Sökning: onr:"swepub:oai:lup.lub.lu.se:8e876198-93d8-46ff-8e67-70e085287ac7" > C-12 vs C-3 substit...
Fältnamn | Indikatorer | Metadata |
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000 | 04317naa a2200469 4500 | |
001 | oai:lup.lub.lu.se:8e876198-93d8-46ff-8e67-70e085287ac7 | |
003 | SwePub | |
008 | 191115s2020 | |||||||||||000 ||eng| | |
024 | 7 | a https://lup.lub.lu.se/record/8e876198-93d8-46ff-8e67-70e085287ac72 URI |
024 | 7 | a https://doi.org/10.1016/j.colsurfb.2019.1105562 DOI |
040 | a (SwePub)lu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a art2 swepub-publicationtype |
072 | 7 | a ref2 swepub-contenttype |
100 | 1 | a Cautela, Jacopou Sapienza University of Rome4 aut |
245 | 1 0 | a C-12 vs C-3 substituted bile salts : An example of the effects of substituent position and orientation on the self-assembly of steroid surfactant isomers |
264 | 1 | b Elsevier BV,c 2020 |
520 | a Biomolecule derivatives are transversally used in nanotechnology. Deciphering their aggregation behavior is a crucial issue for the rational design of functional materials. To this end, it is necessary to build libraries of selectively functionalized analogues and infer general rules. In this work we enrich the highly applicative oriented collection of steroid derivatives, by reporting a rare example of C-12 selectively modified bile salt. While nature often exploits such position to encode functions, it is unusual and not trivial to prepare similar analogues in the laboratory. The introduction of a tert-butyl phenyl residue at C-12 provided a molecule with a self-assembly that remarkably switched from rigid pole-like structures to twisted ribbons at a biologically relevant critical temperature (∼25 °C). The system was characterized by microscopy and spectroscopy techniques and compared with the C-3 functionalized analogue. The twisted ribbons generate samples with a gel texture and a viscoelastic response. The parallel analysis of the two systems suggested that the observed thermoresponsive self-assemblies occur at similar critical temperatures and are probably dictated by the nature of the substituent, but involve aggregates with different structures depending on position and orientation of the substituent. This study highlights the self-assembly properties of two appealing thermoresponsive systems. Moreover, it adds fundamental insights hereto missing in the investigations of the relation between self-assembly and structure of synthetic steroids, which are valuable for the rational design of steroidal amphiphiles. | |
650 | 7 | a NATURVETENSKAPx Kemix Materialkemi0 (SwePub)104032 hsv//swe |
650 | 7 | a NATURAL SCIENCESx Chemical Sciencesx Materials Chemistry0 (SwePub)104032 hsv//eng |
650 | 7 | a NATURVETENSKAPx Biologix Biokemi och molekylärbiologi0 (SwePub)106022 hsv//swe |
650 | 7 | a NATURAL SCIENCESx Biological Sciencesx Biochemistry and Molecular Biology0 (SwePub)106022 hsv//eng |
653 | a Bile acid | |
653 | a Hydrogel | |
653 | a Steroid derivatives | |
653 | a Thermoresponsive self-assembly | |
700 | 1 | a Severoni, Emiliau Sapienza University of Rome4 aut |
700 | 1 | a Redondo-Gómez, Carlosu University of Costa Rica4 aut |
700 | 1 | a di Gregorio, Maria Chiarau Sapienza University of Rome4 aut |
700 | 1 | a Del Giudice, Alessandrau Sapienza University of Rome4 aut |
700 | 1 | a Sennato, Simonau Sapienza University of Rome4 aut |
700 | 1 | a Angelini, Robertau Sapienza University of Rome4 aut |
700 | 1 | a D'Abramo, Marcou Sapienza University of Rome4 aut |
700 | 1 | a Schillén, Karinu Lund University,Lunds universitet,Fysikalisk kemi,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Physical Chemistry,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH4 aut0 (Swepub:lu)fk1-ksc |
700 | 1 | a Galantini, Lucianou Sapienza University of Rome4 aut |
710 | 2 | a Sapienza University of Romeb University of Costa Rica4 org |
773 | 0 | t Colloids and Surfaces B: Biointerfacesd : Elsevier BVg 185q 185x 0927-7765 |
856 | 4 | u http://dx.doi.org/10.1016/j.colsurfb.2019.110556y FULLTEXT |
856 | 4 | u https://iris.uniroma1.it/bitstream/11573/1341758/1/Cautela_Bile-salts_2020.pdf |
856 | 4 8 | u https://lup.lub.lu.se/record/8e876198-93d8-46ff-8e67-70e085287ac7 |
856 | 4 8 | u https://doi.org/10.1016/j.colsurfb.2019.110556 |
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