2021
DOI: 10.1039/d0qo01110j
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Exploring the tubular self-assembly landscape of dinucleobase amphiphiles in water

Abstract: The tubular aqueous assembly of dinucleobase amphiphilic monomers endowed with anionic, neutral or cationic groups is investigated under diverse conditions.

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Cited by 6 publications
(4 citation statements)
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“…Dinucleobase derivatives GC and AU (Figure c) share a common structure designed to yield self-assembled nanotubes based on our own previous experience. The complementary nucleobases were connected through a rigid and linear p- phenylene block attached at the purine 8- and pyrimidine 5-positions. In this way, association through Watson–Crick pairing provides a 90° angle between monomers, which can favor the formation of unstrained rectangular assemblies ( i .…”
Section: Resultsmentioning
confidence: 99%
“…Dinucleobase derivatives GC and AU (Figure c) share a common structure designed to yield self-assembled nanotubes based on our own previous experience. The complementary nucleobases were connected through a rigid and linear p- phenylene block attached at the purine 8- and pyrimidine 5-positions. In this way, association through Watson–Crick pairing provides a 90° angle between monomers, which can favor the formation of unstrained rectangular assemblies ( i .…”
Section: Resultsmentioning
confidence: 99%
“…Some water soluble C 60 derivatives are also soluble in polar organic solvents. For example, water soluble C 60 derivatives bearing PEO chains (17,18) can also form spherical aggregates in THF. 81 For other C 60 -based amphiphiles bearing hydrophilic or polar groups, they may not be dissolved in pure water due to their relatively small HLB values.…”
Section: Self-assembly In Nonaqueous Solutionsmentioning
confidence: 99%
“…Organic amphiphilic molecules, including both artificial and naturally occurring surfactants, are important building blocks to construct supramolecular structures in solutions such as micelles, vesicles, tubes, and lyotropic liquid crystals. [11][12][13][14][15][16][17][18] Each of these amphiphiles has one or several alkyl chains as the hydrophobic part. The hydrophobic/hydrophobic interaction and van der Waals attraction among these alkyl chains, together with the hydration forces and/or electrostatic interaction caused by the hydrophilic headgroups, drive the selfassembly and finally lead to the formation of various supramolecular structures.…”
Section: Introductionmentioning
confidence: 99%
“…5, respectively). 44 The investigation of the aggregation was performed as a function of temperature, concentration and environment (which included solvent composition and pH). Even though, nanotube formation was reached for all compounds in varied experimental conditions, remarkable results were obtained when subtle changes in specific parameters or compound structure were applied.…”
Section: Nucleobasesmentioning
confidence: 99%