IP Library Granted Patent US 7,074,536
Granted Patent B2
US 7,074,536 · App. 10/485,461 · Granted Jul 11, 2006

Alkylenebisnaphtol derivative and charge control agent which consists of the same

Assignee: Kabushiki Kaisha Ueno Seiyaku Oyo Kenkyujo
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Quick Facts
Patent No.
US 7,074,536
App. No.
10/485,461
Granted
Jul 11, 2006
Kind
B2
Abstract

The present invention provides an alkylenebisnaphthol derivative represented by formula [I]: and a salt thereof. The compound of the present invention has an excellent triboelectric charge property and useful as charge control agent for electrophotographic toners.

Claims (27)

1. An alkylenebisnaphthol derivative represented by formula [I]:

wherein Y 1 , Y 2 , Y 1 ′ and Y 2 ′ may be same or different and each of them is selected from the group consisting of a carboxyl group, an esterified carboxyl group, a group of —(CONH)n-X (wherein X is an optionally branched and optionally substituted hydrocarbon group which may have an unsaturated bond, an optionally substituted aromatic group and a heterocyclic group having conjugated double bonds, n is an integer of 1 or 2);

k is an integer of 1–12;

R and R′ are selected from the group consisting of hydrogen atom, an alkaline metal, an optionally branched and optionally substituted alkyl or acyl group of 1–6 carbon atoms and a phenylalkyl group;

Q and Q′ are selected from the group consisting of an optionally branched alkyl or alkoxy group of 1–6 carbon atoms, a halogen atom, nitro group, nitroso group, amino group and sulfo group; and

m and m′ each represents an integer of 0–3

or a salt thereof.

2. The alkylenebisnaphthol derivative or a salt thereof of claim 1 , wherein k is 1.

3. The alkylenebisnaphthol derivative or a salt thereof of claim 1 , wherein said derivative is negatively chargeable and the absolute value of the triboelectric charge is equal to or greater than 1.3 μC/g.

4. A charge control agent consisting of an alkylenebisnaphthol derivative represented by formula [I]:

wherein Y 1 , Y 2 , Y 1 ′ and Y 2 ′ may be same or different and each of them is selected from the group consisting of a carboxyl group, an esterified carboxyl group, a group of —(CONH)n-X (wherein X is an optionally branched and optionally substituted hydrocarbon group which may have an unsaturated bond, an optionally substituted aromatic group and a heterocyclic group having conjugated double bonds, n is an integer of 1 or 2);

k is an integer of 1–12;

R and R′ are selected from the group consisting of hydrogen atom, an alkaline metal, an optionally branched and optionally substituted alkyl or acyl group of 1–6 carbon atoms and a phenylalkyl group;

Q and Q′ are selected from the group consisting of an optionally branched alkyl or alkoxy group of 1–6 carbon atoms, a halogen atom, nitro group, nitroso group, amino group and sulfo group; and

m and m′ each represents an integer of 0–3

or a salt thereof;

provided that said derivative is negatively chargeable and the absolute value of the triboelectric charge is equal to or greater than 1.3 μC/g.

5. A method of using an alkylenebisnaphthol derivative,

comprising providing an alkylenebisnaphthol derivative as defined in claim 1 or a salt thereof as a charge control agent, provided that said derivative is negatively chargeable and the absolute value of the triboelectric charge is equal to or greater than 1.3 μC/g.

6. An electrophotographic toner, comprising at least a binder resin, a colorant and an alkylenebisnaphthol derivative of formula [I]:

wherein Y 1 , Y 2 , Y 1 ′ and Y 2 ′ may be same or different and each of them is selected from the group consisting of a carboxyl group, an esterified carboxyl group, a group of —(CONH)n-X (wherein X is an optionally branched and optionally substituted hydrocarbon group which may have an unsaturated bond, an optionally substituted aromatic group and a heterocyclic group having conjugated double bonds, n is an integer of 1 or 2);

k is an integer of 1–12;

R and R′ are selected from the group consisting of hydrogen atom, an alkaline metal, an optionally branched and optionally substituted alkyl or acyl group of 1–6 carbon atoms and a phenylalkyl group;

Q and Q′ are selected from the group consisting of an optionally branched alkyl or alkoxy group of 1–6 carbon atoms, a halogen atom, nitro group, nitroso group, amino group and sulfo group; and

m and m′ each represents an integer of 0–3

or a salt thereof;

provided that said derivative is negatively chargeable and the absolute value of the triboelectric charge is equal to or greater than 1.3 μC/g.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 22, 2008
From: UENO TECHNOLOGY CO., LTD.
To: UENO FINE CHEMICALS INDUSTRY, LTD.
Reel/Frame 021561/0559 →
CHANGE OF NAME Recorded Sep 12, 2008
From: KABUSHIKI KAISHA UENO SEIYAKU OYO KENKYUJO
To: UENO TECHNOLOGY CO., LTD.
Reel/Frame 021523/0034 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2004
From: UENO, RYUZO; KITAYAMA, MASAYA; MINAMI, KENJI; WAKAMORI, HIROYUKI; YONETANI, NOBUHIRO
To: KABUSHIKI KAISHA UENO SEIYAKU OYO KENKYUJO
Reel/Frame 015619/0598 →
Priority Claims (1)
JP 2001-236303 · Aug 3, 2001 · national
Continuity (1)
Related Publication 20040248026A1 · Dec 9, 2004