Naphthacene
Naphthacene (Benz[b]anthracene) is a fused polycyclic aromatic compound exhibiting an electron field-effect mobility of approximately 10 cm2/Vs; it is an ethylnylated acene that functions as a conducting polymer, making it suitable for use as a donor material. Its exceptional photoluminescence and quantum yield position naphthacene as a highly promising candidate for the advancement of single crystal electronic materials.
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- CAS No.: 92-24-0
- 화학식: C18H12
- 분자량:228.29
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보관:Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
All Endogenous Metabolite Isoforms
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Biological Activity
Chemical Information
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CAS No. 92-24-0
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Appearance Solid
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분자량 228.29
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화학식 C18H12
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Color Yellow to brown
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SMILES
C12=CC=CC=C1C=C3C=C4C=CC=CC4=CC3=C2
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Synonyms
Benz[b]anthracene
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Powder -20°C 3 years In solvent -80°C 6 months -20°C 1 month
순도&문서
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Data Sheet (268 KB)
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SDS (761 KB)
- English - EN (761 KB)
- Français - FR (761 KB)
- Deutsch - DE (761 KB)
- Norwegian - NO (761 KB)
- Español - ES (761 KB)
- Swedish - SV (761 KB)
- Italian - IT (761 KB)
- Korean - KR (761 KB)
- Portuguese - PT (761 KB)
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Handling Instructions (2659 KB)
References
[1]. Electronic functionalization of the surface of organic semiconductors with self-assembled monolayers
[2]. Ambipolar light-emitting transistors of a tetracene single crystal
[3]. Singlet exciton fission in nanostructured organic solar cells
[4]. An organic solid state injection laser
[5]. Trap healing and ultralow-noise Hall effect at the surface of organic semiconductors
[6]. 25th Anniversary Article: Key Points for High-Mobility Organic Field-Effect Transistors
[7]. Molecular and morphological influences on the open circuit voltages of organic photovoltaic devices
[8]. Tetracene derivatives as potential red emitters for organic LEDs
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)