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Photo-isomerisation of alkenyl complexes of platinum(II): structural, spectroscopic, kinetic and computational investigations

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  • Carmen R. Barone
  • Cecilia Coletti
  • Ruth J. McQuitty
  • Nicola J. Farrer
  • Giuseppe Lorusso
  • Luciana Maresca
  • Alessandro Marrone
  • Giovanni Natile
  • Concetta Pacifico
  • Simon Parsons
  • Nazzareno Re
  • Peter J. Sadler
  • Fraser J. White

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http://pubs.rsc.org/en/content/articlehtml/2013/dt/c3dt32354d
Original languageEnglish
Pages (from-to)6840-6851
Number of pages12
JournalDalton Transactions
Volume42
Issue number19
Early online date20 Feb 2013
DOIs
Publication statusPublished - 21 May 2013

Abstract

In this work UVA and blue light have been used to study photo-isomerisation about the CvC double bond in complexes of the type [PtCl(-CH=CHAr)(tmeda)] [Ar = C6H5, (E)-2a; 4-CH3O-C6H4, (E)-2b; 3-NO2-C6H4, (E)-2c; and 3-CH3O-C6H4, (E)-2d]. The progress of the reaction has been monitored by NMR spectroscopy following irradiation of the NMR sample. The NMR data have been complemented with X-ray diffractometric analysis of compounds (E)-2a-c and (Z)-2a. The kinetic data clearly indicate that a monomolecular mechanism is operating with the energy of the irradiating light influencing the rate of isomerisation but not the equilibrium composition, which is only slightly in favour of the Z isomer. DFT and TD-DFT theoretical investigations have been carried out to elucidate the nature of the main electronic transitions in the UV-Vis region and the mechanism of the photo-isomerisation reaction appears to proceed through a C=C bond twist process similar to that involved in purely organic molecules such as stilbene. In the Z isomer, one ortho proton of the phenyl group can come close to platinum (Pt···Hortho distance of 2.632 Å in (Z)-2a). In the case of 2c, the difference in chemical shift between the two ortho protons varies from 3.30 ppm in the Z isomer, where interaction with Pt is possible, to 0.60 ppm in the E isomer, where such interaction cannot take place. The analysis of the DFT orbitals indicates that the most shifted Hortho is that with a greater positive charge, pointing to an H-bond type of interaction.

    Research areas

  • RAY CRYSTAL-STRUCTURE, EFFECTIVE CORE POTENTIALS, DENSITY-FUNCTIONAL METHODS, HYDRIDO CARBONYL CLUSTER, PLANAR METAL-COMPLEXES, H-C INTERACTIONS, X-RAY, TRANSITION-METAL, HYDROGEN-BONDS, MOLECULAR CALCULATIONS

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