Faculty Publications
Permanent URI for this communityhttps://idr.nitk.ac.in/handle/123456789/18736
Publications by NITK Faculty
Browse
5 results
Search Results
Item Chemical syntheses and salient features of azulenecontaining homo- And copolymers(Beilstein-Institut Zur Forderung der Chemischen Wissenschaften, 2021) Shetti, V.S.Azulene is a non-alternant, aromatic hydrocarbon with many exciting characteristics such as having a dipole moment, bright color, stimuli responsiveness, anti-Kasha photophysics, and a small HOMO-LUMO gap when compared to its isomer, naphthalene. These properties make azulene-containing polymers an intriguing entity in the field of functional polymers, especially for organic electronic applications like organic field-effect transistors (OFET) and photovoltaic (PV) cells. Since azulene has a fused five and seven-membered ring structure, it can be incorporated onto the polymer backbone through either of these rings or by involving both the rings. These azulene-connection patterns can influence the properties of the resulting polymers and the chemical synthesis in comparison to the electrochemical synthesis can be advantageous in obtaining desired patterns of substitution. Hence, this review article presents a comprehensive overview of the developments that have taken place in the last three decades in the field of chemical syntheses of azulene-containing homo- and copolymers, including brief descriptions of their key properties. © 2021 Beilstein-Institut Zur Forderung der Chemischen Wissenschaften. All rights reserved.Item Supramolecular columnar self-assembly of wedge-shaped rhodanine based dyes: Synthesis and optoelectronic properties(Elsevier B.V., 2019) Vinayakumara, D.R.; Kumar, S.; Vasudeva Adhikari, A.V.The development of small ?-conjugated functional organic molecules capable of forming supramolecular columnar self-assembly, is a rapidly growing area of material research. In this context, the present work describes the design and synthesis of a new series of wedge-shaped rhodanine derivatives with D-A configuration, viz. RA1–RA5. Their LC properties were studied by employing DSC, POM and XRD techniques. The mesophase behavior was investigated as a function of chain length, density and position of alkoxy terminals to understand structure-property relationship. Interestingly, the longer chain analog, i.e. RA3 demonstrated H-bonded disc-like macrocyclic structures, causing an imperative columnar hexagonal phase at ambient temperature. Further, their photophysical and electrochemical properties were evaluated. They showed a good dye property attributing to effective intramolecular interactions, as confirmed by experimental and theoretical studies. Conclusively, RA3 has been considered to be a potential candidate for its application in organic electronics. © 2018Item Boronic Acid-Based n-Type Semiconductor for Electronic Device Application(Springer, 2022) Kagatikar, S.; Dhanya, D.; Kekuda, D.; Satyanarayana, M.N.; Kulkarni, S.D.; Karkera, C.Electron transporting, or n-type, semiconductors can serve as charge-transport materials, and are ideal for use in organic electronic devices. Boron-based small organic molecules have garnered immense research attention as the heteroatom can effectively alter the electronic structures leading to excellent photophysical and electrochemical properties. A luminescent Schiff base (E)-(4-((2-(2-hydroxybenzoyl)hydrazono)methyl)phenyl)boronic acid (SHB) was prepared by a one-pot condensation reaction between salicyloyl hydrazide and formylphenylboronic acid. The synthesized molecule was chemically characterized by infrared spectroscopy, nuclear magnetic resonance spectroscopy, and mass spectrometry. The blue-emitting boronic acid-derived molecule displayed intramolecular charge transfer, high carrier concentration, good thermal stability, a reversible reduction tendency and formation of uniform amorphous thin films. A diode was successfully fabricated via a solution processing technique with an ideality factor of 7.76. Further, AC conductivity, dielectric constant, dielectric loss, and capacitance values in a frequency range of 10–1000 Hz were extracted from dielectric studies. The dielectric constant of SHB was found to be 9.71 with an AC conductivity of 6.34 × 10−9 Ω−1 cm−1 at 1000 Hz. Graphical Abstract: [Figure not available: see fulltext.] © 2022, The Author(s).Item Pyrene-based chalcones as functional materials for organic electronics application(Elsevier Ltd, 2023) Kagatikar, S.; Dhanya, D.; Kekuda, D.; Satyanarayana, M.N.; Kulkarni, S.D.; Sudhakar, Y.N.; Vatti, A.K.; Sadhanala, A.Though new generation organic electronic devices have evolved from mere scientific perceptions to real-life marketed applications, considerably less research attention has been focused on n-type or electron transporting small molecule semiconductors. The present study is focused on the exploration of structural, thermal, electrochemical, electrical, and optical properties of two pyrene-based chalcones: PC1 and PC2, synthesized through Claisen Schmidt condensation reaction. The chalcones displayed good thermal stability and wide bandgap n-type semiconducting behaviour with high charge carrier concentration and dielectric constant. The experimental evidences including fluorescence measurements, nanoaggregate size, and morphology analysis, supported by DFT calculations and molecular dynamic simulations advocated the intramolecular charge transfer and aggregation-induced enhanced emission features of the molecules. Successful fabrication of a diode in combination with the current-voltage characteristics established the candidature of PC1 and PC2 for electro-optical devices. The dielectric studies were performed to measure dielectric constant and AC conductivity at different frequency ranges. The cyclic voltammetry and AC impedance response of PC2 differed from PC1 due to the inclusion of a fluorine atom in the molecular scaffold. Further, the functional implication of PC2 as an electrode material was explored by constructing a supercapacitor, which offered a specific capacitance of 220 Fg-1 at a scan rate of 10 mV s−1. Moreover, these chalcone-based organic semiconductors displayed high thermal and charge carrier concentration as well as compatibility with other layers in an OLED device. Hence PC1/PC2 can be further investigated as dopants along with other emissive layers as host materials in OLEDs. © 2022 Elsevier B.V.Item Orthovanillin azine ester as a potential functional material for organic electronic devices(Elsevier B.V., 2023) Kagatikar, S.; Acharya, S.; Mp, Y.; Dhanya, D.; Kekuda, D.; Abdul Salam, A.A.; Sudhakar, S.N.; Mn, S.; De, S.The present study reports the synthesis of OVAE, an ester of ortho-vanillin azine, and its structural characterization using spectral and single crystal-XRD studies. Intermolecular interactions of OVAE are investigated using the Hirshfield surface analysis, 3D Hirshfield surface maps, 2D fingerprint plots, and electrostatic energy frameworks. Good thermal stability in thermogravimetric analysis, irreversible redox peaks in electrochemical studies, high carrier concentration and dielectric constant in electrical measurements, uniform films observed upon surface morphology examination, fabrication of a diode, the obtained current-voltage characteristics, dielectric constant and frequency-dependent AC conductivities directed towards the use of OVAE as a potential semiconducting functional material in suitable electronic devices. Based on cyclic voltammetry and AC impedance response, the performance of OVAE as an electrode material is explored by constructing a supercapacitor, which exhibited a specific capacitance of 56 Fg−1 at 10 mV s−1. © 2023 Elsevier B.V.