Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes

被引:3
|
作者
Idzik, Krzysztof R. [1 ]
Beckert, Rainer [1 ]
Tauscher, Eric [1 ]
Ledwon, Przemyslaw [2 ]
Golba, Sylwia [2 ]
Lapkowski, Mieczyslaw [2 ,3 ]
Rapta, Peter [4 ,5 ]
Dunsch, Lothar [6 ]
Frydel, Jaroslaw [6 ]
机构
[1] Jena FSU, Inst Organ & Macromol Chem, D-07743 Jena, Germany
[2] Silesian Technol Univ, Fac Chem, PL-44100 Gliwice, Poland
[3] Polish Acad Sci, Ctr Polymer & Corbon Mat, PL-44121 Gliwice, Poland
[4] Grp Electrochem & Conduct Polymer, Leibniz Inst Solid State & Mat Res, D-01171 Dresden, Germany
[5] Slovak Univ Technol Bratislava, Fac Chem & Food Technol, Dept Phys Chem, SK-81237 Bratislava, Slovakia
[6] Tech Univ Darmstadt, Eduard Zintl Inst Anorganische Physik, Petersenstr 30, D-64287 Darmstadt, Germany
来源
OPTOELECTRONIC MATERIALS, PTS 1AND 2 | 2010年 / 663-665卷
关键词
Stille coupling procedure; Electrochemical polymerization; Hyperbranched polymers; Cyclic voltammetry; SOLAR-CELLS; DESIGN;
D O I
10.4028/www.scientific.net/MSF.663-665.876
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
A series of various substituted 1,3,5-triarylbenzenes, 2,4,6-triaryl-1-phenoles, 1,3,5-triaryl-1-methoxybenzenes and 2,4,6-triaryl-1,3,5-trimethoxybenzenes were synthesized by a Stille cross-coupling procedure. Their structures were confirmed by H-1 NMR, C-13 NMR, and elemental analysis. Containing thienyl, fury! and EDOT groups polymers obtained in the process of electropolymerization could be carefully considered as a building material in a wide range of organic-electronic devices. We compare properties of monomers and related polymers depending on aryls moieties and their influence of hydroxyl and methoxyl groups attached to the central benzene core.
引用
收藏
页码:876 / +
页数:2
相关论文
共 50 条
  • [21] Stille cross-coupling applied to get higher molecular weight polymers: Synthesis, optoelectronic, Voc properties, and solar cell application
    Hanif, Muddasir
    Chen, Linlin
    Zhu, Li
    Zhao, Dan
    Xiong, Tianrou
    Hou, Haoqing
    JOURNAL OF APPLIED POLYMER SCIENCE, 2015, 132 (26)
  • [22] Magnetic MIL-101-SO3H: a highly efficient bifunctional nanocatalyst for the synthesis of 1,3,5-triarylbenzenes and 2,4,6-triaryl pyridines
    Boroujeni, Mahmoud Borjian
    Hashemzadeh, Alireza
    Faroughi, Mohammad-Tayeb
    Shaabani, Ahmad
    Amini, Mostafa Mohammadpour
    RSC ADVANCES, 2016, 6 (102): : 100195 - 100202
  • [23] Hydrostannation of diyne and triyne π-electron bridges:: Efficient stille cross-coupling of 1,3,5-Tris[(E)-2-(tributylstannyl)vinyl]benzene
    Jung, I
    Lee, TW
    Kang, SO
    Ko, JJ
    SYNTHESIS-STUTTGART, 2005, (06): : 986 - 992
  • [24] Synthesis of 3-Thiophenchromone by Stille Cross-coupling Palladium on Charcoal-Catalyzed Ligand-Free
    Yang, Qian
    Zhang, Zunting
    Liang, Bo
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2015, 52 (01) : 310 - 316
  • [25] Synthesis of fluorene-based oligomeric organoboron reagents via Kumada, Heck, and stille cross-coupling reactions
    Zhang, Xiaojie
    Tian, Hongkun
    Liu, Qin
    Wang, Lixiang
    Geng, Yanhou
    Wang, Fosong
    JOURNAL OF ORGANIC CHEMISTRY, 2006, 71 (11): : 4332 - 4335
  • [26] Synthesis of differentially substituted hexaethynylbenzenes based on tandem Sonogashira and Negishi cross-coupling reactions
    Sonoda, M
    Inaba, A
    Itahashi, K
    Tobe, Y
    ORGANIC LETTERS, 2001, 3 (15) : 2419 - 2421
  • [27] Development of a sp2-sp3 Stille Cross-Coupling for Rapid Synthesis of HIV NNRTI Doravirine Analogues
    ElMarrouni, Abdellatif
    Campbell, Mark
    Perkins, James J.
    Converso, Antonella
    ORGANIC LETTERS, 2017, 19 (12) : 3071 - 3074
  • [28] Facile Synthesis of 1,3,5-Triarylbenzenes and 4-Aryl-NH-1,2,3-Triazoles Using Mesoporous Pd-MCM-41 as Reusable Catalyst
    Saha, Arijit
    Wu, Chia-Ming
    Peng, Rui
    Koodali, Ranjit
    Banerjee, Subhash
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2019, 2019 (01) : 104 - 111
  • [29] A straightforward synthesis of 1,3-dichloro-5,8-dihydroisoquinoline by consecutive Stille cross-coupling and metathesis reactions
    van den Hoogenband, Adri
    den Hartog, Jack A. J.
    Faber-Hilhorst, Nancy
    Lange, Jos H. M.
    Terpstra, Jan Willem
    TETRAHEDRON LETTERS, 2009, 50 (35) : 5040 - 5043
  • [30] Electrochemical Reductive Cross-Coupling of Vinyl Bromides for the Synthesis of 1,3-Dienes
    Zhang, Hong
    Ye, Zenghui
    Wu, Yanqi
    Zhang, Xi
    Ma, Weiyuan
    Zhan, Zha-Jun
    Zhang, Fengzhi
    ORGANIC LETTERS, 2024, 26 (05) : 994 - 999