Synthesis, structure, and photoluminescence properties of coordination polymers of 4,4′,4′′,4′′′-tetrakiscarboxyphenylsilane and 3,5-bis(1′,2′,4′-triazol-1′-yl)pyridine
Three coordination polymers (CPs) incorporating both 4,4′,4′′,4′′′-tetrakiscarboxyphenylsilane (H 4 tcps) and 3,5-bis(1′,2′,4′-triazol-1′-yl)pyridine (btap), namely [Co 2 (tcps)(btap)(H 2 O) 3 ] ( 1 ), [Co 3 (Htcps) 2 (btap)(H 2 O) 6 ] ( 2 ) and [Cd 3 (Htcps) 2 (btap)(H 2 O) 6 ] ( 3 ), were synthesi...
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Veröffentlicht in: | CrystEngComm 2020-01, Vol.22 (3), p.534-545 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Three coordination polymers (CPs) incorporating both 4,4′,4′′,4′′′-tetrakiscarboxyphenylsilane (H
4
tcps) and 3,5-bis(1′,2′,4′-triazol-1′-yl)pyridine (btap), namely [Co
2
(tcps)(btap)(H
2
O)
3
] (
1
), [Co
3
(Htcps)
2
(btap)(H
2
O)
6
] (
2
) and [Cd
3
(Htcps)
2
(btap)(H
2
O)
6
] (
3
), were synthesized by a solvothermal method. Compound
1
features a 3D (3,4,5)-connected framework with the (6·7
5
·8
4
)(6
4
·8
2
)(7
2
·9) topology. Compounds
2
and
3
are isostructural, which display an unusual 1D + 3D → 3D polythreaded supramolecular architecture with the 1D chain inserted into the channels of the two-fold interpenetrating 3D motif. Hydrogen bonds among the 3D anionic motif and the 1D cationic motif further stabilize the compounds. The structure of compounds
2
and
3
is a 3D 3-connected framework with the point symbol (10
3
)
4
. The luminescence properties of compound
3
in their solid state and as dispersed in various solvents were investigated. Luminescence studies have revealed that compound
3
exhibits high sensitivity and stable anti-interference towards Fe
3+
and Cu
2+
cations in aqueous solution.
Three coordination polymers based on 4,4′,4′′,4′′′-tetrakiscarboxyphenylsilane and 3,5-bis(1′,2′,4′-triazol-1′-yl)pyridine ligands were synthesized. Luminescence studies revealed that [Cd
3
(Htcps)
2
(btap)(H
2
O)
6
] exhibits a luminescence quenching response towards Fe
3+
and Cu
2+
. |
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ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/c9ce01529a |