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Merck
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767743

Sigma-Aldrich

2,5-Dihydro-3,6-di-2-thienyl-pyrrolo[3,4-c]pyrrole-1,4-dione

97%

동의어(들):

3,6-Di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione, DPP

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크기 선택

5 G
₩2,352,872

₩2,352,872

예상 입고일2025년 4월 21일세부사항

벌크 견적 요청
모든 사진(1)

크기 선택

보기 변경
5 G
₩2,352,872

About This Item

실험식(Hill 표기법):
C14H8N2O2S2
CAS Number:
850583-75-4
Molecular Weight:
300.36
MDL number:
MFCD20257907
UNSPSC 코드:
12352103
PubChem Substance ID:
329767335
NACRES:
NA.23

₩2,352,872

예상 입고일2025년 4월 21일세부사항

벌크 견적 요청

Quality Level

100

분석

97%

양식

solid

SMILES string

O=C1NC(c2cccs2)=C3C(=O)NC(c4cccs4)=C13

InChI

1S/C14H8N2O2S2/c17-13-9-10(12(16-13)8-4-2-6-20-8)14(18)15-11(9)7-3-1-5-19-7/h1-6H,(H,15,18)(H,16,17)

InChI key

YIUHGBNJJRTMIE-UHFFFAOYSA-N

관련 카테고리

일반 설명

2,5-Dihydro-3,6-di-2-thienyl-pyrrolo[3,4-c]pyrrole-1,4-dione is a diketopyrrolopyrrole (DPP) based copolymer and are used widely in thin-film transistors and solar cell devices. This aromatic polymer has electron withdrawing groups and hence is very useful for the synthesis of narrow band gap donor-acceptor polymers which are used as active semiconductors for organic electronics. They give rise to high power conversion efficiency (PCE) in Organic Photovoltaic (OPV) Cells. [1]

애플리케이션

Used in the synthesis of donor-acceptor polymers which are used in polymer field-effect transistors and bulk heterojunction solar cells. [2][3]

특징 및 장점

Diketopyrrolopyrrole is planar and can accept hydrogen bonds/other electrostatic interactions which results in copolymers that have pi-pi stacking.

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

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시험 성적서(COA)

Lot/Batch Number
MKCV9220
MKCV5561
MKCP5085
MKCQ6446
MKCJ9520

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이미 열람한 고객

Slide 1 of 2

1 of 2

Thieno[3,2-b]thiophene 95%

Sigma-Aldrich

702668

Thieno[3,2-b]thiophene

3,4-Thiophenedicarboxylic acid

Sigma-Aldrich

795577

3,4-Thiophenedicarboxylic acid

Synthesis and characterization of phenanthrocarbazole-diketopyrrolopyrrole copolymer for high-performance field-effect transistors
Chen, H., Guo, Y., Sun, X., Gao, D., Liu, Y., & Yu, G.
Journal of Polymer Science Part A: Polymer Chemistry, 51(10), 2208-2215 (2013)
David Rais et al.
ChemPlusChem, 85(12), 2689-2703 (2020-12-18)
The singlet fission (SF) process discovered in bis(thienyl)diketopyrrolopyrroles (TDPPs) can boost their potential for photovoltaics (PV). The crystal structures of TDPP analogs carrying n-hexyl, n-butyl, or 2-(adamant-1-yl)ethyl substituents are similar, but contain increasingly slipped stacked neighbor molecules. The observed SF
Influence of Side-Chain on Structural Order and Photophysical Properties in Thiophene Based Diketopyrrolopyrroles: A Systematic Study.
Naik, M. A., Venkatramaiah, N., Kanimozhi, C., & Patil, S.
The Journal of Physical Chemistry C, 116(50), 26128-26137 (2012)
Hugo Bronstein et al.
Journal of the American Chemical Society, 133(10), 3272-3275 (2011-02-22)
We report the synthesis and polymerization of a novel thieno[3,2-b]thiophene-diketopyrrolopyrrole-based monomer. Copolymerization with thiophene afforded a polymer with a maximum hole mobility of 1.95 cm(2) V(-1) s(-1), which is the highest mobility from a polymer-based OFET reported to date. Bulk-heterojunction

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