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231226s2022 xx |||||o 00| ||eng c |
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|a 10.1021/acs.langmuir.2c01246
|2 doi
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|a pubmed24n1154.xml
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|a (DE-627)NLM346384664
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|a (NLM)36121768
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|a DE-627
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|a eng
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|a Costa, Telma
|e verfasserin
|4 aut
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|a Nanostructuring with Surfactants
|b The Self-Assembly of a New Poly(thiophene-phenylene) Conjugated Polymer Bearing Azacrown Ether Pendant Groups
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|c 2022
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|a Text
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Revised 04.10.2022
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a We report the synthesis of a new conjugated polymer bearing crown ether moieties, poly[(N(1-aza-[18]crown-6)carbamido)thiophene-2,5-diyl-alt-1,4-phenylene] (BG2). In water, BG2 forms a dispersion with a slightly cloudy appearance. We have studied the effect of adding surfactants, with different polar head groups, on these polymer-polymer aggregates. Special attention is given to the system with the anionic surfactant, sodium dodecyl sulfate (SDS). The combination of photophysical techniques with electrical conductivity, NMR (1H, 13C, and 27Na), DFT calculations, molecular dynamics simulations, and small-angle neutron scattering (SANS) provides a detailed picture on the behavior of the SDS/BG2 system in aqueous solution and in thin films. NMR, electric conductivity, and DFT results suggest that hydrophilic interactions occur between the polar headgroup of the surfactant (OSO3- Na+) and the aza-[18]-crown-6 moiety. DFT calculations confirmed the capability of BG2 to form stable complexes with the Na+ cations, where the cation can be either inside the azacrown cavity or sandwiched between the cavity and the polymer chain, which seem to determine the position of the surfactant hydrocarbon chain and, therefore, be responsible for the disruption of the BG2 aggregates and subsequent increase in the photoluminescence quantum yields. SANS measurements, made with hydrogenated and deuterated SDS in D2O, clearly show how micron-sized aggregates of BG2 are broken down by SDS and then how BG2 becomes preferentially incorporated within joint colloidal particles of BG2 and SDS with increasing [SDS]/[BG2] molar ratio
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|a Journal Article
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|a Knaapila, Matti
|e verfasserin
|4 aut
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|a Stewart, Beverly
|e verfasserin
|4 aut
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|a Ramos, M Luísa
|e verfasserin
|4 aut
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|a Justino, Licinia L G
|e verfasserin
|4 aut
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|a Valente, Artur J M
|e verfasserin
|4 aut
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|a Dalgliesh, Robert
|e verfasserin
|4 aut
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|a Rogers, Sarah E
|e verfasserin
|4 aut
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|a Kraft, Mario
|e verfasserin
|4 aut
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|a Allard, Sybille
|e verfasserin
|4 aut
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|a Scherf, Ullrich
|e verfasserin
|4 aut
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|a Burrows, Hugh D
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 38(2022), 39 vom: 04. Okt., Seite 11845-11859
|w (DE-627)NLM098181009
|x 1520-5827
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|g volume:38
|g year:2022
|g number:39
|g day:04
|g month:10
|g pages:11845-11859
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|u http://dx.doi.org/10.1021/acs.langmuir.2c01246
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