The Organometallic Reader

Dedicated to the teaching and learning of modern organometallic chemistry.

Posts Tagged ‘total electron count

What is an Open Coordination Site?

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The concept of coordinative unsaturation can be confusing for the student of organometallic chemistry, but recognizing open coordination sites in OM complexes is a critical skill. Why? Let’s begin with a famous example of coordinative unsaturation from organic chemistry.

An analogy from organic chemistry. The reactivity of the carbene flows from its open coordination site.

An analogy from organic chemistry. The reactivity of the carbene flows from its open coordination site.

Carbenes are both nucleophilic and electrophilic, but the essence of their electrophilicity comes from the fact that they don’t have their fair share of electrons (8). They have not been saturated with electrons—carbenes want more! To achieve saturation, carbenes may inherit a pair of electrons from a σ bond (σ-bond insertion), π bond (cyclopropanation), or lone pair (ylide formation). Notice that, simply by spotting coordinative unsaturation, we’ve been able to fully describe the carbene’s reactivity! We can do the same with organometallic complexes—open coordination sites suggest specific reactivity patterns. That’s why understanding coordinative unsaturation and recognizing its telltale sign (the open coordination site) are essential skills for the organometallic chemist. Read the rest of this entry »

Simplifying the Organometallic Complex (Part 3)

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So far, we’ve seen how deconstruction can reveal useful “bookkeeping” properties of organometallic complexes: number of electrons donated by ligands, coordination number, oxidation state, and d electron count (to name a few). Now, let’s bring everything together and discuss total electron count, the sum of non-bonding and bonding electrons associated with the metal center. Like oxidation state, total electron count can reveal the likely reactivity of OM complexes—in fact, it is often more powerful than oxidation state for making predictions. We’ll see that there is a definite norm for total electron count, and when a complex deviates from that norm, reactions are likely to happen.

Let’s begin with yet another new complex. This molecule features the common and important cyclopentadienyl and carbon monoxide ligands, along with an X-type ethyl ligand.

What's the total electron count of this d6, Fe(II) complex?

What is the total electron count of this Fe(II) complex?

The Cp or cyclopentadienyl ligand is a polydentate, six-electron L2X ligand. The two pi bonds of the free anion are dative, L-type ligands, which we’ll see again in a future post on ligands bound through pi bonds. Think of the electrons of the pi bond as the source of a dative bond to the metal. Since both electrons come from the ligand, the pi bonds are L-type binders. The anionic carbon in Cp is a fairly standard, anionic X-type binder. The carbon monoxide ligands are interesting examples of two-electron L-type ligands—notice that the free ligands are neutral, so these are considered L-type! Carbon monoxide is an intriguing ligand that can teach us a great deal about metal-ligand bonding in OM complexes…but more on that later. Read the rest of this entry »

Written by Michael Evans

January 6, 2012 at 1:40 pm