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Key Documents

525936

Sigma-Aldrich

Poly(thiophene-2,5-diyl), bromine terminated

powder

Synonym(s):

Thiophene, polymers

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
12352103
NACRES:
NA.23

form

powder

Quality Level

mp

>350 °C

InChI

1S/C4H4S/c1-2-4-5-3-1/h1-4H

InChI key

YTPLMLYBLZKORZ-UHFFFAOYSA-N

General description

Conducting polymer.

Packaging

Packaged in glass bottles

Legal Information

Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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.
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

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