Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yvonne Abel"'
Autor:
Yvonne Abel, Sergei N. Smirnov, Enno Lork, Marat R. Talipov, Ivan Vlassiouk, Franz-Peter Montforts
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
In donor–acceptor dyads undergoing photoinduced electron transfer (PET), a direction or pathway for electron movement is usually dictated by the redox properties and the separation distance between the donor and acceptor subunits, while the effect
Autor:
Ilkka Kilpeläinen, Andrei Y. Tauber, Nikolai V. Tkachenko, Paavo H. Hynninen, Yvonne Abel, Helge Lemmetyinen, Juho Helaja
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2403-2408
The first chlorin–fullerene electron donor–acceptor (DA) compounds have been synthesized. The synthesis produced C-2′ R and S epimers, both of which exhibited atropisomerism regarding the mutual orientation of the fullerene ball and the propion
Autor:
Gerold Haake, Yvonne Abel, Franz-Peter Montforts, Andreas Walter, D. Struve, Wolfgang Schmidt, Elmar Haake
Publikováno v:
Helvetica Chimica Acta. 81:1978-1996
Synthesis of a novel chlorin-quinone system for the investigation of light induced electron transfer
Autor:
Franz-Peter Montforts, Yvonne Abel
Publikováno v:
Tetrahedron Letters. 38:1745-1748
In order to investigate the effect of the molecular symmetry on the light induced electron transfer in chlorin-quinone dyades we aimed at the synthesis of chlorin-quinone models 18a and 18b in which the quinone is situated at ring D adjacent to the r
Autor:
Franz-Peter Montforts, Gerold Haake, Yvonne Abel, Wolfgang Schmidt, D. Struve, Andreas Walter, Elmar Haake
Publikováno v:
ChemInform. 30
Autor:
Andrei Y. Tauber, Yvonne Abel, Helge Lemmetyinen, Ilkka Kilpelaeinen, Nikolai V. Tkachenko, Paavo H. Hynninen, Juho Helaja
Publikováno v:
ChemInform. 30
Publikováno v:
ChemInform. 34
This paper describes the development of novel aromatic platforms for supramolecular construction. By the Suzuki cross-coupling protocol, a variety of functionalized m-terphenyl derivatives were prepared (Schemes 1–4). Macrolactamization of bis(ammo
Publikováno v:
Vox Sanguinis. 65:335-336