Host–Guest Chemistry of Helical Copper(I) Coordination Polymers
Source abstract
Abstract
In this paper, we present a series of one-dimensional coordination polymers built of achiral components: relatively small and rigid halogenated triazole Schiff base and copper(I) salts. The coordination polymer exhibits quite rare helicity, in which the metal ions are arranged in a helical pattern. Self-recognition of the neighboring polymeric chains leads to the formation of one-dimensional channels occupied by solvent molecules, which can be easily removed by thermal treatment, resulting in the formation of a porous material that reveals its ability to capture CO 2 and small organic particles. The anion, situated at the corners of the channels, exerts a negligible influence on the structure. However, it has an impact on the physicochemical properties, including sorption and spectroscopic properties. Unusually for copper(I) compounds, the title polymers exhibit emission in the deep-red region.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications · Supramolecular Chemistry and Complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Faculty of Chemistry, University of Wrocław, ul. Joliot-Curie 14, Wrocław 50-383, Poland
Institute of Low Temperature and Structure Research, Polish Academy of Sciences, ul. Okólna 2, Wrocław 50-422, Poland
References (77)
Show source-provided references
1. 10.1016/j.ccr.2021.21406410.1016/j.ccr.2021.214064 ↗
2. Steed, J. L.; Atwood, J. W. Crystal Engineering. In Supramolecular Chemistry ; Wiley: 2022; pp 537–646.
3. 10.1039/B207466B10.1039/B207466B ↗
4. 10.1002/anie.20030061010.1002/anie.200300610 ↗
5. 10.1021/ja067374y10.1021/ja067374y ↗
6. 10.1080/00958972.2018.143916310.1080/00958972.2018.1439163 ↗
7. 10.1021/cr200324t10.1021/cr200324t ↗
8. 10.1016/j.ccr.2019.21314510.1016/j.ccr.2019.213145 ↗
9. 10.1021/acs.cgd.1c0040610.1021/acs.cgd.1c00406 ↗
10. 10.1016/j.mattod.2017.07.00610.1016/j.mattod.2017.07.006 ↗
11. 10.1002/anie.20070393410.1002/anie.200703934 ↗
12. 10.1107/S205252062300673X10.1107/S205252062300673X ↗
13. 10.1039/c3ce41461b10.1039/c3ce41461b ↗
14. 10.1021/acs.cgd.1c0095510.1021/acs.cgd.1c00955 ↗
15. 10.1002/ejic.20039020210.1002/ejic.200390202 ↗
16. 10.1016/j.poly.2011.05.00610.1016/j.poly.2011.05.006 ↗
17. 10.1021/cg101018b10.1021/cg101018b ↗
18. 10.1021/ja408870910.1021/ja4088709 ↗
19. 10.1039/B407253G10.1039/B407253G ↗
20. 10.1021/acs.inorgchem.2c0142110.1021/acs.inorgchem.2c01421 ↗
21. 10.1246/cl.16079410.1246/cl.160794 ↗
22. 10.1039/a804249g10.1039/a804249g ↗
23. 10.1016/j.ccr.2015.03.02210.1016/j.ccr.2015.03.022 ↗
24. 10.1039/D2RA06986E10.1039/D2RA06986E ↗
25. 10.1016/j.ccr.2022.21470010.1016/j.ccr.2022.214700 ↗
26. 10.1021/acs.chemrev.2c0003310.1021/acs.chemrev.2c00033 ↗
27. 10.1016/j.ccr.2006.02.01310.1016/j.ccr.2006.02.013 ↗
28. 10.1002/(SICI)1521-3773(19990215)38:4<492::AID-ANIE492>3.3.CO;2-R10.1002/(SICI)1521-3773(19990215)38:4<492::AID-ANIE492>3.3.CO;2-R ↗
29. 10.1039/D0CS01236J10.1039/D0CS01236J ↗
30. 10.1039/C5DT00205B10.1039/C5DT00205B ↗
31. 10.1039/c3cc00299c10.1039/c3cc00299c ↗
32. 10.1021/acs.cgd.6b0105210.1021/acs.cgd.6b01052 ↗
33. 10.1039/b305705b10.1039/b305705b ↗
34. 10.1021/ja001618b10.1021/ja001618b ↗
35. 10.1002/1521-3773(20010417)40:8<1529::AID-ANIE1529>3.0.CO;2-B10.1002/1521-3773(20010417)40:8<1529::AID-ANIE1529>3.0.CO;2-B ↗
36. 10.1002/1521-3765(20010917)7:18<4007::AID-CHEM4007>3.0.CO;2-J10.1002/1521-3765(20010917)7:18<4007::AID-CHEM4007>3.0.CO;2-J ↗
37. 10.1039/b104284j10.1039/b104284j ↗
38. 10.1021/ic971579d10.1021/ic971579d ↗
39. 10.1016/S0020-1693(99)00522-810.1016/S0020-1693(99)00522-8 ↗
40. 10.1002/cber.1997130092110.1002/cber.19971300921 ↗
41. 10.1002/(SICI)1099-0682(199911)1999:11<1859::AID-EJIC1859>3.0.CO;2-410.1002/(SICI)1099-0682(199911)1999:11<1859::AID-EJIC1859>3.0.CO;2-4 ↗
42. 10.1039/a800083b10.1039/a800083b ↗
43. 10.1002/(SICI)1521-3773(19991004)38:19<2945::AID-ANIE2945>3.0.CO;2-D10.1002/(SICI)1521-3773(19991004)38:19<2945::AID-ANIE2945>3.0.CO;2-D ↗
44. 10.1021/acs.inorgchem.7b0068110.1021/acs.inorgchem.7b00681 ↗
45. 10.1039/C5CE00776C10.1039/C5CE00776C ↗
46. 10.1021/acs.cgd.5b0135910.1021/acs.cgd.5b01359 ↗
47. 10.1039/C5CC05566K10.1039/C5CC05566K ↗
48. 10.1021/ic400853r10.1021/ic400853r ↗
49. 10.1039/a807522k10.1039/a807522k ↗
50. 10.1039/a807450j10.1039/a807450j ↗
51. 10.1021/ic00125a01910.1021/ic00125a019 ↗
52. 10.1002/anie.19972327110.1002/anie.199723271 ↗
53. 10.1002/1521-3773(20000703)39:13<2317::AID-ANIE2317>3.0.CO;2-B10.1002/1521-3773(20000703)39:13<2317::AID-ANIE2317>3.0.CO;2-B ↗
54. 10.1002/(SICI)1521-3773(19980420)37:7<920::AID-ANIE920>3.0.CO;2-O10.1002/(SICI)1521-3773(19980420)37:7<920::AID-ANIE920>3.0.CO;2-O ↗
55. 10.1021/acs.cgd.9b0025210.1021/acs.cgd.9b00252 ↗
56. 10.1039/C8CE01242C10.1039/C8CE01242C ↗
57. 10.1039/c1cc12914g10.1039/c1cc12914g ↗
58. 10.1016/j.ica.2013.04.01910.1016/j.ica.2013.04.019 ↗
59. 10.1021/cg400060t10.1021/cg400060t ↗
60. 10.1039/c0ce00054j10.1039/c0ce00054j ↗
61. 10.1021/acs.cgd.9b0023510.1021/acs.cgd.9b00235 ↗
62. 10.1107/S010876730704393010.1107/S0108767307043930 ↗
63. 10.1107/S205327331402637010.1107/S2053273314026370 ↗
64. 10.1107/S205322961402421810.1107/S2053229614024218 ↗
65. 10.1039/B918159H10.1039/B918159H ↗
66. Quiang G. · Angew. Chem., Int. Ed. · 2016 · 15027
67. 10.1107/S090744490804362X10.1107/S090744490804362X ↗
68. 10.1080/08927022.2018.142685510.1080/08927022.2018.1426855 ↗
69. 10.1016/j.inoche.2003.11.00810.1016/j.inoche.2003.11.008 ↗
70. 10.1016/j.molstruc.2017.05.03010.1016/j.molstruc.2017.05.030 ↗
71. 10.1039/D3CE00758H10.1039/D3CE00758H ↗
72. 10.47014/16.2.510.47014/16.2.5 ↗
73. 10.1016/j.jphotochem.2008.10.02310.1016/j.jphotochem.2008.10.023 ↗
74. 10.1021/acs.inorgchem.3c0190810.1021/acs.inorgchem.3c01908 ↗
75. 10.1039/C8DT00069G10.1039/C8DT00069G ↗
76. 10.1002/adom.20240266610.1002/adom.202402666 ↗
77. 10.1021/acs.inorgchem.3c0290010.1021/acs.inorgchem.3c02900 ↗