Chalcogen bonds provide supramolecular association of beta-octamolybdate and chalconium cations
The interactions of triple σ-(Q IV )-hole donating chalconium cations ([Q(bPh)R] + , when Q = S, Se, and Te) with nucleophilic beta-octamolybdate ([β-Mo 8 O 26 ] 4− ) result in supramolecular association. The main focus of such assembly is on σ-(Q IV )-hole recognition by the molybdate in cations wi...
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Published in | Inorganic chemistry frontiers Vol. 11; no. 24; pp. 892 - 8915 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Royal Society of Chemistry
03.12.2024
|
Subjects | |
Online Access | Get full text |
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Summary: | The interactions of triple σ-(Q
IV
)-hole donating chalconium cations ([Q(bPh)R]
+
, when Q = S, Se, and Te) with nucleophilic beta-octamolybdate ([β-Mo
8
O
26
]
4−
) result in supramolecular association. The main focus of such assembly is on σ-(Q
IV
)-hole recognition by the molybdate in cations with a biphenyl aromatic fragment. This leads to a remarkable diversity of the association patterns producing: (i) neutral 4 : 1 {[Q(bPh)R]
4
[β-Mo
8
O
26
]} complexes with cations stacked by π-π interactions; (ii) (Bu
4
N)
+
, [Q(bPh)R]
+
and [β-Mo
8
O
26
]
4−
complexes of 2 : 2 : 1 stoichiometry with π-π interactions; (iii) (Bu
4
N)
+
, [Q(bPh)R]
+
and [β-Mo
8
O
26
]
4−
complexes of a 2 : 2 : 1 stoichiometry without π-π interactions; and (iv) {[Q(bPh)R]
2
}
2
[β-Mo
8
O
26
] salts with π-π stacked cations but lacking any (Q
IV
) O interactions. Moreover, interactions in the system can drive the reorganization of [β-Mo
8
O
26
]
4−
into [α-Mo
8
O
26
]
4−
. The halogen-bonded (Q
IV
) O {(Q(bPh)R)
x
[β-Mo
8
O
26
]
4−
} (
x
= 2 and 4) assemblies, π-π stacked cationic dimers {(Q(bPh)R)
2
}
2+
and complicated associates based on both types of interactions have been the subjects of crystallographic and computational studies.
Organic-inorganic supramolecular associates of chalconium cations and beta-octamolybdate anion unlock the potential of lacunary type polyoxometalates to serve as noncovalent ligands in the comparison with classical coordination chemistry of POM. |
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Bibliography: | https://doi.org/10.1039/d4qi02258k Electronic supplementary information (ESI) available. CCDC 2381722-2381728, 2358696 and 2358690. For ESI and crystallographic data in CIF or other electronic format see DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ISSN: | 2052-1553 2052-1545 2052-1553 |
DOI: | 10.1039/d4qi02258k |