Polylutidines: Multifunctional Surfaces through Vaporâ Based Polymerization of Substituted Pyridinophanes
dc.contributor.author | Bally‐le gall, Florence | |
dc.contributor.author | Hussal, Christoph | |
dc.contributor.author | Kramer, Joshua | |
dc.contributor.author | Cheng, Kenneth | |
dc.contributor.author | Kumar, Ramya | |
dc.contributor.author | Eyster, Thomas | |
dc.contributor.author | Baek, Amy | |
dc.contributor.author | Trouillet, Vanessa | |
dc.contributor.author | Nieger, Martin | |
dc.contributor.author | Bräse, Stefan | |
dc.contributor.author | Lahann, Joerg | |
dc.date.accessioned | 2017-10-23T17:31:57Z | |
dc.date.available | 2018-11-01T16:42:01Z | en |
dc.date.issued | 2017-09-27 | |
dc.identifier.citation | Bally‐le gall, Florence ; Hussal, Christoph; Kramer, Joshua; Cheng, Kenneth; Kumar, Ramya; Eyster, Thomas; Baek, Amy; Trouillet, Vanessa; Nieger, Martin; Bräse, Stefan ; Lahann, Joerg (2017). "Polylutidines: Multifunctional Surfaces through Vaporâ Based Polymerization of Substituted Pyridinophanes." Chemistry â A European Journal 23(54): 13342-13350. | |
dc.identifier.issn | 0947-6539 | |
dc.identifier.issn | 1521-3765 | |
dc.identifier.uri | https://hdl.handle.net/2027.42/138923 | |
dc.description.abstract | We report a new class of functionalized polylutidine polymers that are prepared by chemical vapor deposition polymerization of substituted [2](1,4)benzeno[2](2,5)pyridinophanes. To prepare sufficient amounts of monomer for CVD polymerization, a new synthesis route for ethynylpyridinophane has been developed in three steps with an overall yield of 59â %. Subsequent CVD polymerization yielded wellâ defined films of poly(2,5â lutidinyleneâ coâ pâ xylylene) and poly(4â ethynylâ 2,5â lutidinyleneâ coâ pâ xylylene). All polymers were characterized by infrared reflectionâ absorption spectroscopy, ellipsometry, contact angle studies, and Xâ ray photoelectron spectroscopy. Moreover, ζâ potential measurements revealed that polylutidine films have higher isoelectric points than the corresponding polyâ xylylene surfaces owing to the nitrogen atoms in the polymer backbone. The availability of reactive alkyne groups on the surface of poly(4â ethynylâ 2,5â lutidinyleneâ coâ pâ xylylene) coatings was confirmed by spatially controlled surface modification by means of Huisgen 1,3â dipolar cycloaddition. Compared to the more hydrophobic polyâ pâ xylylyenes, the presence of the heteroatom in the polymer backbone of polylutidine polymers resulted in surfaces that supported an increased adhesion of primary human umbilical vein endothelial cells (HUVECs). Vaporâ based polylutidine coatings are a new class of polymers that feature increased hydrophilicity and increased cell adhesion without limiting the flexibility in selecting appropriate functional side groups.Coat of many nitrogens! Chemical vapor deposition based polymers have been widely used as biomedical interfaces, but all of these coatings are restricted to simple allâ carbon backbones. For the first time, a class of functionalized lutidine polymers has been prepared by chemical vapor deposition (see figure). This reactive coating opens new perspectives for the design of new cell biomedical applications. | |
dc.publisher | Springer Science+Business Media | |
dc.publisher | Wiley Periodicals, Inc. | |
dc.subject.other | alkynes | |
dc.subject.other | click chemistry | |
dc.subject.other | pyridinophanes | |
dc.subject.other | reactive coatings | |
dc.subject.other | chemical vapor deposition | |
dc.title | Polylutidines: Multifunctional Surfaces through Vaporâ Based Polymerization of Substituted Pyridinophanes | |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | |
dc.subject.hlbsecondlevel | Chemistry | |
dc.subject.hlbtoplevel | Science | |
dc.description.peerreviewed | Peer Reviewed | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/138923/1/chem201700901.pdf | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/138923/2/chem201700901_am.pdf | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/138923/3/chem201700901-sup-0001-misc_information.pdf | |
dc.identifier.doi | 10.1002/chem.201700901 | |
dc.identifier.source | Chemistry â A European Journal | |
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dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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