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PBBTSiD


Product Code M2258A1-100mg
Price $600

Specifications | MSDS | Literature and Reviews | Technical Support


PBBTSiD (CAS number 1334032-16-4) is a small bandgap copolymer (Eg = ~ 0.7 eV ) with a backbone alternating electron donating dithienosilole (DTS) and electron accepting fused-ring benzobisthiadiazole (BBT) units.

The balanced ambipolarity of the BBT moiety of the polymer makes PBBTSiD a good candidate for logic circuit applications. Integrating BBT backboned semiconducting polymers into the bottom gate/top contact TFTs resulted in balanced ambipolar performances with the high µh and µe charge mobility values.

For 5 - 10 grams order quantity, the lead time is 4-6 weeks.

The Luminosyn™ Range


High Purity Materials: Purified by Soxhlet extraction with methanol, hexane, and chlorobenzene under argon atmosphere.
Batch-Specific Data: Confidence in your materials with batch-specific GPC data for your thesis or publications.
Large Quantity Orders: Plan your experiments with confidence using polymers from the same batch.

General Information


Full name Poly[(4,7-bis(3-hexylthien-2-yl)- 2λ4δ2-benzo[1,2-c;4,5-c′]bis[1,2,5] thiadiazole)-alt-(3,3'-bis(2-ethylhexylsilyene-2,2'-bithiophene)]
Synonyms PBBTSiD
Chemical formula (C50H64N4S 6Si )n
CAS number 1334032-16-4
HOMO / LUMO HOMO = -4.80 eV, LUMO = -4.10 eV; Eg = ~ 0.7 eV [1]
Soluble in Chloroform, chlorobenzene and dichlorobenzene
Recommended Processing Solvents at 10mg/ml Dichlorobenzene
Classification / Family Organic semiconducting materials, Very low-bandgap polymers, Ambipolar semiconducting polymers, OFET polymers, High charge mobility polymers, Photodetectors, Thin-film Transistors

Batch Details


Batch Mw Mn PDI Stock Info
M2258A1 17,975 7,554
2.38 In stock

Chemical Structure


pbbtsid chemical structure
Chemical structure of PBBTSiD, CAS 1334032-16-4

UV-Vis-NIR Absorption


pbbtsid un-vis-nir absorption in chloroform
UV-Vis-NIR absorption of PBBTSiD in chloroform.

MSDS Documentation


PBBTSiD MSDSPBBTSiD MSDS sheet

Literature and Reviews


  1. Ambipolarity in Benzobisthiadiazole-Based Donor–Acceptor Conjugated Polymers, J. D. Yuen et al., Adv. Mater., 23, 3780–3785 (2011); DOI: 10.1002/adma.201101134.
  2. Organic Transistors in the New Decade: Toward n-Channel, Printed, and Stabilized Devices, S. Kola et al., J. Polym. Sci. B: Polym. Phys., 50, 1090–1120 (2012); DOI: 10.1002/polb.23054.
  3. Benzothiadiazole and its π-extended heteroannulated derivatives: useful acceptor building blocks for high-performance donor–acceptor polymers in organic electronics, Y. Wang et al., J. Mater. Chem. C, 4, 6200 (2016); DOI: 10.1039/c6tc01860b.

Technical Support


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