Quadruple bond between two carbon atoms

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The discussion centers on the feasibility of a quadruple bond between two carbon atoms, specifically in the context of dicarbon (C2). The Wikipedia article on dicarbon is criticized for lacking clarity. Valence bond theory suggests that carbon can form a double bond due to its two unpaired electrons, but it does not strictly require adherence to the octet rule. There is ongoing debate regarding whether the bonding in dicarbon is more accurately represented as a double or quadruple bond, with some theories proposing that higher bond orders could exist in electronically excited states of C2. The assignment of bond orders is described as a characteristic of the models used to explain bonding, with the possibility of interpreting C2's bonding as quadruple, double, or triple based on the orbital configurations. Ultimately, the discussion highlights that bond order is less significant than observable bond lengths and strengths, making it a topic of interest for theorists.
pierce15
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I was wondering if a quadruple bond between two carbon atoms would be possible. I found this on wikipedia about "dicarbon": http://en.wikipedia.org/wiki/Diatomic_carbon, which is related to this question, since what I'm describing is an isomer of dicarbon. Anyone have any ideas?
 
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The wikipedia article is not very good. Valence bond theory also predicts a double bond as carbon atoms have two unpaired electrons. It is not a requirement of VB theory for the molecule to obey the octet rule.
Higher bond orders may be present in electronically excited state of C2.
 
So what do you think about a quadruple bond?
 
Whether bonding in dicarbon is better described as a double or quadruple bond is still being debated, see http://www.ch.imperial.ac.uk/rzepa/blog/?p=10733 .

Assigning definite integer-valued bond orders to chemical bonds is just a property of the approximative model used to describe bonding.
 
Whatever else one may or may not say about C2, if it is described with a single closed-shell determinant wave function (i.e., with Hartree-Fock or Kohn-Sham), one can rotate its occupied orbitals into two equivalent doubly-occupied non-standard sigma bond orbitals and two standard doubly occupied pi bond orbitals via orbital localization (Pipek-Mezey-like).

As the theoretical basis for bond order concept is closely related to this form of MO theory (which, for C2, is not entirely beyond question--it has low lying excited states), one could formally interpret this as a quadruple bond. Or as a double bond or triple bond, depending on how one wishes to interpret the non-standard sigma system.

In short, it is the perfect fighting ground for bored theorists 8).
 
Another question is what a number like "bond order" really tells you.
What we observe are bond lengths and strengths and not bond orders.
 
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