Literature DB >> 25781631

Chalcogen bonding in solution: interactions of benzotelluradiazoles with anionic and uncharged Lewis bases.

Graham E Garrett1, Gregory L Gibson1, Rita N Straus1, Dwight S Seferos1, Mark S Taylor1.   

Abstract

Chalcogen bonding is the noncovalent interaction between an electron-deficient, covalently bonded chalcogen (Te, Se, S) and a Lewis base. Although substantial evidence supports the existence of chalcogen bonding in the solid state, quantitative data regarding the strengths of the interactions in the solution phase are lacking. Herein, determinations of the association constants of benzotelluradiazoles with a variety of Lewis bases (Cl(-), Br(-), I(-), NO3(-) and quinuclidine, in organic solvent) are described. The participation of the benzotelluradiazoles in chalcogen bonding interactions was probed by UV-vis, (1)H and (19)F NMR spectroscopy as well as nano-ESI mass spectrometry. Trends in the free energy of chalcogen bonds upon variation of the donor, acceptor and solvent are evident from these data, including a linear free energy relationship between chalcogen bond donor ability and calculated electrostatic potential at the tellurium center. Calculations using the dispersion-corrected B97-D3 functional were found to give good agreement with the experimental free energies of chalcogen bonding.

Entities:  

Year:  2015        PMID: 25781631     DOI: 10.1021/ja512183e

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  22 in total

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4.  Redox-Switchable Chalcogen Bonding for Anion Recognition and Sensing.

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5.  Carbon-Halogen Bond Activation by Selenium-Based Chalcogen Bonding.

Authors:  Patrick Wonner; Lukas Vogel; Maximilian Düser; Luís Gomes; Florian Kniep; Bert Mallick; Daniel B Werz; Stefan M Huber
Journal:  Angew Chem Int Ed Engl       Date:  2017-07-06       Impact factor: 15.336

6.  Catalysis with chalcogen bonds: neutral benzodiselenazole scaffolds with high-precision selenium donors of variable strength.

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Journal:  Chem Sci       Date:  2017-10-16       Impact factor: 9.825

7.  Resolving orbital pathways for intermolecular electron transfer.

Authors:  Cameron W Kellett; Wesley B Swords; Michael D Turlington; Gerald J Meyer; Curtis P Berlinguette
Journal:  Nat Commun       Date:  2018-11-21       Impact factor: 14.919

8.  Supramolecular macrocycles reversibly assembled by Te(…)O chalcogen bonding.

Authors:  Peter C Ho; Patrick Szydlowski; Jocelyn Sinclair; Philip J W Elder; Joachim Kübel; Chris Gendy; Lucia Myongwon Lee; Hilary Jenkins; James F Britten; Derek R Morim; Ignacio Vargas-Baca
Journal:  Nat Commun       Date:  2016-04-19       Impact factor: 14.919

9.  Catalytic Carbon-Chlorine Bond Activation by Selenium-Based Chalcogen Bond Donors.

Authors:  Patrick Wonner; Lukas Vogel; Florian Kniep; Stefan M Huber
Journal:  Chemistry       Date:  2017-11-14       Impact factor: 5.236

10.  Catalysis with Pnictogen, Chalcogen, and Halogen Bonds.

Authors:  Sebastian Benz; Amalia I Poblador-Bahamonde; Nicolas Low-Ders; Stefan Matile
Journal:  Angew Chem Int Ed Engl       Date:  2018-03-20       Impact factor: 15.336

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