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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Xu, Lu T. Dunning, Thom H. |
| Description | Author Affiliation: Xu LT ( Department of Chemistry, University of Illinois at Urbana-Champaign , 600 S. Mathews Avenue, Urbana, Illinois 61801, United States.); Dunning TH ( Department of Chemistry, University of Illinois at Urbana-Champaign , 600 S. Mathews Avenue, Urbana, Illinois 61801, United States.) |
| Abstract | The inertness of molecular nitrogen and the reactivity of acetylene suggest there are significant variations in the nature of triple bonds. To understand these differences, we performed generalized valence bond as well as more accurate electronic structure calculations on three molecules with putative triple bonds: N2, HCN, and HC2H. The calculations predict that the triple bond in HC2H is quite different from the triple bond in N2, with HCN being an intermediate case but closer to N2 than HC2H. The triple bond in N2 is a traditional triple bond with the spins of the electrons in the bonding orbital pairs predominantly singlet coupled in the GVB wave function (92%). In HC2H, however, there is a substantial amount of residual CH(a(4)Σ(-)) fragment coupling in the triple bond at its equilibrium geometry with the contribution of the perfect pairing spin function dropping to 82% (77% in a full valence GVB calculation). This difference in the nature of the triple bond in N2 and HC2H may well be responsible for the differences in the reactivities of N2 and HC2H. |
| ISSN | 10895639 |
| Issue Number | 26 |
| Journal | The Journal of Physical Chemistry A |
| Volume Number | 120 |
| e-ISSN | 15205215 |
| Language | English |
| Publisher | American Chemical Society (United States) |
| Publisher Date | 2016-07-07 |
| Publisher Place | United States |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Physical chemistry |
| Content Type | Text |
| Resource Type | Article |
| Subject | Medicine Physical and Theoretical Chemistry |
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