IP Library Granted Patent US 11,873,432
Granted Patent B2
US 11,873,432 · App. 16/695,867 · Granted Jan 16, 2024

Luminescent materials including a luminescent benzothiazole, articles including a security feature, and methods of forming luminescent particles including a luminescent benzothiazole

Inventors: Thomas Potrawa (Seelze, DE); Michael Kessler (Neustadt, DE)
Assignee: HONEYWELL INTERNATIONAL INC.
C09K11/06C09K2211/1037
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Quick Facts
Patent No.
US 11,873,432
App. No.
16/695,867
Granted
Jan 16, 2024
Kind
B2
Abstract

Luminescent materials that include a luminescent phosphor compound, articles including a security feature, and methods for producing the luminescent phosphor compounds are provided herein. In an embodiment, a luminescent material includes a medium and luminescent particles. The luminescent particles include a luminescent benzothiazole having a ureido linkage. The luminescent benzothiazole has a peak intensity within a wavelength of from about 555 to about 630 nm in response to excitation with electromagnetic radiation at a wavelength of about 366 nm.

Claims (26)

1. A luminescent material comprising:

a medium chosen from the group of an ink, an ink additive, a glue, a polymer, a plastic, plastic base resin, a glass, a ceramic, a metal, a textile, wood, fiber, paper pulp, and paper; and

luminescent particles comprising a luminescent benzothiazole having a ureido linkage, wherein

the ureido linkage joins a benzothiazolyl-containing group and an optionally halogenated phenyl group in the luminescent benzothiazole;

the benzothiazolyl-containing group is a phenylbenzothiazolyl group wherein the ureido linkage joins the phenylbenzothiazolyl group to the optionally halogenated phenyl group in the luminescent benzothiazole; and

the phenylbenzothiazolyl group is free from pendant hydroxyl groups;

wherein the luminescent particles comprise the luminescent benzothiazole in an amount of at least 99 weight % based upon a total weight of the luminescent particles.

2. The luminescent material of claim 1 , wherein the luminescent benzothiazole has the following structure:

wherein R 1 is H, a halogen radical, an alkyl group, an ester group, an ether group, an aromatic group, or an alkoxy group; R 2 is H, a halogen radical, an alkyl group, an ester group, an ether group, an aromatic group, or an alkoxy group, wherein R 1 and R 2 may represent bonds of an aromatic group to the phenyl group to form a polycyclic aromatic group; and R 3 is H, a halogen radical, or an alkyl group.

3. The luminescent material of claim 2 , wherein R 1 is H, a halogen radical, an alkyl group, an ester group, an ether group, an aromatic group, or an alkoxy group; R 2 is H; and R 3 is H.

4. The luminescent material of claim 1 , wherein the luminescent benzothiazole is the reaction product of 2-aminophenylbenzothiazole and an optionally halogenated phenylisocyanate.

5. A method of forming luminescent particles, wherein the method comprises:

heating a mixture comprising an amino-functional benzothiazole reactant and an organic solvent to a temperature of greater than about 60° C.;

adding an isocyanate-containing compound to the mixture after heating to the temperature of greater than about 60° C. to form a reaction mixture;

maintaining the reaction mixture at the temperature of greater than about 60° C. for a reaction period to form luminescent particles comprising a luminescent benzothiazole having a ureido linkage.

6. The method of claim 5 , further comprising separating the luminescent particles as precipitate from a liquid portion of the reaction mixture after the reaction period.

7. The method of claim 5 , wherein heating the mixture comprises heating the mixture to reflux conditions wherein vapor from the mixture is returned to the mixture prior to adding the isocyanate-containing compound.

8. The method of claim 5 , wherein the luminescent particles are formed at a yield of at least 75 weight % based upon a theoretical yield of the luminescent particles from the reaction.

9. The method of claim 5 , wherein the amino-functional benzothiazole reactant is 2-aminophenylbenzothiazole and the isocyanate-containing compound is an optionally halogenated phenylisocyanate.

10. The method of claim 9 , wherein the isocyanate-containing compound is a halogenated phenylisocyanate.

11. A luminescent material comprising:

a medium chosen from the group of an ink, an ink additive, a glue, a polymer, a plastic, plastic base resin, a glass, a ceramic, a metal, a textile, wood, fiber, paper pulp, and paper; and

luminescent particles comprising a luminescent benzothiazole having a ureido linkage, wherein

the ureido linkage joins a benzothiazolyl-containing group and an optionally halogenated phenyl group in the luminescent benzothiazole;

the benzothiazolyl-containing group is a phenylbenzothiazolyl group wherein the ureido linkage joins the phenylbenzothiazolyl group to the optionally halogenated phenyl group in the luminescent benzothiazole;

wherein the phenylbenzothiazolyl group is free from pendant hydroxyl groups.

Assignments (3)
SECURITY INTEREST Recorded Jan 12, 2026
From: SOLSTICE ADVANCED MATERIALS US, INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 074569/0260 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 12, 2022
From: POTRAWA, THOMAS; KESSLER, MICHAEL
To: HONEYWELL INTERNATIONAL INC.
Reel/Frame 061056/0385 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2019
From: POTRAWA, THOMAS; KESSLER, MICHAEL
To: HONEYWELL INTERNATIONAL INC.
Reel/Frame 051119/0060 →