Bis-urea gelators for curable ink applications
View Patent ↗The disclosure provides curable inks including a bis-urea gelator having the structure of Formula I. wherein R and R′ each, independently of the other, is a saturated aliphatic hydrocarbon group selected from the group consisting of (1) linear aliphatic groups, (2) branched aliphatic groups, (3) cyclic aliphatic groups, (4) aliphatic groups containing both cyclic and acyclic portions, any carbon atom of the saturated aliphatic hydrocarbon group may be optionally substituted with an alkyl group (cyclic or acyclic), wherein (1) and (2) groups have a carbon number of from about 1 to about 22 carbons, and wherein (3) and (4) groups have a carbon number of from about 4 to about 10 carbons; and X is selected from the group consisting of: (i) an alkylene group, (ii) an arylene group, (iii) an arylalkylene group, and (iv) an alkylarylene group.
1. A bis-urea gelator having a structure of Formula I:
wherein R 1 and R 1 ′ are different from each other, and each independently of the other, is saturated aliphatic hydrocarbon group selected from the group consisting of (1) linear aliphatic groups, (2) branched aliphatic groups, (3) cyclic aliphatic groups, (4) aliphatic groups containing both cyclic and acyclic portions, any carbon atom of the saturated aliphatic hydrocarbon group may be optionally substituted with an alkyl group (cyclic or acyclic), wherein (1) and (2) groups have a carbon number of from 14 to 18 carbons, and wherein (3) and (4) groups have a carbon number of from 4 to 10 carbons; and X is an aliphatic group containing both cyclic and acyclic portions, any carbon atom of the aliphatic hydrocarbon group may be optionally substituted with an alkyl group (cyclic or acyclic).
2. A bis-urea gelator having a structure of Formula I:
wherein each one of R 1 and R 1 ′ is a linear aliphatic group containing from 14 to 18 carbon atoms substituted with one or more C 1 -C 3 alkyl; and X is an aliphatic group containing both cyclic and acyclic portions, any carbon atom of the aliphatic hydrocarbon group may be optionally substituted with an alkyl group (cyclic or acyclic).
3. The gelator according to claim 2 , wherein R 1 and R 1 ′ are the same as each other.
4. The gelator according to claim 2 , wherein each one of the one or more cyclic portions is independently selected from the group consisting of cyclopropylene, 1,2-cyclobutylene, 1,3-cyclobutylene, cyclopentylene, 1,3-cyclopenylene, cyclohexylene, 1,3-cyclohexylene, and 1,4-cyclohexylene.
5. The gelator according to claim 2 , wherein the acyclic portion comprises a C 1 -C 8 alkylene.
6. A bis-urea gelator having a structure of Formula II:
wherein each R 2 each R 2 ′ each R 3 and each R 3 ′, independently of one another is H or C 1 -C 3 alkyl; R 4 , R 4 ′, R 5 , and R 5 ′ are methyl; n and n′ each, independently of the other, is from 10 to 15; p is from 1 to 10; and Z and Z′ each, independently of the other, is selected from the group consisting of null, cyclopropylene, 1,2-cyclobutylene, 1,3-cyclobutylene, cyclopentylene, 1,3-cyclopenylene, cyclohexylene, 1,3-cyclohexylene, and 1,4-cyclohexylene, wherein at least one of Z and Z′ is not null.
7. The gelator according to claim 6 , wherein the Z and Z′ are each 1,4-cyclohexylene and p is from 1 to 4.
8. The gelator according to claim 6 , wherein the each one of the one or more cyclic portions is 1,4-cyclohexylene.
9. The gelator according to claim 6 , wherein the acyclic portion is methylene.
10. The gelator according to claim 6 , wherein at least one of Z and Z′ is not null.
11. A bis-urea gelator having a structure of Formula III:
wherein R 4 , R 4 ′, R 5 , and R 5 ′ are methyl; and p is from 1 to 10.
12. The gelator according to claim 6 , p is 1.