Skip to Content
Merck
CN
All Photos(1)

Documents

646652

Sigma-Aldrich

Poly(2,5-di(hexyloxy)cyanoterephthalylidene)

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

About This Item

Linear Formula:
(C42H58N2O4)n
CAS Number:
151897-69-7
MDL number:
MFCD06412341
UNSPSC Code:
12352103
NACRES:
NA.23

form

solid

semiconductor properties

N-type (mobility~10−5 cm2/V·s)

General description

Poly(2,5-di(hexyloxy)cyanoterephthalylidene) (CN-PPV) is an electron conducting polymer (n-type) that is a cyano-derivative of poly(phenylenevinylene) (PPV). It can be used in combination with other PPVs for organic photovoltaics.
Light emitting conjugated polymer.

Application

CN-PPV can be used in the formation of conducting films for the fabrication of polymeric light emitting diodes (PLEDs) and photovoltaic cells.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Influence of annealing and blending of photoactive polymers on their crystalline structure
Ruderer MA, et al.
The Journal of Physical Chemistry B, 114(47), 15451-15458 (2010)
Organic light-emitting devices for solid-state lighting
So F, et al.
Mrs Bulletin, 33(7), 663-669 (2008)
Optically observed multiple inter-chain interactions in polyblend semiconducting polymer nanoparticles
Hashim Z, et al.
Royal Society of Chemistry Advances, 7(76), 48308-48314 (2017)
Change of photoluminescence properties of cyano-substituted poly p-phenylene vinylene controlled by photoirradiation
Kuzuoka Y and Yamaguchi Y
Synthetic Metals, 158(12), 489-496 (2008)

Articles

High-Performance Semiconductor Polymers Based on Diketopyrrolopyrrole and Thienothiophene

The development of high-performance conjugated organic molecules and polymers has received widespread attention in industrial and academic research.

Polymer Semiconductors for Intrinsically Stretchable Organic Transistors

Intrinsically stretchable active layers for organic field-effect transistors (OFET) are discussed. Polymer structural modification & post-polymerization modifications are 2 methods to achieve this.

Soluble Pentacene Precursors

Fabrication procedure of organic field effect transistor device using a soluble pentacene precursor.

Organic Transistors for Biomedical Applications

Thin, lightweight, and flexible electronic devices meet widespread demand for scalable, portable, and robust technology.

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