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Dive into the research topics where Jonas Hellberg is active.

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Featured researches published by Jonas Hellberg.


Tetrahedron Letters | 2002

A convenient and improved synthesis of dithieno[3,2-b:2′,3′-d]thiophene

Fredrik Allared; Jonas Hellberg; Tommi Remonen

Abstract An improved synthesis of dithieno[3,2- b :2′,3′- d ]thiophene 1 is presented. By starting from 2,3-dibromothiophene 2 the total yield was improved from 35 to 58%. We also describe a more convenient synthesis of one of the reagents, benzenesulfonic acid thioanhydride 3 .


Journal of The Chemical Society, Chemical Communications | 1987

Conducting polymers from dimethyl-2,2′-bithiophenes

Bernd Krische; Jonas Hellberg; Christina Lilja

Electrochemical oxidation of symmetrical dimethylbithiophenes with free α-positions yields electroactive polymers with excellent cycling ability.


Journal of Organometallic Chemistry | 1985

A general procedure for the synthesis of methylthio-, methylseleno- and methyltelluro-substituted aromatic compounds

Lars Engman; Jonas Hellberg

Abstract A one-pot procedure is described which allows the facile introduction of one or two methylchalcogeno groups into a variety of monobromo or dibromo aromatics. The bromo compounds were converted to their corresponding lithio derivatives by treatment with t-butyllithium in tetrahydrofuran at −78°C, and these derivatives were then treated, at ambient temperature with elemental sulfur, selenium, or tellurium. The resulting lithium thiolates, selenolates and tellurolates were finally methylated with methyl iodide to afford good yields (typically 50–80%) of the various methylchalcogeno-substituted aromatic compounds. The procedure could not be used for the synthesis of ortho -disubstituted compounds, or for the simultaneous introduction of three methylchalcogeno groups.


Synthetic Metals | 1993

Fabrication and characterization of schottky gate poly(3-alkylthiophene) planar field-effect transistors

A. Assadi; M. Willamder; Christer Svensson; Jonas Hellberg

Abstract In this paper fabrication and characterization of Schottky gate planar field-effect transistors using poly(3-alkylthiophene) as an active semiconductor region are reported. This is the first time that planar MESFET transistors utilizing a polymer semiconductor have been fabricated and measured. Aluminum metal is used for the rectifying contact and two gold electrodes are constructed as source and drain. From the MESFET characteristic the channel carrier mobility is evaluated as 10 −5 cm 2 V −1 s −s , which is one order of magnitude larger than a MOSFET utilizing the same polymer.


Synthetic Metals | 1997

New monomers for polythiophenes

Jonas Hellberg; Tommi Remonen; Mats Johansson; Olle Inganäs; M. Theander; L Engman; P Eriksson

Two series of chalcogen substituted thiophene monomers have been synthesised; 3-(4-alkylchalcogenophenyl)thiophenes 1a-c and 3-(4-alkylphenylchalcogeno)thiophenes 2a-d. Polymerisations of examples of these with iron(III)chloride gave regiorandom polymers. Light-emitting diodes with low efficiency could be fabricated from poly-1a and poly-1b.


Journal of The Chemical Society-perkin Transactions 1 | 1988

New alkoxylated dibenzo[1,4]dichalcogenines as donors for low-dimensional materials: electrochemistry and cation-radical salts

Lars Engman; Jonas Hellberg; Christina Ishag; Svante Söderholm

The synthesis of new alkoxylated dibenzo[1,4]dichalcogenines (3a–c), (3e–f), (3h), (4a–h), and (5a) is presented. The first cyclovoltammetric half-wave potentials of these compounds range from 0.62 to 1.06 V vs. standard calomel electrode (s.c.e.). Cation radical salts of several different stoicheiometries have been prepared from the new donors.


Synthetic Metals | 1993

Bithiophenes as starting monomers for polythiophene syntheses

Bernd Krische; Malgorzata Zagorska; Jonas Hellberg

Abstract Bithiophenes, when used as starting material for polythiophene synthesis, offer advantages over corresponding thiophenes. Polymerization proceeds at lower oxidation potentials and lower monomer concentration and gives polymers with higher yield and better regularity as shown by cyclic voltammetry and 1H NMR spectroscopy.


Tetrahedron Letters | 1994

Synthesis of annulated dioxins and their use as donors for cation radical salts

Jonas Hellberg; Margit E. Pelcman

Abstract The synthesis of a series of new alkoxylated annulated dioxins is described together with their cyclovoltammetric behaviour.


Synthetic Metals | 1999

Ethylenedithio end-capped oligothiophenes (bEDTnT); Dimer, trimer and tetramer

Tommi Remonen; Jonas Hellberg; Johnny Slätt

Two new ethylenedithio substituted thiophenes (I; R = H, Br) have been synthesized. Starting from I (R = Br), oligomers II (n = 0, 1, 2) were synthesized. Their cyclic voltammetric behavior and ele ...


Molecular Crystals and Liquid Crystals | 1985

A New Cation Radical Salt: (bMDODBF)2AsF6

Jonas Hellberg; Göran Ahlgren; Svante Söderholm; Gunnar Olovsson; J.U. von Schütz

Abstract The AsF− 6 cation radical salt of 2,3,6,7-bis-methylene-dioxydibenzofuran has been synthesized. Its structural, electrical and ESR properties are presented.

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S. Söderholm

Royal Institute of Technology

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Mikael Moge

Royal Institute of Technology

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Emma Dahlstedt

Royal Institute of Technology

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Tommi Remonen

Royal Institute of Technology

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Fredrik Allared

Royal Institute of Technology

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Göran Ahlgren

Royal Institute of Technology

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