Multi-end functionalised polymer additives synthesised by living anionic polymerisation—the impact of additive molecular structure upon surface properties
Literature Information
Lian R. Hutchings, Richard L. Thompson
Numerous applications require specific properties at polymer surfaces that differ from the bulk. Herein we describe the novel synthesis of a series of multi-end functionalised poly(styrene) and poly(isoprene) additives carrying 1 to 3 fluoroalkyl (CF) groups. The additives were prepared by endcapping the living chain ends of polymers prepared via living anionic polymerisation. The resulting polymers have been used as additives to render the surface of polymer films hydrophobic/lipophobic and we have characterised these polymer films using static contact angle measurements with water as the contact fluid. We have found that the additive molecular weight, the number of CF groups, additive concentration and annealing conditions have a significant impact upon the resulting surface properties. Increasing the additive concentration and/or number of CF groups resulted in higher contact angles whereas increasing the molecular weight of additive reduced contact angles and surface hydrophobicity. It has been discovered that these additives undergo rapid adsorption to the surface of a thin film in the time taken to produce the film by spin coating and the result is significantly enhanced surface properties. Annealing polystyrene films above the glass transition temperature revealed some interesting behaviour in so much that it demonstrated that on many occasions it is preferable to anneal films containing very small quantities of additive rather than to simply add greater quantities of additive. In addition to contact angles measurements, Rutherford backscattering (RBS) analysis has been carried out on examples of modified poly(isoprene) films to quantitatively analyse the effect of additive molecular weight and number of fluoroalkyl groups on the near surface elemental composition of the modified thin films and confirming the relationship (described above) between these additive molecular parameters and surface adsorption. Finally, we have described a model which compares the behaviour of the additives in thin films to surfactants in solution.
Recommended Journals
Related Literature
Photoelectron spectroscopy and density functional calculations of CnSm− (n = 2–7; m = 1, 2) clusters
Xi-Ling Xu, Xiao-Jiao Deng, Hong-Guang Xu, Wei-Jun Zheng
DOI: 10.1039/C5CP04482K
Solvent-shared pairs of densely charged ions induce intense but short-range supra-additive slowdown of water rotation
Ana Vila Verde, Mark Santer, Reinhard Lipowsky
DOI: 10.1039/C5CP05726D
Interactions of hydrogen with the iron and iron carbide interfaces: a ReaxFF molecular dynamics study
Chenyu Zou, Sumathy Raman
DOI: 10.1039/C5CP06108C
Effective rate constant for nanostructured heterogeneous catalysts
Leila Rajabi, S. C. Hendy
DOI: 10.1039/C5CP04448K
Enhanced field-emission of silver nanoparticle–graphene oxide decorated ZnO nanowire arrays
Guojing Wang, Jiecui Liao, Chienhua Chen, Shasha Lv, Chuanqing Shi
DOI: 10.1039/C5CP05036G
The effect of iron re-deposition on the corrosion of impurity-containing magnesium
Daniel Höche, Carsten Blawert, Sviatlana V. Lamaka, Nico Scharnagl, Chamini Mendis
DOI: 10.1039/C5CP05577F
Physicochemical perspectives (aggregation, structure and dynamics) of interaction between pluronic (L31) and surfactant (SDS)
G. K. S. Prameela, B. V. N. Phani Kumar, A. Pan, V. K. Aswal, J. Subramanian, A. B. Mandal, S. P. Moulik
DOI: 10.1039/C5CP04910E
Probing electrode/electrolyte interfaces in situ by X-ray spectroscopies: old methods, new tricks
Robert S. Weatherup
DOI: 10.1039/C5CP04058B
Methane partial oxidation using FeOx@La0.8Sr0.2FeO3−δ core–shell catalyst – transient pulse studies
Arya Shafiefarhood, Joseph Clay Hamill, Luke Michael Neal, Fanxing Li
DOI: 10.1039/C5CP05583K
S-doped mesoporous nanocomposite of HTiNbO5 nanosheets and TiO2 nanoparticles with enhanced visible light photocatalytic activity
Ruirui Han, Hongmei Ji, Tao Sun, Jin Zhao, Ningna Chen, Jing Chen, Xuefeng Guo, Wenhua Hou, Weiping Ding
DOI: 10.1039/C5CP06555K
You might also like
What is 3-Fluoro-2-methylbenzylamine (CAS: 771573-36-5)?
3-Fluoro-2-methylbenzylamine is an organic compound with the CAS number 771573-3...
Is Tert-butyl 2-(oxetan-3-ylidene)acetate (CAS: 1207175-03-8) safe?
Tert-butyl 2-(oxetan-3-ylidene)acetate is considered safe for its intended uses ...
What precautions should be taken when handling 4-Acetyl-2-fluorobenzonitrile (CAS: 214760-18-6)?
Proper personal protective equipment (PPE) such as gloves, goggles, and a lab co...
How is 2-Ethyl-4-methyl-1,3-thiazole (CAS: 15679-12-6) typically synthesized?
2-Ethyl-4-methyl-1,3-thiazole is commonly synthesized via the reaction of thiour...
How should 5',5''-([2,2'-Bithiophene]-5,5'-diyl)bis(([1,1':3',1''-terphenyl]-4,4''-dicarboxylic acid)) (CAS: 1227780-71-3) be stored?
This compound should be stored in a cool, dry place away from direct sunlight an...
What regulatory guidelines apply to L-Lysine Acetate Salt (CAS: 52315-92-1)?
L-Lysine Acetate Salt (CAS: 52315-92-1) is subject to various regulatory guideli...
Is 6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) safe?
6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) is generally conside...
What are the physical and chemical properties of 1,1'-Sulfonylbis(1H-imidazole) (CAS: 7189-69-7)?
1,1'-Sulfonylbis(1H-imidazole) is a crystalline solid with a molecular weight of...
What industries use 4-methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5)?
4-Methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5) is primarily used i...
How should waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) be handled?
Waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) should be ...
Source Journal
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.











![2-Methyl-2-propanyl [(2S)-1-hydroxy-3-(4-hydroxyphenyl)-2-propanyl]carbamate structure 2-Methyl-2-propanyl [(2S)-1-hydroxy-3-(4-hydroxyphenyl)-2-propanyl]carbamate structure](https://static.chemtradehub.com/structs/833/83345-46-4-eec2.webp)


