Routes to trans A,B-substituted bacteriochlorins
US-9365722-B2 · Jun 14, 2016 · US
US2017174888A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017174888-A1 |
| Application number | US-201615338720-A |
| Country | US |
| Kind code | A1 |
| Filing date | Oct 31, 2016 |
| Priority date | Dec 22, 2015 |
| Publication date | Jun 22, 2017 |
| Grant date | — |
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Provided is a transparent conductive film that suppresses deterioration of display characteristics due to reduced contrast and that has excellent long-term conductivity, even when exposed to harsh conditions. The transparent conductive film includes one or more metal nanowire bodies and a colored compound adsorbed onto the metal nanowire bodies. The colored compound includes a first dye that includes a macrocyclic π-conjugated moiety and a moiety having a functional group that exhibits adsorptivity with respect to a constituent metal of the metal nanowire bodies.
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1 . A transparent conductive film comprising: one or more metal nanowire bodies; and a colored compound adsorbed onto the metal nanowire bodies, wherein the colored compound includes a first dye that includes a macrocyclic π-conjugated moiety and a moiety having a functional group that exhibits adsorptivity with respect to a constituent metal of the metal nanowire bodies. 2 . The transparent conductive film of claim 1 , wherein the functional group that exhibits adsorptivity with respect to the constituent metal is at least one selected from the group consisting of a sulfo group, a sulfonyl group, a sulfonamide group, a carboxylic acid group, an aromatic amino group, an amide group, a phosphate group, a phosphino group, a silanol group, an epoxy group, an isocyanate group, a cyano group, a vinyl group, a thiol group, a sulfide group, a carbinol group, an ammonium group, a pyridinium group, a hydroxy group, and a methyl group. 3 . The transparent conductive film of claim 1 , wherein the number of functional groups in the first dye that exhibit adsorptivity with respect to the constituent metal is at least two per each macrocyclic π-conjugated moiety in the first dye. 4 . The transparent conductive film of claim 1 , wherein the macrocyclic π-conjugated moiety is at least one selected from the group consisting of a porphyrin, a chlorin, a corrole, a norcorrole, a subporphyrin, a phthalocyanine, a naphthalocyanine, a subphthalocyanine, an anthracocyanine, a tetraazaporphyrin, a bacteriochlorin, and a benzoporphyrin. 5 . The transparent conductive film of claim 1 , wherein the first dye has a number-average molecular mass of from 1,000 to 2,000. 6 . The transparent conductive film of claim 1 , wherein the colored compound further includes a second dye including a chromophore that absorbs visible region light, but does not have a macrocyclic π-conjugated moiety, and a moiety having a functional group that exhibits adsorptivity with respect to the constituent metal of the metal nanowire bodies. 7 . The transparent conductive film of claim 6 , wherein the chromophore that absorbs visible region light, but does not have a macrocyclic π-conjugated moiety, is at least one selected from the group consisting of a stilbene derivative, an indophenol derivative, a diphenylmethane derivative, an anthraquinone derivative, a triphenylmethane derivative, a diazine derivative, an indigoid derivative, a xanthene derivative, an oxazine derivative, an acridine derivative, a thiazine derivative, an azo compound, and a metal-containing complex. 8 . The transparent conductive film of claim 6 , wherein either or both of the first dye and the second dye have a number-average molecular mass of from 1,000 to 2,000. 9 . The transparent conductive film of claim 1 , wherein the constituent metal of the metal nanowire bodies is silver. 10 . An electrode production method comprising forming the transparent conductive film of claim 1 on a substrate, wherein pressing is not performed after the forming of the transparent conductive film. 11 . A structure comprising: a substrate; and the transparent conductive film of claim 1 on the substrate. 12 . An information input device comprising the structure of claim 11 .
Porphines; Azaporphines {(non-dyeing compounds C07D487/22)} · CPC title
Phthalocyanines {abbreviation: Pc} · CPC title
Manufacturing, i.e. details related to manufacturing processes specially suited for touch sensitive devices · CPC title
having six-membered heterocyclic rings · CPC title
Obtaining compounds having —COOH or —SO3H radicals, or derivatives thereof, directly bound to the phthalocyanine radical · CPC title
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