TY - JOUR A1 - Täuber, K. A1 - Zimathies, Annett A1 - Yuan, J. T1 - Porous membranes built up from hydrophilic poly(ionic liquid)s N2 - Porous polymer membranes made via electrostatic complexation are fabricated from a water-soluble poly(ionic liquid) (PIL) for the first time. The porous structure is formed as a consequence of simultaneous phase separation of the PIL and ionic complexation with an acid, which occurred in a basic solution of a nonsolvent for the PIL. These membranes have a stimuli-responsive porosity, with open and closed pores in isopropanol and in water, respectively. This property is quantitatively demonstrated in filtration experiments, where water is passing much slower through the membranes than isopropanol. KW - Crosslinking KW - Phase separation KW - Poly(ionic liquid) KW - Porous membranes KW - Responsive materials PY - 2015 DO - https://doi.org/10.1002/marc.201500480 SN - 1022-1336 SN - 1521-3927 VL - 36 IS - 24 SP - 2176 EP - 2180 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-35135 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Steinkönig, J. A1 - Bloesser, F. R. A1 - Huber, B. A1 - Welle, A. A1 - Trouillet, V. A1 - Weidner, Steffen A1 - Barner, L. A1 - Roesky, P. W. A1 - Yuan, J. A1 - Goldmann, A. S. A1 - Barner-Kowollik, C. T1 - Controlled radical polymerization and in-depth mass-spectrometric characterization of poly(ionic liquid)s and their photopatterning on surfaces N2 - The preparation and characterization of poly(ionic liquid)s (PILs) bearing a polystyrene backbone via reversible addition fragmentation chain transfer (RAFT) polymerization and their photolithographic patterning on silicon wafers is reported. The controlled radical polymerization of the styrenic ionic liquid (IL) monomers ([BVBIM]X, X = Cl− or Tf2N−) by RAFT polymerization is investigated in detail. We provide a general synthetic tool to access this class of PILs with controlled molecular weight and relatively narrow molecular weight distribution (2000 g mol−1 ≤ Mn ≤ 10 000 g mol−1 with dispersities between 1.4 and 1.3 for p([BVBIM]Cl); 2100 g mol−1 ≤ MP ≤ 14 000 g mol−1 for p([BVBIM]Tf2N)). More importantly, we provide an in-depth characterization of the PILs and demonstrate a detailed mass spectrometric analysis via matrix-assisted laser desorption ionization (MALDI) as well as – for the first time for PILs – electrospray ionization mass spectrometry (ESI-MS). Importantly, p([BVBIM]Cl) and p([DMVBIM]Tf2N) were photochemically patterned on silicon wafers. Therefore, a RAFT agent carrying a photoactive group based on ortho-quinodimethane chemistry – more precisely photoenol chemistry – was photochemically linked for subsequent controlled radical polymerization of [BVBIM]Cl and [DMVBIM]Tf2N. The successful spatially-resolved photografting is evidenced by surface-sensitive characterization methods such as X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS). The presented method allows for the functionalization of diverse surfaces with poly(ionic liquid)s. KW - reversible addition fragmentation chain transfer (RAFT) polymerization KW - polyionic liquids KW - mass spectrometry KW - surface modification PY - 2016 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-355202 DO - https://doi.org/10.1039/C5PY01320H VL - 7 SP - 451 EP - 461 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-35520 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -