Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Martin S. Vollmer"'
Publikováno v:
Synthesis. 2000:1229-1236
Publikováno v:
Angewandte Chemie International Edition. 38:1598-1601
The new photochromic supramolecular system 1 is based on the E→Z isomerization of an azobenzene substituted with cyclic peptides with alternating D- and L-α-amino acids. This system allows reversible switching between inter- and intramolecularly a
Publikováno v:
Langmuir. 15:3956-3964
A new photoswitchable peptide system composed of two flat, ring-shaped cyclic octapeptides with the sequence cyclo-[(l-Phe-d-MeN-Ala)3-l-Cys-d-MeN-Ala] tethered via an azobenzene moiety was investigated at the air−water interface, on mica, germaniu
Publikováno v:
Chemistry - A European Journal. 5:96-101
Spontaneously ordered monolayers on graphite are formed by the new synthezised class of steroid-bridged oligothiophenes 1 a–c; in STM images these appear in all cases as bright (thiophene) and dark (steroid) areas due to different energy gaps of th
Autor:
Achim Hartschuh, Martin S. Vollmer, Helmut Port, Thomas Stümpfig, Hans Christoph Wolf, Franz Effenberger
Publikováno v:
The Journal of Organic Chemistry. 63:5080-5087
The novel steroid-bridged energy transfer system 2 was prepared starting from epi-androsterone. The linkage of both the anthrylthienyl and the bithienyl group in the 3- and 17-position of the steroid was achieved by Grignard reaction of the respectiv
Autor:
Peter Emele, Frank Würthner, Dirk Meyer, Hans Christoph Wolf, Helmut Port, Franz Effenberger, Martin S. Vollmer, Thomas Stümpfig
Publikováno v:
Chemistry - A European Journal. 4:260-269
In the new trichromophoric supermolecule 1, a quantitative intramolecular energy transfer (>98 %) occurs from the anthracene donor to the emitting porphyrin acceptor through the oligothiophene chain after selective UV excitation of anthracene. Energy
Autor:
Franz Effenberger, Martin S. Vollmer, Bruno Gompf, Jörg Petersen, Horst Müller, Wolfgang Eisenmenger, Rainer Strohmaier
Publikováno v:
Advanced Materials. 8:733-737
Autor:
Peter Emele, Franz Effenberger, Helmut Port, Dirk Meyer, Hans Christoph Wolf, Martin S. Vollmer, Frank Wuerthner
Publikováno v:
Journal of the American Chemical Society. 117:8090-8099
Publikováno v:
Liebigs Annalen der Chemie. 1993:255-260
Treatment of methyl 2,3-di-O-acyl-D-glycopyranosides 1 of glucose and mannose with catalytic amounts of trifluoromethanesulfonic acid afforded the corresponding bis(5-O-acyl-3,6-anhydro-D-glycofuranose) 1,2′:2,1′-dianhydrides 6 in 12–58% yield
Publikováno v:
ChemInform. 24
Treatment of methyl 2,3-di-O-acyl-D-glycopyranosides 1 of glucose and mannose with catalytic amounts of trifluoromethanesulfonic acid afforded the corresponding bis(5-O-acyl-3,6-anhydro-D-glycofuranose) 1,2′:2,1′-dianhydrides 6 in 12–58% yield