C3 polypeptide supramolecular helical polymer and preparation method thereof
A supramolecular and polymer technology, which is applied in the field of C3 polypeptide supramolecular helical polymer and its preparation, can solve the problems of lack of functionalization of molecules and expensive raw materials, and achieve the effect of reliable chirality, simple preparation and low price
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Embodiment 1
[0041] Take 2.50mg of C 3 -GA monomer was added into 10 mL of tetrahydrofuran, and then sonicated and heated repeatedly until the monomer was completely dissolved. The solution was then left for 12 hours.
Embodiment 2
[0043] take multiple copies of C 3 -AG monomer, 2.5mg each, was added to 10mL of methanol, 10mL of propanol, 10mL of isopropanol, 10mL of n-butanol, 10mL of sec-butanol and 10mL of tetrahydrofuran, and then repeated ultrasonication and heating, until the monomer is completely dissolved. The solution was then left for 12 hours.
Embodiment 3
[0045] Take 2.50mg of C 3 -VG monomer was added into 10 mL of tetrahydrofuran, and then ultrasonic and heated repeatedly until the monomer was completely dissolved. The solution was then left for 12 hours.
[0046] Performance Tests and Uses
[0047] The circular dichroism of the above solutions was measured by circular dichroism (CD). Through the CD spectrum ( Figure 5 ) It can be seen that C 3 The tetrahydrofuran solution of -GA monomer presents negative and positive peaks at 243nm and 215nm, respectively, confirming that C 3 - The supramolecular helical polymer formed by layer-by-layer self-assembly of GA monomers has a right-handed helix, and the atomic force microscope (see Figure 8 ), observed that C 3 -GA assemblies are multi-strand winding fibers with helices.
[0048] C 3 THF solution of -AG monomer ( Figure 4 ) have negative, positive and negative peaks at 260nm, 245nm and 212nm, respectively, which proves that the supramolecular polymer has a left-hand...
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