TY  - BOOK
A1  - Stillmark, Hans-Christian
A1  - Limberg, Jörg
A1  - Götzmann, Jutta
A1  - Vogt, Jochen
A1  - Eke, Norbert Otto
A1  - Braun, Matthias
A1  - Clare, Jennifer
A1  - Grimm, Christa
A1  - Hofmann, Michael
A1  - Bauer, Gerhard
A1  - Starke, Frank
ED  - Stillmark, Hans-Christian
T1  - Peter Weiss erinnernd - Ansichten und Einsichten
N2  - Der Band versammelt verschiedenen Beiträge, die sich mit dem Leben und Werk von Peter Weiss auseinandersetzen. Die Beiträge wurden auf der Konferenz "Peter Weiss - 100" anläßlich des hundertsten Geburtstages des Autors im Jahre 2016 in Potsdam gehalten. Dabei wirkten unterschiedliche Einrichtungen und Institutionen erstmals gemeinsam im Geburtsort des Künstlers.
KW  - Peter Weiss
KW  - Erinnernungskultur
KW  - Ästhetik des Widerstands
KW  - Collage
KW  - engagierte Kunst
KW  - Auschwitz-Prozess
KW  - Dokumentartheater
Y1  - 2020
SN  - 978-3-89693-747-6
PB  - Weidler Buchverlag
CY  - Berlin
ET  - 150
ER  - 
TY  - JOUR
A1  - Secker, Christian
A1  - Brosnan, Sarah M.
A1  - Limberg, Felix Rolf Paul
A1  - Braun, Ulrike
A1  - Trunk, Matthias
A1  - Strauch, Peter
A1  - Schlaad, Helmut
T1  - Thermally Induced Crosslinking of Poly(N-Propargyl Glycine)
JF  - Macromolecular chemistry and physics
N2  - As polypeptoids become increasingly popular, they present a more soluble and processable alternative to natural and synthetic polypeptides; the breadth of their potential functionality slowly comes into focus. This report analyzes the ability of an alkyne-functionalized polypeptoid, poly(N-propargyl glycine), to crosslink upon heating. The crosslinking process is analyzed by thermal analysis (differential scanning calorimetry and thermogravimetric analysis), Fourier-transform infrared, electron paramagnetic resonance, and solid-state NMR spectroscopy. While a precise mechanism cannot be confidently assigned, it is clear that the reaction proceeds by a radical mechanism that exclusively involves the alkyne functionality, which, upon crosslinking, yields alkene and aromatic products.
KW  - Fourier-transform infrared
KW  - metal-free crosslinking
KW  - polypeptoid
KW  - propargyl
KW  - solid-state NMR
Y1  - 2015
U6  - https://doi.org/10.1002/macp.201500223
SN  - 1022-1352
SN  - 1521-3935
VL  - 216
IS  - 21
SP  - 2080
EP  - 2085
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Wirth, Jonas
A1  - Hatter, Nino
A1  - Drost, Robert
A1  - Umbach, Tobias R.
A1  - Barja, Sara
A1  - Zastrow, Matthias
A1  - Rück-Braun, Karola
A1  - Pascual, Jose Ignacio
A1  - Saalfrank, Peter
A1  - Franke, Katharina J.
T1  - Diarylethene Molecules on a Ag(111) Surface: Stability and Electron-Induced Switching
JF  - The journal of physical chemistry : C, Nanomaterials and interfaces
N2  - Diarylethene derivatives are photochromic molecular switches, undergoing a ring-opening/-closing reaction by illumination with light. The symmetry of the closed form is determined by the WoodWard Hoffinann rules according to which the reaction proceeds by corirotatory rotation -in that case. Here, we show by a cOrnbined approach of scanning tunneling microscopy (STM) and density functional theory (DFT) calculations that the Open isomer of 4,4'-(4,4'-(perfluorocydopent-1-ene-1,2-diyl)bis(5-methyl-thiophent-4,2,4-dipyridine) (PDTE) retains its open form upon adsorption on a Ag(111) surface. It caribe switched into a closed form, which we identify as the digrotatOly cydization product, by controlled manipulation 'With the STM tip, Evidence of an electric-field dependent switching-process 'is interpreted on the basis of a Simple electroStatic Model, which suggests that the reaction proceedS via an "upright" intermediate state. This pathway thus strongly differs from the switching reaction in solution.
Y1  - 2015
U6  - https://doi.org/10.1021/jp5122036
SN  - 1932-7447
VL  - 119
IS  - 9
SP  - 4874
EP  - 4883
PB  - American Chemical Society
CY  - Washington
ER  -