A theoretical study of the aromaticity in neutral and anionic borole compounds-Reference-Cited by-同舟云学术

A theoretical study of the aromaticity in neutral and anionic borole compounds

Published:2015 Issue:15 Volume:44 Page:6740-6747
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Jimenez-Halla J. Oscar C.¹²³⁴,Matito Eduard⁵⁶⁷⁸,Solà Miquel⁵⁶⁷⁸,Braunschweig Holger⁹¹⁰¹¹¹²,Hörl Christian⁹¹⁰¹¹¹²,Krummenacher Ivo⁹¹⁰¹¹¹²,Wahler Johannes⁹¹⁰¹¹¹²

Affiliation:

1. Department of Chemistry (DCNE)

2. University of Guanajuato

3. Noria Alta s/n 36050 Guanajuato

4. Mexico

5. Institut de Química Computacional i Catàlisi (IQCC) and Departament de Química

6. Universitat de Girona

7. 17071 Girona (Catalonia)

8. Spain

9. Institut für Anorganische Chemie

10. Julius-Maximilians-Universität Würzburg

11. 97074 Würzburg

12. Germany

Abstract

A theoretical assessment of the degree of (anti)aromaticity in various borole compounds reveals distinct substituent effects.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/DT/C4DT03445G

Reference71 articles.

1. Antiaromaticity in Open-Shell Cyclopropenyl to Cycloheptatrienyl Cations, Anions, Free Radicals, and Radical Ions

2. Antiaromaticity

3. Heteroarene-fused boroles: what governs the antiaromaticity and Lewis acidity of the borole skeleton?

4. Synthesis of pentaphenylborole, a potentially antiaromatic system

5. Structural Evidence for Antiaromaticity in Free Boroles

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