Dihydroindenofluorenes as building units in organic semiconductors for organic electronics

被引:8
作者
Poriel, Cyril [1 ]
Rault-Berthelot, Joelle [1 ]
机构
[1] Univ Rennes 1, UMR CNRS 6226, ISCR, Campus Beaulieu, F-35042 Rennes, France
关键词
EXTERNAL QUANTUM EFFICIENCY; ACTIVATED DELAYED FLUORESCENCE; LIGHT-EMITTING-DIODES; DES INDENO-FLUORENES; FIELD-EFFECT TRANSISTORS; BIPOLAR HOST MATERIALS; THIN-FILM TRANSISTORS; D-PI-D; N-TYPE; ANODIC-OXIDATION;
D O I
10.1039/d1cs00993a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This review aims to discuss organic semiconductors constructed on dihydroindenofluorene positional isomers, which are key molecular scaffolds in organic electronics. Bridged oligophenylenes are key organic semiconductors that have allowed the development of organic electronic technologies. Dihydroindenofluorenes (DHIFs) belong to the family of bridged oligophenylenes constructed on a terphenyl backbone. They have proven to be very promising building blocks for the construction of highly efficient organic semiconductors for all OE devices, namely organic light emitting diodes (OLEDs), phosphorescent OLEDs, organic field-effect transistors (OFETs), solar cells, etc. The five DHIF cores on which are constructed DHIF-based organic semiconductors used as active materials for organic electronics.
引用
收藏
页码:6754 / 6805
页数:52
相关论文
共 229 条
  • [1] Effect of various host characteristics on blue thermally activated delayed fluorescent devices
    Ahn, Dae Hyun
    Moon, Ji Su
    Kim, Si Woo
    Lee, Seung Yeon
    Karthik, Durai
    Lee, Ju Young
    Kwon, Jang Hyuk
    [J]. ORGANIC ELECTRONICS, 2018, 59 : 39 - 44
  • [2] ALICYCLIC STUDIES .15. PREPARATION AND REACTIONS OF 3,3'-BI-INDENYL AND 2,3-2',3'-DIBENZOBI(CYCLOHEPTA-2,7-DIENYL)
    ALTMAN, Y
    GINSBURG, D
    [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1961, (APR): : 1498 - &
  • [3] SYNTHESIS, CHARACTERIZATION OF A NOVEL CONJUGATED STRUCTURAL OLIGOMER
    An, Dong
    Ye, Zhiwen
    [J]. JOURNAL OF THE CHILEAN CHEMICAL SOCIETY, 2015, 60 (02): : 2971 - 2974
  • [4] Annealing effect on the electrical proprieties of IF(CN2)2-meta based OTFTs: Thermal behavior and modeling of charge transport
    Arfaoui, N.
    Mahdouani, M.
    Bouhadda, I.
    Poriel, C.
    Bourguiga, R.
    Jacques, E.
    Chevrier, M.
    Bebiche, S.
    [J]. SUPERLATTICES AND MICROSTRUCTURES, 2018, 123 : 286 - 296
  • [5] Highly efficient phosphorescent emission from organic electroluminescent devices
    Baldo, MA
    O'Brien, DF
    You, Y
    Shoustikov, A
    Sibley, S
    Thompson, ME
    Forrest, SR
    [J]. NATURE, 1998, 395 (6698) : 151 - 154
  • [6] Experimental and theoretical insights into the sequential oxidations of 3π-2spiro molecules derived from oligophenylenes: A comparative study of 1,2-b-DiSpiroFluorene-IndenoFluorene versus 1,2-b-DiSpiroFluorene(tert-butyl)4-IndenoFluorene
    Barriere, Frederic
    Poriel, Cyril
    Rault-Berthelot, Joelle
    [J]. ELECTROCHIMICA ACTA, 2013, 110 : 735 - 740
  • [7] Predictably Ordered Open Hydrogen-Bonded Networks Built from Indeno[1,2-b]fluorenes
    Beaudoin, Daniel
    Blair-Pereira, Joao-Nicolas
    Langis-Barsetti, Sophie
    Maris, Thierry
    Wuest, James D.
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2017, 82 (16) : 8536 - 8547
  • [8] Influence of the gate bias stress on the stability of n-type organic field-effect transistors based on dicyanovinylene-dihydroindenofluorene semiconductors
    Bebiche, S.
    Cisneros-Perez, P. A.
    Mohammed-Brahim, T.
    Harnois, M.
    Rault-Berthelot, J.
    Poriel, C.
    Jacques, E.
    [J]. MATERIALS CHEMISTRY FRONTIERS, 2018, 2 (09) : 1631 - 1641
  • [9] Performance improvement of IF(CN2)2 meta based N-channel OTFTs and their integration into a stable CMOS inverter
    Bebiche, S.
    Bouhadda, I.
    Mohammed-Brahim, T.
    Coulon, N.
    Bergamini, J. F.
    Poriel, C.
    Jacques, E.
    [J]. SOLID-STATE ELECTRONICS, 2017, 130 : 49 - 56
  • [10] MACROCYCLIC ACETYLENIC COMPOUNDS .2. 1,2,7,8-DIBENZOCYCLODODECA-1,7-DIENE-3,5,9,11-TETRAYNE
    BEHR, OM
    EGLINTON, G
    GALBRAITH, AR
    RAPHAEL, RA
    [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1960, (SEP): : 3614 - 3625