Hollow Spherical Covalent Organic Frameworks from Nonplanar or Planar Monomers for the Fluorescence Detection of Telomere DNA: Role of the 2-(2-Azidoethoxy)ethoxy Group
Source abstract
Abstract
Construction of covalent organic frameworks (COFs) with a hollow and uniform morphology─regardless of whether planar or nonplanar building blocks are employed─is still challenging. Herein, we report a facile strategy for the self-assembly and template-free synthesis of hollow spherical COFs by increasing the percentage content of 2-(2-azidoethoxy)ethoxy groups in the pore skeleton of a COF. Moreover, the morphological diversity dependent on the percentage content of 2-(2-azidoethoxy)ethoxy groups in the COF structure is observed. COF-100%N3, which is formed by the polycondensation of the nonplanar 1,3,5-tris(4-aminophenyl)benzene monomer, having the highest percentage content of the 2-(2-azidoethoxy)ethoxy group (100%), is self-assembled into homogeneous hollow spheres. For the first time, our strategy effectively explores the self-assembly of the planar monomer into a hollow spherical COF. Hollow spherical TPP-COF-100%N3 is formed via the polycondensation of the planar 2,4,6-tris(4-aminophenyl)pyridine monomer and 2-(2-azidoethoxy)ethoxy group (100%). Due to the favorable characteristics of its specific surface area and hollow mesoporous nature, spherical COF-100%N3 functions as an enticing sensing platform for the fluorescence-selective and -sensitive detection of telomere DNA. Consequently, this research study documents a facile strategy for constructing a unique hollow spherical COF and expands the application of COFs as fluorescent platforms for DNA detection.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Covalent Organic Framework Applications · Luminescence and Fluorescent Materials · Metal-Organic Frameworks: Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials and Optoelectronic Science, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan
Institute of Medical Science and Technology, National Sun Yat-sen University, Kaohsiung 804201, Taiwan
Inorganic Chemistry I, Technische Universität Dresden, Bergstraße 66, 01069 Dresden, Germany
Chemistry Department, Faculty of Science, Assiut University, Assiut 71516, Egypt
Funding
Ministry of Science and Technology, Taiwan
References (70)
Show source-provided references
1. 10.1126/science.aal158510.1126/science.aal1585 ↗
2. 10.1002/adfm.20170555310.1002/adfm.201705553 ↗
3. 10.1039/D0CS00199F10.1039/D0CS00199F ↗
4. 10.1039/C8TA04781B10.1039/C8TA04781B ↗
5. 10.1039/D0TA07281H10.1039/D0TA07281H ↗
6. 10.1039/D0TC01872D10.1039/D0TC01872D ↗
7. 10.1021/jacs.9b0048510.1021/jacs.9b00485 ↗
8. 10.1038/s41557-018-0141-510.1038/s41557-018-0141-5 ↗
9. 10.1039/C8CS00919H10.1039/C8CS00919H ↗
10. Ying Y. · Adv. Mater. · 2021 · 2104946
11. 10.1038/s41467-019-11264-z10.1038/s41467-019-11264-z ↗
12. 10.1021/ja409421d10.1021/ja409421d ↗
13. 10.1002/adom.20200064110.1002/adom.202000641 ↗
14. 10.1039/D2TA00328G10.1039/D2TA00328G ↗
15. 10.1039/C6CC00853D10.1039/C6CC00853D ↗
16. 10.1039/D1CS00559F10.1039/D1CS00559F ↗
17. 10.1021/jacs.7b0409610.1021/jacs.7b04096 ↗
18. 10.1002/adma.20170750910.1002/adma.201707509 ↗
19. 10.1021/jacs.7b0092510.1021/jacs.7b00925 ↗
20. 10.1039/C8CS00376A10.1039/C8CS00376A ↗
21. 10.1039/C3NR05192G10.1039/C3NR05192G ↗
22. 10.1002/adma.20160291410.1002/adma.201602914 ↗
23. 10.1039/C8TB02870B10.1039/C8TB02870B ↗
24. 10.1021/acsanm.9b0260310.1021/acsanm.9b02603 ↗
25. 10.1016/j.talanta.2020.12086410.1016/j.talanta.2020.120864 ↗
26. 10.1002/chem.20190473110.1002/chem.201904731 ↗
27. 10.1016/j.memsci.2018.08.04310.1016/j.memsci.2018.08.043 ↗
28. 10.1038/ncomms778610.1038/ncomms7786 ↗
29. 10.1002/anie.20160008710.1002/anie.201600087 ↗
30. 10.1021/jacs.7b0283610.1021/jacs.7b02836 ↗
31. 10.1021/acsami.8b2186710.1021/acsami.8b21867 ↗
32. 10.1016/j.snb.2020.12807710.1016/j.snb.2020.128077 ↗
33. 10.1038/s41467-020-20162-810.1038/s41467-020-20162-8 ↗
34. 10.1002/hep.3084410.1002/hep.30844 ↗
35. 10.3390/cancers1305099410.3390/cancers13050994 ↗
36. 10.3390/cancers1103039610.3390/cancers11030396 ↗
37. 10.1016/j.bios.2019.03.05510.1016/j.bios.2019.03.055 ↗
38. 10.1021/acs.analchem.8b0047710.1021/acs.analchem.8b00477 ↗
39. 10.1016/S0959-8049(97)00062-210.1016/S0959-8049(97)00062-2 ↗
40. 10.3390/genes1004031810.3390/genes10040318 ↗
41. 10.1038/nrm284810.1038/nrm2848 ↗
42. 10.1016/j.celrep.2020.10845710.1016/j.celrep.2020.108457 ↗
43. 10.1158/0008-5472.CAN-08-302810.1158/0008-5472.CAN-08-3028 ↗
44. 10.1096/fba.2019-0008810.1096/fba.2019-00088 ↗
45. 10.1093/nar/30.10.e4710.1093/nar/30.10.e47 ↗
46. 10.1002/bio.359510.1002/bio.3595 ↗
47. 10.1016/j.bioorg.2020.10382110.1016/j.bioorg.2020.103821 ↗
48. 10.3390/genes1009069710.3390/genes10090697 ↗
49. 10.1093/nar/gkx121310.1093/nar/gkx1213 ↗
50. 10.1016/j.snb.2021.12965910.1016/j.snb.2021.129659 ↗
51. 10.20964/2020.11.2810.20964/2020.11.28 ↗
52. 10.1016/j.bios.2021.11299910.1016/j.bios.2021.112999 ↗
53. 10.1016/j.aca.2019.11.03510.1016/j.aca.2019.11.035 ↗
54. 10.1039/C3CC47454B10.1039/C3CC47454B ↗
55. 10.1007/s00604-014-1348-910.1007/s00604-014-1348-9 ↗
56. 10.1021/ja800604z10.1021/ja800604z ↗
57. 10.1039/C3CS60277J10.1039/C3CS60277J ↗
58. 10.1039/C4CS00300D10.1039/C4CS00300D ↗
59. 10.1007/s00604-019-3368-y10.1007/s00604-019-3368-y ↗
60. 10.1021/am404811j10.1021/am404811j ↗
61. 10.1016/j.talanta.2020.12150510.1016/j.talanta.2020.121505 ↗
62. 10.1021/ja510926w10.1021/ja510926w ↗
63. 10.1038/s41467-020-18844-410.1038/s41467-020-18844-4 ↗
64. 10.1002/anie.20171037810.1002/anie.201710378 ↗
65. 10.1002/adma.20160476510.1002/adma.201604765 ↗
66. 10.1002/anie.20140977610.1002/anie.201409776 ↗
67. 10.1002/anie.20170852610.1002/anie.201708526 ↗
68. 10.1039/c0sm01559h10.1039/c0sm01559h ↗
69. 10.1021/acs.analchem.7b0186110.1021/acs.analchem.7b01861 ↗
70. 10.1039/C8AN00816G10.1039/C8AN00816G ↗