What’s An Organometallic?
Last updated: August 18th, 2022 |
What Is The Definition of An Organometallic Compound?
Quick summary for today – the first in a new series on organometallic compounds:
It’s hard to underestimate how important dipoles are in determining the reactivity of a molecule.
Wait: dipoles, you might ask. How do we determine a dipole again?
Let’s start this series by making sure we’re clear on this, because it will be key to understanding the class of molecules we call “organometallics”.
Table of Contents
- A Refresher on “Dipoles”
- Dipoles Provide A Clue To Reactivity
- Some Examples Of How Dipoles Govern Reactivity
- Organometallics: Contain Carbon-Metal Bonds (And Have Nucleophilic Carbons!)
- Summary: Organometallics
Recall that molecules are built of covalent bonds between atoms, but the electrons in covalent bonds aren’t always shared equally between atoms.
- When two atoms of significantly different electronegativity form a covalent bond, the atom with higher electronegativity (“greedier” for electrons, if you’ll pardon the anthropomorphism) will have an unequal share of those electrons, leading to a partial buildup of negative charge on that atom (which we represent by using the symbol δ– ).
- Conversely, the atom with the lower negativity will have a partial deficit of electron density, leading to a partial positive charge (δ+).
- The most likely place to find a large dipole is to look for strongly electronegative atoms such as oxygen (3.5) and nitrogen (3.0) or the halogens fluoride (4.0), chlorine (3.2) and bromine (3.0): if any of those atoms is bound to a less electronegative atom like carbon (2.6) or hydrogen (2.2), a dipole results.
Since opposite charges attract, atoms which are electron rich (δ– ) are attracted to atoms bearing partial positive charge (δ+).
You’ve likely already seen that molecules with large dipoles (so-called, “polar” molecules) tend to have higher boiling points and melting points than molecules of similar molecular weight without them (“non-polar” molecules).
That’s because attractive interactions between oppositely charged dipoles (e.g. hydrogen bonds and dipole-dipole interactions) require additional energy to disrupt.
Another feature of dipoles, less often mentioned, is that they provide us with excellent hypotheses for determining where reactions might happen between two given molecules.
If you’ve started to cover even the simplest of reactions, you’ve already learned that bonds are formed when a Lewis base (electron rich) donates a pair of electrons to a Lewis acid (electron poor).
- When the electron pair is being donated to any atom except hydrogen, we usually call that Lewis base a “nucleophile” [when a lone pair is being donated to hydrogen, we tend to call it a “base”].
- Since atomic nuclei are positively charged, “nucleophile” is shorthand for “positive-charge loving”. Nothing new here: atoms which are (δ– ) are attracted to atoms which are (δ+).
On the other hand, since Lewis acids tend to be electron poor (δ+, negative-charge-loving) and they are attracted to electrons [or to be more specific, atoms with high electron density (δ– ) ], we often call Lewis acids “electrophiles”.
To shorten it to a point, pretty much every reaction you’ll learn is some version of nucleophile (negative charge) attacks electrophile (positive charge). And learning to recognize dipoles will help you to recognize nucleophiles and electrophiles.
This diagram tries to show some interactions between potential nucleophiles and electrophiles based solely on dipoles. Note that this doesn’t mean that reactions between these atoms will necessarily occur – it’s only saying that these are good guesses for where the “action” will be.
Just to illustrate, here are some examples of real reactions you see in Org 1 (or sometimes Org 2) which follow this pattern. Note how the source of electrons (the tail of the blue arrow – the nucleophile) is always the negative end of a dipole, and the electron acceptor (the head of the blue arrow – the electrophile) always the positive end of a dipole. Nucleophile attacks electrophile.
Here, the trick is to see that hydrogen actually has a higher electronegativity (2.2) than boron (2.0) and therefore in the B-H bond, it’s the hydrogen which is δ– . Always pay attention to the dipole more than the formal charge, because formal charge can mislead.
All of this should be review. However, like a dog who needs to walk around their pillow before they finally lie down, sometimes teachers need to get the introduction out of the way before getting deep into a topic.
The reason I began with dipoles is the following. Most of the functional groups you’ll encounter in organic chemistry have one feature in common. Look for the biggest dipole in these functional groups.
Do you notice that in all of these cases, carbon is electropositive [electron poor]? We see carbon as an electrophile so often in introductory organic chemistry, it’s important to realize that carbon can act as a nucleophile as well.
If carbon tends to be electrophilic when attached to a more electronegative group, then under what circumstances might carbon act as a nucleophile?
When it’s attached to a less electronegative atom! After all, carbon is slightly upper-middle class when it comes to electronegativity (2.6). There’s a lot of other elements on the periodic table with lower electronegativities than that. Many of them are metals of some variety, whether they be alkali metals, alkaline earth metals, or transition metals. Even group 13 elements (the old group III) – boron, aluminum and so on – qualify as metals for these purposes.
Molecules that contain a carbon-metal bond are referred to as organometallics.
The common theme in organometallic chemistry is that carbon tends to act as a nucleophile (or a base, if there are Brønsted acids around).
We’ll get to some examples of reactions in subsequent posts, but first, let’s just see some examples of what organometallic compounds look like. Three of them are extremely common in introductory organic chemistry. Organolithium compounds, organomagnesium compounds (which go by the name “Grignard reagents” after their discoverer), and organocuprate reagents (again, usually referred to as “Gilman” reagents after the chemist who first popularized them, Henry Gilman of Iowa State University).
There are, of course, many more examples of organometallic compounds – this is just a dusting of snow on the tip of the iceberg – but for our purposes, these three classes of organometallic compound will carry most of the freight.
In the next post, we’ll show some examples of how these organometallic compounds are made.
- Organocuprates (Gilman Reagents): How They’re Made
- Organometallics Are Strong Bases
- Synthesis of Grignard and Organolithium Reagents
- Watch Out – Formal Charge Can Lie
- How to apply electronegativity and resonance to understand reactivity
P.S. This series will only go into the most superficial aspects of organometallic compounds and their reactions. For much more thorough treatment, I strongly encourage you to visit The Organometallic Reader by Mike Evans, a free online resource that teaches the essentials of this very deep subject.