Why does formation of 1,3-dimethylenecyclobutane-2,4-diyl from 1,3-dimethylenecyclobutane show a large positive deviation from bond enthalpy additivity?-Reference-Cited by-同舟云学术

Why does formation of 1,3-dimethylenecyclobutane-2,4-diyl from 1,3-dimethylenecyclobutane show a large positive deviation from bond enthalpy additivity?

Published:2000-12 Issue:1-3 Volume:556 Page:151-156
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Zhang D.Y,Borden W.T

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference31 articles.

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4. Biradical Thermochemistry from Collision-Induced Dissociation Threshold Energy Measurements. Absolute Heats of Formation of ortho-, meta-, and para-Benzyne

5. Ultraviolet Photoelectron Spectroscopy of the o-, m-, and p-Benzyne Negative Ions. Electron Affinities and Singlet−Triplet Splittings for o-, m-, and p-Benzyne

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1. An Opened Route to 1,3-Dimethylenecyclobutanes via Sequential Ruthenium-Catalyzed [2 + 2] Cycloaddition of Allenyl Boronate and Palladium Suzuki Coupling;Journal of the American Chemical Society;2005-07-30

2. Do Deviations from Bond Enthalpy Additivity Define the Thermodynamic Stabilities of Diradicals?;The Journal of Organic Chemistry;2002-05-03

3. Triradical Thermochemistry from Collision-Induced Dissociation Threshold Energy Measurements. The Heat of Formation of 1,3,5-Trimethylenebenzene;Journal of the American Chemical Society;2001-11-09