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dc.contributor.authorNUTHANAKANTI, ASHOKen_US
dc.contributor.authorSRIVATSAN, SEERGAZHI G.en_US
dc.date.accessioned2019-07-01T05:35:44Z
dc.date.available2019-07-01T05:35:44Z
dc.date.issued2017-07en_US
dc.identifier.citationACS Applied Materials & Interfaces, 9(27), 22864-22874.en_US
dc.identifier.issn1944-8244en_US
dc.identifier.issn1944-8252en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3297
dc.identifier.urihttps://doi.org/10.1021/acsami.7b06037en_US
dc.description.abstractSupramolecular synthons based on nucleic acid components, nucleobases and nucleosides, and their derivatives have been highly useful in constructing wide varieties of nanoarchitectures. While most of the design strategies have focused on developing biocompatible delivery vehicles, the potential of nucleoside hybrids in assembling smart materials with tunable and sensing properties, though challenging, is gaining significant attention. Here, we describe the development of novel functional materials with surface tunability and metal-ion responsiveness by using simple nucleolipid supramolecular synthons derived by attaching various fatty acids to the 3′-O or 3′,5′-O positions of the sugar residue of thymidine nucleoside. 3′,5′-O-Difatty acid-substituted thymidines formed typical organogels in pure organic solvents, whereas, 3′-O-monofatty acid-substituted thymidine nucleolipids formed water-induced gels. A detailed morphological and structural analysis using microscopy, single-crystal and powder X-ray diffraction, and NMR techniques clearly revealed the molecular interactions invoked by nucleobase, sugar, fatty acid chain, and water in setting up the path for hierarchical self-assembly and gelation of thymidine nucleolipids. Interestingly, the surface property of the xerogel film fabricated using 3′-O-monosubstituted nucleolipid gels could be switched from highly hydrophobic to hydrophilic and vice versa depending on the nature of the organic solvent–water mixture used in the gelation process. On the contrary, the gelation process of disubstituted thymidine nucleolipids was highly sensitive to the presence of Hg2+ ions as the metal ion formed a T–Hg–T base pair, thereby disrupting the H-bonding interactions that favored the gelation. Taken together, straightforward synthesis and modification-dependent gelation behavior, surface tunability, and metal-ion responsiveness underscore the potential of these supramolecular nucleolipid synthons in constructing novel functional materials.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectSurface-Tuneden_US
dc.subjectGels Based on Nucleolipidsen_US
dc.subjectMetal-Ion-Responsiveen_US
dc.subjectHierarchical structuresen_US
dc.subjectMetal-ion sensoren_US
dc.subjectNucleolipidsen_US
dc.subjectSelf-assemblyen_US
dc.subjectSuperhydrophobicityen_US
dc.subjectSupramolecular gelsen_US
dc.subject2017en_US
dc.titleSurface-Tuned and Metal-Ion-Responsive Supramolecular Gels Based on Nucleolipidsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleACS Applied Materials & Interfacesen_US
dc.publication.originofpublisherForeignen_US
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