Dithienylpyrrole-based biosensors and methods for their preparation and use
View Patent ↗Dithienylpyrrole compounds, compositions containing dithienylpyrrole polymers, and methods for making the compounds and compositions are disclosed herein. The compositions containing dithienylpyrrole polymers, can for example, be used as conducting polymers in biosensors for detecting analytes in a sample.
1. A method to prepare a nanostructure film on a surface of a substrate, the method comprising:
forming a composition comprising dithienylpyrrole monomers, at least one metal precursor, at least one organic solvent, at least one supporting electrolyte, and at least one amine compound;
allowing metal nanostructures to form in the composition;
contacting the composition having the metal nanostructures with the substrate under a condition effective to covalently bind two or more dithienylpyrrole monomers to form a dithienylpyrrole polymer; and
forming the nanostructure film on at least a portion of the surface of the substrate.
2. The method of claim 1 , wherein forming the composition comprising the dithienylpyrrole monomers, the at least one metal precursor, the at least one organic solvent, the at least one supporting electrolyte, and the at least one amine compound comprises contacting the dithienylpyrrole monomers, the at least one metal precursor, the at least one organic solvent, the at least one supporting electrolyte, and the at least one amine compound in a weight ratio of about 1:1:83:10:5 to about 3:1:66:20:10.
3. The method of claim 1 , wherein forming the composition comprising the dithienylpyrrole monomers, the at least one metal precursor, the at least one organic solvent, the at least one supporting electrolyte, and the at least one amine compound comprises contacting the dithienylpyrrole monomers represented by Formula Ia:
wherein:
Z is a bivalent hydrocarbyl group selected from the group consisting of alkylene, alkenylene, and alkynylene;
R 1 , R 2 , R 3 , and R 4 are each independently C 1 -C 6 alkyl, C 2 -C 6 alkylene, C 2 -C 6 alkyne, hydrogen, or halogen; and
R 5 , R 6 , R 7 , and R 8 are each independently C 1 -C 10 alkyl, C 2 -C 10 alkylene, C 1 -C 10 alkyne, hydrogen, or halogen, with the at least one metal precursor, the at least one organic solvent, the at least one supporting electrolyte, and the at least one amine compound.
4. The method of claim 3 , wherein the dithienylpyrrole monomer is a 2,5-di(2-thienyl)-1-pyrrol-1-(p-phenylacetic acid) monomer or a 2,5-di-(2-thienyl)-1H-pyrrole-1-(p-phenylbutanoic acid) monomer.
5. The method of claim 1 , wherein forming the composition comprising the dithienylpyrrole monomers, the at least one metal precursor, the at least one organic solvent, the at least one supporting electrolyte, and the at least one amine compound comprises contacting the dithienylpyrrole monomers, the at least one organic solvent, the at least one supporting electrolyte, and the at least one amine compound with the at least one metal precursor selected from the group consisting of gold metal precursors, silver gold precursors, palladium metal precursors, copper metal precursors, nickel metal precursors, platinum metal precursors, rhodium nanostructures, ruthenium nanostructures, and a combination thereof.
6. The method of claim 1 , wherein forming the composition comprising the dithienylpyrrole monomers, the at least one metal precursor, the at least one organic solvent, the at least one supporting electrolyte, and the at least one amine compound comprises contacting the dithienylpyrrole monomers, the at least one metal precursor, the at least one supporting electrolyte, and the at least one amine compound with the at least one organic solvent selected from the group consisting of n-hexane, chloroform, dichloromethane, n-heptane, carbon tetrachloride, and a mixture thereof.
7. The method of claim 1 , wherein forming the composition comprising the dithienylpyrrole monomers, the at least one metal precursor, the at least one organic solvent, the at least one supporting electrolyte, and the at least one amine compound comprises contacting the dithienylpyrrole monomers, the at least one metal precursor, the at least one organic solvent, and the at least one amine compound with the at least one supporting electrolyte represented by Formula II: (Y) 4 N + ClO4 − , wherein Y is a C 1 -C 30 alkyl, a C 1 -C 30 alkylene, a C 1 -C 30 alkyne, or an aromatic hydrocarbon group.
8. The method of claim 1 , wherein forming the composition comprising the dithienylpyrrole monomers, the at least one metal precursor, the at least one organic solvent, the at least one supporting electrolyte, and the at least one amine compound comprises contacting the dithienylpyrrole monomers, the at least one metal precursor, the at least one organic solvent, and the at least one supporting electrolyte with the at least one amine compound represented by Formula III:
wherein X is a C 6 -C 10 alkyl.
9. The method of claim 1 , wherein contacting the composition having the metal nanostructures with the substrate comprises contacting the composition with an electrode.
10. The method of claim 1 , wherein contacting the composition having the metal nanostructures with the substrate comprises cyclic voltammetry scanning.
11. A biosensor, comprising:
a working electrode configured to immobilize a bioreactive material, wherein the bioreactive material is reactive with a target material, and wherein the working electrode comprises the nanostructure film prepared according to claim 1 .
12. The biosensor of claim 11 , wherein the biosensor further comprises a reference electrode.
13. The biosensor of claim 11 , wherein the bioreactive material is reactive specifically with the target material.
14. The biosensor of claim 11 , wherein the bioreactive material is selected from the group consisting of enzymes, antibodies, nucleic acids, peptides, peptide nucleic acids (PNA), aptamers, and a combination thereof.
15. The method of claim 5 , wherein the at least one metal precursor is a gold metal precursor, HAuCl 4 , AgNO 3 , or a combination thereof.
16. The method of claim 7 , wherein Y is a C 1 -C 4 linear alkyl.
17. The method of claim 7 , wherein the at least one supporting electrolyte is selected from the group consisting of tetrabutylammonium perchlorate, tetrapropylammonium perchlorate, tetramethylammonium perchlorate, tetraamylammonium perchlorate, tetramethylammonium acetate, hexadecyltrimethylammonium acetate, hexadecyltrimethylammonium perchlorate, and a combination thereof.
18. The method of claim 8 , wherein the at least one amine compound is selected from the group consisting of oleylamine, 7-tetradecenylamine, 8-hexadecenylamine, and 11-docosenylamine.
19. The method of claim 1 , wherein forming the composition comprises stirring the composition at a temperature of about 45° C. to about 60° C. for about 10 hours to about 48 hours.
20. The method of claim 19 , wherein forming the composition further comprises maintaining the stirred composition at about room temperature for about 48 hours to about 72 hours.
21. The method of claim 10 , wherein the cyclic voltammetry scanning is performed at a voltage of about 0 V to about 1 V.
22. The method of claim 10 , wherein the cyclic voltammetry scanning is performed at a scanning rate of about 10 mV/s to about 500 mV/s.