Literature DB >> 21495098

Electron-rich iron/ruthenium arylalkynyl complexes for third-order nonlinear optics: redox-switching between three states.

Nicolas Gauthier1, Gilles Argouarch, Frédéric Paul, Loic Toupet, Abdelkader Ladjarafi, Karine Costuas, Jean-François Halet, Marek Samoc, Marie P Cifuentes, T Christopher Corkery, Mark G Humphrey.   

Abstract

The new [(η(2)-dppe)(η(5)-C(5)Me(5))Fe(C≡C-1,4-C(6)H(4)C≡C)Ru(η(2) -dppe)(2) C≡C(C(6)H(5))] complex (3-H) and its hexanuclear relative [{(η(2)-dppe)(η(5)-C(5) Me(5))Fe(C≡C-1,4-C(6)H(4)-C≡C)Ru(η(2)-dppe)(2)(C≡C-1,4-C(6)H(4)C≡C)(3)(1,3,5-C(6)H(3))] (4) have been synthesized and characterized. The linear and cubic nonlinear optical properties of these compounds in their various redox states have been studied along with those of the analogous complexes [(η(2)-dppe)(η(5)-C(5)Me(5))Fe(C≡C-1,4-C(6)H(4)C≡C)Ru(η(2)-dppe)(2)R][PF(6)](n) (n=0-2; R=Cl, 2-Cl; R=C≡C(4-C(6)H(4)NO(2)),3-NO(2)). We show that molecules exhibiting large third-order nonlinearities can be obtained by assembling such dinuclear Fe/Ru units around a central 1,3,5-substituted C(6)H(3) core. These data are discussed with a particular emphasis on the large changes in their nonlinear (third-order) optical properties brought about by oxidation. Experimental and computational (DFT) evidence for the electronic structures of these compounds in their various redox states is presented using 3-H(n+) as a prototypical model. Single crystals of this complex in its mono-oxidized state (3-H[PF(6)]) provide the first structural data for such carbon-rich Fe(III) /Ru(II) heteronuclear mixed-valent (MV) systems. Although experimental evidence for the structure of the dioxidized states was more difficult to obtain, the theoretical study reveals that 3-H(2+) can be considered to have a biradical structure with two independent spins. The low-lying absorptions that appear in the near-infrared (NIR) range for all these compounds following oxidation correspond to intervalence charge-transfer (IVCT) bands for the mono-oxidized states and to ligand-to-metal charge-transfer (LMCT) transitions for the dioxidized states. These play a crucial role in the strong optical modulation achieved. The possibility of accessing additional states with distinct linear or nonlinear optical properties is also briefly discussed.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Year:  2011        PMID: 21495098     DOI: 10.1002/chem.201003427

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  Computational investigation on redox-switchable nonlinear optical properties of a series of polycyclic p-quinodimethane molecules.

Authors:  Yong-Qing Qiu; Wen-Yong Wang; Na-Na Ma; Cun-Huan Wang; Meng-Ying Zhang; Hai-Yan Zou; Peng-Jun Liu
Journal:  J Mol Model       Date:  2013-11-17       Impact factor: 1.810

2.  Theoretical modelling of photoswitching of hyperpolarisabilities in ruthenium complexes.

Authors:  Benjamin J Coe; Aggelos Avramopoulos; Manthos G Papadopoulos; Kristine Pierloot; Steven Vancoillie; Heribert Reis
Journal:  Chemistry       Date:  2013-10-10       Impact factor: 5.236

3.  Transition metals induce control of enhanced NLO properties of functionalized organometallic complexes under laser modulations.

Authors:  S Taboukhat; N Kichou; J-L Fillaut; O Alévêque; K Waszkowska; A Zawadzka; A El-Ghayoury; A Migalska-Zalas; B Sahraoui
Journal:  Sci Rep       Date:  2020-09-17       Impact factor: 4.379

  3 in total

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