The process of protonation of [2,6-BHOCCH] was investigated both theoretically and experimentally. The most suitable conditions for protonation of the derivative [2,6-BHOCCH] were found. The process of protonation was carried out in the presence of an excess of trifluoromethanesulfonic acid CFSOH at room temperature in dichloromethane solution.
View Article and Find Full Text PDFAs a result of our study on the interaction between the octahydrotriborate anion with nucleophiles (Nu = THF, PhP, PhP-(CH)-PPh (dppe), PhAs, EtN, PhNH, CHN, CHCN, PhCHCN)) in the presence of a wide range of Lewis acids (Ti(IV), Hf(IV), Zr(IV), Al, Cu(I), Zn, Mn(II), Co(II) halides and iodine), a number of substituted derivatives of the octahydrotriborate anion [BHNu] are obtained. It is found that the use of TiCl, AlCl, ZrCl, HfCl, CuCl and iodine leads to the highest product yields. In this case, it is most likely that the reaction proceeds through the formation of an intermediate [BH-HMXn], which was detected by NMR spectroscopy.
View Article and Find Full Text PDFIn the present work, a convenient and straightforward approach to the preparation of borylated amidines based on the -dodecaborate anion [BHNCCHNHR]-, R=H, Alk, Ar was developed. This method has two stages. A nitrile derivative of the general form [BHNCCH] was obtained, using a modified technique, in the first stage.
View Article and Find Full Text PDFThe interaction of hafnium(IV) salts (oxide-dichloride, chloride, and bromide) with nitrilotriacetic acid (NTA), diethylenetriamminepentaacetic acid (DTPA), 1,2-diaminocyclohexanetetraacetic acid (CDTA), 1,3-dipropylmino-2-hydroxy ,,','-tetraacetic acid (dpta), and -(2-hydroxyethyl)ethylenediamine triacetic acid (HEDTA) has been studied. The corresponding complexes Na[Hf(NTA)]·3HO (), Na[HfDTPA]·3HO (), [HfCDTA(HO)] (), and Na[Hf(dpta)]·7.5HO·0.
View Article and Find Full Text PDFThe novel members of the 1,2-diboraoxazoles family have been obtained. In the present work, we have carried out the intramolecular ring-closure reaction of borylated iminols of general type [BHN=C(OH)R] (R = Me, Et, Pr, Pr, Bu, Ph, 4-Cl-Ph). This process is conducted in mild conditions with 83-87% yields.
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