684503

Sigma-Aldrich

[6,6]-Pentadeuterophenyl C61 butyric acid methyl ester

99.5%, 99.5 atom % D

Synonym(s):
3′-(Phenyl-d5) 3′H-cyclopropyl[1,9] [5,6]fullerene-C60-Ih-3′-butanoic acid methyl ester, d5-PCBM, 1-[3-(Methoxycarbonyl)propyl]-1-pentadeuterophenyl-[6.6] C61
Empirical Formula (Hill Notation):
C72D5H9O2
CAS Number:
Molecular Weight:
915.91
NACRES:
NA.23
Pricing and availability is not currently available.

Quality Level

description

functionalized fullerene

isotopic purity

99.5 atom % D

assay

99.5%

mass shift

M+5

SMILES string

[2H]c1c([2H])c([2H])c(c([2H])c1[2H])C2(CCCC(=O)OC)[C]3=4c5c6c7c8c9c%10c(c%11c%12c3c%13c5c%14c%15c6c%16c7c%17c9c%18c%19c%10c%20c%11c%21c%12c%22c%13c%23c%14c%24c%15c%25c%16c%26c%17c%18c%27c%28c%19c%20c%29c%21c%30c%22c%23c%31c%24c%32c%25c%26c%27c%33c%28c%29c%30c%31c%32%33)[C]2=48

Related Categories

General description

[6,6]-Pentadeuterophenyl C61 butyric acid methyl ester (PC60BM) is a deuterated fullerene that can be used as an acceptor molecule. It has a fullerene as the core and deuterium and benzyl as the attachment. The deuterium atoms facilitate an increase in the quantum efficiency of the electrochemical devices.

Application

PC60BM is a conjugating polymer that can be used as an alternative to the conventionally used PCBM for the organic electronic based applications, which include polymeric solar cells and organic light emitting diodes (OLEDs).

Packaging

100 mg in glass insert

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Target Organs

Respiratory system

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis
Certificate of Origin
Deuterium isotope effect on bulk heterojunction solar cells. Enhancement of organic photovoltaic performances using monobenzyl substituted deuteriofullerene acceptors
Lu S, et al.
Organic Letters, 15(22), 5674-5677 (2013)
Manipulating the crystal structure of a conjugated polymer for efficient sequentially processed organic solar cells
Yi A, et al.
Nanoscale, 10(45), 21052-21061 (2018)
Characterization of poly (p-phenylene vinylene)/methanofullerene blends of polymer solar cells by time-of-flight secondary ion mass spectrometry
Bulle-Lieuwma CWT, et al.
Applied Surface Science, 231(45), 274-277 (2004)
Bulle-Lieuwma, C.,; Van Duren, J. et al.
Applied Surface Science, 274, 231-232 (2004)
Articles
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