Iminoacylation Reaction of Iodoaniline with [2-B10H9NCCH3]– Anion as a Route to the Preparation of New Boron-Containing Synthons
The reaction of nucleophilic addition of isomers of iodaniline to the nitrile derivative of the closo-decaborate anion has been studied. The structures of the products have been determined using multinuclear NMR and IR spectroscopy, as well as ESI mass spectrometry. The structure of compound (NBu4)[2-B10H9NHC(CH3)HN(2-C6H4I)] was determined by single-crystal X-ray diffraction.
Authors
- К. Yu. Zhizhin (ORCID: https://orcid.org/0000-0002-4475-124X)
- А. V. Nelyubin (ORCID: https://orcid.org/0000-0002-9990-4231)
- Andrey P. Zhdanov (ORCID: https://orcid.org/0000-0003-4083-386X)
- Н. А. Селиванов (ORCID: https://orcid.org/0000-0001-7426-5982)
- A. Yu. Bykov (ORCID: https://orcid.org/0000-0003-1793-8487)
- I. N. Klyukin (ORCID: https://orcid.org/0000-0001-8940-3049)
- Alexey S. Kubasov (ORCID: https://orcid.org/0000-0002-0156-5535)
- Nikolay T. Kuznetsov (ORCID: https://orcid.org/0000-0002-0131-6387)
Institutions
- NS Kurnakova Institute of General and Inorganic Chemistry (RU)
Publication Details
- Journal
- Russian Journal of Inorganic Chemistry
- Published
- 2024-10-01
- DOI
- https://doi.org/10.1134/s0036023624601934
- Primary Topic
- Boron Compounds in Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00