Synthesis, structures and electrocatalytic properties of coordination polymers of 4,4′,4′′,4′′′-tetrakiscarboxyphenylsilane and 1,3,5-tris(2-methyl-1-imidazol-1-yl)benzene
Four Ni, Co, Cu, Zn-containing coordination polymers incorporating 4,4′,4′′,4′′′-tetrakiscarboxyphenylsilane (H 4 tcps) and 1,3,5-tris(2-methyl-1 H -imidazol-1-yl)benzene (tmib) ligands, namely [Ni 6 (tcps) 3 (tmib) 4 (H 2 O) 2 ] ( 1 ), [Co 6 (tcps) 3 (tmib) 4 ] ( 2 ), [Cu 2 (tcps)(tmib)(H 2 O)] ( 3...
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Published in | CrystEngComm Vol. 26; no. 7; pp. 985 - 994 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
12.02.2024
|
Subjects | |
Online Access | Get full text |
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Summary: | Four Ni, Co, Cu, Zn-containing coordination polymers incorporating 4,4′,4′′,4′′′-tetrakiscarboxyphenylsilane (H
4
tcps) and 1,3,5-tris(2-methyl-1
H
-imidazol-1-yl)benzene (tmib) ligands, namely [Ni
6
(tcps)
3
(tmib)
4
(H
2
O)
2
] (
1
), [Co
6
(tcps)
3
(tmib)
4
] (
2
), [Cu
2
(tcps)(tmib)(H
2
O)] (
3
) and [Zn
2
(tcps)(tmib)] (
4
), were synthesized by the solvothermal method. Compounds
1
and
2
were isostructural with three-dimensional (3D) (3,4)-connected frameworks. Compounds
3
and
4
possessed (3,4)-connected 3D networks with (6·8
2
)(6·8
5
)(6
2
·8
2
·10
2
)(6
2
·8) and (4·6·8)(4·6
3
·8
2
)(6
6
)(6
7
·8
3
) topology, respectively. The thermal derivatives of compounds
1
and
2
, Co-800 and Ni-700, exhibited low OER overpotentials of 338 and 388 mV to achieve a current density of 10 mA cm
−2
and hold their electrocatalytic activity for at least 9 hours in 1 M KOH.
Coordination polymers based on H
4
tcps and tmib were synthesized, and the pristine crystals and thermal derivation composites were converted into their metal hydroxides and oxidized hydroxides in alkaline solution as OER catalysts. |
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Bibliography: | Electronic supplementary information (ESI) available. CCDC For ESI and crystallographic data in CIF or other electronic format see DOI 2299226-2299229 https://doi.org/10.1039/d3ce01266b |
ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/d3ce01266b |