IP Library › Granted Patent US 12,247,008
Granted Patent B2
US 12,247,008 · App. 17/794,525 · Granted Mar 11, 2025

Multi-aziridine compound

Inventors: Patrick Johannes Maria Stals (Geleen, NL); Daan Van Der Zwaag (Geleen, NL); Alfred Jean Paul Bückmann (Geleen, NL); Gerardus Cornelis Overbeek (Geleen, NL); Jan Van Riel (Geleen, NL)
Assignee: Covestro (Netherlands) B.V.
C07D203/10C07D251/32C07D403/12C07D403/14C07D413/14C07D487/14C08F220/1804C08G18/027C08G18/0823C08G18/0866C08G18/12C08G18/227C08G18/246C08G18/282C08G18/2825C08G18/283C08G18/2865C08G18/2875C08G18/302C08G18/3228C08G18/3231C08G18/3275C08G18/348C08G18/3842C08G18/4291C08G18/44C08G18/4808C08G18/4825C08G18/4854C08G18/4862C08G18/4879C08G18/6692C08G18/6715C08G18/73C08G18/755C08G18/758C08G18/765C08G18/792C08G18/798C08G18/833C08K5/3412C08K5/34924C08K5/34926C08L63/00C09D7/20C09D7/45C09D7/63C09D7/65C09D11/101C09D133/02C09D133/04C09D175/04C09D175/08C09D175/12C08G2150/00
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Quick Facts
Patent No.
US 12,247,008
App. No.
17/794,525
Granted
Mar 11, 2025
Kind
B2
Abstract

The present invention relates to a multi-aziridine compound having: ⋅a) from 2 to 6 of the following structural units (A): whereby R 1 is H, R 2 and R 4 are independently chosen from H or an aliphatic hydrocarbon group containing from 1-4 carbon atoms, R 3 is an aliphatic hydrocarbon group containing from 1-4 carbon atoms, R′═H or an aliphatic hydrocarbon group containing from 1 to 4 carbon atoms; R″ and R′″ are independently chosen from an aliphatic hydrocarbon group containing from 1 to 4 carbon atoms, a cycloaliphatic hydrocarbon group containing from 4 to 12 carbon atoms or an aromatic hydrocarbon group containing from 6 to 12 carbon atoms, b) one or more linking chains wherein each one of these linking chains links two of the structural units A; and c) a molecular weight in the range from 600 Daltons to 5000 Daltons.

Claims (42)

1. A multi-aziridine compound having:

a) from 2 to 6 of the following structural units (A):

whereby

R 1 is H,

R 2 and R 4 are independently chosen from H or an aliphatic hydrocarbon group containing from 1 to 4 carbon atoms,

R 3 is an aliphatic hydrocarbon group containing from 1 to 4 carbon atoms,

R′═H or an aliphatic hydrocarbon group containing from 1 to 4 carbon atoms;

R″ and R′″ are independently chosen from an aliphatic hydrocarbon group containing from 1 to 4 carbon atoms, a cycloaliphatic hydrocarbon group containing from 4 to 12 carbon atoms or an aromatic hydrocarbon group containing from 6 to 12 carbon atoms, or R′ and R″ are part of the same saturated cycloaliphatic hydrocarbon group containing from 4 to 8 carbon atoms, optionally containing heteroatoms,

or R″ and R′″ are part of the same saturated cycloaliphatic hydrocarbon group containing from 4 to 8 carbon atoms, optionally containing heteroatoms,

b) one or more linking chains wherein each one of these linking chains links two of the structural units A whereby a linking chain is defined as the shortest chain of consecutive atoms that links two structural units A; and

c) a molecular weight in the range from 600 Daltons to 5000 Daltons, wherein the molecular weight is determined using MALDI-TOF mass spectrometry.

2. The multi-aziridine compound according to claim 1 , wherein R 2 is H, R 3 is CH 3 and R 4 is H.

3. The multi-aziridine compound according to claim 1 , wherein R 2 is H, R 3 is CH 3 and R 4 is CH 3 .

4. The multi-aziridine compound according to claim 1 , wherein R′═H; R″ and R′″ are an aliphatic hydrocarbon group containing from 1 to 4 carbon atoms.

5. The multi-aziridine compound according to claim 1 , wherein R′═H; R″ and R′″ are an aliphatic hydrocarbon group containing from 1 to 2 carbon atoms.

6. The multi-aziridine compound according to claim 1 , wherein R′═H; R″ and R′″ are CH 3 .

7. The multi-aziridine compound according to claim 1 , wherein the multi-aziridine compound contains 2 or 3 structural units (A).

8. The multi-aziridine compound according to claim 1 , wherein the linking chains consist of from 4 to 300 atoms and the linking chains are a collection of atoms covalently connected which collection of atoms consists of i) carbon atoms, ii) carbon and nitrogen atoms, or iii) carbon, oxygen and nitrogen atoms.

9. The multi-aziridine compound according to claim 1 , wherein the multi-aziridine compound has a molecular weight of from 840 to 3800 Daltons, whereby the molecular weight is determined using MALDI-TOF mass spectrometry.

10. The multi-aziridine compound according to claim 1 , wherein the multi-aziridine compound comprises one or more connecting groups wherein each one of these connecting groups connects two of the structural units A, whereby the connecting groups consist of at least one functionality selected from:

aliphatic hydrocarbon functionality, cycloaliphatic hydrocarbon functionality, aromatic hydrocarbon functionality, isocyanurate functionality, iminooxadiazindione functionality, ether functionality, ester functionality, amide functionality, carbonate functionality, urethane functionality, urea functionality, biuret functionality, allophanate functionality, uretdione functionality and any combination thereof.

11. The multi-aziridine compound according to claim 10 , wherein the connecting groups of the multi-aziridine compound consist of at least one functionality selected from:

aliphatic hydrocarbon functionality, cycloaliphatic hydrocarbon functionality, aromatic hydrocarbon functionality, isocyanurate functionality, iminooxadiazindione functionality, urethane functionality, urea functionality, biuret functionality and any combination thereof.

12. The multi-aziridine compound according to claim 1 , wherein the multi-aziridine compound comprises one or more connecting groups wherein each one of these connecting groups connects two of the structural units A, wherein the connecting groups consist of (i) at least two aliphatic hydrocarbon functionality or at least two cycloaliphatic hydrocarbon functionality and (ii) an isocyanurate functionality or an iminooxadiazindione functionality, and wherein a pendant group is present on a connecting group, whereby the pendant group has the following structural formula:

n′ is the number of repeating units and is an integer from 1 to 50,

X is O or NH,

R 7 and R 8 are independently H or CH 3 in each repeating unit,

R 9 is an aliphatic hydrocarbon group or a cycloaliphatic hydrocarbon group and

R 10 contains at most 20 carbon atoms and is an aliphatic, cycloaliphatic or aromatic hydrocarbon group or a combination thereof.

13. The multi-aziridine compound according to claim 12 , wherein X is O and R 7 and R 8 are H.

14. The multi-aziridine compound according to claim 12 , wherein the multi-aziridine compound contains 2 structural units (A).

15. The multi-aziridine compound according to claim 14 , wherein the connecting group consists of the array of the following consecutive functionalities: a first aliphatic hydrocarbon functionality, an isocyanurate or functionality an iminooxadiazindione functionality, and a second aliphatic hydrocarbon functionality, and R 9 is an aliphatic hydrocarbon group, whereby the first and second aliphatic hydrocarbon functionality and R 9 are identical.

16. The multi-aziridine compound according to claim 1 , wherein the multi-aziridine compound contains polyoxyethylene groups in an amount of at least 0.1 wt. %, and in an amount of less than 45 wt. % relative to the multi-aziridine compound.

17. The multi-aziridine compound according to claim 1 , wherein the multi-aziridine compound is obtained by reacting at least a polyisocyanate and a compound B with the following structural formula:

whereby the molar ratio of compound B to polyisocyanate is from 2 to 6.

18. The multi-aziridine compound according to claim 17 , wherein the polyisocyanate is a polyisocyanate with aliphatic reactivity that is a compound in which all of the isocyanate groups are directly bonded to aliphatic or cycloaliphatic hydrocarbon groups, irrespective of whether aromatic hydrocarbon groups are also present.

19. The multi-aziridine compound according to claim 17 , wherein compound B is obtained by reacting at least a non-OH functional monoepoxide compound with an aziridine compound with the following structural formula:

20. The multi-aziridine compound according to claim 19 , wherein the non-OH functional monoepoxide compound is 2,2-dimethyloxirane (CAS number 558-30-5).

21. A crosslinker composition comprising at least one multi-aziridine compound according to claim 1 and further comprising at least one additional component.

22. The crosslinker composition according to claim 21 , wherein the amount of aziridinyl group functional molecules having a molecular weight lower than 580 Daltons is lower than 5 wt. %, relative to the total weight of the crosslinker composition, whereby the molecular weight is determined using LC-MS.

23. The crosslinker composition according claim 21 , wherein the crosslinker composition contains water in an amount of less than 5 wt. % based on the weight of the crosslinker composition.

24. A two-component coating system comprising a first component and a second component each of which is separate and distinct from each other and wherein the first component comprises a carboxylic acid functional polymer dissolved and/or dispersed in an aqueous medium, whereby the carboxylic acid functional polymer contains carboxylic acid groups and/or carboxylate groups and the second component comprises a multi-aziridine compound according to claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2022
From: STALS, PATRICK JOHANNES MARIA; VAN DER ZWAAG, DAAN; BÜCKMANN, ALFRED JEAN PAUL; OVERBEEK, GERARDUS CORNELIS; VAN RIEL, JAN
To: COVESTRO (NETHERLANDS) B.V.
Reel/Frame 060583/0816 →
Priority Claims (14)
EP 20153154 · Jan 22, 2020 · regional
EP 20153159 · Jan 22, 2020 · regional
EP 20153239 · Jan 22, 2020 · regional
EP 20153240 · Jan 22, 2020 · regional
EP 20153242 · Jan 22, 2020 · regional
EP 20153245 · Jan 22, 2020 · regional
EP 20153246 · Jan 22, 2020 · regional
EP 20153249 · Jan 22, 2020 · regional
EP 20153250 · Jan 22, 2020 · regional
EP 20153251 · Jan 22, 2020 · regional
EP 20153253 · Jan 22, 2020 · regional
EP 20153628 · Jan 24, 2020 · regional
EP 20153630 · Jan 24, 2020 · regional
EP 20187717 · Jul 24, 2020 · regional
Continuity (1)
Related Publication 20230136495A1 · May 4, 2023
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