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  • 771627 - 2,9-Bis[(4-methoxyphenyl)methyl]anthra[2,1,9-def:6,5,10-def′]diisoquinoline-1,3,8,10(2H,9H)tetrone

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771627 Sigma-Aldrich

2,9-Bis[(4-methoxyphenyl)methyl]anthra[2,1,9-def:6,5,10-def′]diisoquinoline-1,3,8,10(2H,9H)tetrone

99%

Synonym: N,N′-Bis(4-methoxybenzyl)perylene-3,4:9,10-bis(dicarboximide)

  • Empirical Formula (Hill Notation) C40 H26 N2 O6

  • Molecular Weight 630.64

  •  EC Number 280-472-4

  •  MDL number MFCD23160595

  •  PubChem Substance ID 329767509

  •  NACRES NA.23

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Properties

Related Categories Materials Science, Organic Field Effect Transistor (OFET) Materials, Organic and Printed Electronics, n-Type Organic Semiconductors, n-Type Small Molecules More...
Quality Level   100
assay   99%
form   powder
mp   120-130 °C
λmax   527, 490 nm in dichloromethane
semiconductor properties   (mobility=0.5 cm2/V·s)
SMILES string   COc1ccc(CN2C(=O)c3ccc4c5ccc6C(=O)N(Cc7ccc(OC)cc7)C(=O)c8ccc(c9ccc(C2=O)c3c49)c5c68)cc1
InChI   1S/C40H26N2O6/c1-47-23-7-3-21(4-8-23)19-41-37(43)29-15-11-25-27-13-17-31-36-32(40(46)42(39(31)45)20-22-5-9-24(48-2)10-6-22)18-14-28(34(27)36)26-12-16-30(38(41)44)35(29)33(25)26/h3-18H,19-20H2,1-2H3
InChI key   LQDAMBYDGRGJGA-UHFFFAOYSA-N

Description

Application

High electron transporting character (electron mobility on the order of 0.5 cm2 V-1 s-1); Perylenebis(dicarboximide)s (PDIs) can be used as n-type materials for organic fieldeffect transistors (OFETs);
Excellent candidates as electron accepting building blocks for organic photovoltaics (OPVs);
IR transparent pigment for coating application.

Packaging

1 g in glass bottle

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Target organs 
Respiratory system
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Development of Small Molecule Donors for Solution-Processed Organic Solar Cells

Abby-Jo Payne and Gregory C. Welch Dalhousie University, Department of Chemistry 6274 Coburg Road, Halifax, Nova Scotia, Canada B3H 4R2 Email: gregory.welch@dal.ca
Keywords: Absorption, Bacterial conjugations, Building blocks, Deposition, Infrared spectroscopy, Nucleic acid annealing, Phase transitions, Separation, Solar cells, Solvents, Substitutions

Flexible Organic Transistors for Biomedical Applications

Tsuyoshi Sekitani,* Kazunori Kuribara, Tomoyuki Yokota, Takao Someya Department of Electric and Electronic Engineering, Department of Applied Physics, School of Engineering University of Tokyo, 7-3-1...
Keywords: Absorption, Building blocks, Degradations, Diffraction, Electronics, Evaporation, Microscopy, Nucleic acid annealing, Oxidations, Reductions, Semiconductor, Solar cells, Spectroscopy, Sterilizations, X-Ray diffraction

Polymer Semiconductors for Intrinsically Stretchable Organic Transistors

Department of Chemical Engineering, Stanford University, Stanford, CA 94305-5025, USA *E-mail: zbao@stanford.edu
Ging-Ji Nathan Wang, Zhenan Bao*
Material Matters, 2017, 12.3
Keywords: Bacterial conjugations, Crystallization, Degradations, Diffraction, Electronics, Hydrogenations, Microscopy, Nucleic acid annealing, Optical microscopy, Organic electronics, Polymerization reactions, Semiconductor, Separation, Solar cells, X-Ray diffraction

Soluble Pentacene Precursors

In order to introduce un-functionalized pentacene within a device such as an organic field effect transistor (OFET), soluble pentacene precursors, which readily transform into pentacene upon heating ...
Prof. Cherie R. Kagan

Associate Professor, Department of Materials Science and Engineering,
University of Pennsylvania, Philadelphia, PA 19104
Keywords: Deposition, Evaporation, Semiconductor, Size-exclusion chromatography

Peer-Reviewed Papers
15

References

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