In 1937, the American chemist Louis P. Hammett quantified the electronic effect of functional groups in various types of organic reactions. More than 80 years later, Hammett's research is still widely used to design an efficient reaction or catalysis by modulating the electronic property of target molecules. However, this approach involves a frustrating and inefficient amount of tasks. Since each functional group can render only a specific inductive effect and sometimes, it may not be possible to synthesize target molecules which have desired functional groups due to a synthetic difficulty. These constraints have forced researchers to prepare numerous derivatives for a series of complicated reaction scenarios.

Led by professor BAIK Mu-Hyun [the Center for Catalytic Hydrocarbon Functionalizations within the Institute for Basic Science (IBS) & the Department of Chemistry within the Korea Advanced Institute of Science and Technology, KAIST in Daejeon, South Korea] and HAN Sang Woo (the Department of Chemistry within the Korea Advanced Institute of Science and Technology, KAIST) a research team at the IBS and KAIST discovered what they call the "electro-inductive effect" offering an alternative to the classical approach of chemical synthesis. Employing a gold electrode, the researchers attached the target molecules onto the electrode. "Just like functional groups generate diverse electronic effects, we wished to change the properties of the immobilized molecules using different voltages. The beauty of our discovery is that one electrode fits all reactions as the single electrode can behave like multiple functional groups just with the switch of applied voltage," notes professor Mu-Hyun Baik.

The research team showed that the gold electrode can serve as a "universal functional group" to control the reactivity of a molecule, thus propelling or inhibiting the reaction just by switching the voltage applied to the electrode. In the "base-catalyzed ester hydrolysis reaction," a representative organic reaction that Hammett had used to establish the conventional inductive effect 80 years ago, the application of (+) voltage on the electrode decreased the electron density of the carbonyl carbon in the ester molecule. Thus, the reactivity of the ester molecule was significantly enhanced. Conversely, when (-) voltage was applied, the reaction barely proceeded owing to the high electron density of the reaction site.They have also successfully controlled the reaction rate of the "Suzuki-Miyaura cross-coupling reaction," a major catalytic method for forming carbon-carbon bonds. It is of great significance that the electrode can control the reactivity not only in the organic reaction, but also in the complicated organometallic catalytic reaction.

The researchers also confirmed that this "universal function group" allows for fine-tuning of the electronic property and reactivity of the molecule in the middle of a chemical reaction. (in-situ tuning). EDC [1-ethyl-3-(3-dimethylaminopropyl) carbodiimide]-mediated amidation reaction can be divided into two steps: The first step is accelerated by the electron-donating group, whereas the second step is enhanced by the electron-withdrawing group. EDC-mediated amidation reaction hardly proceeded when one type of voltage was applied. The "universal functional group" successfully changed the reactivity of the molecule while the reaction was in progress.

The idea of covalently attaching molecules to an electrode is not new. However, most of such cases involve redox reactions. "The chemical reactions controlled by the electro-inductive effect do not involve redox processes. The electrode only serves as a functional group with tunable inductive effect. In addition, this study explored how the electro-inductive effect works in actual chemical reactions," explains professor Mu-Hyun Baik.

As researchers confirmed the potential of replacing functional groups with a gold electrode at different voltages, they are going to employ other types of electrodes, such as carbon-based electrodes to ensure a practical and scalable application of this study.

Story Source:

Materials provided by Institute for Basic Science. Note: Content may be edited for style and length.

Journal Reference:

1. Joon Heo, Hojin Ahn, Joonghee Won, Jin Gyeong Son, Hyun Kyong Shon, Tae Geol Lee, Sang Woo Han, and Mu-Hyun Baik. Electro-inductive effect: electrodes as functional groups with tunable electronic properties. Science, 2020 DOI: 10.1126/science.abb6375