About: Ferrocene-Donor and 4,5-Dicyanoimidazole-Acceptor Moieties in Charge- Transfer Chromophores with p Linkers Tailored for Second-Order Nonlinear Optics     Goto   Sponge   NotDistinct   Permalink

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  • A series of new nonlinear optical chromophores (1?15) that were comprised of ferrocene-donor and 4,5-dicyanoimidazole-acceptor moieties and various p linkers of different length were synthesized. Support for the presence of significant DA interactions in these NLO-phores was obtained from the evaluation of the quinoid character of the 1,4-phenylene moieties and their electronic absorption spectra, which featured intense high-energy (HE) bands that were accompanied by less-intense low-energy (LE) bands. The redox behavior of these compounds was investigated by cyclic voltammetry (CV) and by rotating-disc voltammetry (RDV); their electrochemical gaps decreased steadily from 2.64 to 2.09 V. In addition to the experimentally obtained data, DFT calculations of their absorption spectra, HOMO/LUMO levels, and secondorder polarizabilities (b) (2w,w,w) were performed. A structure?property relationship study that was performed by systematically altering the p linker revealed that the intramolecular charge-transfer and nonlinear optical properties of these inorganic?organic hybrid DpA systems (1?15) were primarily affected by: 1) The presence of olefinic/acetylenic subunits; 2) the length of the p linker; and 3) the spatial arrangement (planarity) of the p linker.
  • A series of new nonlinear optical chromophores (1?15) that were comprised of ferrocene-donor and 4,5-dicyanoimidazole-acceptor moieties and various p linkers of different length were synthesized. Support for the presence of significant DA interactions in these NLO-phores was obtained from the evaluation of the quinoid character of the 1,4-phenylene moieties and their electronic absorption spectra, which featured intense high-energy (HE) bands that were accompanied by less-intense low-energy (LE) bands. The redox behavior of these compounds was investigated by cyclic voltammetry (CV) and by rotating-disc voltammetry (RDV); their electrochemical gaps decreased steadily from 2.64 to 2.09 V. In addition to the experimentally obtained data, DFT calculations of their absorption spectra, HOMO/LUMO levels, and secondorder polarizabilities (b) (2w,w,w) were performed. A structure?property relationship study that was performed by systematically altering the p linker revealed that the intramolecular charge-transfer and nonlinear optical properties of these inorganic?organic hybrid DpA systems (1?15) were primarily affected by: 1) The presence of olefinic/acetylenic subunits; 2) the length of the p linker; and 3) the spatial arrangement (planarity) of the p linker. (en)
Title
  • Ferrocene-Donor and 4,5-Dicyanoimidazole-Acceptor Moieties in Charge- Transfer Chromophores with p Linkers Tailored for Second-Order Nonlinear Optics
  • Ferrocene-Donor and 4,5-Dicyanoimidazole-Acceptor Moieties in Charge- Transfer Chromophores with p Linkers Tailored for Second-Order Nonlinear Optics (en)
skos:prefLabel
  • Ferrocene-Donor and 4,5-Dicyanoimidazole-Acceptor Moieties in Charge- Transfer Chromophores with p Linkers Tailored for Second-Order Nonlinear Optics
  • Ferrocene-Donor and 4,5-Dicyanoimidazole-Acceptor Moieties in Charge- Transfer Chromophores with p Linkers Tailored for Second-Order Nonlinear Optics (en)
skos:notation
  • RIV/00216275:25310/13:39896116!RIV14-GA0-25310___
http://linked.open...avai/predkladatel
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  • I, P(GAP106/12/0392)
http://linked.open...iv/cisloPeriodika
  • 2
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http://linked.open...dnocenehoVysledku
  • 74899
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  • RIV/00216275:25310/13:39896116
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  • nonlinear optics; imidazole; ferrocene; donor?acceptor systems; charge transfer (en)
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  • DE - Spolková republika Německo
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  • [C206D88A5083]
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  • Chemistry - An Asian Journal
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  • 8
http://linked.open...iv/tvurceVysledku
  • Bureš, Filip
  • Kulhánek, Jiří
  • Růžička, Aleš
  • Mikysek, Tomáš
  • Kuznik, Wojciech
  • Kityk, Iwan V.
http://linked.open...ain/vavai/riv/wos
  • 000314177300019
issn
  • 1861-4728
number of pages
http://bibframe.org/vocab/doi
  • 10.1002/asia.201200963
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  • 25310
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