
通讯作者:
B. Valeur
中科院分区:
文献类型:
--
作者:
Monique M. Martin;Andreia Plaza;Y. Meyer;F. Badaoui;J. Bourson;Andre Lefevre;B. Valeur
Reversible photorelease of Li+ and Ca2+ cations from complexes with a crowned derivative of the merocyanine dye DCM (4-(dicyanomethylene)-2-methyl-6-(p-(dimethylamino)styryl)-4H-pyran) in acetonitrile is investigated by steady-state and time-resolved spectroscopy. The results obtained by fluorescence spectroscopy reveal the presence of two emitting species in solutions containing DCM−crown complexes. One species with a 2 ns lifetime is attributed to the free ligand resulting from cation photorelease, with a maximum formation yield of 86% for Li+ and 41% for Ca2+. The other one with a 400 ps slightly blue-shifted emission for both cations is suggested to be due to a loose complex. The mechanism of cation photorelease is studied by transient absorption and gain spectroscopy within 2 ns after excitation with a 0.7 ps pulse at 425 nm. In the 360−660 nm spectral range, the main changes observed take place within 30 ps. For longer time delays the time-resolved differential spectra indicate a dominant decay of 1...