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Light-responsive material containing a dye comprising two cyclodextrin groups |
| OF THE INVENTION The present invention provides a light-responsive material comprising a dye ... |
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Leukotriene antagonists and use thereas |
| AND PREFERRED EMBODIMENT The present invention relates to new organic compounds that are useful in ... |
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Photochromic system and layers produced therewith |
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Preparation of unsaturated and saturated ketones |
| We claim: 1. A process for the preparation of an unsaturated ketone of the formula (I) ##STR9## or ... |
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Ultraviolet protective overcoat for application to heat sensitive record materials |
| AND EXAMPLES OF PREFERRED EMBODIMENT The preferred overcoating compositions of the present ... |
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Method for producing metal films |
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Method of preparing cyclodextrin-coated surfaces |
| OF THE INVENTION The invention herein is based on several key discoveries. One is that in the ... |
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Aqueous ink composition for ink-jet recording
| Details |
Inventors: Shimada, Masaru; Kawanishi, Toshiyuki; Murakami, Kakuji; Aruga, Tamotsu; Uemura, Hiroyuki;
Assignee: Ricoh Company, Ltd. (Tokyo, JP)
Primary Examiner: Yarbrough; Amelia Burgess
Assistant Examiner:
Attorney, Agent or Firm: Oblon, Fisher, Spivak, McClelland & Maier
An aqueous ink composition for ink-jet recording comprising an aqueous solution of a water-soluble dye of formula (I) and a humectant dissolved in water: ##STR1## wherein R.sup.1 and R.sup.2 each represent hydrogen, an alkyl group, an alkoxy group, halogen, a carboxyl group or a sulfonic acid group; R.sup.3 and R.sup.4 each represent a hydroxyl group, halogen, an alkoxy group, an unsubstituted or substituted amino group; X represents --O--, --CH.sub.2 --, --C.sub.2 H.sub.4 --, --CH.dbd.CH--, --S--, --SO.sub.2 -- or --; Ar.sup.1 and Ar.sup.2 each represent an unsubstituted or substituted phenyl group, an unsubstituted or substituted naphthyl group; M represents hydrogen ion, an alkali metal cation, amine cation or an ammonium ion; and n is an integer of 1, 2 or 3. |
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DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS An aqueous ink composition according to the present invention comprises a water-soluble dye of the above described formula, water and a humectant. In the following table 1, there are listed representative examples of the water-soluble dyes having the above formula for use in the present invention:
TABLE 1
(1)
##STR3##
(2)
##STR4##
(3)
##STR5##
(4)
##STR6##
(5)
##STR7##
(6)
##STR8##
(7)
##STR9##
(8)
##STR10##
(9)
##STR11##
(10)
##STR12##
(11)
##STR13##
(12)
##STR14##
The above dyes can be prepared by a conventional method. For example, the dye (5) can be prepared as follows: One mole of 4,4'-diaminostilbene 2,2'-disulfonic acid is dissolved in water. To this solution, (1) 2 moles of cyanuric chloride dissolved in acetone and (2) an aqueous solution of sodium carbonate are simultaneously added at temperatures below 0. degree. C. , with the mixuture kept unalkaline, thereby allowing the added components to react for 2 hours. To the above reaction mixture is added a monoazo dye obtained by a conventional reaction of H-acid and o-toluidine. The monoazo dye is dissolved in the reaction mixture. To this reaction mixture, an aqueous solution of sodium carbonate is further added, with the reaction mixture kept unalkaline, so that the reaction mixture is allowed to react at room temperature for 10 hours. Thereafter, the temperature of the reaction mixture is gradually raised to 60. degree. C. and the reaction is continued for 1 hour. Aniline and sodium carbonate are then added to the reaction mixture and the temperature of the reaction mixture is raised to 90. degree. C. , so that the reaction is further continued for 3 hours. After cooling the reaction mixture, the dye (5) is obtained by a salting-out technique using a 20% aqueous solution of sodium chloride. In the present invention, it is preferable that the dye be contained in an amount of 0
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