Dominant Role of the π Framework in Cyclobutadiene-Reference-Cited by-同舟云学术

Dominant Role of the π Framework in Cyclobutadiene

Published:2004-09-25 Issue:42 Volume:108 Page:9126-9133
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Kovačević Borislav¹,Barić Danijela¹,Maksić Zvonimir B.¹,Müller Thomas¹

Affiliation:

1. Quantum Organic Chemistry Group, Department of Organic Chemistry and Biochemistry, “Ruđer Bošković” Institute, POB 180, 10002 Zagreb, Croatia, and Central Institute of Applied Mathematics Research Centre Juelich, D-52425 Juelich, Germany

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp0489626

Reference44 articles.

1. Antiaromaticity

2. Cyclobutadiene- and Benzocyclobutadiene-Iron Tricarbonyl Complexes1

3. Properties of the [4]annulene system. Induced paramagnetic ring current

4. Rapid double bond shift in a donor-acceptor substituted cyclobutadiene. Evidence from 584-Ang and x-ray photoelectron spectroscopy

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Quantum mechanical tunneling in the automerization of cyclobutadiene;The Journal of Chemical Physics;2018-03-14

2. The Nature of the Chemical Bond from a Quantum Mechanical Interference Perspective;ChemistrySelect;2017-01-13

3. The Nature of the Singlet and Triplet States of Cyclobutadiene as Revealed by Quantum Interference;ChemPhysChem;2015-12-03

4. Is cyclobutadiene really highly destabilized by antiaromaticity?;Chemical Communications;2012

5. Homodesmotic reactions for thermochemistry;Wiley Interdisciplinary Reviews: Computational Molecular Science;2011-06-29