Superelectrophilic Behavior of an Anion Demonstrated by the Spontaneous Binding of Noble Gases to [B12Cl11]−. Issue 27 (31st May 2017)
- Record Type:
- Journal Article
- Title:
- Superelectrophilic Behavior of an Anion Demonstrated by the Spontaneous Binding of Noble Gases to [B12Cl11]−. Issue 27 (31st May 2017)
- Main Title:
- Superelectrophilic Behavior of an Anion Demonstrated by the Spontaneous Binding of Noble Gases to [B12Cl11]−
- Authors:
- Rohdenburg, Markus
Mayer, Martin
Grellmann, Max
Jenne, Carsten
Borrmann, Tobias
Kleemiss, Florian
Azov, Vladimir A.
Asmis, Knut R.
Grabowsky, Simon
Warneke, Jonas - Abstract:
- Abstract: It is common and chemically intuitive to assign cations electrophilic and anions nucleophilic reactivity, respectively. Herein, we demonstrate a striking violation of this concept: The anion [B12 Cl11 ] − spontaneously binds to the noble gases (Ngs) xenon and krypton at room temperature in a reaction that is typical of "superelectrophilic" dications. [B12 Cl11 Ng] − adducts, with Ng binding energies of 80 to 100 kJ mol −1, contain B−Ng bonds with a substantial degree of covalent interaction. The electrophilic nature of the [B12 Cl11 ] − anion is confirmed spectroscopically by the observation of a blue shift of the CO stretching mode in the IR spectrum of [B12 Cl11 CO] − and theoretically by investigation of its electronic structure. The orientation of the electric field at the reactive site of [B12 Cl11 ] − results in an energy barrier for the approach of polar molecules and facilitates the formation of Ng adducts that are not detected with reactive cations such as [C6 H5 ] + . This introduces the new chemical concept of "dipole‐discriminating electrophilic anions." Abstract : Unexpected reactivity : The binding of the noble gases Xe and Kr to the anion [B12 Cl11 ] − is explained with the exceptional properties of the electric field in the vicinity of the undercoordinated boron atom. Whereas polar nucleophiles such as water face a barrier, neutral unpolar species such as N2 or noble gases are preferred, rendering [B12 Cl11 ] − a "dipole‐discriminating electrophilicAbstract: It is common and chemically intuitive to assign cations electrophilic and anions nucleophilic reactivity, respectively. Herein, we demonstrate a striking violation of this concept: The anion [B12 Cl11 ] − spontaneously binds to the noble gases (Ngs) xenon and krypton at room temperature in a reaction that is typical of "superelectrophilic" dications. [B12 Cl11 Ng] − adducts, with Ng binding energies of 80 to 100 kJ mol −1, contain B−Ng bonds with a substantial degree of covalent interaction. The electrophilic nature of the [B12 Cl11 ] − anion is confirmed spectroscopically by the observation of a blue shift of the CO stretching mode in the IR spectrum of [B12 Cl11 CO] − and theoretically by investigation of its electronic structure. The orientation of the electric field at the reactive site of [B12 Cl11 ] − results in an energy barrier for the approach of polar molecules and facilitates the formation of Ng adducts that are not detected with reactive cations such as [C6 H5 ] + . This introduces the new chemical concept of "dipole‐discriminating electrophilic anions." Abstract : Unexpected reactivity : The binding of the noble gases Xe and Kr to the anion [B12 Cl11 ] − is explained with the exceptional properties of the electric field in the vicinity of the undercoordinated boron atom. Whereas polar nucleophiles such as water face a barrier, neutral unpolar species such as N2 or noble gases are preferred, rendering [B12 Cl11 ] − a "dipole‐discriminating electrophilic anion". … (more)
- Is Part Of:
- Angewandte Chemie international edition. Volume 56:Issue 27(2017)
- Journal:
- Angewandte Chemie international edition
- Issue:
- Volume 56:Issue 27(2017)
- Issue Display:
- Volume 56, Issue 27 (2017)
- Year:
- 2017
- Volume:
- 56
- Issue:
- 27
- Issue Sort Value:
- 2017-0056-0027-0000
- Page Start:
- 7980
- Page End:
- 7985
- Publication Date:
- 2017-05-31
- Subjects:
- bond theory -- borates -- ion–molecule reactions -- noble gases
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3773 ↗
http://www.interscience.wiley.com/jpages/1433-7851 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/anie.201702237 ↗
- Languages:
- English
- ISSNs:
- 1433-7851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2833.xml