Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

901058

Sigma-Aldrich

J51

greener alternative

Synonym(s):

Poly[(5,6-difluoro-2-octyl-2H-benzotriazole-4,7-diyl)-2,5-thiophenediyl[4,8-bis[5-(2-hexyldecyl)-2-thienyl]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl]-2,5-thiophenediyl]

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(C72H93F2N3S6)n
CAS Number:
1393529-03-7
UNSPSC Code:
12352103
NACRES:
NA.23

description

Band gap: 1.99 eV

Quality Level

100

form

solid

mol wt

Mw 40,000-80,000 by GPC (PS standard)

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

>200 °C

solubility

organic solvents: soluble (Soluble in chlorobenzene and dichlorobenzene, Limited solubility in CHCl3)

Orbital energy

HOMO -5.29 eV 
LUMO -3.3 eV 

PDI

2.0‑3.0

greener alternative category

Enabling,

Related Categories

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product belongs to Enabling category of greener alternatives thus aligns with "Design for energy efficency". Hole transport organic materials allow perfect energy level alignment with the absorber layer and therefore efficient charge collection, are prone to degradation in ambient conditions.Click here for more information.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCF3031

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Mapping Polymer Donors toward High-Efficiency Fullerene Free Organic Solar Cells.
Lin Y, et al.
Advanced Materials, 29(3) (2017)
Indacenodithienothiophene-naphthalene diimide copolymer as an acceptor for all-polymer solar cells.
Xue L, et al.
Journal of Material Chemistry A, 4(16), 5810-5816 (2016)
Conjugated Side-Chain-Isolated D-A Copolymers Based on Benzo[1,2-b:4,5-b']dithiophene-alt-dithienylbenzotriazole: Synthesis and Photovoltaic Properties.
Min J, et al.
Chemistry of Materials, 24(16), 3247-3254 (2012)
Liang Gao et al.
Advanced materials (Deerfield Beach, Fla.), 28(37), 8288-8295 (2016-07-09)
A nonfullerene polymer solar cell with a high efficiency of 9.26% is realized by using benzodithiophene-alt-fluorobenzotriazole copolymer J51 as a medium-bandgap polymer donor and the low-bandgap organic semiconductor ITIC with high extinction coefficients as the acceptor.

Articles

Solution Gated Field Effect Transistors for Biosensing Applications

Novel biosensing devices, like bio-FET sensors, offer label-free analysis by detecting ionic and biomolecular charges, crucial for diagnostics and biological research.

Solution Gated Field Effect Transistors for Biosensing Applications

Novel biosensing devices, like bio-FET sensors, offer label-free analysis by detecting ionic and biomolecular charges, crucial for diagnostics and biological research.

Solution Gated Field Effect Transistors for Biosensing Applications

Novel biosensing devices, like bio-FET sensors, offer label-free analysis by detecting ionic and biomolecular charges, crucial for diagnostics and biological research.

Solution Gated Field Effect Transistors for Biosensing Applications

Novel biosensing devices, like bio-FET sensors, offer label-free analysis by detecting ionic and biomolecular charges, crucial for diagnostics and biological research.

See All

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service