525936
Poly(thiophene-2,5-diyl), bromine terminated
powder
Sinónimos:
Thiophene, polymers
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About This Item
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Formulario
powder
mp
>350 °C
cadena SMILES
[s]1cccc1
InChI
1S/C4H4S/c1-2-4-5-3-1/h1-4H
Clave InChI
YTPLMLYBLZKORZ-UHFFFAOYSA-N
Categorías relacionadas
Descripción general
Conducting polymer.
Envase
Packaged in glass bottles
Información legal
Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
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Yi Huang et al.
Biosensors & bioelectronics, 44, 41-47 (2013-02-09)
We report here on a facile enzymatic polymerization protocol to prepare enzyme-poly(thiophene-3-boronic acid) (PTBA) polymeric biocomposites (PBCs) for high-performance mono-/bi-enzyme amperometric biosensing. Horseradish peroxidase (HRP)-catalyzed polymerization of thiophene-3-boronic acid (TBA) monomer was conducted in aqueous solution containing HRP (or plus
Rajesh Kumar et al.
Journal of the American Chemical Society, 134(36), 14869-14876 (2012-08-04)
A three terminal molecular memory device was monitored with in situ Raman spectroscopy during bias-induced switching between two metastable states having different conductivity. The device structure is similar to that of a polythiophene field effect transistor, but ethylviologen perchlorate was
C Zanardi et al.
Analytical and bioanalytical chemistry, 405(2-3), 509-531 (2012-09-04)
This overview of polythiophene-based materials provides a critical examination of meaningful examples of applications of similar electrode materials in electroanalysis. The advantages arising from the use of polythiophene derivatives in such an applicative context is discussed by considering the organic
Dmytro Dudenko et al.
Angewandte Chemie (International ed. in English), 51(44), 11068-11072 (2012-10-06)
To tilt or not to tilt: The crystal structure for bulk P3HT (phase I) was determined by "multi-technique crystallography", which combines X-ray diffraction, solid-state NMR spectroscopy, and DFT calculations. The results showed that this semiconducting polymer crystallizes in the monoclinic space
Hiroyuki Tamura et al.
The Journal of chemical physics, 137(22), 22A540-22A540 (2012-12-20)
Following up on our recent study of ultrafast charge separation at oligothiophene-fullerene interfaces [H. Tamura, I. Burghardt, and M. Tsukada, J. Phys. Chem. C 115, 10205 (2011)], we present here a detailed quantum dynamical perspective on the charge transfer process.
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