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Merck

684503

Sigma-Aldrich

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

99.5%, 99.5 atom % D

Sinónimos:

1-[3-(Methoxycarbonyl)propyl]-1-pentadeuterophenyl-[6.6] C61, 3′-(Phenyl-d5)3′H-cyclopropyl[1, 9] [5, 6] fullerene-C60-Ih-3′-butanoic acid methyl ester, d5-[60]PCBM

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About This Item

Fórmula empírica (notación de Hill):
C72D5H9O2
Número de CAS:
Peso molecular:
915.91
UNSPSC Code:
12352103
NACRES:
NA.23

description

functionalized fullerene

isotopic purity

99.5 atom % D

assay

99.5%

form

powder

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

InChI

1S/C72H14O2/c1-74-11(73)8-5-9-70(10-6-3-2-4-7-10)71-66-58-50-40-30-22-14-12-13-16-20-18(14)26-34-28(20)38-32-24(16)25-17(13)21-19-15(12)23(22)31-37-27(19)35-29(21)39-33(25)43-42(32)52-46(38)56-48(34)54(44(50)36(26)30)62(66)64(56)68-60(52)61-53(43)47(39)57-49(35)55-45(37)51(41(31)40)59(58)67(71)63(55)65(57)69(61)72(68,70)71/h2-4,6-7H,5,8-9H2,1H3/i2D,3D,4D,6D,7D

InChI key

FIGVSQKKPIKBST-QRKCWBMQSA-N

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).

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Visite la Librería de documentos

Bulle-Lieuwma, C.,; Van Duren, J. et al.
Applied Surface Science, 274, 231-232 (2004)
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)
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)
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)

Artículos

Since the first publication in 1995 describing a bulk heterojunction photodiode incorporating a methanofullerene, significant progress has been made in improving device performance and the scope of device research has broadened widely.

Find various photovoltaic and bioscience-based applications of fullerenes.

Single-walled carbon nanotubes (SWCNTs) are promising materials for use in the active channel of field-effect transistors (FETs), photoabsorbing layers of solar cells and photodetectors because of their ultrafast charge transport mobility.

Solution-processed organic photovoltaic devices (OPVs) have emerged as a promising clean energy generating technology due to their ease of fabrication, potential to enable low-cost manufacturing via printing or coating techniques, and ability to be incorporated onto light weight, flexible substrates.

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