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Publikace detail

The reactivity of N,C,N-intramolecularly coordinated antimony(III) and bismuth(III) oxides with the sterically encumbered organoboronic acid 2,6-i-Pr2C6H3B(OH)(2)
Autoři: Kořenková Monika | Erben Milan | Jambor Roman | Růžička Aleš | Dostál Libor
Rok: 2014
Druh publikace: článek v odborném periodiku
Název zdroje: Journal of Organometallic Chemistry
Strana od-do: 287-291
Tituly:
Jazyk Název Abstrakt Klíčová slova
cze Reaktivita NCN-chelatovaných antimonitých a bismutitých oxidů se stericky náročnou organoboronovou kyselinou Byla studována reaktivita NCN-chelatovaných antimonitých a bismutitých oxidů se stericky náročnou organoboronovou kyselinou2,6-i-Pr2C6H3B(OH)(2). Reakce vedly k novým sloučeninám LM[OB(Dip) (OH)](2). Reaktivita; NCN-chelatovaných; antimonitých; bismutitých; oxidů; stericky; náročnou; organoboronovou; kyselinou
eng The reactivity of N,C,N-intramolecularly coordinated antimony(III) and bismuth(III) oxides with the sterically encumbered organoboronic acid 2,6-i-Pr2C6H3B(OH)(2) The reactivity of N,C,N-intramolecularly coordinated antimony(III) and bismuth(III) oxides (LMO)(2) [where M = Sb 1, Bi 2 and L is an abbreviation for (2,6-Me2NCH2)(2)C6H3] with sterically demanding organoboronic acid DipB(OH)(2) (where Dip = 2,6-i-Pr2C6H3) was studied. Stoichiometric reactions of 1 and 2 with DipB(OH)2 in 1:4 molar ratio gave compounds LM[OB(Dip) (OH)](2) (where M = Sb 3, Bi 4). Compounds 3 and 4 are in solution liable to further dehydration leading to the formation of sixmembered heteroboroxine rings LM[OB(Dip)](2)O (where M = Sb 5, Bi 6). Changing of the stoichiometry to 1(oxide):2(acid) led to the isolation of eight-membered heteroboroxine rings LM[OB(Dip)O](2)ML (where M = Sb 7, Bi 8), but both compounds are unstable in solution and slowly decomposed to 5 (or 6) with concomitant elimination of oxides 1 (or 2). Studied compounds were characterized by the help of multinuclear NMR spectroscopy, IR spectroscopy and in the case of 5 by single-crystal X-ray diffraction analysis. Antimony; Bismuth; Chelating ligands; Boroxines; NMR spectroscopy