A new class of processable, chemically stable, and easily synthesized and purified alpha,omega-bis(dimethyl-tert-butylsilyl) oligothiophenes is described. Information on the solid-state properties was obtained by single crystal X-ray diffraction and CPMAS NMR spectroscopy. Molecular packing was characterized by a sandwich-type organization, with the molecular planes between adjacent layers along the stacking direction being exactly parallel. Vacuum-evaporated thin films of the tetramer, pentamer, and hexamer displayed field effect transistor activity, with charge mobilities increasing with the substrate deposition temperatures in the range 28-80 degrees C. The best FET performance was achieved with the pentamer which was characterized by an on/off ratio > 10(3), reproducibility, and a device stability in air of months.

Structural and electrical characterization of processable bis-silylated thiophene oligomers

Barbarella G;Maccagnani P;
1998

Abstract

A new class of processable, chemically stable, and easily synthesized and purified alpha,omega-bis(dimethyl-tert-butylsilyl) oligothiophenes is described. Information on the solid-state properties was obtained by single crystal X-ray diffraction and CPMAS NMR spectroscopy. Molecular packing was characterized by a sandwich-type organization, with the molecular planes between adjacent layers along the stacking direction being exactly parallel. Vacuum-evaporated thin films of the tetramer, pentamer, and hexamer displayed field effect transistor activity, with charge mobilities increasing with the substrate deposition temperatures in the range 28-80 degrees C. The best FET performance was achieved with the pentamer which was characterized by an on/off ratio > 10(3), reproducibility, and a device stability in air of months.
1998
Istituto per la Microelettronica e Microsistemi - IMM
Inglese
10
11
3683
3689
Sì, ma tipo non specificato
FIELD-EFFECT TRANSISTORS
X-RAY STRUCTURE
SOLID-STATE
SUBSTITUTED OLIGOTHIOPHENES
ORGANIC SEMICONDUCTORS
7
info:eu-repo/semantics/article
262
Barbarella, G; Ostoja, P; Maccagnani, P; Pudova, O; Antolini, L; Casarini, D; Bongini, A
01 Contributo su Rivista::01.01 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/203743
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