Picosecond Structural Relaxation of Abietic Acid Based Amine End Capped Para-Phenylenevinylene Trimers in Solution

被引:20
作者
Di Paolo, Roberto E. [1 ]
Gigante, Barbara [2 ]
Esteves, Maria A. [2 ]
Pires, Natercia [2 ]
Santos, Celia [2 ]
Lameiro, Maria H. [3 ]
Seixas de Melo, Joao [4 ]
Burrows, Hugh D. [4 ]
Macanita, Antonio L. [1 ]
机构
[1] Inst Super Tecn, Dept Engn Quim & Biol, Ctr Quim Estrutural, P-1049001 Lisbon, Portugal
[2] INETI, Dept Tecnol Ind Quim, P-1649038 Lisbon, Portugal
[3] Inst Tecnol Quim & Biol, P-2781901 Oeiras, Portugal
[4] Univ Coimbra, Dept Quim, P-3004535 Coimbra, Portugal
关键词
amines; conformational relaxation; dehydroabietic acid; photophysics; time-resolved spectroscopy;
D O I
10.1002/cphc.200800374
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 [物理化学]; 081704 [应用化学];
摘要
The synthesis and photophysical properties of six new abietic acid based amine end-capped p-phenylenevinylene trimers (AECPV3) in their lowest excited singlet states are presented. The AECPV3 compounds show a large red-shift of both the absorption (25-30 nm) and emission (37-42 nm) maxima with respect to those of the corresponding trimers. Picosecond time-resolved fluorescence data reveal the presence of a fast conformational relaxation process (40-62 ps) of the initially excited compounds, leading to more planar conformers. The conformational relaxation time is proportional to the volume of both the side chain and the amine groups.
引用
收藏
页码:2214 / 2220
页数:7
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