Mixed Self‐Assembled Monolayers with Internal Urea Group on Silica Surface. Issue 35 (19th December 2017)
- Record Type:
- Journal Article
- Title:
- Mixed Self‐Assembled Monolayers with Internal Urea Group on Silica Surface. Issue 35 (19th December 2017)
- Main Title:
- Mixed Self‐Assembled Monolayers with Internal Urea Group on Silica Surface
- Authors:
- Meillan, Matthieu
Buffeteau, Thierry
Le Bourdon, Gwenaëlle
Thomas, Laurent
Degueil, Marie
Heuzé, Karine
Bennetau, Bernard
Vellutini, Luc - Abstract:
- Abstract: In this study, we report the successful grafting on silica surfaces by the coadsorption method, of mixed nitrobenzyl ester‐/methyl‐terminated self‐assembled monolayers (SAMs), with ratios of two coupling agents (30/70) and (10/90). We show that the preparation of mixed monolayers using two organosilanes with internal urea groups in the alkyl chain seems to be appropriate to obtain a monolayer composition similar to the molar ratio of the two silanes in the deposition solution. This behavior could be due to the presence of the polar urea groups in the molecular structure of both organosilanes which allows them to have the same ability of self‐assembly by hydrogen‐bonding and also the same affinity with the hydrophilic surface. To locate the ester functions at the surface of the mixed monolayers, we investigated the covalent immobilization of amino functionalized gold nanoparticles (GNPs) as nanoscale marker. Polarization modulation infrared reflection‐adsorption spectroscopy (PM‐IRRAS) and atomic force microscopy (AFM) were used to monitor the chemical modifications of the silica surfaces and to demonstrate the successful attachment of gold nanoparticles onto the modified surfaces. Finally, we show that the mixed SAMs were grafted with a phase separation. Abstract : Successful grafting on silica surfaces by the coadsorption method, of mixed nitrobenzyl ester‐/methyl‐terminated SAMs, with ratios of two coupling agents (30/70) and (10/90). The preparation of mixedAbstract: In this study, we report the successful grafting on silica surfaces by the coadsorption method, of mixed nitrobenzyl ester‐/methyl‐terminated self‐assembled monolayers (SAMs), with ratios of two coupling agents (30/70) and (10/90). We show that the preparation of mixed monolayers using two organosilanes with internal urea groups in the alkyl chain seems to be appropriate to obtain a monolayer composition similar to the molar ratio of the two silanes in the deposition solution. This behavior could be due to the presence of the polar urea groups in the molecular structure of both organosilanes which allows them to have the same ability of self‐assembly by hydrogen‐bonding and also the same affinity with the hydrophilic surface. To locate the ester functions at the surface of the mixed monolayers, we investigated the covalent immobilization of amino functionalized gold nanoparticles (GNPs) as nanoscale marker. Polarization modulation infrared reflection‐adsorption spectroscopy (PM‐IRRAS) and atomic force microscopy (AFM) were used to monitor the chemical modifications of the silica surfaces and to demonstrate the successful attachment of gold nanoparticles onto the modified surfaces. Finally, we show that the mixed SAMs were grafted with a phase separation. Abstract : Successful grafting on silica surfaces by the coadsorption method, of mixed nitrobenzyl ester‐/methyl‐terminated SAMs, with ratios of two coupling agents (30/70) and (10/90). The preparation of mixed monolayers using two organosilanes with internal urea groups in the alkyl chain seems to be appropriate to obtain a monolayer composition similar to the molar ratio of the two silanes in the deposition solution. … (more)
- Is Part Of:
- ChemistrySelect. Volume 2:Issue 35(2017)
- Journal:
- ChemistrySelect
- Issue:
- Volume 2:Issue 35(2017)
- Issue Display:
- Volume 2, Issue 35 (2017)
- Year:
- 2017
- Volume:
- 2
- Issue:
- 35
- Issue Sort Value:
- 2017-0002-0035-0000
- Page Start:
- 11868
- Page End:
- 11874
- Publication Date:
- 2017-12-19
- Subjects:
- Coatings -- Self-Assembled Monolayers -- Surface Reactions -- Thin Films
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.201702434 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.241000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5568.xml