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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Gigantic Two-Photon Absorption Cross Sections and Strong Two-Photon Excited Fluorescence in Pyrene Core Dendrimers with Fluorene/Carbazole as Dendrons and Acetylene as Linkages
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Gigantic Two-Photon Absorption Cross Sections and Strong Two-Photon Excited Fluorescence in Pyrene Core Dendrimers with Fluorene/Carbazole as Dendrons and Acetylene as Linkages

机译:Fluor /咔唑为树枝状和乙炔为键的P核树枝状大分子中的巨大双光子吸收截面和强双光子激发荧光

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We report a series of stiff dendrimers (referred to as T1, T2, T3, and T4) that have both gigantic two-photon absorption (TPA) cross sections up to 25 000 GM and strong two-photon excited fluorescence (TPEF) with fluorescence quantum yield of ~0.5. The large TPA cross sections and high quantum yields of these dendrimers are directly related to their geometrical structures, where the polycyclic aromatic pyfene is chosen as the chromophoric core because of its planar and highly π-conjugated structure, fluorene moieties as dendrons extend the conjugation length through the planar structure, and carbazole moieties are modified at three-, six-, and nine-positions as electron donor. All of these groups are linked with acetylene linkage for effective π-electron delocalization, leading to large TPA cross section and high fluorescence quantum yield. The spectral properties of all dendrimers are investigated by one- and two-photon excitations. Furthermore, steady-state fluorescence excitation anisotropy and quantum chemical calculation are also employed to determine the structure-related mechanism of these dendrimers with gigantic TPA cross sections and high TPEF efficiency. We then show that the improvement of branched chains in the T-series dendrimers enhances the light-harvesting ability. The core emission spectra, fluorescence quantum yield, and fluorescence lifetime are almost invariable by directly exciting the dendrons. These results will provide a guideline for the design of useful two-photon materials with structural motifs that can enhance the TPA cross-section and fluorescence quantum yield of a molecule without causing a red shift of the one- and two-photon excitation wavelengths for specific applications.
机译:我们报告了一系列刚性树枝状分子(称为T1,T2,T3和T4),它们具有高达25000 GM的巨大双光子吸收(TPA)截面和具有荧光的强双光子激发荧光(TPEF)量子产率为〜0.5。这些树枝状聚合物的大TPA横截面和高量子产率与它们的几何结构直接相关,其中多环芳族由于其平面和高度π共轭结构而被选择为发色核,芴作为树枝状分子而延长了共轭长度通过平面结构,咔唑部分在三个,六个和九个位置被修饰为电子供体。所有这些基团均通过乙炔键连接以有效地进行π电子离域,从而导致大的TPA截面和高荧光量子产率。所有树状聚合物的光谱性质都通过单光子和双光子激发来研究。此外,稳态荧光激发各向异性和量子化学计算也被用来确定这些具有大TPA横截面和高TPEF效率的树枝状分子的结构相关机理。然后,我们表明在T系列树状聚合物中支链的改进增强了光收集能力。通过直接激发树突,核心发射光谱,荧光量子产率和荧光寿命几乎不变。这些结果将为设计有用的具有结构图案的双光子材料提供指导,该结构可以增强分子的TPA横截面和荧光量子产率,而不会引起特定分子的单光子和双光子激发波长的红移。应用程序。

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