Molecular orbitals of the oxocarbons (CO)n, n = 2-6: why does (CO)4 have a triplet ground state?
Cyclobutane-1,2,3,4-tetrone has been both predicted and found to have a triplet ground state, in which a b2g σ MO and an a2u π MO are each singly occupied. The nearly identical energies of these two orbitals of (CO)4 can be attributed to the fact that both of these MOs are formed from a bonding comb...
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| Hauptverfasser: | , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
June 11, 2012
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| In: |
Journal of the American Chemical Society
Year: 2012, Jahrgang: 134, Heft: 24, Pages: 10259-10270 |
| ISSN: | 1520-5126 |
| DOI: | 10.1021/ja3034087 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1021/ja3034087 Verlag, Volltext: https://doi.org/10.1021/ja3034087 
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| Verfasserangaben: | Xiaoguang Bao, Xin Zhou, Charity Flener Lovitt, Amruth Venkatraman, David A. Hrovat, Rolf Gleiter, Roald Hoffmann, and Weston Thatcher Borden |
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| 245 | 1 | 0 | |a Molecular orbitals of the oxocarbons (CO)n, n = 2-6 |b why does (CO)4 have a triplet ground state? |c Xiaoguang Bao, Xin Zhou, Charity Flener Lovitt, Amruth Venkatraman, David A. Hrovat, Rolf Gleiter, Roald Hoffmann, and Weston Thatcher Borden |
| 246 | 3 | 3 | |a Molecular orbitals of the oxocarbons (CO) n, n = 2-6 |
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| 520 | |a Cyclobutane-1,2,3,4-tetrone has been both predicted and found to have a triplet ground state, in which a b2g σ MO and an a2u π MO are each singly occupied. The nearly identical energies of these two orbitals of (CO)4 can be attributed to the fact that both of these MOs are formed from a bonding combination of C-O π* orbitals in four CO molecules. The intrinsically stronger bonding between neighboring carbons in the b2g σ MO compared to the a2u π MO is balanced by the fact that the non-nearest-neighbor, C-C interactions in (CO)4 are antibonding in b2g, but bonding in a2u. Crossing between an antibonding, b1g combination of carbon lone-pair orbitals in four CO molecules and the b2g and a2u bonding combinations of π* MOs is responsible for the occupation of the b2g and a2u MOs in (CO)4. A similar orbital crossing occurs on going from two CO molecules to (CO)2, and this crossing is responsible for the triplet ground state that is predicted for (CO)2. However, such an orbital crossing does not occur on formation of (CO)2n+1 from 2n + 1 CO molecules, which is why (CO)3 and (CO)5 are both calculated to have singlet ground states. Orbital crossings, involving an antibonding, b1, combination of lone-pair MOs, occur in forming all (CO)2n molecules from 2n CO molecules. Nevertheless, (CO)6 is predicted to have a singlet ground state, in which the b2u σ MO is doubly occupied and the a2u π MO is left empty. The main reason for the difference between the ground states of (CO)4 and (CO)6 is that interactions between 2p AOs on non-nearest-neighbor carbons, which stabilize the a2u π MO in (CO)4, are much weaker in (CO)6, due to the much larger distances between non-nearest-neighbor carbons in (CO)6 than in (CO)4. | ||
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