2013
DOI: 10.1016/j.solmat.2012.11.008
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Electrochromic devices based on surface-confined Prussian blue or Ruthenium purple and aqueous solution-phase di-n-heptyl viologen

Abstract: • AbstractPrototype electrochromic devices (ECDs) based on anodically-colouring thin-film Prussian blue (PB) or Ruthenium purple (RP) and cathodically-colouring aqueous solution-phase di-n-heptyl viologen are described. The initial ('off') state of each ECD is set with the PB (or RP) in the colourless reduced form and the di-n-heptyl viologen as the colourless di-cation. Switching the ECDs to the coloured state ('on'), forms on oxidation the coloured mixed-valence PB (or RP), with simultaneous reduction of th… Show more

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Cited by 16 publications
(19 citation statements)
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“…1 H NMR (300.18 MHz, DMSO-d 6 ): δ 12.27 (s, 1H, OH), 8.78 (m, 1H, H3), 8.74 (m, 1H, H3′), 8.59 (d, 3 J = 7.9 Hz, 1H, H6), 8.52 (d, 3 J = 7.9 Hz, 1H, H6′), 8.11 (td, 3 J = 7.8 Hz, 4 J = 1.7 Hz, 1H, H5), 8.03 (td, 3 J = 7.7 Hz, 4 J = 1.8 Hz, 1H, H5′), 7.69 (ddd, 3 J = 4.8 Hz, 4 J = 1.1 Hz, 1H, H4), 7.56 (ddd, 3 J = 4.7 Hz, 4 J = 1.1 Hz, 1H, H4′), 7.28 (s, 1H, H9) ppm. 13 Synthesis of 4-Chloro-2,6-bis(2-pyridyl)pyrimidine (8). 4-Hydroxy-2,6-bis(2-pyridyl)pyrimidine 7 (0.88 g, 3.52 mmol) was added slowly to the freshly distilled thionyl chloride (30 mL) under an inert atmosphere.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
See 1 more Smart Citation
“…1 H NMR (300.18 MHz, DMSO-d 6 ): δ 12.27 (s, 1H, OH), 8.78 (m, 1H, H3), 8.74 (m, 1H, H3′), 8.59 (d, 3 J = 7.9 Hz, 1H, H6), 8.52 (d, 3 J = 7.9 Hz, 1H, H6′), 8.11 (td, 3 J = 7.8 Hz, 4 J = 1.7 Hz, 1H, H5), 8.03 (td, 3 J = 7.7 Hz, 4 J = 1.8 Hz, 1H, H5′), 7.69 (ddd, 3 J = 4.8 Hz, 4 J = 1.1 Hz, 1H, H4), 7.56 (ddd, 3 J = 4.7 Hz, 4 J = 1.1 Hz, 1H, H4′), 7.28 (s, 1H, H9) ppm. 13 Synthesis of 4-Chloro-2,6-bis(2-pyridyl)pyrimidine (8). 4-Hydroxy-2,6-bis(2-pyridyl)pyrimidine 7 (0.88 g, 3.52 mmol) was added slowly to the freshly distilled thionyl chloride (30 mL) under an inert atmosphere.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…1 H NMR (300.18 MHz, CDCl 3 ): δ 8.89 (m, 1H, H3), 8.74 (m, 1H, H3′), 8.68 (d, 3 J = 7.9 Hz, 1H, H6), 8.62 (d, 3 J = 8.0 Hz, 1H, H6′), 8.44 (s, 1H, H9), 7.90 (m, 2H, H5, H5′), 7.45 (m, 2H, H4, H4′) ppm. 13 C NMR (75.48 MHz, CDCl 3 ): δ 165.17 Synthesis of 2-Pyridalacetophenone (11). 31 Acetophenone 10 (3.85 g, 32 mmol) and DBU 3 (4.79 mL, 32 mmol) were added to a solution of 2-pyridinecarboxaldehyde 2 (6.08 mL, 64 mmol) in anhydrous tetrahydrofuran (80 mL).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…When comparing electrochromic materials derived from metal oxides 1 with molecular organic [2][3][4] and polymeric 5 electrochromes, the latter stand out for the broad array of colours that can switch to highly transmissive states. Due to their solubility allowing them to be processed via spin, [6][7][8] spray, 9,10 blade, 11 and slot-die 12 coating along with inkjet printing, 11,13 fully conjugated electrochromic polymers (ECPs) provide a full palette of colours from which to develop devices.…”
Section: Introductionmentioning
confidence: 99%
“…11 In another report, electrochromic devices with aqueous solution phase di-heptyl viologen (N,N 0 -diheptyl-4,4 0bipyridylium) as the cathodic electrochrome and surface conned Prussian blue or Ruthenium purple as the anodic electrochrome were fabricated and in situ spectroelectrochemistry and color measurement were studied. 12,13 In yet another study, a poly(butyl viologen) and Prussian blue based electrochromic device was fabricated using a solid electrolyte based on succinonitrile and a large coloration efficiency was obtained. 14 In another study, layer-by-layer (LbL) self-assembled multilayer lms were fabricated using a perylenediimide-viologen dyad and poly(3,4-ethylenedioxythiophene)-poly-(styrenesulfonate) (PEDOT:PSS) and a three stage color change from red to blue to violet was attained.…”
Section: Introductionmentioning
confidence: 99%