2013
DOI: 10.1002/marc.201300845
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Directing Self‐Assembly of Nanoscopic Cylindrical Diblock Brush Terpolymers into Films with Desired Spatial Orientations: Expansion of Chemical Composition Scope

Abstract: Diblock brush terpolymers (DBTs) with different fluorinated methacrylate-based block segments are synthesized through sequential ring-opening metathesis polymerizations and are used to prepare polymer thin films with predictable film thicknesses. These DBTs exhibit preferable substrate vertical alignments within the films, induced by the relatively lower surface energy of the fluorinated structural components, together with the overall cylindrical morphology of the brush architecture.

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Cited by 20 publications
(17 citation statements)
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“…Pairs of fluorine‐related ions F − , CF 3 − , C 2 F 6 CHO − , and C 2 F 6 OC 5 H 9 O − at m/z 19, 69, 167, and 239 were chosen to calculate the fluorine fractional surface coverage K (%) for the thin films using Eqns . The fluorine surface coverages of DBT and HB films were ~88% and ~93%, respectively, which was in agreement with previous studies . This result indicates virtually complete surface coverage of fluorinated components, as designed.…”
Section: Resultssupporting
confidence: 92%
See 1 more Smart Citation
“…Pairs of fluorine‐related ions F − , CF 3 − , C 2 F 6 CHO − , and C 2 F 6 OC 5 H 9 O − at m/z 19, 69, 167, and 239 were chosen to calculate the fluorine fractional surface coverage K (%) for the thin films using Eqns . The fluorine surface coverages of DBT and HB films were ~88% and ~93%, respectively, which was in agreement with previous studies . This result indicates virtually complete surface coverage of fluorinated components, as designed.…”
Section: Resultssupporting
confidence: 92%
“…This ratio (Φ) can be calculated as follows: normalΦ=YAYR×100% where Y A and Y R are the SI yields of the detected ions from analyte and reference, respectively. The F − ratio for DBT films was 50%, which is comparable to a previous X‐ray photoelectron spectroscopy result with similar components . However, the ratios for larger fluorine molecular ions (CF 3 − , C 2 F 6 CHO − , and C 2 F 6 OC 5 H 9 O − ) were substantially lower than that of the F − ion.…”
Section: Resultssupporting
confidence: 80%
“…The RAFT polymerization of 1,1,1‐trifluoro‐2‐(trifluoromethyl)−2‐hydroxy‐4‐methyl‐5‐pentyl methacrylate (BTFHMBMA) was used to synthesize the fluorinated macromonomers 3 and 4 ( M3 , NB‐PBTFHMBMA 17 and M4 , NB‐PBTFHMBMA 19 ). The preparation and characterization of these macromonomers are reported elsewhere …”
Section: Resultsmentioning
confidence: 99%
“…[290], polylactate groups [291,292,293], polypeptide chains [294], polyacrylate or substituted polystyrene chains [295], nitroxide groups [296], fluorescent groups [297], a perfluorooctyl group [298], perfluorocarboxylic acid groups [299], and a fullerene-carbene adduct [300]; (2) norbornene in the presence of Fe 3 O 4 nanoparticles [301]; (3) norbornenes in the presence of an allylated lanthanide salen complex [302]; (4) norbornyl-acac-like systems complexed to terbium [303] or to an iridium-pyrazolone complex (e.g. 71) [304];…”
Section: Polymerization Reactionsmentioning
confidence: 99%