Handbook of Aggregation-Induced Emission, Volume 3. Группа авторов. Читать онлайн. Newlib. NEWLIB.NET

Автор: Группа авторов
Издательство: John Wiley & Sons Limited
Серия:
Жанр произведения: Химия
Год издания: 0
isbn: 9781119643067
Скачать книгу
Chihaya, A. Third‐generation organic electroluminescence materials. Jpn. J. Appl. Phys. 2014; 53(6):060101.

      118 118 Furue, R., Nishimoto, T., Park, I. S., Lee, J., Yasuda, T. Aggregation‐induced delayed fluorescence based on donor/acceptor‐tethered Janus Carborane Triads: unique photophysical properties of nondoped OLEDs. Angew. Chem. Int. Ed. 2016; 55(25):7171–5.

      119 119 Guo, J. J., Li, X. L., Nie, H., Luo, W. W., Gan, S. F., Hu, S. M., et al. Achieving high‐performance nondoped OLEDs with extremely small efficiency roll‐off by combining aggregation‐induced emission and thermally activated delayed fluorescence. Adv. Funct. Mater. 2017; 27(13):9.

      120 120 Guo, J., Li, X.‐L., Nie, H., Luo, W., Hu, R., Qin, A., et al. Robust luminescent materials with prominent aggregation‐induced emission and thermally activated delayed fluorescence for high‐performance organic light‐emitting diodes. Chem. Mater. 2017; 29(8):3623–31.

      121 121 Guo, J., Li, X.‐L., Nie, H., Luo, W., Gan, S., Hu, S., et al. Achieving high‐performance nondoped OLEDs with extremely small efficiency roll‐off by combining aggregation‐induced emission and thermally activated delayed fluorescence. Adv. Funct. Mater. 2017; 27(13):1606458–n/a.

      122 122 Li, M., Liu, Y., Duan, R., Wei, X., Yi, Y., Wang, Y., et al. Aromatic‐imide‐based thermally activated delayed fluorescence materials for highly efficient organic light‐emitting diodes. Angew. Chem. Int. Ed. 2017; 56(30):8818–22.

      123 123 Keller, R. A. Excited triplet–singlet intersystem crossing. Chem. Phys. Lett. 1969; 3(1):27–9.

      124 124 Islam, A., Zhang, D., Peng, R., Yang, R., Hong, L., Song, W., et al. Non‐doped sky‐blue OLEDs based on simple structured AIE emitters with high efficiencies at low driven voltages. Chem. Asian J. 2017; 12(17):2189–96.

      125 125 Chen, L., Jiang, Y., Nie, H., Hu, R., Kwok, H. S., Huang, F., et al. Rational design of aggregation‐induced emission luminogen with weak electron donor–acceptor interaction to achieve highly efficient undoped bilayer OLEDs. ACS Appl. Mater. Interfaces. 2014; 6(19):17215–25.

      126 126 Han, X., Bai, Q., Yao, L., Liu, H., Gao, Y., Li, J., et al. Highly efficient solid‐state near‐infrared emitting material based on triphenylamine and diphenylfumaronitrile with an EQE of 2.58% in nondoped organic light‐emitting diode. Adv. Funct. Mater. 2015; 25(48):7521–9.

      127 127 Fan, J., Cai, L., Lin, L., Wang, C.‐K. Excited state dynamics for hybridized local and charge transfer state fluorescent emitters with aggregation‐induced emission in the solid phase: a QM/MM study. Phys. Chem. Chem. Phys. 2017; 19(44):29872–9.

      128 128 Yuan, W. Z., Bin, X., Chen, G., He, Z., Liu, J., Ma, H., et al. Achieving hybridized local and charge‐transfer excited state and excellent OLED performance through facile doping. Adv. Opt. Mater. 2017; 5(21):1700466–n/a.

      129 129 Li, C., Hanif, M., Li, X., Zhang, S., Xie, Z., Liu, L., et al. Effect of cyano‐substitution in distyrylbenzene derivatives on their fluorescence and electroluminescence properties. J. Mater. Chem. C. 2016; 4(31):7478–84.

      130 130 Kondakov, D. Y., Pawlik, T. D., Hatwar, T. K., Spindler, J. P. Triplet annihilation exceeding spin statistical limit in highly efficient fluorescent organic light‐emitting diodes. J. Appl. Phys. 2009; 106(12):124510.

      131 131 Zhou, J., Chen, P., Wang, X., Wang, Y., Wang, Y. Li, F., et al. Charge‐transfer‐featured materials‐promising hosts for fabrication of efficient OLEDs through triplet harvesting via triplet fusion. Chem. Commun. 2014; 50(57):7586–9.

      132 132 Singh, S., Jones, W. J., Siebrand, W., Stoicheff, B. P., Schneider, W. G. Laser generation of excitons and fluorescence in anthracene crystals. J. Chem. Phys. 1965; 42(1):330–42.

       Fuwei Gan, Chengshuo Shen, and Huibin Qiu

       School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai, China

      Electronic circular dichroism (ECD) measures the differential molar absorption coefficient (Δε) between a left‐handed circularly polarized light (εL) and a right‐handed circularly polarized light (εR) for electronic transitions:

equation

      ECD is the chiroptical counterpart of UV–vis absorption and is utilized extensively in most chiral systems including small molecules, biomolecules, supramolecular assemblies, polymers, liquid crystals (LCs), etc., providing valuable information of the ground states.

      For a luminescent chiral system, one can investigate its circularly polarized luminescence (CPL), which measures the differential emission (ΔI) between a left‐handed circularly polarized light (IL) and a right‐handed circularly polarized light (IR):

equation

      Unlike ECD measurement, determination of the absolute emission intensity of CPL is quite difficult, and it is customary to quantify the intensity difference using its relative value, namely, luminescence dissymmetry factor (glum):

equation

      The value of glum should be limited between −2 and +2, and 0 represents the absence of circularly polarized emission. Similar to its absorption analog ECD, CPL reflects the information of the excited states of a chiral system.

      Generally, systems with intrinsically chiral luminophores or luminophores situated in a chiral environment can generate CPL signals. However, due to the detection limit, most early reported examples were restricted to lanthanide complexes since their ff Laporte‐forbidden transitions can give relatively high CPL activities (glum ~ 10−2 to 10−1) [5]. This situation is changing recently following the discovery of several categories of SOMs with intense CPL [6–8], such as chiral ketones, cyclophanes, binaphthyl derivatives, helicenes, and boron dipyrromethenes (BODIPYs), and their promising applications in circularly polarized organic light‐emitting diodes (CP‐OLEDs), circularly polarized organic semiconductor transistor, and other optoelectronic devices [9–12].

      For CPL measurements, the most examples were done in dilute solutions, while for devices, materials need to generate CPL in the aggregated state. For the most luminophores, severe ππ stacking can be observed in the aggregated state, resulting in strong luminescence quenching and hence, less or even no emission. Aggregation‐induced emission (AIE) creates a highly efficient way to solve the aggregation‐caused quenching (ACQ) problem. To construct aggregation‐induced circularly polarized luminescence (AICPL) materials, one can introduce nonemissive chiral moieties into an AIE system, rendering the AIEgens chiral, or in several cases, chiral luminophores linked together with AIEgens can also give an efficient AICPL performance. Besides, constructing a chiral environment using supramolecular chemistry or placing AIEgens in chiral polymers or LCs is emerging as another practical way to build AICPL systems.

      Tang and Wong et al.