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Usage

Uses

Used in Organic Electronics Industry:
DPP(TBFu2)2 is employed as a semiconductor material for its high charge carrier mobility, which is essential for the efficient functioning of transistors and other electronic components. Its ability to conduct electrical charges with minimal resistance makes it a preferred choice for enhancing the performance of organic electronic devices.
Used in Optoelectronic Devices:
In the optoelectronics field, DPP(TBFu2)2 is used for its strong absorption in the visible light spectrum, making it suitable for applications in solar cells and other light-sensitive electronic devices. Its light absorption properties allow for improved energy conversion efficiency, which is vital for the advancement of solar energy technologies.
Used in Transistors:
DPP(TBFu2)2 is utilized as a material in transistors due to its high charge carrier mobility, which is crucial for the speed and efficiency of transistor operation. This property is particularly important in the development of high-performance electronic circuits and systems.
Used in Solar Cells:
2,5-bis(2-ethylhexyl)-3,6-bis(5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)pyrrolo[3 is also used in solar cell technology, where its light absorption capabilities contribute to the generation of electric power from sunlight. DPP(TBFu2)2's role in solar cells is to facilitate the conversion of photons into electrons, thereby enhancing the overall energy yield of the solar panels.
Overall, DPP(TBFu2)2 is a versatile compound with a wide range of applications in the electronics and photonics industries, driven by its unique properties and molecular structure.

Upstream product

• 1000623-95-9 3,6-bis(5-bromothiophen-2-yl)-2,5-bis(2-ethylhexyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione 
• 73183-34-3 bis(pinacol)diborane 
• 1185885-86-2 2,5-bis(2-ethylhexyl)-3,6-di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4-dione 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Relevant academic research and scientific papers

Effect of side chain conjugation lengths on photovoltaic performance of two-dimensional conjugated copolymers that contain diketopyrrolopyrrole and thiophene with side chains

Two new two-dimensional conjugated copolymers that contain diketopyrrolopyrrole and thiophene with different π conjugation lengths as side chains, called PDPPMTD and PDPPBTD, were designed and synthesized for use in polymer solar cells (PSCs). The resulti

Synthesis and characterization of optical and redox properties of bithiophene-functionalized diketopyrrolopyrrole chromophores

A series of six new 2,2′-bithiophene-functionalized diketopyrrolopyrrole (DPP) dyes 7a-f bearing different electron-donating and electron-withdrawing substituents at the terminal thiophene units was synthesized by palladium-catalyzed cross-coupling reactions. The to date unknown diiodinated DPP 2 and the corresponding boronic ester derivative 3 could be prepared in high yields, and these are shown to be versatile building blocks for the synthesis of DPP-based molecular materials by Negishi, Stille, and Suzuki coupling. The influence of the peripheral substituents on the optical and electrochemical properties of the present series of DPP dyes 7a-f were investigated by UV/vis and steady-state fluorescence spectroscopy and cyclic voltammetry, revealing an appreciable effect on the electronic nature of these dyes. The diamino-substituted DPP derivative 7e exhibits a strong absorption band reaching in the near-infrared (NIR) region, which is a highly desirable feature for application in organic photovoltaics.

Compound, a polymeric compound obtained by polymerizing the compound and method of manufacturing the compound, as well as polymeric compounds and organic semiconductor thin film

PROBLEM TO BE SOLVED: To provide a novel compound used as a raw material of a polymer which is useful for manufacturing an organic transistor excellent in field effect mobility and for manufacturing an organic solar cell excellent in photoelectric conversion efficiency.SOLUTION: The compound is represented by formula (1). (In the formula, Rand Reach independently represent a C1-C30 alkyl group, a C6-C30 aryl group or a C2-C30 monovalent heterocyclic group, and these groups may have a substituent; Zand Zeach independently represent a hydrogen atom, a halogen atom, a boric acid ester residue, a boric acid residue (a group represented by -B(OH)), or an organic tin residue; and ring A and ring B each independently represent a heterocyclic ring which may have a substituent.)