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Key Documents

900854

Sigma-Aldrich

FBR

Synonym(s):

5,5′-[(9,9-Dioctyl-9H-fluorene-2,7-diyl)bis(2,1,3-benzothiadiazole-7,4-diylmethylidyne)]bis[3-ethyl-2-thioxo-4-thiazolidinone]

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About This Item

Empirical Formula (Hill Notation):
C53H56N6O2S6
CAS Number:
Molecular Weight:
1001.44
UNSPSC Code:
12352101
NACRES:
NA.23

description

Band gap: 1.59 eV

Quality Level

Assay

≥97%

form

solid

solubility

chlorobenzene: soluble
chloroform: soluble
dichlorobenzene: soluble

Orbital energy

HOMO -5.61 eV 
LUMO -4.02 eV 

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Derya Baran et al.
Nature materials, 16(3), 363-369 (2016-11-22)
Technological deployment of organic photovoltaic modules requires improvements in device light-conversion efficiency and stability while keeping material costs low. Here we demonstrate highly efficient and stable solar cells using a ternary approach, wherein two non-fullerene acceptors are combined with both
Sarah Holliday et al.
Journal of the American Chemical Society, 137(2), 898-904 (2014-12-30)
A novel small molecule, FBR, bearing 3-ethylrhodanine flanking groups was synthesized as a nonfullerene electron acceptor for solution-processed bulk heterojunction organic photovoltaics (OPV). A straightforward synthesis route was employed, offering the potential for large scale preparation of this material. Inverted

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Professor Chen (Nankai University, China) and his team explain the strategies behind their recent record-breaking organic solar cells, reaching a power conversion efficiency of 17.3%.

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