IP Library Granted Patent US 8,975,212
Granted Patent B2
US 8,975,212 · App. 13/822,991 · Granted Mar 10, 2015

Phenolsulfonic acid aryl ester derivative, and heat-sensitive recording material using same

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Quick Facts
Patent No.
US 8,975,212
App. No.
13/822,991
Granted
Mar 10, 2015
Kind
B2
Abstract

The invention provides a phenolsulfonic acid aryl ester represented by formula (1) wherein each symbol is as defined in the description. The phenolsulfonic acid aryl ester is useful as a developer to provide a thermal recording material with good color-developing sensitivity, image density when printed at a low application energy (i.e., high start-up sensitivity), and heat and plasticizer resistance. The invention also provides a thermal recording material using the developer.

Claims (29)

1. A phenolsulfonic acid aryl ester represented by the following formula:

wherein

R 1 and R 2 are each independently an alkyl group having 1 to 8 carbon atoms;

R 3 is an alkyl group having 1 to 8 carbon atoms;

R 4 is an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, a cyano group, an aryl group having 6 to 14 carbon atoms or an aralkyl group having 7 to 15 carbon atoms;

m is an integer of 0-3;

and n is an integer of 0-4.

2. A developer for a thermal recording material, comprising at least one kind of the phenolsulfonic acid aryl ester according to claim 1 .

3. A thermal recording material comprising a support and a thermal recording layer comprising a colorless or pale-colored basic leuco dye and a developer for color development of the basic leuco dye, which layer is laminated on at least one surface of the support, wherein the developer contains at least one kind of phenolsulfonic acid aryl ester according to claim 1 .

4. The thermal recording material according to claim 3 , wherein the developer further contains at least one kind of a second developer selected from the group consisting of a bisphenol compound, a bisphenol sulfone compound, a urea compound and a novolac type phenol compound.

5. The thermal recording material according to claim 3 , wherein the thermal recording layer contains at least one kind of sensitizer selected from the group consisting of 1,2-di-(3-methylphenoxy)ethane, fatty acid amide having 10 to 21 carbon atoms, β-benzyloxynaphthalene and diaphenylsulfone.

6. The thermal recording material according to claim 3 , wherein the thermal recording layer contains a hindered phenol compound.

7. The thermal recording material according to claim 6 , wherein the hindered phenol compound is at least one kind selected from the group consisting of a compound represented by the following formula (3), a compound represented by the following formula (5) and a compound represented by the following formula (6):

wherein R 5 , R 8 and R 11 are each independently an alkyl group having 1 to 8 carbon atoms or a cycloalkyl group having 3 to 8 carbon atoms, R 6 , R 7 , R 9 , R 10 , R 12 and R 13 are each independently a hydrogen atom, an alkyl group having 1 to 8 carbon atoms or a cycloalkyl group having 3 to 6 carbon atoms,

wherein p is 1 or 2.

8. The thermal recording material according to claim 7 , wherein the compound represented by the formula (3) is a compound represented by the following formula (4):

wherein R 5a , R 8a and R 11a are each a tert-butyl group or a cyclohexyl group, R 6a , R 9a , and R 12a are methyl groups, and R 7a , R 10a and R 13a are hydrogen atoms.

9. A phenolsulfonic acid aryl ester, which is represented by the following formula (2):

wherein R 1a and R 2a are each independently a hydrogen atom, an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, and R 1a and R 2a are not simultaneously hydrogen atoms; R 3a is an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, a halogen atom, a nitro group, a hydroxy group, a cyano group, an aryl group having 6 to 14 carbon atoms or an aralkyl group having 7 to 15 carbon atoms; and ma is an integer of 0-3.

10. A developer for a thermal recording material, comprising at least one kind of the phenolsulfonic acid aryl ester according to claim 9 .

11. A thermal recording material comprising a support and a thermal recording layer comprising a colorless or pale-colored basic leuco dye and a developer for color development of the basic leuco dye, which layer is laminated on at least one surface of the support, wherein the developer contains at least one kind of phenolsulfonic acid aryl ester according to claim 9 .

12. The thermal recording material according to claim 11 , wherein the developer further contains at least one kind of a second developer selected from the group consisting of a bisphenol compound, a bisphenol sulfone compound, a urea compound and a novolac type phenol compound.

13. The thermal recording material according to claim 11 , wherein the thermal recording layer contains at least one kind of sensitizer selected from the group consisting of 1,2-di-(3-methylphenoxy)ethane, fatty acid amide having 10 to 21 carbon atoms, β-benzyloxynaphthalene and diaphenylsulfone.

14. The thermal recording material according to claim 11 , wherein the thermal recording layer contains a hindered phenol compound.

15. The thermal recording material according to claim 14 , wherein the hindered phenol compound is at least one kind selected from the group consisting of a compound represented by the following formula (3), a compound represented by the following formula (5) and a compound represented by the following formula (6):

wherein R 5 , R 8 , and R 11 are each independently an alkyl group having 1 to 8 carbon atoms or a cycloalkyl group having 3 to 8 carbon atoms, R 6 , R 7 , R 9 , R 10 , R 12 and R 13 are each independently a hydrogen atom, an alkyl group having 1 to 8 carbon atoms or a cycloalkyl group having 3 to 6 carbon atoms,

wherein p is 1 or 2.

16. The thermal recording material according to claim 15 , wherein the compound represented by the formula (3) is a compound represented by the following formula (4):

wherein R 5a , R 8a and R 11a are each a tert-butyl group or a cyclohexyl group, R 6a , R 9a and R 12a are methyl groups, and R 7a , R 10a and R 13a are hydrogen atoms.

Assignments (5)
CHANGE OF NAME Recorded Sep 5, 2017
From: MITSUBISHI RAYON CO., LTD.
To: MITSUBISHI CHEMICAL CORPORATION
Reel/Frame 043750/0834 →
MERGER Recorded Sep 4, 2017
From: MITSUBISHI CHEMICAL CORPORATION
To: MITSUBISHI RAYON CO., LTD.
Reel/Frame 043750/0207 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2015
From: API CORPORATION
To: MITSUBISHI CHEMICAL CORPORATION
Reel/Frame 034793/0507 →
NOTICE OF CHANGE OF ASSIGNEE'S ADDRESS Recorded Jan 21, 2015
From: API CORPORATION
To: API CORPORATION
Reel/Frame 034783/0220 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2013
From: HIGUCHI, MAI; AOSAKI, YOSHIMUNE; INADA, KEIICHIRO; SUGA, MAMORU; OHSE, KATSUTO; MIDORIKAWA, YOSHIMI; SATO, YUKIKO
To: API CORPORATION; NIPPON PAPER INDUSTRIES CO., LTD.
Reel/Frame 030357/0344 →