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Tuning the surface activity and micellization of closo-dodecaborate-based dianionic surfactants via linker and counterion selection
ID Hleli, Belhssen (Author), ID Ogrin, Peter (Author), ID Tošner, Zdeněk (Author), ID Medoš, Žiga (Author), ID Křížek, Tomáš (Author), ID Šarac, Bojan (Author), ID Urbič, Tomaž (Author), ID Bešter-Rogač, Marija (Author), ID Matějíček, Pavel (Author)

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Abstract
o understand the impact of alkaline counterions on the self-assembly of atypical dianionic surfactants, we synthesized a series of novel amphiphilic compounds featuring a bulky dianionic head based on closo-dodecaborate and a hydrophobic alkoxy tail connected via short linkers of different complexation ability toward alkaline cations. The synthetic strategy relied on the opening of cyclic oxonium derivatives by activated alcohol, enabling the attachment of hydrophobic chains to the boron cluster framework. The synthesis of novel surfactants with high cationic purity free from contaminating ions or additional inorganic salts is described. Self-assembly of the dodecaborate-based surfactants at the air–water interface and in aqueous solutions was investigated using tensiometry, various NMR spectroscopy techniques, dynamic light scattering, and all-atom MD simulations. Interestingly, despite their dianionic heads, the surfactants form compact monolayers in cases in which efficient binding of counterions to surfactant dianions occurs. MD simulations suggested relatively small surfactant micelles above the critical micelle concentration, which was confirmed by light scattering analysis. There is evidence that their aggregation number and morphology are strongly dependent on counterion immobilization. The mobility of counterions was observed directly by $^7$Li, $^{23}$Na, $^{39}$K, and $^{133}$Cs NMR spectroscopy, which allowed us to understand the binding abilities of linkers and dianionic heads toward counterions.

Language:English
Keywords:surface activity, micellization, closo-dodecaborate-based surfactants, counterions
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Publication status:Published
Publication version:Version of Record
Year:2025
Number of pages:Str. 32650-32661
Numbering:Vol. 41, iss. 48
PID:20.500.12556/RUL-179692 This link opens in a new window
UDC:544.72
ISSN on article:0743-7463
DOI:10.1021/acs.langmuir.5c04598 This link opens in a new window
COBISS.SI-ID:263697923 This link opens in a new window
Publication date in RUL:20.02.2026
Views:142
Downloads:21
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Record is a part of a journal

Title:Langmuir
Shortened title:Langmuir
Publisher:American Chemical Society
ISSN:0743-7463
COBISS.SI-ID:3267855 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:površinska aktivnost, micelizacija, surfaktanti na osnovi closo-dodekaborana, protiioni

Projects

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:N1-0186-2021
Name:Metalcarborani kot edinstveno izhodišče za pripravo funkcionalnih nanostrukturiranih in polimernih materialov

Funder:Czech Science Foundation
Funding programme:LA CEUS bilateral grant
Project number:21-20008K

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