Te⋯N secondary-bonding interactions in tellurium crystals: Supramolecular aggregation patterns and a comparison with their lighter congeners
Supramolecular aggregation patterns featuring Te…N secondary-bonding interactions have been identified in the crystals of tellurium(II) and tellurium(IV) compounds through a survey of the Cambridge Structural Database; 77% of examples involve tellurium(II) centres. The presence of Te…N secondary-bon...
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| Format: | Article |
| Language: | English |
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Elsevier
2022
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| Online Access: | http://eprints.sunway.edu.my/1948/ http://eprints.sunway.edu.my/1948/1/Tiekink%20Te%20N%20secondary.pdf |
| _version_ | 1848802165485731840 |
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| author | Tiekink, Edward R. T. * |
| author_facet | Tiekink, Edward R. T. * |
| author_sort | Tiekink, Edward R. T. * |
| building | SU Institutional Repository |
| collection | Online Access |
| description | Supramolecular aggregation patterns featuring Te…N secondary-bonding interactions have been identified in the crystals of tellurium(II) and tellurium(IV) compounds through a survey of the Cambridge Structural Database; 77% of examples involve tellurium(II) centres. The presence of Te…N secondary-bonding interactions has been established in approximately 11% of crystals having molecules containing tellurium and nitrogen atoms. Of the 148 Te…N contacts identified in the survey, the overwhelming majority can be classified in terms of chalcogen-bonding invoking the σ-hole bonding concept; there are five examples of π-hole
interactions. Of the aggregates featuring Te…N interactions, just over half occur within one-dimensional architectures, being chains or tapes, over a third occur with zero-dimensional aggregates with 11 examples of two-dimensional arrays and one three-dimensional architecture. While in most aggregates the tellurium atom participated in a single Te…N
interaction only, a sizeable minority (24%) featured tellurium forming two interactions. Certain classes of molecules exhibited very high propensities to form Te…N interactions: [1,3]tellurazolo[5,4-b]pyridines (80%), 2,1,3-benzotelluradiazoles (75%) and 1,3-benzotellurazoles (80%). Compared to the supramolecular association in crystals featuring 2 Se…N interactions, Te…N interactions are more likely to form, have relatively shorter Te…N distances and tend to form higher-dimensional aggregates, all observations consistent with the greater polarizability of the tellurium atom and the more pronounced σ-hole. |
| first_indexed | 2025-11-14T21:19:01Z |
| format | Article |
| id | sunway-1948 |
| institution | Sunway University |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-14T21:19:01Z |
| publishDate | 2022 |
| publisher | Elsevier |
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| spelling | sunway-19482022-01-31T00:38:46Z http://eprints.sunway.edu.my/1948/ Te⋯N secondary-bonding interactions in tellurium crystals: Supramolecular aggregation patterns and a comparison with their lighter congeners Tiekink, Edward R. T. * QD Chemistry Supramolecular aggregation patterns featuring Te…N secondary-bonding interactions have been identified in the crystals of tellurium(II) and tellurium(IV) compounds through a survey of the Cambridge Structural Database; 77% of examples involve tellurium(II) centres. The presence of Te…N secondary-bonding interactions has been established in approximately 11% of crystals having molecules containing tellurium and nitrogen atoms. Of the 148 Te…N contacts identified in the survey, the overwhelming majority can be classified in terms of chalcogen-bonding invoking the σ-hole bonding concept; there are five examples of π-hole interactions. Of the aggregates featuring Te…N interactions, just over half occur within one-dimensional architectures, being chains or tapes, over a third occur with zero-dimensional aggregates with 11 examples of two-dimensional arrays and one three-dimensional architecture. While in most aggregates the tellurium atom participated in a single Te…N interaction only, a sizeable minority (24%) featured tellurium forming two interactions. Certain classes of molecules exhibited very high propensities to form Te…N interactions: [1,3]tellurazolo[5,4-b]pyridines (80%), 2,1,3-benzotelluradiazoles (75%) and 1,3-benzotellurazoles (80%). Compared to the supramolecular association in crystals featuring 2 Se…N interactions, Te…N interactions are more likely to form, have relatively shorter Te…N distances and tend to form higher-dimensional aggregates, all observations consistent with the greater polarizability of the tellurium atom and the more pronounced σ-hole. Elsevier 2022 Article PeerReviewed text en cc_by_nc_4 http://eprints.sunway.edu.my/1948/1/Tiekink%20Te%20N%20secondary.pdf Tiekink, Edward R. T. * (2022) Te⋯N secondary-bonding interactions in tellurium crystals: Supramolecular aggregation patterns and a comparison with their lighter congeners. Coordination Chemistry Reviews, 457. p. 214397. ISSN 0010-8545 (In Press) http://doi.org/10.1016/j.ccr.2021.214397 doi:10.1016/j.ccr.2021.214397 |
| spellingShingle | QD Chemistry Tiekink, Edward R. T. * Te⋯N secondary-bonding interactions in tellurium crystals: Supramolecular aggregation patterns and a comparison with their lighter congeners |
| title | Te⋯N secondary-bonding interactions in tellurium crystals: Supramolecular aggregation patterns and a comparison with their lighter congeners |
| title_full | Te⋯N secondary-bonding interactions in tellurium crystals: Supramolecular aggregation patterns and a comparison with their lighter congeners |
| title_fullStr | Te⋯N secondary-bonding interactions in tellurium crystals: Supramolecular aggregation patterns and a comparison with their lighter congeners |
| title_full_unstemmed | Te⋯N secondary-bonding interactions in tellurium crystals: Supramolecular aggregation patterns and a comparison with their lighter congeners |
| title_short | Te⋯N secondary-bonding interactions in tellurium crystals: Supramolecular aggregation patterns and a comparison with their lighter congeners |
| title_sort | te⋯n secondary-bonding interactions in tellurium crystals: supramolecular aggregation patterns and a comparison with their lighter congeners |
| topic | QD Chemistry |
| url | http://eprints.sunway.edu.my/1948/ http://eprints.sunway.edu.my/1948/ http://eprints.sunway.edu.my/1948/ http://eprints.sunway.edu.my/1948/1/Tiekink%20Te%20N%20secondary.pdf |