IP Library Granted Patent US 12709711
Granted Patent B2
US 12709711 · App. 19/201,726 · Granted Aug 18, 2026

Liquid crystal elastomer compositions and methods of making the same

Inventors: Timothy White (Longmont, CO); Tayler Hebner (Longmont, CO); Joselle Mccracken (Westminster, CO); Brian Donovan (Redwood City, CA); Christopher Bowman (Boulder, CO); Grant Bauman (Boulder, CO)
Assignee: THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE
C09K19/3809
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Quick Facts
Patent No.
US 12709711
App. No.
19/201,726
Granted
Aug 18, 2026
Kind
B2
Abstract

Described herein are various embodiments for liquid crystal elastomers (LCE) formed from liquid crystalline monomers having 4-(6-(acryloyloxy)n-oxy)phenyl-4-(6-(acryloyloxy)m-oxy)benzoate (CnBAPE) as the mesogenic core. The LCEs described herein have improved thermotropic characteristics, including lower thermotropic activation temperatures. The LCEs described herein may also incorporate azobenzene to thereby also enhance the phototropic properties of the LCE.

Claims (24)

1 . A liquid crystal elastomer, comprising:

a first liquid crystalline monomer having a first mesogenic core;

a second liquid crystalline monomer having a second mesogenic core;

a third liquid crystalline monomer having a third mesogenic core;

wherein the first mesogenic core, the second mesogenic core, and the third mesogenic core are all different; and

wherein the first mesogenic core comprises 4-(6-(acryloyloxy)n-oxy)phenyl-4-(6-(acryloyloxy)m-oxy)benzoate, with n being any one of pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, and m being any one of pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl.

2 . The liquid crystal elastomer of claim 1 , wherein n and m in 4-(6-(acryloyloxy)n-oxy)phenyl-4-(6-(acryloyloxy)m-oxy)benzoate are hexyl.

3 . The liquid crystal elastomer of claim 1 , wherein the second mesogenic core comprises more than two aromatic rings.

4 . The liquid crystal elastomer of claim 1 , wherein the second mesogenic core comprises 1,4-Bis[4-(n-acryloyloxybutyloxy)benzoyloxy]-2-methylbenzene.

5 . The liquid crystal elastomer of claim 4 , wherein the value of n in 1,4-Bis[4-(n-acryloyloxybutyloxy)benzoyloxy]-2-methylbenzene is from 3 to 11.

6 . The liquid crystal elastomer of claim 4 , wherein the molar ratio of 4-(6-(acryloyloxy)n-oxy)phenyl-4-(6-(acryloyloxy)m-oxy)benzoate to 1,4-Bis[4-(n-acryloyloxybutyloxy)benzoyloxy]-2-methylbenzene is about 1:1.

7 . The liquid crystal elastomer of claim 1 , wherein a thermotropic actuation temperature of the liquid crystal elastomer is less than 50° C.

8 . The liquid crystal elastomer of claim 1 , further comprising:

one or more thiol monomers.

9 . The liquid crystal elastomer of claim 1 , further comprising:

at least one first thiol monomer serving as a chain extender; and

at least one second thiol monomer serving as a crosslinker.

10 . The liquid crystal elastomer of claim 1 , wherein the liquid crystal elastomer is one of surface aligned, mechanically aligned, or rheologically aligned.

11 . The liquid crystal elastomer of claim 1 , further comprising:

an azobenzene.

12 . The liquid crystal elastomer of claim 11 , wherein the second mesogenic core comprises 1,4-Bis[4-(n-acryloyloxybutyloxy)benzoyloxy]-2-methylbenzene, wherein the value of n in 1,4-Bis[4-(n-acryloyloxybutyloxy)benzoyloxy]-2-methylbenzene is from 3 to 11.

13 . The liquid crystal elastomer of claim 12 , wherein the value of n in 1,4-Bis[4-(n-acryloyloxybutyloxy)benzoyloxy]-2-methylbenzene is 6.

14 . The liquid crystal elastomer of claim 12 , wherein the weight ratio of 4-(6-(acryloyloxy)n-oxy)phenyl-4-(6-(acryloyloxy)m-oxy)benzoate to 1,4-Bis[4-(n-acryloyloxybutyloxy)benzoyloxy]-2-methylbenzene is from about 1:1 to about 1:3.

15 . The liquid crystal elastomer of claim 11 , wherein the liquid crystal elastomer is surface aligned.