Oligothiophene Versus β‐Sheet Peptide: Synthesis and Self‐Assembly of an Organic Semiconductor‐Peptide Hybrid
Source abstract
Abstract
A first representative of a novel class of bioinspired materials is introduced, a fully symmetric hybrid between an oligothiophene and a β-sheet peptide. The conjugate is synthesized via “click chemistry”, and employs a switch-peptide segment to gain control over the self-assembly motif of the peptide part. The self-organization properties of the hybrid are investigated.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supramolecular Self-Assembly in Materials · Polydiacetylene-based materials and applications · Click Chemistry and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (50)
Show source-provided references
1. 10.1038/4435910.1038/44359 ↗
2. 10.1038/3211810.1038/32118 ↗
3. 10.1002/smll.20040013010.1002/smll.200400130 ↗
4. 10.1016/S0379-6779(97)80718-710.1016/S0379-6779(97)80718-7 ↗
5. 10.1002/(SICI)1521-4095(199803)10:4<324::AID-ADMA324>3.0.CO;2-E10.1002/(SICI)1521-4095(199803)10:4<324::AID-ADMA324>3.0.CO;2-E ↗
6. 10.1016/S0379-6779(98)00274-410.1016/S0379-6779(98)00274-4 ↗
7. 10.1002/1521-3765(20021115)8:22<5072::AID-CHEM5072>3.0.CO;2-M10.1002/1521-3765(20021115)8:22<5072::AID-CHEM5072>3.0.CO;2-M ↗
8. 10.1021/ja011209v10.1021/ja011209v ↗
9. 10.1002/(SICI)1522-2675(19991215)82:12<2160::AID-HLCA2160>3.0.CO;2-410.1002/(SICI)1522-2675(19991215)82:12<2160::AID-HLCA2160>3.0.CO;2-4 ↗
10. 10.1016/j.bmcl.2005.07.00410.1016/j.bmcl.2005.07.004 ↗
11. 10.1016/j.tetlet.2005.09.12310.1016/j.tetlet.2005.09.123 ↗
12. 10.1021/ol703090f10.1021/ol703090f ↗
13. 10.1021/bc000026f10.1021/bc000026f ↗
14. 10.1039/B415454A10.1039/B415454A ↗
15. 10.1021/ja045835e10.1021/ja045835e ↗
16. 10.1002/adma.20050018310.1002/adma.200500183 ↗
17. 10.1039/b413974g10.1039/b413974g ↗
18. 10.1016/j.tet.2008.06.03310.1016/j.tet.2008.06.033 ↗
19. 10.1021/ja805491d10.1021/ja805491d ↗
20. 10.1002/(SICI)1521-3765(20000218)6:4<735::AID-CHEM735>3.0.CO;2-A10.1002/(SICI)1521-3765(20000218)6:4<735::AID-CHEM735>3.0.CO;2-A ↗
21. 10.1002/1521-3773(20000804)39:15<2679::AID-ANIE2679>3.0.CO;2-210.1002/1521-3773(20000804)39:15<2679::AID-ANIE2679>3.0.CO;2-2 ↗
22. 10.1016/0968-0896(96)00051-X10.1016/0968-0896(96)00051-X ↗
23. 10.1039/B615985K10.1039/B615985K ↗
24. 10.1002/pola.2052710.1002/pola.20527 ↗
25. 10.1039/b105185g10.1039/b105185g ↗
26. 10.1039/b503275j10.1039/b503275j ↗
27. 10.1002/adma.20030637910.1002/adma.200306379 ↗
28. 10.1021/ma034124i10.1021/ma034124i ↗
29. 10.1021/ma702278a10.1021/ma702278a ↗
30. 10.1021/ja803026j10.1021/ja803026j ↗
31. 10.1021/ja076553s10.1021/ja076553s ↗
32. 10.1002/chem.20070132510.1002/chem.200701325 ↗
33. 10.1039/b800860d10.1039/b800860d ↗
34. 10.1021/ma800976e10.1021/ma800976e ↗
35. 10.1021/ja060759w10.1021/ja060759w ↗
36. 10.1021/bi99051010.1021/bi990510 ↗
37. 10.1111/j.1399-3011.1986.tb01826.x10.1111/j.1399-3011.1986.tb01826.x ↗
38. 10.1021/ja064987210.1021/ja0649872 ↗
39. Quibbel M. · 2000 · 115
40. 10.1021/ja961509q10.1021/ja961509q ↗
41. 10.1002/anie.20045404510.1002/anie.200454045 ↗
42. 10.1016/j.tetlet.2004.07.16210.1016/j.tetlet.2004.07.162 ↗
43. 10.1039/B312129A10.1039/B312129A ↗
44. 10.1021/ma071810z10.1021/ma071810z ↗
45. 10.1021/jo011148j10.1021/jo011148j ↗
46. 10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-410.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4 ↗
47. 10.1021/ol061657d10.1021/ol061657d ↗
48. 10.1002/ange.1995107031010.1002/ange.19951070310 ↗
49. 10.1021/ja981363q10.1021/ja981363q ↗
50. Previous experiments conducted by directly mixing dichloromethane and methanol 1:1 then adding the solvent to the sample did not lead to any comparable suprastructure formation after 2 days.