IP Library Granted Patent US 10,988,687
Granted Patent B2
US 10,988,687 · App. 15/825,339 · Granted Apr 27, 2021

Phthalocyanine formulation and uses thereof

Inventors: Xinshe Xu (Lincoln, NE); Rose Skopp (Lincoln, NE); Mark Cradduck (Lincoln, NE); Nisha Padhye (Lincoln, NE)
Assignee: LI-COR, INC.
C09K11/07B43K1/12F21K2/06C09K2211/1029C09K2211/188
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Quick Facts
Patent No.
US 10,988,687
App. No.
15/825,339
Granted
Apr 27, 2021
Kind
B2
Abstract

The present invention provides a chemiluminescent ink formulation, comprising: a phthalocyanine metal catalyst; a visible dye; and a solvent. The formulation is useful in catalyzing a chemiluminescent reaction, by admixing for example, luminol or isoluminol with an oxidizing agent, a base and the chemiluminescent ink formulation to emit light.

Claims (22)

1. A chemiluminescent pen, the chemiluminescent pen comprising:

a barrel comprising a reservoir for holding a chemiluminescent ink formulation;

and a nib, wherein the ink formulation comprises a phthalocyanine metal catalyst at a range from 0.0024 to 1.5 mg/mL, wherein the metal is a member selected from the group consisting of Ni, Mn, Fe, Co, and Ru;

a visible dye, other than the phthalocyanine metal catalyst, wherein the visible dye provides visible orientation for the phthalocyanine metal catalyst, and wherein the phthalocyanine metal catalyzes a chemiluminescent reaction of luminol, isoluminol or luminol derivatives with an oxidizing agent.

2. The chemiluminescent pen of claim 1 , wherein the reservoir further comprising a fiber to adsorb the chemiluminescent ink formulation.

3. The chemiluminescent pen of claim 1 , wherein the barrel further comprising a cap.

4. The chemiluminescent pen of claim 1 , wherein the phthalocyanine metal catalyst has the formula:

wherein M is a member selected from the group consisting of Ni, Mn, Fe, Co, and Ru;

R 1 , R 2 , R 3 and R 4 are each independently selected from the group consisting of hydrogen, amino, amido, alkyl, alkenyl, alkoxy, carboxyl, cyano, halo, hydroxyl, sulfonato, phospho, hydroxyalkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, alkylthioalkyl, carboxyalkyl, alkoxycarbonylalkyl, sulfonatoalkyl, alkoxycarbonyl, and alkoxyalkyl, a sugar residue, a polysaccharide residue, and a PEG; and

m, y, z and n are each independently selected from the group consisting of 0, 1, 2, 3 and 4.

5. The chemiluminescent pen of claim 4 , wherein M is Mn.

6. The chemiluminescent pen of claim 4 , wherein M is Ru.

7. The chemiluminescent pen of claim 4 , wherein R 1 , R 2 , R 3 and R 4 are each alkoxy.

8. The chemiluminescent pen of claim 4 , wherein m, y, z and n are each 2.

9. The chemiluminescent pen of claim 1 , wherein the visible dye is a member selected from the group consisting of Solvent Green, Sudan Blue, Safranin, 1-(methylamino)anthraquinone and Nile Blue A.

10. The chemiluminescent pen of claim 9 , wherein the visible dye is Nile Blue A.

11. The chemiluminescent pen of claim 1 , wherein the chemiluminescent ink formulation comprises a solvent which is a member selected from the group consisting of water, an alcohol, an ester, an amine, an amide, a hydrocarbon, a halogenated hydrocarbon, a ketone, an organic oxide and a mixture thereof.

12. The chemiluminescent pen of claim 11 , wherein the solvent is a mixture of an alcohol and a hydrocarbon.

13. The chemiluminescent pen of claim 11 , wherein the solvent is a mixture of toluene and isopropyl alcohol.

14. A chemiluminescent pen, the chemiluminescent pen comprising:

a barrel comprising a reservoir for holding a chemiluminescent ink formulation; and a nib, wherein the ink formulation comprises a solvent and a phthalocyanine metal catalyst at a range from 0.0024 to 1.5 mg/mL, wherein the metal is a member selected from the group consisting of Ni, Mn, Fe, Co, and Ru;

a visible dye, other than the phthalocyanine metal catalyst, wherein the visible dye provides visible orientation for the phthalocyanine metal catalyst, and wherein the phthalocyanine metal catalyzes a chemiluminescent reaction of luminol, isoluminol or luminol derivatives with an oxidizing agent, wherein the solvent is a mixture of an alcohol and a hydrocarbon.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 2, 2023
From: LI-COR, INC.
To: LI-COR BIOTECH, LLC
Reel/Frame 065436/0255 →
SECURITY INTEREST Recorded Oct 30, 2023
From: LI-COR BIOTECH, LLC
To: MIDCAP FINANCIAL TRUST
Reel/Frame 065396/0454 →
SECURITY INTEREST Recorded Dec 1, 2021
From: LI-COR, INC.
To: MIDCAP FINANCIAL TRUST
Reel/Frame 058293/0889 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2017
From: XU, XINSHE; SKOPP, ROSE; CRADDUCK, MARK; PADHYE, NISHA
To: LI-COR, INC.
Reel/Frame 044252/0881 →
Continuity (3)
Division 14262659 · Apr 25, 2014
Provisional Application 61955743 · Mar 19, 2014
Related Publication 20180079954A1 · Mar 22, 2018