Dispersion Interaction and Crystal Packing Realize an Ultralong C–C Single Bond: A Theoretical Study on Dispirobis(10-methylacridan) Derivatives
Author:
Affiliation:
1. Graduate School of Chemical Sciences and Engineering, Hokkaido University, Kita 10, Nishi 8, Kita-ku, Sapporo, Hokkaido 060-0810, Japan
2. Faculty of Science, Hokkaido University, Kita 10, Nishi 8, Kita-ku, Sapporo, Hokkaido 060-0810, Japan
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/cl.180864
Reference20 articles.
1. Overcoming lability of extremely long alkane carbon–carbon bonds through dispersion forces
2. Theoretical Study of Extremely Long yet Stable Carbon–Carbon Bonds: Effect of Attractive C···H Interactions and Small Radical Stabilization of Diamondoids
3. Extremely Long C−C Bond in (−)-trans-1,2-Di-tert-butyl-1,2-diphenyl- and 1,1-Di-tert-butyl-2,2-diphenyl-3,8-dichlorocyclobuta[b]naphthalenes
4. The x-ray crystal structure of the first quaternary 1-bicyclo[1.1.1]pentane salt. The shortest nonbonding carbon-carbon interaction documented
5. The Relation between Bond Lengths and Dissociation Energies of Carbon−Carbon Bonds
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1. Designing Principles for Ultrashort H⋯H Nonbonded Contacts and Ultralong CC Bonds;Electron Density;2024-07-05
2. Long but Strong C−C Single Bonds: Challenges for Theory;The Chemical Record;2023-06-26
3. The synergetic and multifaceted nature of carbon–carbon rotation reveals the origin of conformational barrier heights with bulky alkane groups;Journal of Physical Organic Chemistry;2022-04-05
4. Expandability of the Covalent Bond: A New Facet Discovered in Extremely Long Csp3-Csp3 Single Bonds;Bulletin of the Chemical Society of Japan;2021-04-15
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