Ambient Temperature Ligation of Diene Functional Polymer and Peptide Strands onto Cellulose via Photochemical and Thermal Protocols. Issue 12 (6th April 2014)
- Record Type:
- Journal Article
- Title:
- Ambient Temperature Ligation of Diene Functional Polymer and Peptide Strands onto Cellulose via Photochemical and Thermal Protocols. Issue 12 (6th April 2014)
- Main Title:
- Ambient Temperature Ligation of Diene Functional Polymer and Peptide Strands onto Cellulose via Photochemical and Thermal Protocols
- Authors:
- Tischer, Thomas
Claus, Tanja K.
Oehlenschlaeger, Kim K.
Trouillet, Vanessa
Bruns, Michael
Welle, Alexander
Linkert, Katharina
Goldmann, Anja S.
Börner, Hans G.
Barner‐Kowollik, Christopher - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>In the present contribution, two novel ambient temperature avenues are introduced to functionalize solid cellulose substrates in a modular fashion with synthetic polymer strands (poly(trifluoro ethyl methacrylate), PTFEMA, <italic>M</italic><sub>n</sub> = 4400 g mol<sup>−1</sup>, <italic>Đ</italic> = 1.18) and an Arg‐Gly‐Asp (RGD) containing peptide sequence. Both protocols rely on a hetero Diels–Alder reaction between an activated thiocarbonyl functionality and a diene species. In the first—thermally activated—protocol, the cellulose features surface‐expressed thiocarbonylthio compounds, which readily react with diene terminal macromolecules at ambient temperature. In the second protocol, the reactive ene species are photochemically generated based on a phenacyl sulfide‐decorated cellulose surface, which upon irradiation expresses highly reactive thioaldehyde species. The generated functional hybrid surfaces are characterized in‐depth via ToF‐SIMS and XPS analysis, revealing the successful covalent attachment of the grafted materials, including the spatially resolved patterning of both synthetic polymers and peptide strands using the photochemical protocol. The study thus provides a versatile platform technology for solid cellulose substrate modification via efficient thermal and photochemical ligation strategies. <boxed-text content-type="graphic" position="anchor"<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>In the present contribution, two novel ambient temperature avenues are introduced to functionalize solid cellulose substrates in a modular fashion with synthetic polymer strands (poly(trifluoro ethyl methacrylate), PTFEMA, <italic>M</italic><sub>n</sub> = 4400 g mol<sup>−1</sup>, <italic>Đ</italic> = 1.18) and an Arg‐Gly‐Asp (RGD) containing peptide sequence. Both protocols rely on a hetero Diels–Alder reaction between an activated thiocarbonyl functionality and a diene species. In the first—thermally activated—protocol, the cellulose features surface‐expressed thiocarbonylthio compounds, which readily react with diene terminal macromolecules at ambient temperature. In the second protocol, the reactive ene species are photochemically generated based on a phenacyl sulfide‐decorated cellulose surface, which upon irradiation expresses highly reactive thioaldehyde species. The generated functional hybrid surfaces are characterized in‐depth via ToF‐SIMS and XPS analysis, revealing the successful covalent attachment of the grafted materials, including the spatially resolved patterning of both synthetic polymers and peptide strands using the photochemical protocol. The study thus provides a versatile platform technology for solid cellulose substrate modification via efficient thermal and photochemical ligation strategies. <boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pghmh7d1rb" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></boxed-text></p> </abstract> … (more)
- Is Part Of:
- Macromolecular rapid communications. Volume 35:Issue 12(2014:Jun.)
- Journal:
- Macromolecular rapid communications
- Issue:
- Volume 35:Issue 12(2014:Jun.)
- Issue Display:
- Volume 35, Issue 12 (2014)
- Year:
- 2014
- Volume:
- 35
- Issue:
- 12
- Issue Sort Value:
- 2014-0035-0012-0000
- Page Start:
- 1121
- Page End:
- 1127
- Publication Date:
- 2014-04-06
- Subjects:
- Macromolecules -- Periodicals
Polymers -- Periodicals
Chemistry -- Periodicals
547.705 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/marc.201400088 ↗
- Languages:
- English
- ISSNs:
- 1022-1336
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5330.400000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3536.xml