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Key Documents

525936

Sigma-Aldrich

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

powder

Sinonimo/i:

Thiophene, polymers

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About This Item

Numero CAS:
Numero MDL:
Codice UNSPSC:
12352103
NACRES:
NA.23

Forma fisica

powder

Livello qualitativo

Punto di fusione

>350 °C

InChI

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

Descrizione generale

Conducting polymer.

Confezionamento

Packaged in glass bottles

Note legali

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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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
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
Therése Klingstedt et al.
Biochemical Society transactions, 40(4), 704-710 (2012-07-24)
The deposition of protein aggregates in various parts of our body gives rise to several devastating diseases, and the development of probes for the selective detection of aggregated proteins is crucial to advance our understanding of the pathogenesis underlying these
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.
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

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