Turchetti Denis Augusto, Nolasco Mariela Martins, Szczerbowski Daiane, Carlos Luís Dias, Akcelrud Leni Campos
Chemistry Department, Paulo Scarpa Polymer Laboratory (LaPPS), Federal University of Parana, P.O. Box 19081, 81531-990, Curitiba, Parana, Brazil.
Phys Chem Chem Phys. 2015 Oct 21;17(39):26238-48. doi: 10.1039/c5cp03567h.
The photophysical properties of a new alternating copolymer containing fluorene, terpyridine, and complexed sites with trivalent europium (Eu(3+)) ions (LaPPS66Eu) were investigated, using the non-complexed backbone (LaPPS66) and a low molecular weight compound of similar chemical structure of the ligand/Eu(3+) site (LaPPS66M) as a model compound. The analogous gadolinium complex (LaPPS66Gd) was also synthesized to determine the triplet state of the complex. (1)H and (13)C nuclear magnetic resonance (NMR) analysis, Fourier transform infrared (FT-IR) spectroscopy, inductively coupled plasma optical emission spectroscopy (ICP-OES), elemental analyses, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA) characterized the chemical structure and thermal properties of the synthesized materials. A level of Eu(3+) insertion of 37% (molar basis) in the polymer backbone was achieved. The photoluminescence studies were performed in the solid state showing the occurrence of polymer-to-Eu(3+) energy transfer brought about by the spectral overlap between the absorption spectra of the Eu(3+) complex and the emission of the polymer backbone. A detailed theoretical photoluminescence study performed using time-dependent DFT (TD-DFT) calculations and the recently developed LUMPAC luminescence package is also presented. The high accuracy of the theoretical calculations was achieved on comparison with the experimental values. Aiming at a deeper level of understanding of the photoluminescence process, the ligand-to-Eu(3+) intramolecular energy transfer and back-transfer rates were predicted. The complexed materials showed a dominant pathway involving the energy transfer between the triplet of the dbm (dibenzoylmethane) ligand and the (5)D1 and (5)D0 Eu(3+) levels.
研究了一种新型含芴、三联吡啶以及与三价铕(Eu(3+))离子络合位点的交替共聚物(LaPPS66Eu)的光物理性质,使用非络合主链(LaPPS66)以及具有与配体/Eu(3+)位点相似化学结构的低分子量化合物(LaPPS66M)作为模型化合物。还合成了类似的钆络合物(LaPPS66Gd)以确定该络合物的三重态。通过(1)H和(13)C核磁共振(NMR)分析、傅里叶变换红外(FT-IR)光谱、电感耦合等离子体发射光谱(ICP-OES)、元素分析、差示扫描量热法(DSC)和热重分析(TGA)对合成材料的化学结构和热性质进行了表征。在聚合物主链中实现了37%(摩尔基准)的Eu(3+)插入水平。在固态下进行了光致发光研究,结果表明由于Eu(3+)络合物的吸收光谱与聚合物主链发射之间的光谱重叠,发生了从聚合物到Eu(3+)的能量转移。还展示了使用含时密度泛函理论(TD-DFT)计算和最近开发的LUMPAC发光程序包进行的详细理论光致发光研究。与实验值比较,实现了理论计算的高精度。为了更深入地理解光致发光过程,预测了配体到Eu(3+)的分子内能量转移和反向转移速率。络合材料显示出一条主要途径,涉及二苯甲酰甲烷(dbm)配体的三重态与Eu(3+)的(5)D1和(5)D0能级之间的能量转移。