Synergistic Interplay between Intermolecular Halogen and Chalcogen Bonds in the Dihalogen Adducts of 2,5-Bis(pyridine-2-yl)tellurophene: Reactivity Insights and Structural Trends

The reactivity of 2,5-bis(pyridine-2-yl)tellurophene (<b>L</b>) toward elemental dihalogens XY (X = Y = I, Br; X = I, Y = Cl, Br) was explored. The oxidative addition of the dihalogen molecules to the Te(II) center was observed in <b>L</b>I<sub>2</sub> (<b>1</b>), <b>L</b>I<sub>2</sub>·1/2I<sub>2</sub> (<b>2</b>), <b>L</b>Br<sub>2</sub> (<b>3</b>), <b>L</b>Br<sub>1.63</sub>I<sub>0.37</sub> (<b>4</b>), and <b>L</b>Cl<sub>1.86</sub>I<sub>0.14</sub> (<b>5</b>), which were characterized in the solid state by X-ray diffraction analysis and Raman spectroscopy. In all cases, a seesaw geometry at the chalcogen atom was observed with the linear X-Te-X moiety almost perpendicular to the tellurophene ring. The crystal packing in these compounds displays a peculiar and synergistic interplay of halogen and chalcogen bonds. A comparison with analogous compounds reported in the literature was carried out to establish the key factors determining the supramolecular arrays of noncovalent intermolecular interactions (NCIs) observed in this class of compounds.

Authors

Institutions

Publication Details

Journal
Inorganic Chemistry
Published
2025-05-29
DOI
https://doi.org/10.1021/acs.inorgchem.5c01084
Citations
3
Primary Topic
Organic Chemistry Cycloaddition Reactions
Type
article
Field-Weighted Citation Impact
2.81

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Synergistic Interplay between Intermolecular Halogen and Chalcogen Bonds in the Dihalogen Adducts of 2,5-Bis(pyridine-2-yl)tellurophene: Reactivity Insights and Structural Trends

Anna Pintus, Paulo H. Schneider, Vito Lippolis, Douglas B. Paixão et al.
3 citations
Inorganic Chemistry
Organic Chemistry Cycloaddition Reactions
2.81
article

Synergistic Interplay between Intermolecular Halogen and Chalcogen Bonds in the Dihalogen Adducts of 2,5-Bis(pyridine-2-yl)tellurophene: Reactivity Insights and Structural Trends

Anna Pintus, Paulo H. Schneider, Vito Lippolis, Douglas B. Paixão, M. Carla Aragoni, Massimiliano Arca, Enrico Podda, Claudia Caltagirone, Eduardo G. O. Soares
article en
3 citations

Abstract

The reactivity of 2,5-bis(pyridine-2-yl)tellurophene (<b>L</b>) toward elemental dihalogens XY (X = Y = I, Br; X = I, Y = Cl, Br) was explored. The oxidative addition of the dihalogen molecules to the Te(II) center was observed in <b>L</b>I<sub>2</sub> (<b>1</b>), <b>L</b>I<sub>2</sub>·1/2I<sub>2</sub> (<b>2</b>), <b>L</b>Br<sub>2</sub> (<b>3</b>), <b>L</b>Br<sub>1.63</sub>I<sub>0.37</sub> (<b>4</b>), and <b>L</b>Cl<sub>1.86</sub>I<sub>0.14</sub> (<b>5</b>), which were characterized in the solid state by X-ray diffraction analysis and Raman spectroscopy. In all cases, a seesaw geometry at the chalcogen atom was observed with the linear X-Te-X moiety almost perpendicular to the tellurophene ring. The crystal packing in these compounds displays a peculiar and synergistic interplay of halogen and chalcogen bonds. A comparison with analogous compounds reported in the literature was carried out to establish the key factors determining the supramolecular arrays of noncovalent intermolecular interactions (NCIs) observed in this class of compounds.

Inorganic ChemistryVol. 64(22)
Universidade Federal do Rio Grande do Sul (BR), University of Cagliari (IT), Istituto Nazionale di Fisica Nucleare, Sezione di Cagliari (IT)
Fondazione di Sardegna, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul, Instituto Nacional de Ciência e Tecnologia de Catálise em Sistemas Moleculares e Nanoestruturados, Ministero dell'Ambiente e della Tutela del Territorio e del Mare
Openalex Percentile: Top 10%
Organic Chemistry Cycloaddition Reactions
2.81
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.