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P(g2T-TT)

CAS Number 2058240-28-9

Luminosyn™ Polymers, Materials

Product Code M2475A1-100mg
Price $390 ex. VAT

High Performance Stretchable Redox-active Semiconducting Polymer

Designed for organic electrochemical transistors (OECTs) with fast switching speed on the microsecond scale


Specifications | MSDS | Literature and Reviews


P(g2T-TT) is a copolymer with a backbone alternating thienothiophene (TT) and 2,2'-bithiophene (BT) units with triethylene glycol (TEG) side chains in the 3,3′ positions of the bithiophene repeating units. The triethylene glycol side chains can facilitate hydration and ion penetration without compromising electronic mobility by shifting the mode of operation of aqueous electrolyte-gated transistors from interfacial to bulk doping/transport.

With triethylene glycol side chains, P(g2T-TT) films can uptake a much higher density of ions while showing a much lower degree of hydration than the PEDOT:PSS films. The p(g2T-TT) films can also show high degree of molecular ordering during electrochemical switching, demonstrating complete and reversible electrochromism and high volumetric capacitance at low operating biases.

Conjugated semiconducting polymer

Conjugated Polymer

Highly desirable for OECTs

High purity P(g2T-TT)

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High purity with batch-specific GPC data

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High quality P(g2T-TT)

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Soxhlet purification

The bulk doping of p(g2T-TT) by hydrated ions allows for extraction of the volumetric capacitance of C*=240 F/cm3, a value almost six times higher than that of PEDOT:PSS, indicating a higher density of ion-accessible sites.

Luminosyn™ P(g2T-TT)


Luminosyn™ P(g2T-TT) is now available.

High Purity

P(g2T-TT) is purified by Soxhlet extraction with methanol, hexane and chlorobenzene under an argon atmosphere

Batch-specific GPC Data

Have confidence in what you are ordering; batch-specific GPC data for your thesis or publications

Large Quantity Orders

Plan your experiments with confidence with polymers from the same batch

General Information


CAS Number 2058240-28-9
Full Name Poly[2-(3,3′-bis(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)-[2,2’-bithiophen]-5-yl)thieno[3,2-b]thiophene]
Chemical Formula (C28H34O8S4)n
HOMO/LUMO HOMO = 5.2 eV (Eg = 1.74 eV) [1]
Absorption λmax = 597 nm (in film)
Form Blue powder/fibres
Processing Solvents DMF, Chloroform (typically 5 mg/ml in chloroform)
Synonyms pg2T-TT, g2T-TT
Classification / Family Polythiophenes, Redox-active semiconducting polymer (RASP), Organic electrochemical transistors (OECTs), Electrocardiogram (ECG) recording, Biosensors

Batch Details


Batch Number Mw Mn PDI Stock Info
M2475A1 5,778 3,777 1.53 In stock

Chemical Structure


Chemical structure of P(g2T-TT)
Chemical structure of P(g2T-TT), CAS No: 2058240-28-9

MSDS Documentation


P(g2T-TT)P(g2T-TT) MSDS Sheet

Literature and Reviews


  1. R. Hallani et al. (2021); Regiochemistry-Driven Organic Electrochemical Transistor Performance Enhancement in Ethylene Glycol-Functionalized Polythiophenes, J. Am. Chem. Soc., 143 (29), 11007–11018; DOI: 10.1021/jacs.1c03516.
  2. Y. Zhang et al. (2023); Combined Optical, Gravimetric, and Electrical Operando Investigation of Structural Variations in Polymeric Mixed Conductors, Adv. Funct. Mater., 33 (16), 2214380. DOI: 10.1002/adfm.202214380.
  3. A. Giovannitti et al. (2016); Controlling the mode of operation of organic transistors through side-chain engineering, PNAS, 113 (43), 12017–12022; DOI: 10.1073/pnas.1608780113.

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