Surfactant‐Templated Synthesis of 1D Single‐Crystalline Polymer Nanostructures
Source abstract
Abstract
Single-crystalline poly(furfuryl alcohol) nanostructures have been synthesized in toluene solvent systems via a simple solvothermal reaction. The π–π stacking interaction is proved to be quite efficient and necessary in fabricating the 1D crystalline nanostructures. This approach may be useful for studying mechanisms of nanoscale structural organization and transformation processes in various organic–organic assembly systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Synthesis and Properties of Aromatic Compounds · Synthesis and properties of polymers
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (42)
Show source-provided references
1. 10.1021/nl025698o10.1021/nl025698o ↗
2. 10.1021/nl034917i10.1021/nl034917i ↗
3. 10.1021/la990194010.1021/la9901940 ↗
4. 10.1021/la025731m10.1021/la025731m ↗
5. 10.1126/science.275.5301.81010.1126/science.275.5301.810 ↗
6. 10.1021/jp051673c10.1021/jp051673c ↗
7. 10.1002/adma.20039009110.1002/adma.200390091 ↗
8. 10.1021/nl035102c10.1021/nl035102c ↗
9. 10.1295/polymj.37.39110.1295/polymj.37.391 ↗
10. Yue D. M. · Chem. Res. Chin. Univ. · 2003 · 19 · 112
11. 10.1021/ja036697g10.1021/ja036697g ↗
12. 10.1021/nl035102c10.1021/nl035102c ↗
13. 10.1021/jp013214r10.1021/jp013214r ↗
14. 10.1002/adma.20039009110.1002/adma.200390091 ↗
15.
16. 10.1002/ange.20035115810.1002/ange.200351158 ↗
17. 10.1002/1521-3757(20021004)114:19<3808::AID-ANGE3808>3.0.CO;2-B10.1002/1521-3757(20021004)114:19<3808::AID-ANGE3808>3.0.CO;2-B ↗
18. 10.1002/1521-3773(20021004)41:19<3656::AID-ANIE3656>3.0.CO;2-710.1002/1521-3773(20021004)41:19<3656::AID-ANIE3656>3.0.CO;2-7 ↗
19. 10.1021/ja029620l10.1021/ja029620l ↗
20. 10.1039/b304505f10.1039/b304505f ↗
21. 10.1021/ja036939c10.1021/ja036939c ↗
22. 10.1002/ange.20046010410.1002/ange.200460104 ↗
23. 10.1002/anie.20046010410.1002/anie.200460104 ↗
24. 10.1002/macp.1992.02193010110.1002/macp.1992.021930101 ↗
25. 10.1016/S0376-7388(00)00444-010.1016/S0376-7388(00)00444-0 ↗
26. 10.1002/app.1325210.1002/app.13252 ↗
27. 10.1016/S0142-9418(98)00006-310.1016/S0142-9418(98)00006-3 ↗
28. 10.1021/jp000861u10.1021/jp000861u ↗
29. 10.1002/ange.20035175210.1002/ange.200351752 ↗
30. 10.1002/anie.20035175210.1002/anie.200351752 ↗
31. 10.1016/j.micromeso.2004.12.00710.1016/j.micromeso.2004.12.007 ↗
32. 10.1021/cm000435l10.1021/cm000435l ↗
33. 10.1002/macp.1983.02184060810.1002/macp.1983.021840608 ↗
34. 10.1002/macp.1983.02184021510.1002/macp.1983.021840215 ↗
35. 10.1002/app.1974.07018052210.1002/app.1974.070180522 ↗
36. 10.1016/S0014-3057(01)00091-X10.1016/S0014-3057(01)00091-X ↗
37. 10.1016/S0014-3057(01)00090-810.1016/S0014-3057(01)00090-8 ↗
38. 10.1016/0008-6223(94)90107-410.1016/0008-6223(94)90107-4 ↗
39. 10.1002/app.1963.07007010410.1002/app.1963.070070104 ↗
40. 10.1016/S0014-3057(96)00138-310.1016/S0014-3057(96)00138-3 ↗
41. 10.1016/S0008-6223(02)00130-610.1016/S0008-6223(02)00130-6 ↗
42. 10.1021/ma00135a01910.1021/ma00135a019 ↗