The effect of substituents on triply bonded boronantimony molecules: a theoretical approach
Author:
Affiliation:
1. Department of Applied Chemistry
2. National Chiayi University
3. Chiayi 60004
4. Taiwan
5. Department of Medicinal and Applied Chemistry
Abstract
Theoretical calculations using the M06-2X, B3PW91 and B3LYP levels of theory demonstrate that the attached substituents (R) play a decisive role in determining the stability of triply bonded RBSbR molecules. Theoretical evidence shows that, from the kinetic viewpoint, only bulkier substituents have a significant stabilizing effect on the formation of the triply bonded RBSbR compounds.
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2017/CP/C7CP00421D
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