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Product Code B971-1g
Price $125.00 ex. VAT


A naturally occurring isomer of indigo to develop a large number of molecular and polymeric materials for organic electronics with exceptional optical and electrical properties

6,6′-Dibromoisoindigo contains two identical fused benzolactam rings that are joined by a double bond as a trans isomer, (E)-6,6'-Dibromo-[3,3'-biindolinylidene]-2,2'-dione. Isoindigo is a naturally occurring isomer of indigo which is one of the oldest known dyes found in the leaves of Isatis tinctoria.

6,6′-Dibromoisoindigo is strongly electron deficient character with multiple functional groups and it has proven successful as an electron-accepting component for the preparation of electroactive materials for organic electronics. The N-H functional groups provide opportunity for adding alkyl chain to improve solubility and the Br groups enable to extend the conjugation to the core structure. The high yielding and scalable synthesis have made it possible for rapid development of a large number of isoindigo based molecular and polymeric materials with remarkable physical properties.

synthesis of 6,6′-dibromoisoindigo

6,6′-Dibromoisoindigocan be prepared from an condensation reaction in acetic/hydrogen chloride acid between 6-Bromoindoline-2,3-dione and 6-Bromoindolin-2-one . Poly(isoindigo-alt-benzothiadiazole) (PIIG-BT), a copolymer alternating isoindigo and benzothiadiazole as the main backbone shows record high electron mobility of up to 0.22 cm2 V-1s-1.

General Information

CAS number 1147124-21-7
Chemical formula C16H8Br2N2O2
Full name 6,6′-Dibromoisoindigo
Molecular weight 420.05 g/mol
Synonyms 6-Bromo-3-(6-bromo-1,2-dihydro-2-oxo-3H-indol-3-ylidene)-1,3-dihydro-2H-indol-2-one
Classification / Family Isoindigo, semiconductor synthesis intermediates, low band gap polymers, OLED, OFETs, organic photovoltaics

Chemical Structure

6,6′-Dibromoisoindigo chemical structure, CAS 1147124-21-7
6,6′-Dibromoisoindigo chemical structure, CAS 1147124-21-7

Product Details

Purity >98% (by 1H NMR)
Melting point n.a.
Appearance Dark red/brown powder/crystals

MSDS Documentation

6,6′-Dibromoisoindigo MSDS Sheet


Literature and Reviews

  1. Acceptor–acceptor type isoindigo-based copolymers for high-performance n-channel field-effect transistors, G. Kim et al., Chem. Commun., 50, 2180-2183 (2014); 10.1039/C3CC48013E.
  2. Synthesis of N,N′-dialkyl-6,6′-dibromoisoindigo Derivatives by Continuous Flow, V. Maes et al., J. Flow Chem., 5(4), 201–209 (2015); DOI: 10.1556/1846.2015.00033 DOI: 10.1556/1846.2015.00033.
  3. Chlorination as a useful method to modulate conjugated polymers: balanced and ambient-stable ambipolar high-performance field-effect transistors and inverters based on chlorinated isoindigo polymers, T. Lei et al., Chem. Sci., 4, 2447-2452 (2013); 10.1039/C3SC50245G.
  4. Isoindigo, a Versatile Electron-Deficient Unit For High-Performance Organic Electronics, R. Stalder et al., Chem. Mater., 26, 1, 664–678 (2014); DOI: 10.1021/cm402219v.
  5. Isoindigo-based copolymers for polymer solar cells with efficiency over 7%, C. Ho et al., J. Mater. Chem. A, 2, 8026-8032 (2014); DOI: 10.1039/C4TA01083C.
  6. Synthesis, characterization, and electronic properties of a thermally-labile isoindigo, T. Pappenfus et al., J. Mol. Struct., 1095, 96-99 (2015); DOI: 10.1016/j.molstruc.2015.04.021.
  7. High efficiency organic photovoltaic devices based on isoindigo conjugated polymers with a thieno[3,2-b]thiophene p-bridge, L. Zhu et al., J. Mater. Chem. A, 4, 16064-16072 (2016); DOI: 10.1039/C6TA07138D.

To the best of our knowledge the information provided here is accurate. However, Ossila assume no liability for the accuracy of this page. The values provided are typical at the time of manufacture and may vary over time and from batch to batch. All products are for laboratory and research and development use only, and may not be used for any other purpose including health care, pharmaceuticals, cosmetics, food or commercial applications.

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