About: Property Tuning in Charge-Transfer Chromophores by Systematic Modulation of the Spacer between Donor and Acceptor     Goto   Sponge   NotDistinct   Permalink

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Description
  • Byla připravena série D-A chromoforů ve kterých byl systematicky obměňován spacer mezi DMA donory a CN akceptory. Všechny nové pusch-pull systémy jsou termálně stabilní kromě chromoforu 4b. V sérii a jsou DMA akceptory přímo navázány na centrální spacer, zatímco v sérii b jsou DMA donory odděleny dalším acetylenovým spacerem. X-ray krystalové struktury byly získány pro sedm nových, intenzivně barevných cílových sloučenin. V serii a jsou DMA kruhy vytočeny z roviny zbytku p-systému, zatímco celý konjuogvaný systém v sérii b je téměř planární. Silná D-A interakce byla zkoumána pomocí chinoidního charakteru DMA kruhů a pomocí IR a NMR spektroskopie. UV/Vis spektra vykazovala intenzivní bathochromě posunuté CT pásy, kdy nejnižší energetické přechody a optické mezery byly naměřeny pro dvoudimenzionální chromofory 6a a 6b. Redox chování připravených push-pull molekul bylo sledováno pomocí cyklické voltametrie (CV) a diferenční pulsní voltametri (DPV). V sérii 1b, 2b, 4b a 5b kdy je centrální spacer systema (cs)
  • A series of donor?acceptor chromophores was prepared in which the spacer separating 4-dimethylanilino (DMA) donor and C(CN)2 acceptor moieties is systematically varied. All of the new push?pull systems, except 4b, are thermally stable molecules. In series a, the DMA rings are directly attached to the central spacer, whereas in series b additional acetylene moieties are inserted. X-ray crystal structures were obtained for seven of the new, intensely colored target compounds. In series a, the DMA rings are sterically forced out of the mean plane of the residual p system, whereas the entire conjugated p system in series b is nearly planar. Support for strong donor?acceptor interactions was obtained through evaluation of the quinoid character of the DMA ring and by NMR and IR spectroscopy. The UV/Vis spectra feature bathochromically shifted, intense charge-transfer bands, with the lowest energy transitions and the smallest optical gap being measured for the two-dimensionally extended chromophores 6a and
  • A series of donor?acceptor chromophores was prepared in which the spacer separating 4-dimethylanilino (DMA) donor and C(CN)2 acceptor moieties is systematically varied. All of the new push?pull systems, except 4b, are thermally stable molecules. In series a, the DMA rings are directly attached to the central spacer, whereas in series b additional acetylene moieties are inserted. X-ray crystal structures were obtained for seven of the new, intensely colored target compounds. In series a, the DMA rings are sterically forced out of the mean plane of the residual p system, whereas the entire conjugated p system in series b is nearly planar. Support for strong donor?acceptor interactions was obtained through evaluation of the quinoid character of the DMA ring and by NMR and IR spectroscopy. The UV/Vis spectra feature bathochromically shifted, intense charge-transfer bands, with the lowest energy transitions and the smallest optical gap being measured for the two-dimensionally extended chromophores 6a and (en)
Title
  • Property Tuning in Charge-Transfer Chromophores by Systematic Modulation of the Spacer between Donor and Acceptor
  • Property Tuning in Charge-Transfer Chromophores by Systematic Modulation of the Spacer between Donor and Acceptor (en)
  • Modulace vlastností CT chromoforů systematickou změnou spaceru mezi donorem a akceptorem (cs)
skos:prefLabel
  • Property Tuning in Charge-Transfer Chromophores by Systematic Modulation of the Spacer between Donor and Acceptor
  • Property Tuning in Charge-Transfer Chromophores by Systematic Modulation of the Spacer between Donor and Acceptor (en)
  • Modulace vlastností CT chromoforů systematickou změnou spaceru mezi donorem a akceptorem (cs)
skos:notation
  • RIV/00216275:25310/07:00006064!RIV08-MSM-25310___
http://linked.open.../vavai/riv/strany
  • 5378-5387
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM0021627501)
http://linked.open...iv/cisloPeriodika
  • 13
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 445445
http://linked.open...ai/riv/idVysledku
  • RIV/00216275:25310/07:00006064
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • conjugation; nonlinear optics; charge transfer; donor?acceptor chromophores; electrochemistry (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • DE - Spolková republika Německo
http://linked.open...ontrolniKodProRIV
  • [D0253B9BBF33]
http://linked.open...i/riv/nazevZdroje
  • Chemistry - A European Journal
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...iv/tvurceVysledku
  • Bureš, Filip
  • Diederich, Francois
  • May, Joshua C.
  • Gisselbrecht, Jean-Paul
  • Boudon, Corinne
  • Gross, Maurice
  • Biaggio, Ivan
  • Scheizer, Bernd W.
http://linked.open...n/vavai/riv/zamer
issn
  • 0947-6539
number of pages
http://localhost/t...ganizacniJednotka
  • 25310
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