نتایج جستجو برای: Oligothiophene

تعداد نتایج: 259  

2017
Y Almadori L Alvarez R Le Parc R Aznar F Fossard A Loiseau Bruno Jousselme S Campidelli Y. Almadori L. Alvarez R. Aznar

We report an experimental study on the confinement of oligothiophene derivatives into single-walled carbon nanotubes over a large range of diameter (from 0.68 to 1.93 nm). We evidence by means of Raman spectroscopy and transmission electron microscopy that the supramolecular organizations of the confined oligothiophenes depend on the nanocontainer size. The Raman Radial Breathing Mode frequency...

Journal: :Biosensors & bioelectronics 2015
Leif B G Johansson Rozalyn Simon Gunnar Bergström Mikaela Eriksson Stefan Prokop Carl-Fredrik Mandenius Frank L Heppner Andreas K O Åslund K Peter R Nilsson

Ligands for identifying protein aggregates are of great interest as such deposits are the pathological hallmark of a wide range of severe diseases including Alzheimer's and Parkinson's disease. Here we report the synthesis of an azide functionalized fluorescent pentameric oligothiophene that can be utilized as a ligand for multimodal detection of disease-associated protein aggregates. The azide...

Journal: :Chemical communications 2009
Yutaka Ie Toshihiko Uto Nobuhiro Yamamoto Yoshio Aso

A dendritic oligothiophene containing perylene bis(dicarboximide) units was synthesized and its electronic properties and photovoltaic performance were investigated.

2014
Jun Terao Yohei Konoshima Akitoshi Matono Hiroshi Masai Tetsuaki Fujihara Yasushi Tsuji

We synthesized symmetrically insulated oligo(para-phenylene) and oligothiophene with a pseudo-linked [3]rotaxane structure by full rotation of glucopyranose units via a flipping (tumbling) mechanism in the π-conjugated guest having two permethylated β-cyclodextrin units at both ends. We also succeeded in the synthesis of an organic-soluble fixed [3]rotaxane by a cross-coupling or complexation r...

Journal: :The journal of physical chemistry. B 2006
Nicholas E Singh-Miller Damian A Scherlis Nicola Marzari

The functionality of conjugated polymer systems often relies on oxidations or reductions, in most cases mediated by the presence of counterions. The effect that the common counterion hexafluorophosphate (PF6-) has on the intermolecular interactions between charged oligothiophenes is investigated here using ab initio quantum chemistry methods. Counterions are explicitly included in the simulatio...

Journal: :Chemical communications 2006
Sudarshan Natarajan Seong H Kim

In contrast to the traditional thermally-activated Ullmann coupling, a photo-activated Ullmann coupling for facile synthesis of oligothiophene and polythiophene films and micropatterns is reported.

Journal: :Chemical communications 2009
Jennifer E Klare Ian P Murray Joshua Goldberger Samuel I Stupp

We report the design and synthesis of an oligothiophene molecule that noncovalently functionalizes carbon nanotubes to create a hybrid material for photovoltaic devices.

Journal: :Chemistry 2005
Shin-Ichiro Kawano Norifumi Fujita Seiji Shinkai

A series of quater-, quinque-, and sexithiophene derivatives bearing two cholesteryl groups at the alpha-position, which are abbreviated as 4 T-(chol)(2), 5 T-(chol)(2), and 6 T-(chol)(2), respectively, have been synthesized. It has been found that these oligothiophene derivatives act as excellent organogelators for various organic fluids and show the unique thermochromic behaviors through the ...

Journal: :Chemical communications 2007
Frédéric Oswald D-M Shafiqul Islam Yasuyuki Araki Vincent Troiani Ruben Caballero Pilar de la Cruz Osamu Ito Fernando Langa

Photoinduced energy transfer and electron transfer processes have been found between the excited singlet state of Zn-porphyrin and C(60) via an oligothienylenevinylene bridge depending on the length of the oligothiophene and solvent polarity.

Journal: :Chemical communications 2009
Yutaka Ie Aihong Han Tetsuo Otsubo Yoshio Aso

A series of oligothiophenes covered with tert-butyldiphenylsilyl (TBDPS) groups was synthesized, and the spectroscopic measurements and X-ray analyses revealed that the oligothiophene backbone is completely encapsulated by bulky TBDPS groups.

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