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https://dspace.iiti.ac.in/handle/123456789/8751
Title: | Interfacing High-Energy Charge-Transfer States to a Near-IR Sensitizer for Efficient Electron Transfer upon Near-IR Irradiation |
Authors: | Pinjari, Dilip Patil, Yuvraj Misra, Rajneesh |
Keywords: | Charge transfer;Electron transport properties;Solvents;Charge transfer state;Computational studies;Effect of solvents;Electron exchange;Electron transfer;Excitation wavelength;Near-IR excitations;Optoelectronic applications;Excited states |
Issue Date: | 2020 |
Publisher: | Wiley-VCH Verlag |
Citation: | Pinjari, D., Alsaleh, A. Z., Patil, Y., Misra, R., & D'Souza, F. (2020). Interfacing high-energy charge-transfer states to a near-IR sensitizer for efficient electron transfer upon near-IR irradiation. Angewandte Chemie - International Edition, 59(52), 23697-23705. doi:10.1002/anie.202013036 |
Abstract: | Push–pull systems comprising of triphenylamine–tetracyanobutadiene (TPA-TCBD), a high-energy charge-transfer species, are linked to a near-IR sensitizer, azaBODIPY, for promoting excited-state CS. These systems revealed panchromatic absorption owing to intramolecular CT and near-IR absorbing azaBODIPY. Using electrochemical and computational studies, energy levels were established to visualize excited state events. Fs-TA studies were performed to monitor excited state CT events. From target analysis, the effect of solvent polarity, number of linked CT entities, and excitation wavelength dependence in governing the lifetime of CS states was established. Electron exchange between two TPA-TCBD entities in 3 seem to prolong lifetime of the CS state. We have been successful in demonstrating efficient CS upon both high-energy CT and low-energy near-IR excitations, signifying importance of these push–pull systems for optoelectronic applications operating in the wide optical window. © 2020 Wiley-VCH GmbH |
URI: | https://doi.org/10.1002/anie.202013036 https://dspace.iiti.ac.in/handle/123456789/8751 |
ISSN: | 1433-7851 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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