525936
Poly(thiophene-2,5-diyl), bromine terminated
powder
Sinônimo(s):
Thiophene, polymers
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About This Item
Produtos recomendados
forma
powder
pf
>350 °C
InChI
1S/C4H4S/c1-2-4-5-3-1/h1-4H
chave InChI
YTPLMLYBLZKORZ-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
Conducting polymer.
Embalagem
Packaged in glass bottles
Informações legais
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 classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
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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