Naphthalimide luminogens: structure-property relationships and sensing applications

dc.contributor.authorMeher, Niranjan
dc.date.accessioned2020-07-03T12:24:29Z
dc.date.accessioned2023-10-19T12:11:23Z
dc.date.available2020-07-03T12:24:29Z
dc.date.available2023-10-19T12:11:23Z
dc.date.issued2019
dc.descriptionSupervisor: Parameswar Krishnan Iyeren_US
dc.description.abstractThe research works presented in this thesis is focused on developing new strategies to control the ACQ/AIE phenomenon in naphthalimide (NI) derivatives. In particular, these research projects include the systematic tuning of condensed state properties and supramolecular self-assembly of the NIs by simple yet judicious structural manipulations. It has been unveiled that the intermolecular packing orientations play a significant role to control the supramolecular self-assembly and photophysical properties of the NIs over the electronic influence of the attached motifs. Apart from the different strategies developed to generate and tailor the condensed state properties of the NIs, the spontaneously formed fluorescent nanoassembly of the NIs have been employed for the detection of various environmentally toxic and biologically active analytes in physiological conditions.The content of this thesis entitled “Naphthalimide Luminogens: Structure-Property Relationships and Sensing Applications” has been divided into five chapters. Chapter 1 commences with a brief essay on the need and discovery of condensed state emission followed by its mechanistic aspects, applications and a short briefing on naphthalimide luminogens. Chapter 2 demonstrates the influence of non-conjugated pendant chains on the supramolecular self-assembly and solid-state emission properties in naphthalimide luminogens. This chapter also includes the detection and unfolding of multifunctional nonheme protein ferritin under physiological conditions using the fluorescent nanoassembly based on naphthalimides. Chapter 3 provides a conceptual insight on the functional group assisted fine-tuning of supramolecular self-assembly and condensed state luminescence in naphthalimides. Chapter 4 demonstrates the formyl group driven ultra-detection of hydrazine on multiple platforms. Chapter 5 demonstrates the spontaneous formation of long alkyl chain incited fluorescent naphthalimide nanosheets for sensitive detection of organic volatile contaminants in water via acceptor excited photoinduced electron transfer (a-PET) mechanism.Overall, development of new strategies to generate and systematically tune the condensed state emission and supramolecular self-assembly properties in traditional fluorophores have been reported. Besides, the spontaneously formed fluorescent supramolecules were used to detect biologically active and environmentally active analytes in aqueous media.en_US
dc.identifier.otherROLL NO.146122018
dc.identifier.urihttps://gyan.iitg.ac.in/handle/123456789/1449
dc.language.isoenen_US
dc.relation.ispartofseriesTH-2114;
dc.subjectCHEMISTRYen_US
dc.titleNaphthalimide luminogens: structure-property relationships and sensing applicationsen_US
dc.typeThesisen_US
Files
Original bundle
Now showing 1 - 2 of 2
No Thumbnail Available
Name:
Abstract-TH-2114_146122018.pdf
Size:
146.02 KB
Format:
Adobe Portable Document Format
Description:
ABSTRACT
No Thumbnail Available
Name:
TH-2114_146122018.pdf
Size:
27.91 MB
Format:
Adobe Portable Document Format
Description:
THESIS
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Plain Text
Description: