Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ara Anja Palmans"'
Publikováno v:
Soft matter. 4(3)
Materials with selective bio-responsiveness could have potential in medical applications. Here we report the synthesis of chiral microspheres obtained from non-crystalline aliphatic polyesters, with the aim to use chirality to program polymer microsp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b404651af36cf9c9490590ab8fdd1ad8
https://pubmed.ncbi.nlm.nih.gov/32907226
https://pubmed.ncbi.nlm.nih.gov/32907226
Autor:
Chi Yuan Cheng, E. W. Meijer, Lotte Van Beek, Songi Han, Ara Anja Palmans, Patrick J. M. Stals, AC Annelies Wauters
Publikováno v:
Chemical Science, 7(3), 2011-2015. Royal Society of Chemistry
A library of water-soluble dynamic single-chain polymeric nanoparticles (SCPN) was prepared using a controlled radical polymerisation technique followed by the introduction of functional groups, including probes at targeted positions. The combined to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e8ec126955a9386ffc852fb9014a38a
https://doi.org/10.1039/c5sc02319j
https://doi.org/10.1039/c5sc02319j
Autor:
Ara Anja Palmans, Robert Graf, Martin Wegner, Dmytro Dudenko, Daniel Sebastiani, de Tfa Tom Greef, Hans-Wolfgang Spiess
Publikováno v:
Chemical Science, 2(10), 2040-2049. Royal Society of Chemistry
Solid-state NMR experiments as well as extensive Car–Parrinello Molecular Dynamics simulations are used to study the dependence of supramolecular self-organization of benzene-1,3,5-tricarboxamides (BTA) on the local orientation of the amide functio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08bf91aa8e01ef9d3eccdc990d49b6e2
https://research.tue.nl/en/publications/2983b64e-794e-4bff-ad59-890ceb870368
https://research.tue.nl/en/publications/2983b64e-794e-4bff-ad59-890ceb870368
Autor:
Peter A. J. Hilbers, Rutger A. van Santen, Iaw Ivo Filot, Tfa Tom de Greef, Evgeny A. Pidko, Ara Anja Palmans
Publikováno v:
Journal of Physical Chemistry B, 114(43), 13667-13674. American Chemical Society
Understanding the molecular mechanism of cooperative self-assembly is a key component in the design of self-assembled supramolecular architectures across multiple length scales with defined function and composition. In this work, we use density funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8090e8d5372b3b83e626d0f33a6cf606
https://doi.org/10.1021/jp1072928
https://doi.org/10.1021/jp1072928
Autor:
TM Thomas Pauloehrl, Lorenzo Albertazzi, Y Yiliu Liu, Ara Anja Palmans, Stanislav I. Presolski, E. W. Meijer
Publikováno v:
Journal of the American Chemical Society, 137(40), 13096-13105. American Chemical Society
Single-chain polymeric nanoparticles (SCPNs) are intriguing systems for multiple applications. In order to arrive at a controlled, but random, positioning of the different side groups to the polymer backbone, alternative synthetic routes have to be d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8501d1d5a64d05bcc15518e1d1093232
https://pubmed.ncbi.nlm.nih.gov/26388188
https://pubmed.ncbi.nlm.nih.gov/26388188
Publikováno v:
Langmuir, 31(1), 57-64. American Chemical Society
A robust method is described for precisely functionalizing silica colloids with short-chain alkanes and self-associating o-nitrobenzyl protected benzene-1,3,5-tricarboxamides (BTAs). Controlled deprotection affords activation of the latent supramolec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d939221e58a5b2f04e9af8c25b45a31
https://research.tue.nl/nl/publications/22b026f8-95f0-4009-9498-e16f32994455
https://research.tue.nl/nl/publications/22b026f8-95f0-4009-9498-e16f32994455
Publikováno v:
Journal of Polymer Science, Part A: Polymer Chemistry, 44(14), 4290-4297. Wiley
The synthetic parameters for the chemoenzymatic cascade synthesis of block copolymers combining enzymatic ring-opening polymerization (EROP) and atom transfer radical polymerization (ATRP) in one pot were investigated. A detailed analysis of the mutu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff05416c47201bf04572811d8274193e
https://doi.org/10.1002/pola.21528
https://doi.org/10.1002/pola.21528
Autor:
Martin Wolffs, CE Cor Koning, Thomas M. Hermans, Ara Anja Palmans, Joris W. Peeters, M Matthijs de Geus, Andreas Heise
Publikováno v:
Macromolecules, 38(10), 4220-4225. American Chemical Society
The chemoenzymatic synthesis of block copolymers from a bifunctional initiator using enzymatic ring-opening polymerization (eROP) and ATRP in two consecutive steps was investigated. First, a polycaprolactone (PCL) macroinitiator was obtained via an e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1e0c13081c8af3e87a7b6e3bb206e82
https://doi.org/10.1021/ma0473871
https://doi.org/10.1021/ma0473871
Autor:
Ara Anja Palmans, Andreas Heise
Publikováno v:
Advances in Polymer Science ISBN: 9783642163753
Lipases show high activity in the polymerization of a range of monomers using ring-opening polymerization and polycondensation. The range of polymer structures from this enzymatic polymerization can be further increased by combination with chemical m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bba537c5fee2cd36d671f363613ba242
https://doi.org/10.1007/12_2010_74
https://doi.org/10.1007/12_2010_74
Autor:
Tfa Tom de Greef, Ejm Emiel Hensen, Peter A. J. Hilbers, Ara Anja Palmans, Evgeny A. Pidko, Iaw Ivo Filot
Publikováno v:
Physical Chemistry Chemical Physics, 14(40), 13997-14002. Royal Society of Chemistry
The molecular origin of the isotope-induced diastereomeric enrichment in helical supramolecular polymers consisting of trialkylbenzene-1,3,5-tricarboxamides (BTAs) is studied using plane-wave DFT calculations. We demonstrate that the creation of a ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e21bde1b11276a5dbef63610513b070
https://doi.org/10.1039/c2cp42302b
https://doi.org/10.1039/c2cp42302b