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Sigma-Aldrich

1H,1H,2H,2H-Perfluorooctanephosphonic acid

95%

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About This Item

Formule empirique (notation de Hill):
C8H6F13O3P
Numéro CAS:
252237-40-4
Poids moléculaire :
428.08
Numéro MDL:
MFCD18910708
Code UNSPSC :
12352300
ID de substance PubChem :
329765203
Nomenclature NACRES :
NA.23

Pureté

95%

Forme

solid

Pf

168-173 °C

Température de stockage

2-8°C

Chaîne SMILES 

OP(O)(=O)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C8H6F13O3P/c9-3(10,1-2-25(22,23)24)4(11,12)5(13,14)6(15,16)7(17,18)8(19,20)21/h1-2H2,(H2,22,23,24)

Clé InChI

DEXIXSRZQUFPIK-UHFFFAOYSA-N

Description générale

1H,1H,2H,2H-Perfluorooctanephosphonic (PFOPA) acid is a fluoroalkyl phosphonic acid that contains 8 fluorinated carbon atoms. It forms a self-assembled layer on the substrate due to the adhesion of the phosphonates. The surface adhesion is a component of the acid base linkage that is enhanced by the hydroxyl groups.

Application

PFOPA can functionalize gallium nitride (GaN) to tune the optical properties, which can potentially be used in chemical sensor based applications. It can modify the surface characteristics of copper substrates that find usage in printed circuit boards as copper foils. PFOPA can also be coated on the indium tin oxide substrate, which may be utilized in organic light emitting diodes (OLEDs) and organic photovoltaics (OPVs).

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

Advanced surface modification of indium tin oxide for improved charge injection in organic devices.
Hanson EL, et al.
Journal of the American Chemical Society, 127(28), 10058-10062 (2005)
Modified surface chemistry, potential, and optical properties of polar gallium nitride via long chained phosphonic acids.
Wilkins SJ, et al.
Applied Surface Science, 327(38), 498-503 (2015)
Direct Patterning of Self-Assembled Monolayers by Stamp Printing Method and Applications in High Performance Organic Field-Effect Transistors and Complementary Inverters.
Zhang Z, et al.
Advances in Functional Materials, 25(38), 6112-6121 (2015)
Phosphonic acid modification of indium- tin oxide electrodes: Combined XPS/UPS/contact angle studies.
Paniagua SA, et al.
The Journal of Physical Chemistry C, 112(21), 7809-7817 (2008)
Surface characterization of copper substrates modified with carboxyl terminated phosphonic acids.
Nothdurft P, et al.
International Journal of Adhesion and Adhesives, 84(38), 143-152 (2018)

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