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Substituent and solvent effects on geometric and electronic structure of C5H5Ir(PH3)3 iridabenzene: A theoretical insight

  • Structure and Properties of Coordination Compounds
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Abstract

Using MPW1PW91 quantum chemical calculations, we report structures, frontier orbital analysis, natural bond analysis, and aromaticity of the C5H5Ir(PH3)3 iridabenzene and XC5H4Ir(PH3)3 para-substituted iridabenzenes. The substituent effects were estimated from the donor–acceptor interaction energies of the natural bond orbitals of substituent and iridabenzene frame. Nucleus-independent chemical shift (NICS) has been evaluated to understand the aromaticity. Time dependent density functional theory (TD-DFT) is used to calculate the energy, oscillatory strength and wavelength absorption maxima (λmax) of electronic transitions and their nature. Changes in hyperpolarizability of molecules are studied. Influence of solvent on the structure, frontier orbital energies, λmax, and hyperpolarizability of C5H5Ir(PH3)3 iridabenzene has been studied.

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Authors and Affiliations

  1. Department of Chemistry, Faculty of Basic Science, East Tehran Branch, Islamic Azad University, Qiam Dasht, Tehran, Iran

    R. Ghiasi & E. Amini

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  1. R. Ghiasi
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  2. E. Amini
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Correspondence to R. Ghiasi.

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Original Russian Text © 2015 R. Ghiasi, E. Amini.

The text was submitted by the authors in English. Zhurnal Strukturnoi Khimii, Vol. 56, No. 8, pp. 1545-1556, December, 2015.

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Ghiasi, R., Amini, E. Substituent and solvent effects on geometric and electronic structure of C5H5Ir(PH3)3 iridabenzene: A theoretical insight. J Struct Chem 56, 1483–1494 (2015). https://doi.org/10.1134/S0022476615080053

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  • DOI: https://doi.org/10.1134/S0022476615080053

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