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Synthesis and characterization of electroactive films based on benzo(a)pyrene

✍ Scribed by Michal Wagner; Kai Yu; Carita Kvarnström; Ari Ivaska


Book ID
103828389
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
658 KB
Volume
56
Category
Article
ISSN
0013-4686

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✦ Synopsis


The polycyclic aromatic hydrocarbons (PAHs) are a group of compounds that might have practical applications due to their graphene-like properties. Derivatized PAHs can self-assemble in liquid crystal form. The chemical synthesis of large size PAHs can however be complicated and problematic. Electrochemical synthesis of PAHs molecules was studied in this work by cyclic voltammetry. Benzo(a)pyrene was used as the monomer. The resulting electroactive films consist of different PAHs in both size and symmetry. We call this mixture poly(benzopyrene) (PBP). The synthesis conditions of PBP were optimized to obtain thick and electrochemically stable films. The best film quality was achieved by potential scanning in propylene carbonate at low scan rate resulting in continues polymer growth during 10 scans giving approx. a 1 m thick PBP film. During p-and n-doping studies the reduction and oxidation peaks were observed at 1.0 V and -1.6 V, respectively, with an electrochemical band gap of approx. 2.6 eV. The in situ UV-vis characterization of the PBP films was made by applying a constant potential with increasing steps. The optical band gap was approx. 2.5 eV and the absorption maximum was observed at ca. 420 nm. During p-and n-doping new induced bands were formed in the range 575-600 nm. UV-vis spectroscopy indicate that PBP mainly consist of units consisting of more than 40 carbon atoms and large number of -electrons.


📜 SIMILAR VOLUMES


Synthesis of (+)- and (−)-benzo[a]pyrene
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The concept of stereoselectivity during monooxygenase catalyzed addition of an oxygen atom to the stereoheterotopic faces of a polycyclic aromatic hydrocarbon (PAH) was initially proposed' on the basis of (a) liver microsomal metabolism studies on naphthalene and (+)-naphthalene 1,2-oxide and (b) sy

13C labeled benzo[a]pyrenes and derivati
✍ J. Ernest Simpson; Guido H. Daub; David L. Vanderjagt 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 French ⚖ 240 KB

## Abstract The synthesis of benzo[a]pyrene‐6‐^13^C is described. Perinaphthane was converted to 6‐benzoyl‐carbonyl‐^13^C‐perinaphthane which was cyclized to 2,3‐dihydrobenzo[a]pyren‐6(1H)‐one‐6‐^13^C. Subsequent reduction of the ketone followed by dehydration and dehydrogenation gave benzo[a]pyren