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Eduard Preis

Researcher at University of Wuppertal

Publications -  45
Citations -  946

Eduard Preis is an academic researcher from University of Wuppertal. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 20, co-authored 34 publications receiving 824 citations.

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Semiconducting Polymers via Microwave-Assisted Suzuki and Stille Cross-Coupling Reactions

TL;DR: In this paper, a fully conjugated para-phenylene ladder polymer (P1) and the alternating copolymers {2,7-[9,9-bis(2-ethylhexyl)fluorene]-5,5′-(2,2′-bithiophene)} (P3) and { 2,7]-9, 9-dioctylfluorene]5, 5′(2, 2,2,bithiohene) (P4) have been prepared via metal-mediated cross-coupling
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Does Conjugation Help Exciton Dissociation? A Study on Poly(p-phenylene)s in Planar Heterojunctions with C60 or TNF

TL;DR: Internal photocurrent quantum yields near 100% can be obtained from the separation of loosely bound geminate pairs when sufficiently large electric fields are applied to organic heterojunctions.
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Microwave-Assisted Synthesis of 1,5- and 2,6-Linked Naphthylene-Based Ladder Polymers

TL;DR: Arylene ladder polymers incorporating conjugated 1,5- and 2,6-naphthylene building blocks were synthesized in this article using a palladium-mediated Suzuki-type crosscoupling reaction using both conventional and microwave heating.
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Mobility relaxation and electron trapping in a donor/acceptor copolymer

TL;DR: In this paper, transient and steady-state charge transport measurements have been conducted on the prototype donor/acceptor copolymer poly[2,7-(9,9-dialkyl-fluorene)-alt-5,5-(4,7'-di-2-thienyl-2,1,3'-benzothiadiazole)] (PFTBTT).
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Novel, Metal-Free, Superacid-Catalyzed “Click” Reactions of Isatins with Linear, Nonactivated, Multiring Aromatic Hydrocarbons

TL;DR: In this article, a series of linear, high-molecular-weight polymers were synthesized by one-pot, metal-free superacid-catalyzed reaction of isatins (1a−d) with linear, nonactivated, multiring aromatic hydrocarbons: biphenyl (A), pterphenyl (B), p-quaterphenyl(C), 2-(4-biphenylyl)-6-phenylbenzoxazole (D), 9H-fluorene (E), 9,9-dim