Show simple item record

dc.contributor.advisorMaitra, Uday
dc.contributor.authorSahu, Manaranjan
dc.date.accessioned2025-01-01T11:37:51Z
dc.date.available2025-01-01T11:37:51Z
dc.date.submitted2024
dc.identifier.urihttps://etd.iisc.ac.in/handle/2005/6750
dc.description.abstractMetal ions play indispensable roles across diverse processes, both biological and abiological, but their significance in the formation of complex self-assembled structures is only beginning to be understood. Sodium cholate, a facially amphiphilic molecule, exhibits intriguing properties by self-assembling with metal ions to form gels. Studying its interaction with cadmium ions revealed the formation of diverse structures like particles, nanofibers, and nanorods/plates over time due to a pathway complexity involved in the gelation process. During our studies, it was discovered that the transformation from the nanofiber to the nanorod proceeds via fragmentation, followed by a secondary nucleation mechanism. We also enhanced the mechanical properties of silver cholate hydrogel (AgCh) by co-assembling it with a small amount of gadolinium ions, achieving a 4-fold increase in mechanical strength. This improvement resulted from a morphological transformation from nanoparticles to networks of nanofibrous, which led to a robust gel. Additionally, the silver cholate hydrogel was used as a host matrix for induction of room temperature phosphorescence from organic chromophores 1,3,5 tris(4 carboxyphenyl)benzene (TCB, green emission) and 1,4,5,8-naphthalenetetracarboxylate (NTCA, red emission). The phosphorescence was enhanced further in a co-assembled hydrogel matrix (GdAgCh). We also explored energy transfer from the triplet state of the phosphors to the singlet state of various fluorophores. It led to delayed luminescence and enhanced lifetime of the acceptor and can be considered an artificial light-harvesting system. This system shows good color tunability with persistence and stable luminescent hydrogel. Furthermore, we developed a lanthanide-based ‘turn-off’ sensor for the detection of water in organic solvents. We systematically quantify the water content in the organic solvents such as MeOH, EtOH, CH3CN, and THF. Our developed protocol is simple yet superior and can detect the presence of 0.1 to 5% water in these samples.en_US
dc.language.isoen_USen_US
dc.relation.ispartofseries;ET00760
dc.rightsI grant Indian Institute of Science the right to archive and to make available my thesis or dissertation in whole or in part in all forms of media, now hereafter known. I retain all proprietary rights, such as patent rights. I also retain the right to use in future works (such as articles or books) all or part of this thesis or dissertationen_US
dc.subjectSupramolecular Self-assemblyen_US
dc.subjectHydrogelen_US
dc.subjectPhosphorescenceen_US
dc.subjectSensingen_US
dc.subjectnanofiberen_US
dc.subjectnanoroden_US
dc.subjectsilver cholate hydrogelen_US
dc.subjectnanoparticlesen_US
dc.subject.classificationResearch Subject Categories::INTERDISCIPLINARY RESEARCH AREASen_US
dc.subject.classificationResearch Subject Categories::NATURAL SCIENCES::Chemistry::Organic chemistryen_US
dc.titleUnlocking the Potential of Metal Ions in the Formation of Diverse Self-assembled Structures, Room Temperature Phosphorescence, and Sensingen_US
dc.typeThesisen_US
dc.degree.namePhDen_US
dc.degree.levelDoctoralen_US
dc.degree.grantorIndian Institute of Scienceen_US
dc.degree.disciplineFaculty of Scienceen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record