Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Volodymyr Senkovskyy"'
Autor:
Wei Zhao, Tetyana Beryozkina, Yevhen Karpov, Jakob Zessin, Roman Tkachov, Volodymyr Senkovskyy, Vasiliy A. Bakulev, Ivan Raguzin, Anton Kiriy, Albena Lederer, Antonio Facchetti, Brigitte Voit, Manfred Stamm
Publikováno v:
Macromolecules. 47:3845-3851
For the fabrication of efficient photovoltaic devices and thin-film transistors, π-conjugated polymers with high molecular weight are desirable as they frequently show superior charge transport, morphological, and film-forming properties. Herein, we
Autor:
Anton Kiriy, Antonio Facchetti, Marcel Schubert, Roman Tkachov, Volodymyr Senkovskyy, Dieter Neher, Z. Wei, W. Liu, Hartmut Komber
Publikováno v:
Polym. Chem.. 5:3404-3411
Herein, we report the chain-growth tin-free room temperature polymerization method to synthesize n-type perylene diimide-dithiophene-based conjugated polymers (PPDIT2s) suitable for solar cell and transistor applications. The palladium/electron-rich
Autor:
Anton Kiriy, Roman Tkachov, Hartmut Komber, Volodymyr Senkovskyy, Jens-Uwe Sommer, Andreas John
Publikováno v:
Macromolecules. 45:7770-7777
Ni-catalyzed polymerization of anion-radical complexes formed upon mixing of 2,6-bis(2-bromothien-5-yl)naphthalene-1,4,5,8-tetracarboxylic-N,N′-bis(2-octyldodecyl) diimide and activated Zn powder was investigated. We provide experimental evidence t
Publikováno v:
Macromolecules. 45:4101-4114
A new synthetic method for the covalent linking of fullerenes to polymers is introduced. The Bingel-reaction was used to prepare bromine-functionalized fullerene building blocks that could be covalently linked to hydroxyl groups of model copolymers b
Autor:
Sven Huettner, Richard H. Friend, Anton Kiriy, Wilhelm T. S. Huck, Volodymyr Senkovskyy, Jens-Uwe Sommer, Michael Sommer, Ullrich Steiner, Roman Tkachov, Peter Kohn, Hartmut Komber
Publikováno v:
Journal of the American Chemical Society, 134, 4790-4805
Journal of the American Chemical Society, 134, 10, pp. 4790-4805
Journal of the American Chemical Society, 134, 10, pp. 4790-4805
Identifying structure formation in semicrystalline conjugated polymers is the fundamental basis to understand electronic processes in these materials. Although correlations between physical properties, structure formation, and device parameters of re
Publikováno v:
Macromolecular Rapid Communications. 32:1503-1517
Kumada catalyst-transfer polycondensation (KCTP) is a new but rapidly developing method with great potential for the preparation of well-defined conjugated polymers (CPs). The recently discovered chain-growth mechanism is unique among the various tra
Publikováno v:
IEEE Journal of Selected Topics in Quantum Electronics. 16:1821-1826
The challenges associated with obtaining the desired nanomorphology of the active layer in polymer solar cells were addressed through preparation of conjugated polymer chains grown from the surface of seed nanoparticles with a well-defined size. Poly
Publikováno v:
Colloid and Polymer Science. 289:603-612
Poly(N-isopropylacrylamide) (PNIPAM)-based microgels covered with hydrophobic but water-permeable shell were used for modification of a hydrophilic substrate with the aim to provide a ‘contraphilic’ wetting behaviour, namely, to make the surface
Autor:
Marta Horecha, Ulrich Oertel, Anton Kiriy, Roman Tkachov, Volodymyr Senkovskyy, Alla Synytska
Publikováno v:
Macromolecular Rapid Communications. 31:2146-2150
A 'grafting-from' approach to synthesize microparticle-supported conjugated polyelectrolyte brushes is presented. Poly(3-bromohexylthiophene) is selectively grown from monodisperse organosilica microparticles by surface-initiated Kumada catalyst-tran
Autor:
Roman Tkachov, Nikolai Severin, Volodymyr Senkovskyy, Manfred Stamm, Anton Kiriy, Vera Bocharova, Albena Lederer, Hartmut Komber, Jürgen P. Rabe, Tetyana Beryozkina
Publikováno v:
Macromolecular Symposia. :17-25
A new and facile method for the preparation of mono- and hexa-functional Ni-bipyridyl-based initiators that mediate Kumada polycondensation of 2 -bromo- 5 -chloromagnesio- 3 -hexylthiophene into head-to-tail regioregular poly(3-hexylthiophene), P 3 H