Abstract
In the present work, a convenient and straightforward approach to the preparation of borylated amidines based on the closo-dodecaborate anion [B(12)H(11)NCCH(3)NHR]-, R=H, Alk, Ar was developed. This method has two stages. A nitrile derivative of the general form [B(12)H(11)NCCH(3)](-) was obtained, using a modified technique, in the first stage. On the second stage the resulting molecular system interacted with primary amines to form the target amidine products. This approach is characterised by a simple chemical apparatus, mild conditions and high yields of the final products. The mechanism of the addition of amine to the nitrile derivative of the closo-dodecaborate anion was studied, using quantum-chemical methods. The interaction between NH(3) and [B(12)H(11)NCCH(3)](-) ammonia was chosen as an example. It was found that the structure of the transition state determines the stereo-selectivity of the process. A study of the biological properties of borylated amidine sodium salts indicated that the substances had low toxicity and could accumulate in cancer cells in significant amounts.