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Patent

Electrochromic marking systems

TLDR
In this article, the color formers are prepared by the interaction of the corresponding 5-(N-R1 -amino)-9-(NR2 -N-r3 -aminosinium halide) or 9-(n-R2-n-r-3-amino)phenoxazin-5-one with a reducing agent and subsequently interacting the leuco compound with at least two molecular proportions of an acylating agent.
Abstract
5-[N-(RCO)-N-R1 -amino] or (RCOO)-9-(N-R2 -N-R3 -amino)-12-(RCO)benzo[a]phenoxazines useful as color formers, particularly in electrochromic recording systems, are prepared by the interaction of the corresponding 5-(N-R1 -amino)-9-(N-R2 -N-R3 -amino)benzo[a]phenoxazinium halide or 9-(N-R2 -N-R3 -amino)benzo[a]phenoxazin-5-one with a reducing agent to obtain the corresponding leuco compound and subsequently interacting the leuco compound with at least two molecular proportions of an acylating agent.

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Compounds for electronic devices

TL;DR: In this paper, the present invention relates to compounds of the formula (I) and to the use thereof in organic electronic devices, and to organic devices which comprise compounds of I, preferably as holetransport materials and/or as matrix materials, in particular in combination with a further matrix material.
Patent

Method for reducing current leakage and enhancing uv stability in electrochemichromic solutions and devices

TL;DR: In this paper, a method for reducing current leakage and enhancing UV stability by using electrochemichromic solutions whose solvents include glutaronitrile (GNT) either solely or in combination with other solvers, was described.
Patent

Method of reducing leakage current in electrochemichromic solutions and solutions based thereon

TL;DR: In this article, the authors describe electrochemichromic solutions and devices based on the use of from about 5% by volume of a nonpolymeric material having a high volume resistivity and high dielectric constant to reduce leakage current without unduly increasing solution viscosity.
Patent

High performance electrochemichromic solutions and devices thereof

TL;DR: In this article, the specification discloses electrochemichromic solutions and devices based on the use of solvents comprising at least about 25% 3-hydroxypropionitrile, 3,3'-oxydipropionitriles, 2-acetylbutyrolactone, 2 -methylglutaronitrile and 3-methylsulfolane and mixtures thereof.
Patent

Electrochemichromic solutions, processes for preparing and using the same, and devices manufactured with the same

TL;DR: In this paper, a method for pre-treating at least one of the electrochemichromic compounds with a redox agent prior to placing it in contact with the other is presented.
References
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Patent

Pressure sensitive copying paper

TL;DR: A pressure sensitive copying paper is prepared using a color former of the general formula whereIN R1 and R2 each represent an alkyl group having 1 to 5 carbon atoms or a benzyl group, and X1, X2, X3 and X4 each represent a hydrogen atom, a halogen atom, an alkoxyl group or a methyl group as mentioned in this paper.
Patent

Electrochromic recording paper

TL;DR: A medium for electrochromic recording is provided by treating paper with a water soluble leuco methylene blue compound having the formula ##STR1## wherein R is a sulfonated aromatic or sulfonate aliphatic moiety as mentioned in this paper.
Patent

Pressure-sensitive copying paper containing phenoxazine compounds

TL;DR: A pressure sensitive copying paper comprising an adsorbent solid acid and a microencapsulated color former capable of forming a distinct color when reacted with the adorbent acid coated on the same or a different surface of a support or supports is defined in this paper.
Journal ArticleDOI

Polymer induced aggregation of dye molecules. Influence of the attachment of dye molecules as side groups

TL;DR: By radical polymerization, 7-(N-acryloyl-N-methyl)-3-dimethyliminio-3H-phenothiazine chloride (1) has been transformed in the N-substituted polyacrylamide carrying Azure B side groups, poly{1]-N-(3dimethylmethyl-7-yl)-N-methylaminocarbonyl]ethylene chloride.
Patent

Compound and pigment having halogen-containing active group

TL;DR: In this article, a compound having halogen-containing active group of formula I is presented. But the compound of formula III is not shown to have a halogen active group.