Synthesis, prodigious two-photon absorption cross sections and electrochemical properties of a series of triphenylamine-based chromophores

被引:4
|
作者
Li, Rui [1 ]
Li, Dandan [1 ]
Fei, Wenwen [1 ]
Tan, Jingyun [1 ]
Li, Shengli [1 ]
Zhou, Hongping [1 ]
Zhang, Shengyi [1 ]
Wu, Jieying [1 ]
Tian, Yupeng [1 ,2 ]
机构
[1] Anhui Univ, Key Lab Funct Inorgan Mat Chem Anhui Prov, Dept Chem, Hefei 230601, Peoples R China
[2] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Triphenylamine; Phenylenevinylene; Polyether; Two-photon absorbing; Two-photon across-section; Electrochemistry; PHOTOPHYSICAL PROPERTIES; CHARGE-TRANSFER; ENERGY-TRANSFER; ONE-PHOTON; FLUORESCENCE; PORPHYRIN; MOLECULE; OLIGOMER; DESIGN;
D O I
10.1016/j.optmat.2014.03.003
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A series of triphenylamine-based chromophores (L1-3) with donor-pi-donor (D-pi-D) model have been designed and synthesized via solid phase Wittig reaction. Their one/two-photon fluorescence and electrochemical properties have been investigated. The results show that L2 and L3 exhibited strong and wide-dispersed two-photon-excited fluorescence (TPEF) in different solvents. Chromophore L3 displays the strongest intensity two-photon absorption activity and large cross-sections (>3600 GM) in the range of 680-840 nm in THF, the largest up to 8899 GM in the near-IR range, and the measured maximum TPA cross-sections per molecular weight (OmaxiMW) is 8.64 GM/g (L3) in THF. Significantly, it also exhibits good solubility in common organic solvents when the chromophore was modified by polyether units as peripheral groups. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1281 / 1288
页数:8
相关论文
共 50 条
  • [41] Synthesis, structures, and two-photon absorption properties of two new heterocycle-based organic chromophores
    Yan, Yun-Xing
    Fan, Hai-Hua
    Lam, Chi-Keung
    Huang, Hong
    Wang, Jing
    Hu, Sheng
    Wang, He-Zhou
    Chen, Xiao-Ming
    BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2006, 79 (10) : 1614 - 1619
  • [42] Bridged Triphenylamine-Based Dendrimers: Tuning Enhanced Two-Photon Absorption Performance with Locked Molecular Planarity
    Fang, Zhen
    Teo, Tang-Lin
    Cai, Liping
    Lai, Yee-Hing
    Samoc, Anna
    Samoc, Marek
    ORGANIC LETTERS, 2009, 11 (01) : 1 - 4
  • [43] Solvent Effect and Two-Photon Optical Properties of Triphenylamine-Based Donor-Acceptor Fluorophores
    Zhang, Yilin
    Jiang, Meijuan
    Han, Guang-Chao
    Zhao, Ke
    Tang, Ben Zhong
    Wong, Kam Sing
    JOURNAL OF PHYSICAL CHEMISTRY C, 2015, 119 (49): : 27630 - 27638
  • [44] Synthesis,structure and nonlinear optical properties of two novel two-photon absorption chromophores
    CHENG LeHua1
    2 Department of Chemistry
    3 Department of Precision Machinery and Precision Instrumentation
    Science in China(Series B:Chemistry), 2009, (04) : 529 - 534
  • [45] Synthesis, structure and nonlinear optical properties of two novel two-photon absorption chromophores
    Cheng LeHua
    Li Lin
    Sun PingPing
    Zhou HongPing
    Tian YuPeng
    Tang HuoHong
    SCIENCE IN CHINA SERIES B-CHEMISTRY, 2009, 52 (04): : 529 - 534
  • [46] Synthesis, structure and nonlinear optical properties of two novel two-photon absorption chromophores
    LeHua Cheng
    Lin Li
    PingPing Sun
    HongPing Zhou
    YuPeng Tian
    HuoHong Tang
    Science in China Series B: Chemistry, 2009, 52 : 529 - 534
  • [47] Two-photon absorption cross sections of dithienothiophene-based molecules
    Chung, MA
    Lee, KS
    Jung, SD
    ETRI JOURNAL, 2002, 24 (03) : 221 - 225
  • [48] Fundamental limits on two-photon absorption cross sections
    Kuzyk, MG
    JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (16): : 8327 - 8334
  • [49] Measurement of two-photon absorption cross-sections.
    Fleitz, PA
    Kirkpatrick, SM
    Sutherland, RL
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1998, 216 : U756 - U756
  • [50] Two-photon absorption cross sections of deoxyribonucleotides and DNA
    Meshalkin, YP
    Alfimov, EE
    Makukha, VK
    QUANTUM ELECTRONICS, 1998, 28 (08) : 725 - 727