Trying To Explain A Bond the formation and Why and when are bonds broken

A team of researchers from Immanuel Kant Baltic Federal University and Saint Petersburg State University has identified the factors that affect the speed of synthesis of organic molecules consisting of several heterocycles. According to the team, an accurate selection of reagents and reaction conditions can help efficiently obtain compounds used in the pharmaceutical industry. An article reporting the results of the study was published in the Tetrahedron Letters journal.

https://network.youthmusic.org.uk/watch-onlinewake-forest-vs-duke-2021-live-free-college-basketball
https://network.youthmusic.org.uk/basketballohio-state-vs-rutgers-live-free-college-game
https://network.youthmusic.org.uk/watch-st-johns-vs-creighton-live-stream-ncaam-online

The development of the so-called small molecules is a promising field of the pharmaceutical industry. Small molecules are organic compounds with a small molecular mass. They are often based on heterocycles—carbon rings that also include atoms of nitrogen and other elements. The synthesis of small molecules is much cheaper than the development of drugs based on antibodies or other biological molecules; however, their properties are still understudied.

Even the slightest modifications can change the characteristics of a small molecule and open a whole new range of practical applications. Therefore, many research teams working in the field of chemical pharmacology improve synthesis methods to create libraries of small molecules and evaluate their biological properties. In the future, this data can be used to develop new drugs.

A team of chemists from Immanuel Kant Baltic Federal University and Saint Petersburg State University has been focusing on the synthesis of new small molecules for a long time. For example, several years ago the researchers successfully developed a method of hydrated imidazoline ring expansion (HIRE). Hydrated imidazolines are based on an imidazole heterocycle (with two nitrogen and three carbon atoms) with three more rings of different composition attached to it.

The reaction created by the chemists provided for the formation of bonds with at least three bigger heterocycles, thus leading to the expansion of the initial imidazole ring. However, further studies showed that sometimes the same reaction can cause one of the tetracyclic imidazoline rings to break. In this case, the reaction product (an ethylenediamine derivative) contains no expanded heterocycles and is less useful in pharmacology because it doesn’t always produce the necessary results.

The team decided to focus on the factors that promote the synthesis of expanded heterocycles. They suggested that the success of the reaction depended on the differences in the electronic properties of substituent groups. Specifically, they assumed that such differences determined the migration of the substitutes from one atom in the cycle to another. To better understand the nature of this dependency, the chemists synthesized 13 ethylenediamine derivatives. An ethylenediamine derivative is an organic substance that contains two amino groups. The derivatives were placed in alkaline solutions at different temperatures: from room temperature to 90°С.

The experiment showed that the nature of the bond between the substituent group and a nitrogen atom determines the reaction speed. If a substitute acts as an electron acceptor, i.e. pulls the electron pair that it has in common with nitrogen closer, the structure of the compound immediately changes. In some cases, it took a substituent group less than 30 seconds to migrate from one atom to another. On the contrary, the compounds with electron-donating substitutes that pushed the electron pair forward reacted slowly, and the reactions required increased temperatures. In two cases, no migration of substituent groups took place at all.

“In this study, we used relatively simple compounds as models to better understand the reaction processes in heterocyclic molecules that are in high demand in the industry. We are already using the obtained data to synthesize small molecules with expanded heterocycles from reaction by-products”, said Mikhail Krasavin, D.Sc.. in Chemistry, Research Professor at the Institute of Living Systems (BFU), and the Head of the Department of the Chemistry of Natural Products (SPbSU).

The concept of a molecule as a unit of bound atoms can be traced to Robert Boyle's 1661 treatise “The Sceptical Chymist” (1). Chemists often depict the strong covalent bonds in molecules formed through electronic interactions of atoms by sticks or springs. By contrast, much weaker attractive forces between molecules in liquids and solids, such as van der Waals forces, are typically unspecific and nondirectional and cannot be represented by sticks or springs. An exception is the hydrogen bond (H-bond) (2), which can create relatively strong directional interactions between molecules when 
t
he atoms that carry opposite partial charges attract each other. Discrimination between very strong H-bonds and covalent bonds can become somewhat arbitrary. On page 160 of this issue, Dereka et al. (3) study what happens if the strength of an intramolecular hydrogen bond becomes comparable to the strength of the intermolecular covalent bonds, blurring the concept of what a “molecule” is.