Electronic effects of the substituted dopants on stability and reactivity of difuranosilapyridine-4-ylidenes: DFT approach
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
https://link.springer.com/content/pdf/10.1007/s11224-023-02151-x.pdf
Reference90 articles.
1. Koohi M (2019) Cyclonona-3,5,7-trienylidene and its Si, Ge, Sn, and Pb analogs versus their α-halogenated derivatives at B3LYP and MP2 methods. J Phys Org Chem 32:e4013
2. Koohi M (2020) Estimating the stability and reactivity of cyclic tetrahalo substituted germylenes: a density functional theory investigation. J Phys Org Chem 33:e4032
3. Koohi M, Bastami H (2020) A quest for stable 2,2,9,9-tetrahaloplumbacyclonona-3,5,7-trienylidenes at density functional theory. Struct Chem 31:877
4. Koohi M, Bastami H (2020) Substituent effects on stability, MEP, NBO analysis, and reactivity of 2,2,9,9-tetrahalosilacyclonona-3,5,7-trienylidenes, at density functional theory. Monatshefte für Chemie - Chemical Monthly 151:11
5. Koohi M, Bastami H (2020) A density functional theory perspective on 2,2,9,9-tetrahalostannacyclonona-3,5,7-trienylidenes. J Phys Org Chem 33:e4031
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