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Vibrations in chemical bonds can be used to contribute to design of better catalysts

16 March 2014

University of Utah chemists have discovered how vibrations in chemical bonds can be used to predict chemical reactions and thus design better catalysts to speed reactions that make medicines, industrial products and new materials. Their study is published in the journal Nature.

The vibrations alone are not adequate, but combined with other classical techniques in physical organic chemistry, we are able to predict how reactions can occur. This should be applicable in a broad range of reactions. It streamlines the process of designing molecules for uses in new drugs, industrial chemicals and new materials.

—Matt Sigman, senior author

Postdoctoral researcher Anat Milo, the study’s first author, noted that the use of the new method could assist the design of reactions with fewer byproducts and much less waste, and the reactions would be more efficient.

Chemical bonds are not static; they vibrate. Those vibrations reflect changes in distance between atoms in the molecule. For example, in water, the sole oxygen atom is bound to two hydrogen atoms, and the two bonds constantly change in length.

You can think of it like a spring. You put two different weights on the end of a spring, and the spring vibrates once you put energy into it.

—Matt Sigman

In chemical reactions, the energy is added with heat, light or electricity. This bending and stretching of chemical bonds can be seen if infrared light is bounced off the molecules—a method called infrared spectroscopy.

An infrared laser is aimed at a sample of a chemical—gas, liquid or solid—and certain wavelengths are absorbed. The wavelengths of the absorbed light reveal how the target molecule’s chemical bonds vibrate, which in turn tells about the types and positions of atoms in the molecule, the kinds and strength of bonds among atoms and the symmetry of the molecule, Milo says.

Infrared spectroscopy is a well-established method with decades of predictable results. So it now can be simulated in computers and produce results that reflect real experiments. Sigman, Milo and Bess performed such simulations in their study using the university’s Center for High Performance Computing.

We took several molecules with known bond vibrations, and we used the relationship of these molecules to each other to build a model mathematically of the relative relationship between the bond vibrations in different molecules. We then built a mathematical relationship between these molecules that provides us with the ability to predict how other molecules will react based on their particular vibrations.

—Matt Sigman

To show the method worked, the researchers performed three case studies, each a scenario with a different class of chemicals reacting with each other. They used computer simulations to predict the outcome of the reactions, and then experimentally verified them with real chemical reactions in the laboratory.

One case study involved how chemicals known as bisphenols reacted with acetic anhydride. A small protein known as a peptide served as a catalyst to speed the reactions. The chemists simulated bond vibrations on different bisphenols to predict whether, when reacted with acetic anhydride and the catalyst, the resulting molecule would be “left-handed” or “right-handed”—a chemical property called chirality.

Chirality is important because when we consume a food or medicine, it must have the correct “handedness” or chirality “to essentially handshake with the molecules in your body” and do what it is supposed to do, Milo says. For example, a right-handed drug molecule may work, while the left-handed version of the same medicine may not.

The research team predicted the handedness of the molecules accurately 95% of the time by analyzing bond vibrations.

The second case study was similar to the first, but involved predicting the “handedness” of chemicals made when a catalyst was used to convert a double carbon-carbon bond to a single carbon-carbon bond in a chemical named diarylalkene. In the third case study, the chemists used the method to predict whether a catalyst reacts with one side or the other side of a double carbon-carbon bond in what is called a Heck reaction, commonly used to make pharmaceuticals.

In real world applications, you would compute infrared vibrations for a specific class of molecules that you are interested in reacting, Sigman says.

“You then take a handful of those molecules and you run the reaction and get the results. Then you take the infrared vibrations you think are important and determine the relationship between those vibrations and the reaction results. The resulting mathematical equation allows you to make new predictions about how other chemicals in the class will react.

—Matt Sigman

Sigman is collaborating with a major pharmaceutical company to use the new technique to improve chemical reactions for drug manufacturing.

Milo added that the new technique is able to provide predictions that are not possible with classical chemistry methods. For example, it allows chemists to simultaneously examine “steric” and electronic effects in reactions—something Sigman says now must be done separately. Steric effects are how the size and shape of atoms in a molecule affect how a chemical reaction works. Electronic effects involve how electrons in the atoms are shared within the molecule. Sigman says it is important that the new method can look at both kinds of effects at once because most modern reactions involve both properties.

Resources

  • Anat Milo, Elizabeth N. Bess & Matthew S. Sigman (2014) “Interrogating selectivity in catalysis using molecular vibrations,” Nature 507, 210-214 doi: 10.1038/nature13019

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