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Makale detayı · 2013 · article

Dialkoxybithiazole A New Building Block for Head to Head PolymerSemiconductors

YÖKSİS OpenAlex Üst %1
Yıl2013
Atıf210OpenAlex
Atıf188Semantic Scholar · 1 etkili
Yüzdelik%99,3
FWCI15,021,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q1

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıJOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  • Katalog eşleşmesi (ISSN)Journal of the American Chemical Society
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

Polymer semiconductors have received great attention for organic electronics due to the low fabrication cost offered by solution-based printing techniques. To enable the desired solubility/processability and carrier mobility, polymers are functionalized with hydrocarbon chains by strategically manipulating the alkylation patterns. Note that head-to-head (HH) linkages have traditionally been avoided because the induced backbone torsion leads to poor π-π overlap and amorphous film microstructures, and hence to low carrier mobilities. We report here the synthesis of a new building block for HH linkages, 4,4'-dialkoxy-5,5'-bithiazole (BTzOR), and its incorporation into polymers for high performance organic thin-film transistors. The small oxygen van der Waals radius and intramolecular S(thiazolyl)···O(alkoxy) attraction promote HH macromolecular architectures with extensive π-conjugation, low bandgaps (1.40-1.63 eV), and high crystallinity. In comparison to previously reported 3,3'-dialkoxy-2,2'-bithiophene (BTOR), BTzOR is a promising building block in view of thiazole geometric and electronic properties: (a) replacing (thiophene)C-H with (thiazole)N reduces steric encumbrance in -BTzOR-Ar- dyads by eliminating repulsive C-H···H-C interactions with neighboring arene units, thereby enhancing π-π overlap and film crystallinity; and (b) thiazole electron-deficiency compensates alkoxy electron-donating characteristics, thereby lowering the BTzOR polymer HOMO versus that of the BTOR analogues. Thus, the new BTzOR polymers show substantial hole mobilities (0.06-0.25 cm(2)/(V s)) in organic thin-film transistors, as well as enhanced I(on):I(off) ratios and greater ambient stability than the BTOR analogues. These geometric and electronic properties make BTzOR a promising building block for new classes of polymer semiconductors, and the synthetic route to BTzOR reported here should be adaptable to many other bithiazole-based building blocks.

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

210atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 3 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2020 Recent developments in the synthesis of regioregular thiophene-based conjugated polymers for electronic and optoelectronic applications using nickel and palladium-based catalytic systemsAtıf 83 · OpenAlex
  2. 2014 Perfluoroalkyl Functionalized Thiazole Thiophene Oligomers as N Channel Semiconductors in Organic Field Effect and Light Emitting TransistorsAtıf 80 · OpenAlex
  3. 2021 SYNTHESIS OF 1,3-THIAZOLE DERIVATIVESAtıf 9 · OpenAlex

Yazarlar

10
  1. Xugang Guo 1
  2. Jordan Quinn 2
  3. Zhihua Chen 3
  4. HAKAN USTA ABDULLAH GÜL ÜNİVERSİTESİ 4
  5. Yan Zheng 5
  6. Yu Xia 6
  7. Jonathan W Hennek 7
  8. Rocio Ponce Ortiz 8
  9. Tobin J Marks 9
  10. Antonio Facchetti 10