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Product Code B571-500mg
Price $475 ex. VAT

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IDTTB6-2CHO, for the synthesis of low band gap non-fullerene acceptors

High purity monomer available online for fast, secure dispatch


IDTTB6-2CHO has a fused Indacenodithienothiophene (IDTT) core structure with extended conjugation to the hexylphenyl side chain with large steric hindrance and electron-rich properties.

Electron-rich IDTT is one of the most important building blocks for the design and synthesis of low-bandgap non-fullerene acceptors (NFAs), such as ITIC and ITIC-2F which are among the earliest developed NFAs for highly efficient organic photovoltaic devices.

IDTTB6-2CHO Electron-rich building block

Electron-rich building block

Preparation of low bandgap non-fullerene acceptors

High purity IDTTB6-2CHO

High purity

>98% pure IDTTB6-2CHO

Worldwide shipping for 1878125-76-8

Worldwide shipping

Quick and reliable shipping

High efficient OPVs

High efficient OPVs

Attributed to the extended conjugated molecule

General Information

CAS Number 1878125-76-8
Chemical Formula C70H74O2S4
Molecular Weight 1075.6 g/mol
Full Name 6,6,12,12-Tetrakis(4-hexylphenyl)-6,12-dihydrodithieno[2,3-d:2',3'-d']-s-indaceno[1,2-b:5,6-b']dithiophene-2,8-dicarboxaldehyde
Synonyms

IDTT-CHO

Dithieno[2,3-d:2,3-d]-s-indaceno[1,2-b:5,6-b]dithiophene-2,8-dicarboxaldehyde

6,6,12,12-tetrakis(4-hexylphenyl)-6,12-dihydro

Classification / Family Indacenodithienothiophene (IDTT), Monomer and inermediates, ITIC, None-fullerene acceptors (NFAs), NFA-OSCs, printing electronics

Chemical Structure

idttb6-2cho, 1878125-76-8
Chemical structure of IDTTB6-2CHO)

Product Details

Purity >98% (by NMR)
Melting Point N/A
Appearance Yellow powder/crystals

MSDS Documentation

IDTTB6-2CHO MSDSIDTTB6-2CHO MSDS Sheet

Literature and Reviews

  1. Impact of Nonfullerene Molecular Architecture on Charge Generation, Transport, and Morphology in PTB7-Th-Based Organic Solar Cells, X. Yi et al., Adv. Funct. Mater., 1802702 (2018); DOI: 10.1002/adfm.201802702.
  2. Performance Optimization of Parallel-Like Ternary Organic Solar Cells through Simultaneous Improvement in Charge Generation and Transport, W. Hadmojo et al., Adv. Funct. Mater., 1808731 (2019); DOI: 10.1002/adfm.201808731.
  3. Polymer Donors for High-performance Non-fullerene Organic Solar Cells, H. Fu et al., Angew. Chem. Int. Ed., 58 (14); 4442-4453 (2019); DOI: 10.1002/ange.201806291.
  4. Donor polymer fluorination doubles the efficiency in non-fullerene organic photovoltaics, N. Bauer et al., . Mater. Chem. A, 5, 22536 (2017); DOI: 10.1039/c7ta07882j.
  5. Fused Benzothiadiazole: A Building Block for n-Type Organic Acceptor to Achieve High-Performance Organic Solar Cells, J. Yuan et al., Adv. Mater., 1807577 (2019); DOI: 10.1002/adma.201807577.

To the best of our knowledge the information provided here is accurate. The values provided are typical at the time of manufacture and may vary over time and from batch to batch. Products may have minor cosmetic differences (e.g. to the branding) compared to the photos on our website. All products are for laboratory and research and development use only.

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